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Gemcitabine - Eli Lilly and Company/Genentech

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Drug Profile

Gemcitabine - Eli Lilly and Company/Genentech

Alternative Names: dFdC; dFdCTP; Gemcitabine Hydrochloride; Gemtro; Gemzar; LY-188011

Latest Information Update: 15 Oct 2024

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At a glance

  • Originator Eli Lilly and Company; Genentech; University of Innsbruck
  • Developer AstraZeneca; Beth Israel Deaconess Medical Center; Dana-Farber Cancer Institute; Eli Lilly and Company; Genentech; Mayo Clinic; National Cancer Institute (USA); University of Iowa
  • Class Amines; Antineoplastics; Deoxyribonucleosides; Fluorinated hydrocarbons; Ketones; Pyrimidine nucleosides; Pyrimidines; Small molecules
  • Mechanism of Action Antimetabolites; DNA synthesis inhibitors
  • Orphan Drug Status

    Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.

    No
  • New Molecular Entity Yes

Highest Development Phases

  • Marketed Biliary cancer; Bladder cancer; Breast cancer; Non-small cell lung cancer; Ovarian cancer; Pancreatic cancer
  • Phase III Cervical cancer
  • Phase II Cholangiocarcinoma; Lymphoma; Renal cell carcinoma
  • No development reported Head and neck cancer; Sarcoma; Solid tumours

Most Recent Events

  • 03 Oct 2024 Cheplapharm acquires worldwide (except South Korea) rights to Gemcitabine from Eli Lilly and Company
  • 21 Aug 2023 Phase-II clinical trials in Cholangiocarcinoma (Late-stage disease, Metastatic disease, Inoperable/Unresectable) in USA (IV) (NCT05655949)
  • 06 Jan 2020 No development reported - Phase-I/II for Sarcoma (Combination therapy, First-line therapy, In the elderly, Inoperable/Unresectable, Late-stage disease, Metastatic disease, In adults) in USA (IV) (Eli-Lilly pipeline, January 2020)

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