lurbinectedin 🐶 Veterinary Use | Indications/Contra | FAERs-F | FAERs-M | Orange Bk | BioActivity |

Stem definitionDrug idCAS RN
ecteinascidin derivatives 5398 497871-47-3

Description:

MoleculeDescription

Molfile Inchi Smiles

Synonyms:

  • lurbinectedin
  • zepzelca
  • PM01183
  • PM-01183
  • LY-01017
  • PM-1183
  • tryptamicidin
  • zepsyre
Lurbinectedin is an alkylating drug that binds guanine residues in the minor groove of DNA, forming adducts and resulting in a bending of the DNA helix towards the major groove. Adduct formation triggers a cascade of events that can affect the subsequent activity of DNA binding proteins, including some transcription factors, and DNA repair pathways, resulting in perturbation of the cell cycle and eventual cell death.
  • Molecular weight: 784.88
  • Formula: C41H44N4O10S
  • CLOGP: 3.67
  • LIPINSKI: 2
  • HAC: 14
  • HDO: 4
  • TPSA: 164.28
  • ALOGS: -4.08
  • ROTB: 4

  • Status: ONP

  • Legend:
    OFP - off patent
    OFM - off market
    ONP - on patent

Drug dosage:

None

ADMET properties:

PropertyValueReference
BDDCS (Biopharmaceutical Drug Disposition Classification System) 2 Bocci G, Oprea TI, Benet LZ

Approvals:

DateAgencyCompanyOrphan
June 15, 2020 FDA JAZZ

FDA Adverse Event Reporting System (Female)

None

FDA Adverse Event Reporting System (Male)

None

FDA Adverse Event Reporting System (Geriatric)

None

FDA Adverse Event Reporting System (Pediatric)

None

Pharmacologic Action:

SourceCodeDescription
ATC L01XX69 ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS
ANTINEOPLASTIC AGENTS
OTHER ANTINEOPLASTIC AGENTS
Other antineoplastic agents
FDA MoA N0000000236 Alkylating Activity
FDA EPC N0000175558 Alkylating Drug

Drug Use | Suggest Off label Use Form| |View source of the data|

DiseaseRelationSNOMED_IDDOID
Small cell carcinoma of lung indication 254632001 DOID:5409




🐶 Veterinary Drug Use

None

🐶 Veterinary products

None

Acid dissociation constants calculated using MoKa v3.0.0

None

Orange Book patent data (new drug applications)

Formulation strengthTrade nameApplicantApplication numberApproval dateTypeDose formRoutePatent numberPatent expiration datePatent use
4MG/VIAL ZEPZELCA JAZZ N213702 June 15, 2020 RX POWDER INTRAVENOUS 7763615 Dec. 13, 2024 TREATMENT OF ADULT PATIENTS WITH SMALL CELL LUNG CANCER (SCLC) WITH DISEASE PROGRESSION ON OR AFTER PLATINUM-BASED CHEMOTHERAPY.

Orange Book exclusivity data (new drug applications)

Formulation strengthTrade nameApplicantApplication numberApproval dateTypeDose formRouteExclusivity dateDescription
4MG/VIAL ZEPZELCA JAZZ N213702 June 15, 2020 RX POWDER INTRAVENOUS June 15, 2025 NEW CHEMICAL ENTITY
4MG/VIAL ZEPZELCA JAZZ N213702 June 15, 2020 RX POWDER INTRAVENOUS June 15, 2027 INDICATED FOR THE TREATMENT OF ADULT PATIENTS WITH METASTATIC SMALL CELL LUNG CANCER (SCLC) WITH DISEASE PROGRESSION ON OR AFTER PLATINUM-BASED CHEMOTHERAPY

Bioactivity Summary:

None

External reference:

IDSource
D11644 KEGG_DRUG
2CN60TN6ZS UNII
C3898565 UMLSCUI
CHEMBL4297516 ChEMBL_ID
57327016 PUBCHEM_CID
DB12674 DRUGBANK_ID
10681 IUPHAR_LIGAND_ID
018414 NDDF
879925002 SNOMEDCT_US
879932006 SNOMEDCT_US
4039494 VANDF
2374729 RXNORM
335658 MMSL
38550 MMSL
d09579 MMSL
C568606 MESH_SUPPLEMENTAL_RECORD_UI
9397 INN_ID

Pharmaceutical products:

ProductCategoryIngredientsNDCFormQuantityRouteMarketingLabel
ZEPZELCA HUMAN PRESCRIPTION DRUG LABEL 1 68727-712 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION 0.50 mg INTRAVENOUS NDA 29 sections
ZEPZELCA HUMAN PRESCRIPTION DRUG LABEL 1 68727-712 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION 0.50 mg INTRAVENOUS NDA 29 sections
ZEPZELCA HUMAN PRESCRIPTION DRUG LABEL 1 68727-712 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION 0.50 mg INTRAVENOUS NDA 29 sections