ADVERSE REACTIONS SECTION.

6 ADVERSE REACTIONS. The following clinically significant adverse reactions are described elsewhere in the labeling:Hepatotoxicity [see Warnings and Precautions (5.1)]. Hepatotoxicity [see Warnings and Precautions (5.1)]. Most common adverse reactions (>20%) were increased lactate dehydrogenase, increased aspartate aminotransferase, hair color changes, fatigue, increased alanine aminotransferase, decreased neutrophils, increased cholesterol, increased alkaline phosphatase, decreased lymphocytes, eye edema, decreased hemoglobin, rash, dysgeusia, and decreased phosphate. (6.1) To report SUSPECTED ADVERSE REACTIONS, contact Daiichi Sankyo, Inc. at 1-877-437-7763 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.. 6.1Clinical Trials Experience. Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.The safety of TURALIO was evaluated in ENLIVEN [see Clinical Studies (14.1)]. ENLIVEN excluded patients with ALT, AST, or total bilirubin >1.5 ULN; and known active or chronic infection with hepatitis or virus, or human immunodeficiency virus. Patients received TURALIO without food at dose of 400 mg in the morning and 600 mg in the evening orally for weeks followed by 400 mg orally twice daily until disease progression or unacceptable toxicity. Seventy-nine percent of patients received TURALIO for months or longer and 66% for greater than one year.The median age of TURALIO-treated patients was 44 years (range: 22-75), 57% were females, and 85% were White.Serious adverse reactions were reported in 13% of patients who received TURALIO. Most frequent (occurring in >1 patient) serious adverse reactions included abnormal liver tests (3.3%) and hepatotoxicity (3.3%).Permanent discontinuation due to an adverse reaction occurred in 13% of patients who received TURALIO. Most frequent adverse reactions (occurring in >1 patient) requiring permanent discontinuation included increased ALT (4.9%), increased AST (4.9%) and hepatotoxicity (3.3%).Dose reductions or interruptions occurred in 38% of patients who received TURALIO. Most frequent adverse reactions (occurring in >1 patient) requiring dosage reduction or interruption were increased ALT (13%), increased AST (13%), nausea (8%), increased ALP (7%), vomiting (4.9%), increased bilirubin (3.3%), increased GGT (3.3%), dizziness (3.3%), and abdominal pain (3.3%).The most common (>20%) adverse reactions, including laboratory abnormalities, in patients who received TURALIO were: increased lactate dehydrogenase (LDH), increased AST, hair color changes, fatigue, increased ALT, decreased neutrophils, increased cholesterol, increased ALP, decreased lymphocytes, eye edema, decreased hemoglobin, rash, dysgeusia and decreased phosphate.Tables 4, and summarize the adverse reactions and laboratory abnormalities in ENLIVEN during the randomized phase (Week 25).Table 4: Adverse Reactions (>=10% All Grades or >2% Grade >= 3) in Patients Receiving TURALIO with Difference Between Arms of >5% Compared to Placebo Through Week 25 in ENLIVENTURALION=61PlaceboN=59Adverse ReactionAll Grades(%)Grade >= 3(%)All Grades(%)Grade >= 3(%)Skin and subcutaneous tissue Hair color changes6703.40RashRash includes rash, maculo-papular rash, rash pruritic, urticaria, erythema, dermatitis acneiform, dermatitis allergic. 281.670PruritusPruritis includes pruritus, pruritus generalized. 1803.40General FatigueFatigue includes fatigue, asthenia, malaise. 640410Peripheral edemaPeripheral edema includes face edema, localized edema, edema peripheral, peripheral swelling. 20070Eye Eye edemaEye edema includes periorbital edema, eye edema, eyelid edema, papilledema. 301.650Nervous system DysgeusiaDysgeusia includes dysgeusia, ageusia. 2601.70NeuropathyNeuropathy includes neuropathy peripheral, paresthesia, hypoesthesia, burning sensation. 10050Gastrointestinal Vomiting201.650Constipation12050Metabolism and nutrition Decreased appetite160100Vascular Hypertension154.9100Table 5: Hepatic Laboratory Abnormalities (>=10% All Grades or >2% Grade >= 3) Worsening from Baseline in Patients Receiving TURALIO with Difference Between Arms of >5% Compared to Placebo Through Week 25 in ENLIVENTURALIOEach test incidence is based on the number of patients who had both baseline and at least one on-study measurement TURALIO (n=61) and placebo (n=59). Placebo Laboratory AbnormalityGraded per NCI CTCAE 4.03 Grade 1(%)Grade 2(%)Grade >= 3(%)Grade 1(%)Grade 2(%)Grade >= 3(%)ALT alanine aminotransferase; AST aspartate aminotransferase; ALP alkaline phosphataseLiver TestsIncreased AST6115121500Increased ALT3113202200Increased ALP313.34.91.700Increased bilirubin3.33.33.3000Table 6: Other Laboratory Abnormalities Worsening from Baseline (>=10% All Grades or >2% of Grade >= 3) in Patients Receiving TURALIO with Difference Between Arms of >5% Compared to Placebo Through Week 25 in ENLIVENTURALIOEach test incidence is based on the number of patients who had both baseline and at least one on-study measurement TURALIO (n 61) and placebo (n 58-59). Placebo Laboratory AbnormalityGraded per NCI CTCAE 4.03 except for LDH All Grades(%)Grade >=3(%)All Grades(%)Grade >=3(%)LDH=Lactate DehydrogenaseChemistryIncreased LDHLDH: Grade >ULN to <=2.5 ULN; Grade >2.5 to <=5 ULN; Grade >5 to <=20 ULN; Grade >20 ULN 92050Increased cholesterol444.9250Decreased phosphate253.350HematologyDecreased neutrophils443.390Decreased lymphocytes381.63.40Decreased hemoglobin300141.7Decreased platelets15050Clinically relevant adverse reactions occurring in <10% of patients were:Eye: blurred vision, photophobia, diplopia, reduced visual acuityGastrointestinal: dry mouth, stomatitis, mouth ulcerationGeneral: pyrexiaHepatobiliary: cholangitis, hepatotoxicity, liver disorderNeurological: cognitive disorders (memory impairment, amnesia, confusional state, disturbance in attention, attention deficit/hyperactivity disorder)Skin and subcutaneous tissue: alopecia, skin pigment changes (hypopigmentation, depigmentation, discoloration, hyperpigmentation).

CARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY SECTION.

13.1Carcinogenesis, Mutagenesis, Impairment of Fertility. Carcinogenicity studies were performed in mice and rats. Both studies were negative for carcinogenic findings at exposures up to times the human exposure at the recommended daily dose of 800 mg based on AUC.Pexidartinib was not mutagenic in an in vitro bacterial reverse mutation (AMES) assay or clastogenic in either an in vitro human peripheral blood lymphocyte chromosomal aberrations assay or in an in vivo mouse bone marrow micronucleus assay.Based on nonclinical findings, TURALIO may impair male and female fertility. In fertility study in which pexidartinib was administered orally to male and female rats, there were reductions in pregnancy, as well as increases in pre- and post-implantation loss with corresponding reduction in viable embryos at 40 mg/kg (approximately 1.3 times the human exposure at the recommended dose of 800 mg). Males at this dose level displayed reductions in spermatogenic parameters and adverse effects on sperm concentration, production, motility, and morphology. Lower testicular and epididymal weights occurred in this study at doses of >=10 mg/kg/day (approximately 0.3 times the human exposure at the recommended dose of 800 mg). This is consistent with findings in chronic toxicology studies of germ cell depletion of the testes and hypospermia and cellular debris in the epididymis in male reproductive tissues of both rats and dogs at respective doses as low as 20 and 30 mg/kg/day (approximately 0.6 and 0.1 times the human exposure at the recommended dose of 800 mg). In rats, these changes persisted following 16-week recovery period at the 60 mg/kg/day dose level (approximately 1.5 times the human exposure at the recommended dose of 800 mg).In female rats, necrosis of corpora lutea occurred at doses >=0.5 mg/kg/day (approximately 0.01 times the human exposure at the recommended dose of 800 mg) with pigment deposition within the interstitium of the ovaries, an increased incidence of luteal cysts and incidence/severity of hemorrhage of corpora lutea, and decreased incidence of retained antral follicles and decreased corpora lutea at 60 mg/kg (approximately 1.8 times the human exposure at the recommended dose of 800 mg). In female dogs there were decreased follicle numbers and moderate atrophy of the oviduct, uterus, and cervix at doses as low as mg/kg (approximately 0.01 times the human exposure at the recommended dose of 800 mg).

CLINICAL PHARMACOLOGY SECTION.

12 CLINICAL PHARMACOLOGY. 12.1Mechanism of Action. Pexidartinib is small molecule tyrosine kinase inhibitor that targets colony stimulating factor receptor (CSF1R), KIT proto-oncogene receptor tyrosine kinase (KIT), and FMS-like tyrosine kinase (FLT3) harboring an internal tandem duplication (ITD) mutation. Overexpression of the CSF1R ligand promotes cell proliferation and accumulation in the synovium. In vitro, pexidartinib inhibited proliferation of cell lines dependent on CSF1R and ligand-induced autophosphorylation of CSF1R. Pexidartinib also inhibited the proliferation of CSF1R dependent cell line in vivo.. 12.2 Pharmacodynamics. Exposure-Response RelationshipsThere is an exposure response relationship between pexidartinib steady state exposure and serum transaminase levels (ALT and AST) with higher risk of increased serum transaminases at higher exposure. Additionally, increased transaminases occurred more frequently with higher pexidartinib doses (200 to 1200 mg per day).. Cardiac ElectrophysiologyAt two times the mean maximum exposure of the 400 mg twice daily dose, TURALIO does not prolong the QTc interval to any clinically relevant extent.. 12.3 Pharmacokinetics. The pharmacokinetics of TURALIO was evaluated following single doses in healthy subjects and following multiple doses in patients as summarized in Table 9.Table 9: TURALIO Exposure and Pharmacokinetic ParametersGeneral InformationSteady state exposure [Mean (SD)]Pexidartinib 400 mg twice daily Cmax 8625 (2746) ng/mLAUC0-12h 77465 (24975) ngh/mLDose proportionalityPexidartinib exposure (Cmax and AUC0-INF) increased linearly over the single oral dose range of 200 to 2400 mg (0.5 to times the recommended dose).Time to steady stateEstimated based on half life Approximately daysAccumulation ratio (AUC) [Median] 3.6AbsorptionTmax [Median]2.5 hours Effect of food Administration with high-fat mealThe high-fat meal comprised 800 to 1000 calories with fat being 50% of total caloric content; approximately 150 calories from protein, 250 calories from carbohydrates, and 500-600 calories from fat. Increased pexidartinib Cmax and AUC0-INF by 100%Delayed Tmax by 2.5 hours Administration with low-fat mealThe low-fat meal comprised 387 calories with fat being approximately 25% of total caloric content. Increased Cmax by 56% and AUC0-INF by 59%Delayed Tmax by 1.5 hoursDistributionIn vitro plasma protein bindingGreater than 99%Human serum albumin: 99.9%-1 acid glycoprotein: 89.9% Apparent volume of distribution (Vz/F) [Mean (CV%)]After single oral dose of pexidartinib 400 mg 187 (27%)EliminationApparent clearance [Mean (CV%)] 5.1 L/h (36%)t1/2 [Mean (SD)]26.6 (6.5) hours Metabolism Primary pathwayOxidation: CYP3A4Glucuronidation: UGT1A4 N-glucuronide metaboliteMajor inactive metabolite formed by UGT1A4Approximately 10% higher exposure than pexidartinib after single dose ExcretionAfter single oral dose of radiolabeled pexidartinib 400 mg Feces: 65% (44% as unchanged)Urine: 27% as metabolites (>=10% as N-glucuronide). Increased pexidartinib Cmax and AUC0-INF by 100%. Delayed Tmax by 2.5 hours. Increased Cmax by 56% and AUC0-INF by 59%. Delayed Tmax by 1.5 hours. Greater than 99%. Human serum albumin: 99.9%. -1 acid glycoprotein: 89.9% 187 (27%). 5.1 L/h (36%). 26.6 (6.5) hours. Oxidation: CYP3A4. Glucuronidation: UGT1A4. Major inactive metabolite formed by UGT1A4. Approximately 10% higher exposure than pexidartinib after single dose. Feces: 65% (44% as unchanged). Urine: 27% as metabolites (>=10% as N-glucuronide). Specific PopulationsNo clinically meaningful differences in the pharmacokinetics of pexidartinib were observed based on age (18 to 84 years), sex, race (White and Black), or mild hepatic impairment (total bilirubin <= ULN with AST ULN or total bilirubin 1 to 1.5 ULN with any AST).. Patients with Renal ImpairmentMild (CLcr 60 to 89 mL/min), moderate (CLcr 30 to 59 mL/min) and severe (CLcr 15 to 29 mL/min) renal impairment increased pexidartinib exposure (AUC) by approximately 30%, relative to that in patients with normal renal function (CLcr >=90 mL/min).. Patients with Hepatic ImpairmentModerate hepatic impairment (total bilirubin 1.5 and up to x ULN, not due to Gilberts syndrome, with any AST) increased pexidartinib exposure (AUC) by 43% relative to exposure in patients with normal hepatic function (total bilirubin and AST <= ULN).The pharmacokinetics of pexidartinib have not been studied in patients with severe hepatic impairment (total bilirubin 3 to 10 ULN with any AST).. Drug Interaction Studies. Clinical Studies and Model-Informed Approaches. Effects of Other Drugs on Pexidartinib. Strong CYP3A Inducers: Coadministration of rifampicin (strong CYP3A inducer) decreased pexidartinib Cmax by 33% and AUC0-INF by 65%.. Moderate CYP3A Inducers: Coadministration of efavirenz (moderate CYP3A inducer) is predicted to decrease pexidartinib Cmax by 27% and AUC by 38% at steady state.. Strong CYP3A Inhibitors: Coadministration of itraconazole (strong CYP3A inhibitor) increased pexidartinib Cmax by 48% and AUC0-INF by 70%.. Moderate CYP3A Inhibitors: Coadministration of fluconazole (moderate CYP3A inhibitor) is predicted to increase pexidartinib Cmax by 41% and AUC by 67% at steady state.. UGT Inhibitors: Coadministration of probenecid (UGT inhibitor) increased pexidartinib Cmax by 5% and AUC0-INF by 60%.. Acid-Reducing Agents: Coadministration of esomeprazole (proton pump inhibitor) decreased pexidartinib Cmax by 55% and AUC0-INF by 50%. The effects of H2-receptor antagonists and locally-acting antacids on pexidartinib pharmacokinetics have not been studied.. Effects of Pexidartinib on Other Drugs. CYP2C19 Substrates: Coadministration of single oral dose of TURALIO 1800 mg (4.5 times the approved recommended dose of 400 mg) decreased omeprazole (CYP2C19 substrate) Cmax by 37% and AUC0-INF by 17%.. CYP3A Substrates: Coadministration of TURALIO 400 mg twice daily decreased midazolam (CYP3A substrate) Cmax by 28% and AUC0-INF by 59%.. CYP2C9 Substrates: Coadministration of TURALIO 400 mg twice daily increased tolbutamide (CYP2C9 substrate) AUC0-INF by 28%. The effect of pexidartinib on CYP2C9 substrates is not considered clinically relevant.. P-gp Substrates: Coadministration of single oral dose of TURALIO 1800 mg (4.5 times the approved recommended dose of 400 mg) increased digoxin (P-gp substrate) Cmax by 30% and AUC0-INF by 9%.. CYP2C8 Substrates: The effect of pexidartinib on CYP2C8 substrates is predicted not to be clinically relevant.. In Vitro Studies. CYP/UGT Enzymes: Pexidartinib is likely to inhibit CYP2B6 and induce CYP2B6 at clinically relevant concentrations. Pexidartinib is likely to inhibit UGT1A1 at clinically relevant concentrations.. Transporter Systems: Pexidartinib is not substrate for P-gp, BCRP, OAT1, OAT3, OCT1, OCT2, OATP1B1, OATP1B3, OATP2B1, and BSEP.Pexidartinib is an inhibitor of MATE1, MATE2-K, OATP1B1, OATP1B3 and OATP2B1.

CLINICAL STUDIES SECTION.

14 CLINICAL STUDIES. 14.1Tenosynovial Giant Cell Tumor The efficacy of TURALIO was evaluated in ENLIVEN (NCT02371369), double-blind, randomized (1:1), placebo-controlled, multicenter trial in patients with symptomatic TGCT [also referred to as giant cell tumor of the tendon sheath (GCT-TS) or pigmented villonodular synovitis (PVNS)] for whom surgical removal of the tumor would be associated with worsening functional limitation or severe morbidity. Eligible patients were required to have measurable disease per the Response Evaluation Criteria in Solid Tumors (RECIST) v1.1. Patients were randomized to placebo or TURALIO 400 mg in the morning and 600 mg in the evening for weeks followed by 400 mg twice daily. Treatment continued until unacceptable toxicity or disease progression. Randomization was stratified by geographic region (US vs. non-US countries) and disease location (upper extremity vs. lower extremity involvement).The major efficacy outcome measure was overall response rate (ORR) as assessed by blinded independent central review (BICR) at Week 25 using RECIST v1.1. Additional efficacy outcome measures were mean change from baseline in range of motion of the affected joint at Week 25 and ORR as assessed by BICR at Week 25 using tumor volume score (TVS). Range of motion was measured as percent of normal reference range for the affected joint. Range of motion assessments were performed by third-party clinical assessor using goniometer. TVS was defined in ENLIVEN as the estimated volume of the maximally distended synovial cavity or tendon sheath involved, measured in 10% increments. Patients in the placebo arm were offered TURALIO at Week 25 beginning with 400 mg twice daily dose, as permitted by the study protocol.A total of 120 patients were randomized, 61 to the TURALIO arm and 59 to the placebo arm. The median age was 44 years (range: 18-79); 59% were females; 88% were White; 53% had prior surgery; 88% were diagnosed with diffuse TGCT; and 9% had previously been treated with systemic therapy. Disease locations were knee (61%), ankle (18%), hip (11%), wrist (3%), foot (3%) and other (5%).ENLIVEN demonstrated statistically significant improvement in ORR in patients randomized to TURALIO compared with placebo. Efficacy results are summarized in Table 10.Table 10: Efficacy Results Assessed at Week 25 for ENLIVENEfficacy ParameterTURALION=61PlaceboN=59CI: confidence interval; NA: not applicable; SD: standard deviation; LS: least squares; +: denotes ongoing at last assessmentOverall Response Rate (ORR)Blinded independent central review Data cut-off date January 31, 2018 ORR(95% CI)38%(27%, 50%)0(0, 6%) Complete Response15%0 Partial Response23%0P-valueFishers exact test <0.0001Duration of Response (DOR) Range (months)6.9+, 24.9+NAThe analysis of mean change from baseline in range of motion at Week 25 demonstrated statistically significant improvement in patients randomized to TURALIO compared to placebo. Figure shows the change from baseline in range of motion for each patient at Week 25 (TURALIO N=45, placebo N=43). Results were excluded for patient with missing baseline and 31 patients with missing range of motion assessment at Week 25.Figure 1: Change from Baseline in Range of Motion at Week 25 for ENLIVEN ORR by TVS was 56% (95% CI: 43%, 67%) in patients randomized to the TURALIO arm and 0% in patients randomized to the placebo arm; < 0.0001.. Figure 1.

DOSAGE & ADMINISTRATION SECTION.

2 DOSAGE AND ADMINISTRATION. Important Administration Instructions: Administer TURALIO on an empty stomach, at least hour before or hours after meal or snack. (2.1)Recommended Dosage: 400 mg orally twice daily (2.2)See full prescribing information for dosage modifications due to renal impairment and hepatic impairment. (2.6, 2.7). Important Administration Instructions: Administer TURALIO on an empty stomach, at least hour before or hours after meal or snack. (2.1). Recommended Dosage: 400 mg orally twice daily (2.2). See full prescribing information for dosage modifications due to renal impairment and hepatic impairment. (2.6, 2.7). 2.1 Important Administration Instructions. Administer TURALIO on an empty stomach, at least one hour before or two hours after meal or snack [see Warnings and Precautions (5.1), Clinical Pharmacology (12.2, 12.3)]. 2.2Recommended Dosage The recommended dosage of TURALIO is 400 mg taken twice daily on an empty stomach until disease progression or unacceptable toxicity [see Dosage and Administration (2.1), Clinical Pharmacology (12.3)].Swallow TURALIO capsules whole. Do not open, break, or chew the capsules.If patient vomits or misses dose of TURALIO, instruct the patient to take the next dose at its scheduled time.. 2.3Dosage Modifications for Adverse Reactions. The recommended dose reductions for adverse reactions are provided in Table 1.Table 1: Recommended Dose Reductions for TURALIO for Adverse ReactionsDose ReductionTotal Daily DoseAdministration of Total Daily DoseFirst600 mg200 mg in the morning and 400 mg in the eveningSecond400 mg200 mg twice dailyPermanently discontinue TURALIO in patients who are unable to tolerate 200 mg orally twice daily.The recommended dosage modifications for adverse reactions are summarized in Table 2.Table 2: Recommended Dosage Modifications for TURALIO for Adverse ReactionsAdverse ReactionSeverityTURALIO Dosage ModificationsALT alanine aminotransferase; ALP alkaline phosphatase; AST aspartate aminotransferase; DB direct bilirubin; GGT gamma-glutamyl transferase; TB total bilirubin; ULN upper limit of normalHepatotoxicity [see Warnings and Precautions (5.1)] Increased ALT and/or ASTGreater than to times ULNWithhold and monitor liver tests weekly.If AST and ALT are less than or equal to times ULN within weeks, resume at reduced dose.If AST or ALT is not less than or equal to times ULN in weeks, permanently discontinue TURALIO.Greater than to 10 times ULNWithhold and monitor liver tests twice weekly.If AST and ALT are less than or equal to times ULN within weeks, resume at reduced dose.If AST or ALT is not less than or equal to times ULN in weeks, permanently discontinue TURALIO.Greater than 10 times ULNPermanently discontinue TURALIO.Monitor liver tests twice weekly until AST or ALT is less than or equal to times ULN, then weekly until less than or equal to times ULN.Increased ALPConfirm ALP elevations as liver isozyme fraction. and GGTALP greater than times ULN with GGT greater than times ULNPermanently discontinue TURALIO. Monitor liver tests twice weekly until ALP is less than or equal to times ULN, then weekly until less than or equal to times ULN.Increased bilirubinTB greater than ULN to less than times ULN or DB greater than ULN and less than 1.5 times ULNWithhold and monitor liver tests twice weekly.If an alternate cause for increased bilirubin is confirmed and bilirubin is less than ULN within weeks, resume at reduced dose.If bilirubin is not less than ULN in weeks, permanently discontinue TURALIO.TB greater or equal to times ULN or DB greater than 1.5 times ULNPermanently discontinue TURALIO.Monitor liver tests twice weekly until bilirubin is less than or equal to ULN.Adverse Reactions or Other Laboratory Abnormalities [see Adverse Reactions (6.1)] AnySevere or intolerableWithhold until improvement or resolution.Resume at reduced dose upon improvement or resolution.. Withhold and monitor liver tests weekly.. If AST and ALT are less than or equal to times ULN within weeks, resume at reduced dose.. If AST or ALT is not less than or equal to times ULN in weeks, permanently discontinue TURALIO.. Withhold and monitor liver tests twice weekly.. If AST and ALT are less than or equal to times ULN within weeks, resume at reduced dose.. If AST or ALT is not less than or equal to times ULN in weeks, permanently discontinue TURALIO.. Permanently discontinue TURALIO.. Monitor liver tests twice weekly until AST or ALT is less than or equal to times ULN, then weekly until less than or equal to times ULN.. Permanently discontinue TURALIO. Monitor liver tests twice weekly until ALP is less than or equal to times ULN, then weekly until less than or equal to times ULN.. Withhold and monitor liver tests twice weekly.. If an alternate cause for increased bilirubin is confirmed and bilirubin is less than ULN within weeks, resume at reduced dose.. If bilirubin is not less than ULN in weeks, permanently discontinue TURALIO.. Permanently discontinue TURALIO.. Monitor liver tests twice weekly until bilirubin is less than or equal to ULN.. Withhold until improvement or resolution.. Resume at reduced dose upon improvement or resolution.. 2.4Concomitant Use of Moderate or Strong CYP3A Inhibitors or UGT Inhibitors. Avoid concomitant use of TURALIO with moderate or strong CYP3A inhibitors or UGT inhibitors during treatment with TURALIO. If concomitant use with moderate or strong CYP3A inhibitor or UGT inhibitor cannot be avoided, reduce the TURALIO dose according to the recommendations in Table 3.If concomitant use of moderate or strong CYP3A inhibitor or UGT inhibitor is discontinued, increase the TURALIO dose (after plasma half-lives of the moderate or strong CYP3A inhibitor or UGT inhibitor) to the dose that was used before starting the inhibitor [see Clinical Pharmacology (12.3)].Table 3: Recommended Dosage Reductions for TURALIO for Concomitant Use of Moderate or Strong CYP3A Inhibitors or UGT InhibitorsPlanned Total Daily DoseModified Total Daily DoseAdministration of Modified Total Daily Dose800 mg400 mg200 mg twice daily600 mgPlanned total daily dose refers to recommended dose reductions for TURALIO for adverse reactions based on dosing recommendations in Table 2. 400 mg200 mg twice daily400 mg 200 mg200 mg once daily. 2.5Concomitant Use of Acid-Reducing Agents. Avoid the concomitant use of proton pump inhibitors (PPI) while taking TURALIO. As an alternative to PPI, administer TURALIO hours before or hours after taking locally-acting antacid, or if using histamine (H2)-receptor antagonist, administer TURALIO at least hours before or 10 hours after taking an H2-receptor antagonist [see Clinical Pharmacology (12.3)].. 2.6Dosage Modification for Renal Impairment. The recommended dosage of TURALIO for patients with mild to severe renal impairment (creatinine clearance [CLcr] 15 to 89 mL/min estimated by Cockcroft-Gault using actual body weight) is 200 mg in the morning and 400 mg in the evening [see Clinical Pharmacology (12.3)].. 2.7 Dosage Modification for Hepatic Impairment. The recommended dosage of TURALIO for patients with moderate hepatic impairment (total bilirubin greater than 1.5 and up to times upper limit of normal (ULN), not due to Gilberts syndrome, with any AST) is 200 mg twice daily [see Clinical Pharmacology (12.3)]. TURALIO has not been studied in patients with severe hepatic impairment (total bilirubin greater than to 10 times ULN and any AST).

DRUG INTERACTIONS SECTION.

7 DRUG INTERACTIONS. Use with Hepatotoxic Products: Avoid coadministration of TURALIO with other products known to cause hepatotoxicity. (7.1)Moderate or Strong CYP3A Inhibitors: Reduce the dose of TURALIO if concomitant use of moderate or strong CYP3A inhibitors cannot be avoided. (2.4, 7.2)Strong CYP3A Inducers: Avoid concomitant use of strong CYP3A inducers. (7.2)UGT Inhibitors: Reduce the dose of TURALIO if concomitant use of UGT inhibitors cannot be avoided. (2.4, 7.2)Acid-Reducing Agents: Avoid concomitant use of proton pump inhibitors. Use histamine-2 receptor antagonists or antacids if needed. (2.5, 7.2)CYP3A Substrates: Avoid concomitant use with CYP3A substrates where minimal concentration changes may lead to serious therapeutic failure. (7.3). Use with Hepatotoxic Products: Avoid coadministration of TURALIO with other products known to cause hepatotoxicity. (7.1). Moderate or Strong CYP3A Inhibitors: Reduce the dose of TURALIO if concomitant use of moderate or strong CYP3A inhibitors cannot be avoided. (2.4, 7.2). Strong CYP3A Inducers: Avoid concomitant use of strong CYP3A inducers. (7.2). UGT Inhibitors: Reduce the dose of TURALIO if concomitant use of UGT inhibitors cannot be avoided. (2.4, 7.2). Acid-Reducing Agents: Avoid concomitant use of proton pump inhibitors. Use histamine-2 receptor antagonists or antacids if needed. (2.5, 7.2). CYP3A Substrates: Avoid concomitant use with CYP3A substrates where minimal concentration changes may lead to serious therapeutic failure. (7.3). 7.1Use with Hepatotoxic Products. TURALIO can cause hepatotoxicity. In patients with increased serum transaminases, total bilirubin, or direct bilirubin (>ULN) or active liver or biliary tract disease, avoid coadministration of TURALIO with other products known to cause hepatotoxicity [see Warnings and Precautions (5.1)].. 7.2Effect of Other Drugs on TURALIO. Table 7: Effect of Other Drugs on TURALIOModerate or Strong CYP3A InhibitorsClinical ImpactConcomitant use of moderate or strong CYP3A inhibitor may increase pexidartinib concentrations [see Clinical Pharmacology (12.3)], which may increase the incidence and severity of adverse reactions of TURALIO.ManagementReduce TURALIO dosage if concomitant use of moderate or strong CYP3A inhibitors, including grapefruit or grapefruit juice, cannot be avoided [see Dosage and Administration (2.4)]. Strong CYP3A InducersClinical ImpactConcomitant use of strong CYP3A inducer decreases pexidartinib concentrations [see Clinical Pharmacology (12.3)], which may decrease the efficacy of TURALIO.ManagementAvoid concomitant use of strong CYP3A inducers, including St Johns wort.UGT InhibitorsClinical ImpactConcomitant use of UGT inhibitor increases pexidartinib concentrations [see Clinical Pharmacology (12.3)], which may increase the incidence and severity of adverse reactions of TURALIO.ManagementReduce TURALIO dosage if concomitant use of UGT inhibitors cannot be avoided [see Dosage and Administration (2.4)]. Acid-Reducing AgentsClinical ImpactConcomitant use of PPI decreases pexidartinib concentrations [see Clinical Pharmacology (12.3)], which may decrease the efficacy of TURALIO.ManagementAvoid concomitant use of PPIs with TURALIO. As an alternative to PPIs, use locally-acting antacids or H2-receptor antagonists [see Dosage and Administration (2.5)].. Concomitant use of moderate or strong CYP3A inhibitor may increase pexidartinib concentrations [see Clinical Pharmacology (12.3)], which may increase the incidence and severity of adverse reactions of TURALIO.. Reduce TURALIO dosage if concomitant use of moderate or strong CYP3A inhibitors, including grapefruit or grapefruit juice, cannot be avoided [see Dosage and Administration (2.4)]. Concomitant use of strong CYP3A inducer decreases pexidartinib concentrations [see Clinical Pharmacology (12.3)], which may decrease the efficacy of TURALIO.. Avoid concomitant use of strong CYP3A inducers, including St Johns wort.. Concomitant use of UGT inhibitor increases pexidartinib concentrations [see Clinical Pharmacology (12.3)], which may increase the incidence and severity of adverse reactions of TURALIO.. Reduce TURALIO dosage if concomitant use of UGT inhibitors cannot be avoided [see Dosage and Administration (2.4)]. Concomitant use of PPI decreases pexidartinib concentrations [see Clinical Pharmacology (12.3)], which may decrease the efficacy of TURALIO.. Avoid concomitant use of PPIs with TURALIO. As an alternative to PPIs, use locally-acting antacids or H2-receptor antagonists [see Dosage and Administration (2.5)].. 7.3Effect of TURALIO on Other Drugs. Table 8: Effect of TURALIO on Other DrugsCYP3A SubstratesClinical ImpactTURALIO is moderate CYP3A inducer. Concomitant use of TURALIO decreases the concentration of CYP3A substrates [see Clinical Pharmacology (12.3)], which may reduce the efficacy of these substrates. ManagementAvoid coadministration of TURALIO with hormonal contraceptives [see Warnings and Precautions (5.3), Use in Specific Populations (8.3)]. Avoid concomitant use of TURALIO with other CYP3A substrates, where minimal concentration changes may lead to serious therapeutic failures. If concomitant use is unavoidable, increase the CYP3A substrate dosage in accordance with approved product labeling.. TURALIO is moderate CYP3A inducer. Concomitant use of TURALIO decreases the concentration of CYP3A substrates [see Clinical Pharmacology (12.3)], which may reduce the efficacy of these substrates. Avoid coadministration of TURALIO with hormonal contraceptives [see Warnings and Precautions (5.3), Use in Specific Populations (8.3)]. Avoid concomitant use of TURALIO with other CYP3A substrates, where minimal concentration changes may lead to serious therapeutic failures. If concomitant use is unavoidable, increase the CYP3A substrate dosage in accordance with approved product labeling.

INFORMATION FOR PATIENTS SECTION.

17 PATIENT COUNSELING INFORMATION. Advise the patient to read the FDA-approved patient labeling (Medication Guide).. HepatotoxicityAdvise patients of the risk of hepatotoxicity that could be fatal and that they will need to undergo monitoring for liver injury and to report immediately any signs or symptoms of severe liver injury to their healthcare provider [see Warnings and Precautions (5.1)].. TURALIO REMS ProgramTURALIO is available only through restricted program called TURALIO REMS Program and patients are required to be part of the patient registry [see Warnings and Precautions (5.2)].TURALIO is available only from certified pharmacies participating in the program. Therefore, provide patients with the telephone number and website for information on how to obtain the product.. TURALIO is available only through restricted program called TURALIO REMS Program and patients are required to be part of the patient registry [see Warnings and Precautions (5.2)].. TURALIO is available only from certified pharmacies participating in the program. Therefore, provide patients with the telephone number and website for information on how to obtain the product.. Embryo-Fetal ToxicityAdvise pregnant women and females of reproductive potential of the potential risk to fetus. Advise females of reproductive potential to inform their healthcare provider of known or suspected pregnancy [see Warnings and Precautions (5.3), Use in Specific Populations (8.1, 8.3)].Advise females of reproductive potential to use effective non-hormonal contraception during treatment with TURALIO and for month after the final dose [see Drug Interactions (7.3), Use in Specific Populations (8.3)].Advise male patients with female partners of reproductive potential to use effective contraception during treatment and for week after the final dose [see Use in Specific Populations (8.3), Nonclinical Toxicology (13.1)].. Advise pregnant women and females of reproductive potential of the potential risk to fetus. Advise females of reproductive potential to inform their healthcare provider of known or suspected pregnancy [see Warnings and Precautions (5.3), Use in Specific Populations (8.1, 8.3)].. Advise females of reproductive potential to use effective non-hormonal contraception during treatment with TURALIO and for month after the final dose [see Drug Interactions (7.3), Use in Specific Populations (8.3)].. Advise male patients with female partners of reproductive potential to use effective contraception during treatment and for week after the final dose [see Use in Specific Populations (8.3), Nonclinical Toxicology (13.1)].. LactationAdvise females not to breastfeed during treatment with TURALIO and for week after the final dose [see Use in Specific Populations (8.2)]. InfertilityAdvise females and males of reproductive potential that TURALIO may impair fertility [see Use in Specific Populations (8.3), Nonclinical Toxicology (13.1)]. Drug InteractionsAdvise patients to inform their healthcare providers of all concomitant products, including over-the-counter products and supplements [see Dosage and Administration (2), Drug Interactions (7)].. AdministrationInstruct patients to take TURALIO on an empty stomach (at least hour before or hours after meal or snack). Instruct patients to swallow capsules whole (do not open, break, or chew) [see Dosage and Administration (2.1, 2.2)].

NONCLINICAL TOXICOLOGY SECTION.

13 NONCLINICAL TOXICOLOGY. 13.1Carcinogenesis, Mutagenesis, Impairment of Fertility. Carcinogenicity studies were performed in mice and rats. Both studies were negative for carcinogenic findings at exposures up to times the human exposure at the recommended daily dose of 800 mg based on AUC.Pexidartinib was not mutagenic in an in vitro bacterial reverse mutation (AMES) assay or clastogenic in either an in vitro human peripheral blood lymphocyte chromosomal aberrations assay or in an in vivo mouse bone marrow micronucleus assay.Based on nonclinical findings, TURALIO may impair male and female fertility. In fertility study in which pexidartinib was administered orally to male and female rats, there were reductions in pregnancy, as well as increases in pre- and post-implantation loss with corresponding reduction in viable embryos at 40 mg/kg (approximately 1.3 times the human exposure at the recommended dose of 800 mg). Males at this dose level displayed reductions in spermatogenic parameters and adverse effects on sperm concentration, production, motility, and morphology. Lower testicular and epididymal weights occurred in this study at doses of >=10 mg/kg/day (approximately 0.3 times the human exposure at the recommended dose of 800 mg). This is consistent with findings in chronic toxicology studies of germ cell depletion of the testes and hypospermia and cellular debris in the epididymis in male reproductive tissues of both rats and dogs at respective doses as low as 20 and 30 mg/kg/day (approximately 0.6 and 0.1 times the human exposure at the recommended dose of 800 mg). In rats, these changes persisted following 16-week recovery period at the 60 mg/kg/day dose level (approximately 1.5 times the human exposure at the recommended dose of 800 mg).In female rats, necrosis of corpora lutea occurred at doses >=0.5 mg/kg/day (approximately 0.01 times the human exposure at the recommended dose of 800 mg) with pigment deposition within the interstitium of the ovaries, an increased incidence of luteal cysts and incidence/severity of hemorrhage of corpora lutea, and decreased incidence of retained antral follicles and decreased corpora lutea at 60 mg/kg (approximately 1.8 times the human exposure at the recommended dose of 800 mg). In female dogs there were decreased follicle numbers and moderate atrophy of the oviduct, uterus, and cervix at doses as low as mg/kg (approximately 0.01 times the human exposure at the recommended dose of 800 mg). 13.2Animal Toxicology and/or Pharmacology. In repeat dose toxicity studies of up to 26 weeks in rats, there were findings of myxomatous change in the skin, tongue, and gastrointestinal tract, lymphoid depletion of the bone marrow and thymus, and chronic progressive nephropathy of the kidney at 20 mg/kg/day (approximately 0.6 times the human exposure at the recommended dose of 800 mg). Similar changes occurred in the rat carcinogenicity study along with alterations in the tunica intima of the aorta. Vascular inflammation consistent with polyarteritis nodosa occurred in male rats at 60 mg/kg/day (approximately 1.5 times the human exposure at the recommended dose of 800 mg). There were also dose-dependent findings of minimal to moderate subphyseal or cortical hyperostosis and physeal hypertrophy in the femur that correlated with decreased systemic phosphate levels at doses >= 60 mg/kg.

PHARMACOKINETICS SECTION.

12.3 Pharmacokinetics. The pharmacokinetics of TURALIO was evaluated following single doses in healthy subjects and following multiple doses in patients as summarized in Table 9.Table 9: TURALIO Exposure and Pharmacokinetic ParametersGeneral InformationSteady state exposure [Mean (SD)]Pexidartinib 400 mg twice daily Cmax 8625 (2746) ng/mLAUC0-12h 77465 (24975) ngh/mLDose proportionalityPexidartinib exposure (Cmax and AUC0-INF) increased linearly over the single oral dose range of 200 to 2400 mg (0.5 to times the recommended dose).Time to steady stateEstimated based on half life Approximately daysAccumulation ratio (AUC) [Median] 3.6AbsorptionTmax [Median]2.5 hours Effect of food Administration with high-fat mealThe high-fat meal comprised 800 to 1000 calories with fat being 50% of total caloric content; approximately 150 calories from protein, 250 calories from carbohydrates, and 500-600 calories from fat. Increased pexidartinib Cmax and AUC0-INF by 100%Delayed Tmax by 2.5 hours Administration with low-fat mealThe low-fat meal comprised 387 calories with fat being approximately 25% of total caloric content. Increased Cmax by 56% and AUC0-INF by 59%Delayed Tmax by 1.5 hoursDistributionIn vitro plasma protein bindingGreater than 99%Human serum albumin: 99.9%-1 acid glycoprotein: 89.9% Apparent volume of distribution (Vz/F) [Mean (CV%)]After single oral dose of pexidartinib 400 mg 187 (27%)EliminationApparent clearance [Mean (CV%)] 5.1 L/h (36%)t1/2 [Mean (SD)]26.6 (6.5) hours Metabolism Primary pathwayOxidation: CYP3A4Glucuronidation: UGT1A4 N-glucuronide metaboliteMajor inactive metabolite formed by UGT1A4Approximately 10% higher exposure than pexidartinib after single dose ExcretionAfter single oral dose of radiolabeled pexidartinib 400 mg Feces: 65% (44% as unchanged)Urine: 27% as metabolites (>=10% as N-glucuronide). Increased pexidartinib Cmax and AUC0-INF by 100%. Delayed Tmax by 2.5 hours. Increased Cmax by 56% and AUC0-INF by 59%. Delayed Tmax by 1.5 hours. Greater than 99%. Human serum albumin: 99.9%. -1 acid glycoprotein: 89.9% 187 (27%). 5.1 L/h (36%). 26.6 (6.5) hours. Oxidation: CYP3A4. Glucuronidation: UGT1A4. Major inactive metabolite formed by UGT1A4. Approximately 10% higher exposure than pexidartinib after single dose. Feces: 65% (44% as unchanged). Urine: 27% as metabolites (>=10% as N-glucuronide). Specific PopulationsNo clinically meaningful differences in the pharmacokinetics of pexidartinib were observed based on age (18 to 84 years), sex, race (White and Black), or mild hepatic impairment (total bilirubin <= ULN with AST ULN or total bilirubin 1 to 1.5 ULN with any AST).. Patients with Renal ImpairmentMild (CLcr 60 to 89 mL/min), moderate (CLcr 30 to 59 mL/min) and severe (CLcr 15 to 29 mL/min) renal impairment increased pexidartinib exposure (AUC) by approximately 30%, relative to that in patients with normal renal function (CLcr >=90 mL/min).. Patients with Hepatic ImpairmentModerate hepatic impairment (total bilirubin 1.5 and up to x ULN, not due to Gilberts syndrome, with any AST) increased pexidartinib exposure (AUC) by 43% relative to exposure in patients with normal hepatic function (total bilirubin and AST <= ULN).The pharmacokinetics of pexidartinib have not been studied in patients with severe hepatic impairment (total bilirubin 3 to 10 ULN with any AST).. Drug Interaction Studies. Clinical Studies and Model-Informed Approaches. Effects of Other Drugs on Pexidartinib. Strong CYP3A Inducers: Coadministration of rifampicin (strong CYP3A inducer) decreased pexidartinib Cmax by 33% and AUC0-INF by 65%.. Moderate CYP3A Inducers: Coadministration of efavirenz (moderate CYP3A inducer) is predicted to decrease pexidartinib Cmax by 27% and AUC by 38% at steady state.. Strong CYP3A Inhibitors: Coadministration of itraconazole (strong CYP3A inhibitor) increased pexidartinib Cmax by 48% and AUC0-INF by 70%.. Moderate CYP3A Inhibitors: Coadministration of fluconazole (moderate CYP3A inhibitor) is predicted to increase pexidartinib Cmax by 41% and AUC by 67% at steady state.. UGT Inhibitors: Coadministration of probenecid (UGT inhibitor) increased pexidartinib Cmax by 5% and AUC0-INF by 60%.. Acid-Reducing Agents: Coadministration of esomeprazole (proton pump inhibitor) decreased pexidartinib Cmax by 55% and AUC0-INF by 50%. The effects of H2-receptor antagonists and locally-acting antacids on pexidartinib pharmacokinetics have not been studied.. Effects of Pexidartinib on Other Drugs. CYP2C19 Substrates: Coadministration of single oral dose of TURALIO 1800 mg (4.5 times the approved recommended dose of 400 mg) decreased omeprazole (CYP2C19 substrate) Cmax by 37% and AUC0-INF by 17%.. CYP3A Substrates: Coadministration of TURALIO 400 mg twice daily decreased midazolam (CYP3A substrate) Cmax by 28% and AUC0-INF by 59%.. CYP2C9 Substrates: Coadministration of TURALIO 400 mg twice daily increased tolbutamide (CYP2C9 substrate) AUC0-INF by 28%. The effect of pexidartinib on CYP2C9 substrates is not considered clinically relevant.. P-gp Substrates: Coadministration of single oral dose of TURALIO 1800 mg (4.5 times the approved recommended dose of 400 mg) increased digoxin (P-gp substrate) Cmax by 30% and AUC0-INF by 9%.. CYP2C8 Substrates: The effect of pexidartinib on CYP2C8 substrates is predicted not to be clinically relevant.. In Vitro Studies. CYP/UGT Enzymes: Pexidartinib is likely to inhibit CYP2B6 and induce CYP2B6 at clinically relevant concentrations. Pexidartinib is likely to inhibit UGT1A1 at clinically relevant concentrations.. Transporter Systems: Pexidartinib is not substrate for P-gp, BCRP, OAT1, OAT3, OCT1, OCT2, OATP1B1, OATP1B3, OATP2B1, and BSEP.Pexidartinib is an inhibitor of MATE1, MATE2-K, OATP1B1, OATP1B3 and OATP2B1.

SPL MEDGUIDE SECTION.

This Medication Guide has been approved by the U.S. Food and Drug Administration.Revised: 10/2021 Medication GuideTURALIO(R) (tur-a-lee-oh)(pexidartinib)CapsulesWhat is the most important information should know about TURALIOTURALIO can cause serious side effects, including:Serious Liver Problems which may be severe and can lead to death.Your healthcare provider will do blood tests to check for liver problems:before starting treatment with TURALIO,every week for the first weeks during treatment,every weeks for the next month,then, every months after that.If you develop liver problems during treatment with TURALIO, your healthcare provider may do blood tests more often to monitor you. It is important to stay under the care of your healthcare provider during treatment with TURALIO.Stop taking TURALIO and call your healthcare provider right away if you develop:yellowing of your skin and whites of your eyesdark urineTell your healthcare provider right away if you have any of these symptoms of liver problems while taking TURALIO:lack or loss of appetiteright upper stomach-area (abdomen) pain or tendernessfeeling overly tirednauseavomitingfeverrashitchingTURALIO Risk Evaluation and Mitigation Strategy (REMS): Because of the risk of serious liver problems, TURALIO is available only through restricted program called the TURALIO REMS Program. Your healthcare provider must be enrolled in the program in order for you to be prescribed TURALIO. There is registry that collects information about the effects of taking TURALIO over time. You must complete and sign an enrollment form for the TURALIO REMS Program and the registry. Ask your healthcare provider for more information.What is TURALIOTURALIO is prescription medicine used to treat certain adults who have tenosynovial giant cell tumor (TGCT) that is not likely to improve with surgery. TGCT is also known as giant cell tumor of the tendon sheath (GCT-TS) or pigmented villonodular synovitis (PVNS).It is not known if TURALIO is safe and effective in children.Before taking TURALIO, tell your healthcare provider about all of your medical conditions, including if you:have or had liver problems.are pregnant or plan to become pregnant. TURALIO may harm your unborn baby. If you are female who is able to become pregnant: Your healthcare provider will do pregnancy test before you start treatment with TURALIO.Females who are able to become pregnant should use effective non-hormonal birth control (contraception) during treatment with TURALIO and for month after your final dose of TURALIO. Birth control pills (oral contraceptives) and other hormonal forms of birth control may not be effective if used during treatment with TURALIO. Talk with your healthcare provider about birth control methods you can use during this time.Tell your healthcare provider right away if you become pregnant or think you are pregnant during treatment with TURALIO. If you are male with female partner who is able to become pregnant: Use effective birth control (contraception) during treatment and for week after your final dose of TURALIO.Tell your healthcare provider right away if your female partner becomes pregnant or thinks she is pregnant during your treatment with TURALIO. are breastfeeding or plan to breastfeed. Do not breastfeed during treatment with TURALIO and for at least week after your final dose of TURALIO.Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. Certain medicines may affect the way TURALIO works and TURALIO may affect how other medicines work. Taking TURALIO with certain medicines can increase the amount of TURALIO in your blood. This may make it more likely for you to have side effects and may cause more severe side effects. Avoid taking the following medicines or supplements during treatment with TURALIO because they can affect how TURALIO works: Proton Pump Inhibitor medicines (PPIs)St. Johns wort How should take TURALIOYour healthcare provider will explain to you how you will receive your TURALIO.Take TURALIO exactly as your healthcare provider tells you to.TURALIO is usually taken times day. Your healthcare provider will tell you how much TURALIO to take and when to take it.TURALIO must be taken on an empty stomach, at least hour before or hours after eating meal or snack.Swallow TURALIO capsules whole.Do not open, break, or chew TURALIO capsules.If you need to take an acid-reducing medicine, follow your healthcare providers instructions for which medicine to take and when to take it. See What should avoid while taking TURALIO Antacid medicines: Take TURALIO either hours before or hours after taking an antacid medicine.H2 receptor blocker medicines. Take TURALIO at least hours before or 10 hours after taking an H2 receptor blocker medicine. If you vomit after taking dose, or if you miss dose of TURALIO, take your next dose at your regular time.What should avoid while taking TURALIOAvoid grapefruit or drinking grapefruit juice during treatment with TURALIO. Grapefruit or grapefruit juice can cause you to have too much TURALIO in your blood and may lead to increased side effects and more severe side effects.What are the possible side effects of TURALIOTURALIO can cause serious side effects. See What is the most important information should know about TURALIOThe most common side effects of TURALIO include:changes in blood liver testshair color changestirednessincreased cholesterol level in your blooddecreased white blood cells and red blood cellsswelling in or around your eyesrashloss of taste or changes in the way things tasteTURALIO may affect fertility in females and males, which may affect your ability to have children. Talk to your healthcare provider if you have concerns about fertility.These are not all of the possible side effects of TURALIO.Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. How should store TURALIOStore TURALIO at room temperature between 68F to 77F (20C to 25C).Keep the TURALIO container closed tightly.TURALIO comes with drying agent (desiccant) in the container. Keep the desiccant in the container.Keep TURALIO and all medicines out of the reach of children.General information about the safe and effective use of TURALIOMedicines are sometimes prescribed for purposes other than those listed in Medication Guide. Do not use TURALIO for condition for which it was not prescribed. Do not give TURALIO to other people, even if they have the same symptoms that you have. It may harm them. You can ask your pharmacist or healthcare provider for information about TURALIO that is written for health professionals.What are the ingredients in TURALIOActive Ingredient: pexidartinib Inactive Ingredients: poloxamer 407, mannitol, crospovidone, and magnesium stearate. Capsule shell: hypromellose, titanium dioxide, black iron oxide and yellow iron oxideManufactured for: Daiichi Sankyo, Inc., Basking Ridge, NJ 07920TURALIO(R) is registered trademark of Daiichi Sankyo Company, Limited. (C)2020, Daiichi Sankyo, Inc.USMG-TUR-C4-1021-r003For more information, call 1-877-437-7763 or go to https://www.turalio.com/.. before starting treatment with TURALIO,. every week for the first weeks during treatment,. every weeks for the next month,. then, every months after that.. yellowing of your skin and whites of your eyes. dark urine. lack or loss of appetite. right upper stomach-area (abdomen) pain or tenderness. feeling overly tired. nausea. vomiting. fever. rash. itching. have or had liver problems.. are pregnant or plan to become pregnant. TURALIO may harm your unborn baby. If you are female who is able to become pregnant: Your healthcare provider will do pregnancy test before you start treatment with TURALIO.Females who are able to become pregnant should use effective non-hormonal birth control (contraception) during treatment with TURALIO and for month after your final dose of TURALIO. Birth control pills (oral contraceptives) and other hormonal forms of birth control may not be effective if used during treatment with TURALIO. Talk with your healthcare provider about birth control methods you can use during this time.Tell your healthcare provider right away if you become pregnant or think you are pregnant during treatment with TURALIO. If you are male with female partner who is able to become pregnant: Use effective birth control (contraception) during treatment and for week after your final dose of TURALIO.Tell your healthcare provider right away if your female partner becomes pregnant or thinks she is pregnant during your treatment with TURALIO. Your healthcare provider will do pregnancy test before you start treatment with TURALIO.. Females who are able to become pregnant should use effective non-hormonal birth control (contraception) during treatment with TURALIO and for month after your final dose of TURALIO. Birth control pills (oral contraceptives) and other hormonal forms of birth control may not be effective if used during treatment with TURALIO. Talk with your healthcare provider about birth control methods you can use during this time.. Tell your healthcare provider right away if you become pregnant or think you are pregnant during treatment with TURALIO.. Use effective birth control (contraception) during treatment and for week after your final dose of TURALIO.. Tell your healthcare provider right away if your female partner becomes pregnant or thinks she is pregnant during your treatment with TURALIO.. are breastfeeding or plan to breastfeed. Do not breastfeed during treatment with TURALIO and for at least week after your final dose of TURALIO.. Avoid taking the following medicines or supplements during treatment with TURALIO because they can affect how TURALIO works: Proton Pump Inhibitor medicines (PPIs)St. Johns wort Proton Pump Inhibitor medicines (PPIs). St. Johns wort. Your healthcare provider will explain to you how you will receive your TURALIO.. Take TURALIO exactly as your healthcare provider tells you to.. TURALIO is usually taken times day. Your healthcare provider will tell you how much TURALIO to take and when to take it.. TURALIO must be taken on an empty stomach, at least hour before or hours after eating meal or snack.. Swallow TURALIO capsules whole.. Do not open, break, or chew TURALIO capsules.. If you need to take an acid-reducing medicine, follow your healthcare providers instructions for which medicine to take and when to take it. See What should avoid while taking TURALIO Antacid medicines: Take TURALIO either hours before or hours after taking an antacid medicine.H2 receptor blocker medicines. Take TURALIO at least hours before or 10 hours after taking an H2 receptor blocker medicine. Antacid medicines: Take TURALIO either hours before or hours after taking an antacid medicine.. H2 receptor blocker medicines. Take TURALIO at least hours before or 10 hours after taking an H2 receptor blocker medicine.. If you vomit after taking dose, or if you miss dose of TURALIO, take your next dose at your regular time.. Avoid grapefruit or drinking grapefruit juice during treatment with TURALIO. Grapefruit or grapefruit juice can cause you to have too much TURALIO in your blood and may lead to increased side effects and more severe side effects.. changes in blood liver tests. hair color changes. tiredness. increased cholesterol level in your blood. decreased white blood cells and red blood cells. swelling in or around your eyes. rash. loss of taste or changes in the way things taste. Store TURALIO at room temperature between 68F to 77F (20C to 25C).. Keep the TURALIO container closed tightly.. TURALIO comes with drying agent (desiccant) in the container. Keep the desiccant in the container.

USE IN SPECIFIC POPULATIONS SECTION.

8 USE IN SPECIFIC POPULATIONS. Lactation: Advise not to breastfeed. (8.2)Renal Impairment: Reduce the dose for patients with mild to severe renal impairment. (2.6, 8.6)Hepatic Impairment: Reduce the dose for patients with moderate hepatic impairment. (2.7, 8.7). Lactation: Advise not to breastfeed. (8.2). Renal Impairment: Reduce the dose for patients with mild to severe renal impairment. (2.6, 8.6). Hepatic Impairment: Reduce the dose for patients with moderate hepatic impairment. (2.7, 8.7). 8.1 Pregnancy. Risk SummaryBased on findings from animal studies and its mechanism of action [see Clinical Pharmacology (12.1)], TURALIO may cause embryo-fetal harm when administered to pregnant woman. The available human data do not establish the presence or absence of major birth defects or miscarriage related to the use of TURALIO. Oral administration of pexidartinib to pregnant animals during the period of organogenesis resulted in malformations, post-implantation loss, and abortion at maternal exposures that were approximately equal to the human exposure at the recommended dose of 800 mg (see Data). Advise pregnant women of the potential risk to fetus.In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is to 4% and 15 to 20%, respectively.. Data. Animal DataEmbryo-fetal development studies investigating the administration of pexidartinib during the period of organogenesis were conducted in rats and rabbits. In rats, pexidartinib resulted in increased post-implantation loss and fetal malformations including localized fetal edema, absence of kidney and ureter, abnormalities of the reproductive tract, and developmental variations including misshapen kidney, decreased skeletal ossification and higher mean litter proportions of slightly or moderately malaligned sternebrae at doses of 40 mg/kg (approximately equal to the human exposure at the recommended dose of 800 mg). In rabbits, administration of pexidartinib resulted in increased post-implantation loss, abortion, and fetal malformations including absence of kidney or ureter, rudimentary, misshapen or malpositioned kidney, rib abnormalities, and skeletal variations of accessory skull bones at doses of 60 mg/kg (approximately equal to the human exposure at the recommended dose of 800 mg).. 8.2 Lactation. Risk SummaryThere are no data on the presence of pexidartinib or its metabolites in either human or animal milk or its effects on breastfed child or on milk production. Because of the potential for serious adverse reactions in the breastfed child, advise women not to breastfeed during treatment with TURALIO and for at least week after the final dose.. 8.3 Females and Males of Reproductive Potential. TURALIO may cause fetal harm when administered to pregnant woman [see Use in Specific Populations (8.1)].. Pregnancy TestingVerify pregnancy status in females of reproductive potential prior to the initiation of TURALIO [see Use in Specific Populations (8.1)].. Contraception. FemalesAdvise females of reproductive potential to use effective non-hormonal contraception during treatment with TURALIO and for month after the final dose. Counsel patients to use non-hormonal method(s) of contraception, since TURALIO can render hormonal contraceptives ineffective [see Drug Interactions (7.3), Nonclinical Toxicology (13.1)].. MalesAdvise male patients with female partners of reproductive potential to use effective contraception during treatment with TURALIO and for week after the final dose [see Nonclinical Toxicology (13.1)].. InfertilityBased on findings from animal studies, TURALIO may impair both male and female fertility [see Nonclinical Toxicology (13.1)]. 8.4 Pediatric Use. The safety and effectiveness of TURALIO in pediatric patients have not been established.. 8.5 Geriatric Use. Clinical studies of TURALIO did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects.. 8.6Renal Impairment. Reduce the dose when administering TURALIO to patients with mild to severe renal impairment (CLcr 15 to 89 mL/min, estimated by Cockcroft-Gault [C-G]) [see Dosage and Administration (2.6), Clinical Pharmacology (12.3)]. 8.7Hepatic Impairment. No dosage adjustment is recommended for patients with mild hepatic impairment (total bilirubin less than or equal to upper limit of normal [ULN] with AST greater than ULN or total bilirubin greater than and up to 1.5 times ULN with any AST) [see Clinical Pharmacology (12.3)].Reduce the dosage of TURALIO for patients with moderate hepatic impairment (total bilirubin greater than 1.5 and up to times ULN, not due to Gilberts syndrome, with any AST) [see Dosage and Administration (2.7), Clinical Pharmacology (12.3)].TURALIO has not been studied in patients with severe hepatic impairment (total bilirubin greater than to 10 times ULN and any AST).

WARNINGS AND PRECAUTIONS SECTION.

5 WARNINGS AND PRECAUTIONS. Embryo-Fetal Toxicity: May cause fetal harm. Advise patients of reproductive potential of the potential risk to fetus and to use an effective non-hormonal method of contraception. (5.3, 7.3, 8.1, 8.3). Embryo-Fetal Toxicity: May cause fetal harm. Advise patients of reproductive potential of the potential risk to fetus and to use an effective non-hormonal method of contraception. (5.3, 7.3, 8.1, 8.3). 5.1Hepatotoxicity. TURALIO can cause serious and potentially fatal liver injury and is available only through restricted program under Risk Evaluation and Mitigation Strategy (REMS) [see Warnings and Precautions (5.2)]. Hepatotoxicity with ductopenia and cholestasis occurred in patients treated with TURALIO. Across 768 patients who received TURALIO in clinical trials, there were two irreversible cases of cholestatic liver injury. One patient died with advanced cancer and ongoing liver toxicity and one patient required liver transplant. The mechanism of cholestatic hepatotoxicity is unknown and its occurrence cannot be predicted. It is unknown whether liver injury occurs in the absence of increased transaminases.In ENLIVEN, of 61 (5%) patients who received TURALIO developed signs of serious liver injury, defined as ALT or AST >=3 ULN with total bilirubin >=2 ULN. In these patients, peak ALT ranged from to x ULN, peak total bilirubin ranged from 2.5 to 15 ULN, and alkaline phosphatase (ALP) was >=2 ULN. ALT, AST and total bilirubin improved to <2 ULN in these patients to months after discontinuing TURALIO. Avoid TURALIO in patients with pre-existing increased serum transaminases; total bilirubin or direct bilirubin (>ULN); or active liver or biliary tract disease, including increased ALP. Taking TURALIO with food increases drug exposure by 100% and may increase the risk of hepatotoxicity. Administer TURALIO on an empty stomach, either hour before or hours after meal or snack [see Dosage and Administration (2.1), Clinical Pharmacology (12.2, 12.3)]. Monitor liver tests, including AST, ALT, total bilirubin, direct bilirubin, ALP and gamma-glutamyl transferase (GGT), prior to initiation of TURALIO, weekly for the first weeks, every weeks for the next month and every months thereafter. Withhold and dose reduce, or permanently discontinue TURALIO based on the severity of the hepatotoxicity [see Dosage and Administration (2.2)]. Rechallenge with reduced dose of TURALIO may result in recurrence of increased serum transaminases, bilirubin, or ALP. Monitor liver tests weekly for the first month after rechallenge.. 5.2TURALIO REMS Program. TURALIO is only available through restricted program under REMS, because of the risk of hepatotoxicity [see Warnings and Precautions (5.1)].Notable requirements of the TURALIO REMS Program include the following:Prescribers must be certified with the program by enrolling and completing training.Patients must complete and sign an enrollment form for inclusion in patient registry. Pharmacies must be certified with the program and must only dispense to patients who are authorized to receive TURALIO.Further information is available at www.TURALIOREMS.com or 1-833-887-2546.. Prescribers must be certified with the program by enrolling and completing training.. Patients must complete and sign an enrollment form for inclusion in patient registry. Pharmacies must be certified with the program and must only dispense to patients who are authorized to receive TURALIO.. 5.3Embryo-Fetal Toxicity. Based on animal studies and its mechanism of action, TURALIO may cause fetal harm when administered to pregnant woman. Oral administration of pexidartinib to pregnant rats and rabbits during the period of organogenesis resulted in malformations, increased post-implantation loss, and abortion at exposures approximately equal to the human exposure at the recommended dose of 800 mg based on area under the curve (AUC).Advise pregnant women of the potential risk to fetus. Advise females of reproductive potential to use effective non-hormonal contraception, since TURALIO can render hormonal contraceptives ineffective, during treatment with TURALIO and for month after the final dose. Advise males with female partners of reproductive potential to use effective contraception during treatment with TURALIO and for week after the final dose [see Drug Interactions (7.3), Use in Specific Populations (8.1, 8.3)].