ADVERSE REACTIONS SECTION.

ADVERSE REACTIONS. Clinical experience with trientine hydrochloride has been limited. The following adverse reactions have been reported in clinical study in patients with Wilsons disease who were on therapy with trientine hydrochloride: iron deficiency, systemic lupus erythematosus (see CLINICAL PHARMACOLOGY). In addition, the following adverse reactions have been reported in marketed use: dystonia, muscular spasm, myasthenia gravis. Trientine hydrochloride is not indicated for treatment of biliary cirrhosis, but in one study of patients treated with trientine hydrochloride for primary biliary cirrhosis, the following adverse reactions were reported: heartburn; epigastric pain and tenderness; thickening, fissuring and flaking of the skin; hypochromic microcytic anemia; acute gastritis; aphthoid ulcers; abdominal pain; melena; anorexia; malaise; cramps; muscle pain; weakness; rhabdomyolysis. causal relationship of these reactions to drug therapy could not be rejected or established. To report SUSPECTED ADVERSE EVENTS, contact Rising Pharmaceuticals, Inc. at 1-866-562-4597 or FDA at 1- 800-FDA-1088 or http://www.fda.gov/ for voluntary reporting of adverse reactions.

CARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY SECTION.

Carcinogenesis, Mutagenesis, Impairment of Fertility. Data on carcinogenesis, mutagenesis, and impairment of fertility are not available.

CLINICAL PHARMACOLOGY SECTION.

CLINICAL PHARMACOLOGY. IntroductionWilsons disease (hepatolenticular degeneration) is an autosomal inherited metabolic defect resulting in an inability to maintain near-zero balance of copper. Excess copper accumulates possibly because the liver lacks the mechanism to excrete free copper into the bile. Hepatocytes store excess copper but when their capacity is exceeded copper is released into the blood and is taken up into extrahepatic sites. This condition is treated with low copper diet and the use of chelating agents that bind copper to facilitate its excretion from the body. Clinical Summary Forty-one patients (18 male and 23 female) between the ages of and 54 with diagnosis of Wilsons disease and who were intolerant of d-penicillamine were treated in two separate studies with trientine hydrochloride. The dosage varied from 450 to 2400 mg per day. The average dosage required to achieve an optimal clinical response varied between 1000 mg and 2000 mg per day. The mean duration of trientine hydrochloride therapy was 48.7 months (range to 164 months). Thirty-four of the 41 patients improved, had no change in clinical global response, were lost to follow-up and one showed deterioration in clinical condition. One of the patients who improved while on therapy with trientine hydrochloride experienced recurrence of the symptoms of systemic lupus erythematosus which had appeared originally during therapy with penicillamine. Therapy with trientine hydrochloride was discontinued. No other adverse reactions, except iron deficiency, were noted among any of these 41 patients.One investigator treated 13 patients with trientine hydrochloride following their development of intolerance to d-penicillamine. Retrospectively, he compared these patients to an additional group of 12 patients with Wilsons disease who were both tolerant of and controlled with d-penicillamine therapy, but who failed to continue any copper chelation therapy. The mean age at onset of disease of the latter group was 12 years as compared to 21 years for the former group. The trientine hydrochloride group received d-penicillamine for an average of years as compared to an average of 10 years for the non- treated group.Various laboratory parameters showed changes in favor of the patients treated with trientine hydrochloride. Free and total serum copper, SGOT, and serum bilirubin all showed mean increases over baseline in the untreated group which were significantly larger than with the patients treated with trientine hydrochloride. In the 13 patients treated with trientine hydrochloride, previous symptoms and signs relating to d-penicillamine intolerance disappeared in patients, improved in patients, and remained unchanged in one patient. The neurological status in the trientine hydrochloride group was unchanged or improved over baseline, whereas in the untreated group, patients remained unchanged and worsened. Kayser-Fleischer rings improved significantly during trientine hydrochloride treatment.The clinical outcome of the two groups also differed markedly. Of the 13 patients on therapy with trientine hydrochloride (mean duration of therapy 4.1 years; range to 13 years), all were alive at the data cutoff date, and in the non-treated group (mean years with no therapy 2.7 years; range months to years), of the 12 died of hepatic disease.Chelating Properties Preclinical Studies Studies in animals have shown that trientine hydrochloride has cupriuretic activities in both normal and copper-loaded rats. In general, the effects of trientine hydrochloride on urinary copper excretion are similar to those of equimolar doses of penicillamine, although in one study they were significantly smaller.HumanStudiesRenal clearance studies were carried out with penicillamine and trientine hydrochloride on separate occasions in selected patients treated with penicillamine for at least one year. Six-hour excretion rates of copper were determined off treatment and after single dose of 500 mg of penicillamine or 1.2 of trientine hydrochloride. The mean urinary excretion rates of copper were as follows:No. of PatientsSingle Dose TreatmentBasal Excretion Rate (ug Cu + /6hr)Test-doseExcretionRate(ug Cu+ /6hr)6 Trientine,1.2 19 234 Penicillamine, 500 mg 17 320 In patients not previously treated with chelating agents, similar comparison was made:No. of PatientsSingle Dose TreatmentBasal Excretion Rate (ug Cu++ /6hr)Test-dose Excretion Rate (ug Cu++ /6hr)8 Trientine,1.2 71 1326 Penicillamine, 500 mg 68 1074 These results demonstrate that trientine hydrochloride is effective as cupriuretic agent in patients with Wilsons disease although on molar basis it appears to be less potent or less effective than penicillamine. Evidence from radio-labelled copper study indicates that the different cupriuretic effect between these two drugs could be due to difference in selectivity of the drugs for different copper pools within the body. Pharmacokinetics Data on the pharmacokinetics of trientine hydrochloride are not available. Dosage adjustment recommendations are based upon clinical use of the drug (see DOSAGE AND ADMINISTRATION).

CONTRAINDICATIONS SECTION.

CONTRAINDICATIONS. Hypersensitivity to this product.

DESCRIPTION SECTION.

DESCRIPTION. Trientine hydrochloride, USP is N,N-bis (2-aminoethyl)-1,2-ethanediamine dihydrochloride. It is white to pale yellow crystalline hygroscopic powder. It is freely soluble in water, soluble in methanol, slightly soluble in ethanol, and insoluble in chloroform and ether.The molecular formula is C6H18N4o2HCl with molecular weight of 219.2. The structural formula is: NH2(CH2)2NH(CH2)2NH(CH2)2NH2o2HClTrientine hydrochloride, USP is chelating compound for removal of excess copper from the body.Trientine hydrochloride, USP is available as 250 mg capsules for oral administration. Trientine hydrochloride capsules, USP contain gelatin, iron oxide black, iron oxide red, iron oxide yellow, potassium hydroxide, propylene glycol, shellac, stearic acid and titanium dioxide as inactive ingredients.

DRUG INTERACTIONS SECTION.

Drug Interactions. In general, mineral supplements should not be given since they may block the absorption of trientine hydrochloride. However, iron deficiency may develop, especially in children and menstruating or pregnant women, or as result of the low copper diet recommended for Wilsons disease. If necessary, iron may be given in short courses, but since iron and trientine hydrochloride each inhibit absorption of the other, two hours should elapse between administration of trientine hydrochloride capsules and iron. It is important that trientine hydrochloride capsules be taken on an empty stomach, at least one hour before meals or two hours after meals and at least one hour apart from any other drug, food, or milk. This permits maximum absorption and reduces the likelihood of inactivation of the drug by metal binding in the gastrointestinal tract.

GENERAL PRECAUTIONS SECTION.

General. There are no reports of hypersensitivity in patients who have been administered trientine hydrochloride for Wilsons disease. However, there have been reports of asthma, bronchitis and dermatitis occurring after prolonged environmental exposure in workers who use trientine hydrochloride as hardener of epoxy resins. Patients should be observed closely for signs of possible hypersensitivity.

GERIATRIC USE SECTION.

Geriatric Use. Clinical studies of trientine hydrochloride did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects. Other reported clinical experience is insufficient to determine differences in responses between the elderly and younger patients. In general, dose selection should be cautious, usually starting at the low end of the dosing range, reflecting the greater frequency of decreased hepatic, renal or cardiac function, and of concomitant disease or other drug therapy.

HOW SUPPLIED SECTION.

HOW SUPPLIED. Trientine Hydrochloride Capsules, USP 250 mg, are Size 1 hard gelatin capsule with brown opaque cap/brown opaque body, imprinted C27 on cap with black ink and 250mg on body with black ink filled with white to pale yellow powder. They are supplied as follows: NDC 64980-450-01 Bottles of 100 Capsules. Storage Keep container tightly closed. Store at 2C to 8C (36F to 46F). Manufactured by: Suven Life Sciences Limited Plot No. 262-271, IDA, Pashamylaram, Sangareddy District, Telangana, India 502307Distributed by: Rising Pharmaceuticals, Inc. Saddle brook, NJ 07663 M.L No.: 24/MD/AP/2009/F/RRev. 02/2020.

INDICATIONS & USAGE SECTION.

INDICATIONS AND USAGE. Trientine hydrochloride is indicated in the treatment of patients with Wilsons disease who are intolerant of penicillamine. Clinical experience with trientine hydrochloride is limited and alternate dosing regimens have not been well-characterized; all endpoints in determining an individual patients dose have not been well defined. Trientine hydrochloride and penicillamine cannot be considered interchangeable. Trientine hydrochloride should be used when continued treatment with penicillamine is no longer possible because of intolerable or life endangering side effects.Unlike penicillamine, trientine hydrochloride is not recommended in cystinuria or rheumatoid arthritis. The absence of sulfhydryl moiety renders it incapable of binding cystine and, therefore, it is of no use in cystinuria. In 15 patients with rheumatoid arthritis, trientine hydrochloride was reported not to be effective in improving any clinical or biochemical parameter after 12 weeks of treatment.Trientine hydrochloride is not indicated for treatment of biliary cirrhosis.

INFORMATION FOR PATIENTS SECTION.

Information for Patients. Patients should be directed to take trientine hydrochloride capsules on an empty stomach, at least one hour before meals or two hours after meals and at least one hour apart from any other drug, food, or milk. The capsules should be swallowed whole with water and should not be opened or chewed. Because of the potential for contact dermatitis, any site of exposure to the capsule contents should be washed with water promptly. For the first month of treatment, the patient should have his temperature taken nightly, and he should be asked to report any symptom such as fever or skin eruption.

LABORATORY TESTS SECTION.

Laboratory Tests. The most reliable index for monitoring treatment is the determination of free copper in the serum, which equals the difference between quantitatively determined total copper and ceruloplasmin-copper. Adequately treated patients will usually have less than 10 mcg free copper/dL of serum. Therapy may be monitored with 24-hour urinary copper analysis periodically (i.e., every to 12 months). Urine must be collected in copper-free glassware. Since low copper diet should keep copper absorption down to less than one milligram day, the patient probably will be in the desired state of negative copper balance if 0.5 to 1.0 milligram of copper is present in 24-hour collection of urine.

NURSING MOTHERS SECTION.

Nursing Mothers. It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when trientine hydrochloride is administered to nursing mother.

OVERDOSAGE SECTION.

OVERDOSAGE. There is report of an adult woman who ingested 30 grams of trientine hydrochloride without apparent ill effects. No other data on overdosage are available.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL. CARTON Rising NDC 64980- 450 -01 Trientine Hydrochloride Capsules, USP 250 mg 100 Capsules Rx only CONTAINER LABEL Rising NDC 64980- 450 -01 Trientine Hydrochloride Capsules, USP 250 mg 100 Capsules Rx only Carton label. Label.

PEDIATRIC USE SECTION.

Pediatric Use. Controlled studies of the safety and effectiveness of trientine hydrochloride in pediatric patients have not been conducted. It has been used clinically in pediatric patients as young as years with no reported adverse experiences.

PRECAUTIONS SECTION.

PRECAUTIONS. General. There are no reports of hypersensitivity in patients who have been administered trientine hydrochloride for Wilsons disease. However, there have been reports of asthma, bronchitis and dermatitis occurring after prolonged environmental exposure in workers who use trientine hydrochloride as hardener of epoxy resins. Patients should be observed closely for signs of possible hypersensitivity.. Information for Patients. Patients should be directed to take trientine hydrochloride capsules on an empty stomach, at least one hour before meals or two hours after meals and at least one hour apart from any other drug, food, or milk. The capsules should be swallowed whole with water and should not be opened or chewed. Because of the potential for contact dermatitis, any site of exposure to the capsule contents should be washed with water promptly. For the first month of treatment, the patient should have his temperature taken nightly, and he should be asked to report any symptom such as fever or skin eruption.. Laboratory Tests. The most reliable index for monitoring treatment is the determination of free copper in the serum, which equals the difference between quantitatively determined total copper and ceruloplasmin-copper. Adequately treated patients will usually have less than 10 mcg free copper/dL of serum. Therapy may be monitored with 24-hour urinary copper analysis periodically (i.e., every to 12 months). Urine must be collected in copper-free glassware. Since low copper diet should keep copper absorption down to less than one milligram day, the patient probably will be in the desired state of negative copper balance if 0.5 to 1.0 milligram of copper is present in 24-hour collection of urine.. Drug Interactions. In general, mineral supplements should not be given since they may block the absorption of trientine hydrochloride. However, iron deficiency may develop, especially in children and menstruating or pregnant women, or as result of the low copper diet recommended for Wilsons disease. If necessary, iron may be given in short courses, but since iron and trientine hydrochloride each inhibit absorption of the other, two hours should elapse between administration of trientine hydrochloride capsules and iron. It is important that trientine hydrochloride capsules be taken on an empty stomach, at least one hour before meals or two hours after meals and at least one hour apart from any other drug, food, or milk. This permits maximum absorption and reduces the likelihood of inactivation of the drug by metal binding in the gastrointestinal tract.. Carcinogenesis, Mutagenesis, Impairment of Fertility. Data on carcinogenesis, mutagenesis, and impairment of fertility are not available.. Pregnancy. Pregnancy Category Trientine hydrochloride was teratogenic in rats at doses similar to the human dose. The frequencies of both resorptions and fetal abnormalities, including hemorrhage and edema, increased while fetal copper levels decreased when trientine hydrochloride was given in the maternal diets of rats. There are no adequate and well-controlled studies in pregnant women. Trientine hydrochloride should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.. Nursing Mothers. It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when trientine hydrochloride is administered to nursing mother.. Pediatric Use. Controlled studies of the safety and effectiveness of trientine hydrochloride in pediatric patients have not been conducted. It has been used clinically in pediatric patients as young as years with no reported adverse experiences.. Geriatric Use. Clinical studies of trientine hydrochloride did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects. Other reported clinical experience is insufficient to determine differences in responses between the elderly and younger patients. In general, dose selection should be cautious, usually starting at the low end of the dosing range, reflecting the greater frequency of decreased hepatic, renal or cardiac function, and of concomitant disease or other drug therapy.

PREGNANCY SECTION.

Pregnancy. Pregnancy Category Trientine hydrochloride was teratogenic in rats at doses similar to the human dose. The frequencies of both resorptions and fetal abnormalities, including hemorrhage and edema, increased while fetal copper levels decreased when trientine hydrochloride was given in the maternal diets of rats. There are no adequate and well-controlled studies in pregnant women. Trientine hydrochloride should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.

SPL UNCLASSIFIED SECTION.

DOSAGE AND ADMINISTRATION. Systemic evaluation of dose and/or interval between dose has not been done. However, on limited clinical experience, the recommended initial dose of trientine hydrochloride is 500-750 mg /day for pediatric patients and 750-1250 mg/day for adults given in divided doses two, three or four times daily. This may be increased to maximum of 2000 mg/day for adults or 1500 mg/day for pediatric patients age 12 or under. The daily dose of trientine hydrochloride should be increased only when the clinical response is not adequate or the concentration of free serum copper is persistently above 20 mcg/dL. Optimal long-term maintenance dosage should be determined at to 12 month intervals (see PRECAUTIONS, Laboratory Tests). It is important that trientine hydrochloride capsules be given on an empty stomach, at least one hour before meals or two hours after meals and at least one hour apart from any other drug, food, or milk. The capsules should be swallowed whole with water and should not be opened or chewed.

WARNINGS SECTION.

WARNINGS. Patient experience with trientine hydrochloride is limited (see CLINICAL PHARMACOLOGY). Patients receiving trientine hydrochloride capsules should remain under regular medical supervision throughout the period of drug administration. Patients (especially women) should be closely monitored for evidence of iron deficiency anemia.