Gemcitabine

Generic Name
Gemcitabine
Brand Names
Gemzar
Drug Type
Small Molecule
Chemical Formula
C9H11F2N3O4
CAS Number
95058-81-4
Unique Ingredient Identifier
B76N6SBZ8R
Background

Gemcitabine is a nucleoside analog and a chemotherapeutic agent. It was originally investigated for its antiviral effects, but it is now used as an anticancer therapy for various cancers. Gemcitabine is a cytidine analog with two fluorine atoms replacing the hydroxyl on the ribose. As a prodrug, gemcitabine is transformed into its active metabolites that work by replacing the building blocks of nucleic acids during DNA elongation, arresting tumour growth and promoting apoptosis of malignant cells. The structure, metabolism, and mechanism of action of gemcitabine are similar to cytarabine, but gemcitabine has a wider spectrum of antitumour activity.

Gemcitabine is marketed as Gemzar and it is available as intravenous injection. It is approved by the FDA to treat advanced ovarian cancer in combination with carboplatin, metastatic breast cancer in combination with paclitaxel, non-small cell lung cancer in combination with cisplatin, and pancreatic cancer as monotherapy. It is also being investigated in other cancer and tumour types.

Indication

Gemcitabine is a chemotherapeutic agent used as monotherapy or in combination with other anticancer agents.

In combination with carboplatin, it is indicated for the treatment of advanced ovarian cancer that has relapsed at least 6 months after completion of platinum-based therapy.

Gemcitabine in combination with paclitaxel is indicated for the first-line treatment of patients with metastatic breast cancer after failure of prior anthracycline-containing adjuvant chemotherapy, unless anthracyclines were clinically contraindicated.

In combination with cisplatin, gemcitabine is indicated for the first-line treatment of patients with inoperable, locally advanced (Stage IIIA or IIIB) or metastatic (Stage IV) non-small cell lung cancer (NSCLC). Dual therapy with cisplatin is also used to treat patients with Stage IV (locally advanced or metastatic) transitional cell carcinoma (TCC) of the bladder.

Gemcitabine is indicated as first-line treatment for patients with locally advanced (nonresectable Stage II or Stage III) or metastatic (Stage IV) adenocarcinoma of the pancreas. Gemcitabine is indicated for patients previously treated with fluorouracil.

Associated Conditions
Advanced Ovarian Cancer, Bladder Transitional Cell Carcinoma Stage IV, Carcinoma of the Head and Neck, Cervical Cancer, Cutaneous T-Cell Lymphoma (CTCL), Hodgkins Disease (HD), Mesothelioma, Metastatic Breast Cancer, Pancreatic Adenocarcinoma Locally Advanced, Small Cell Lung Cancer (SCLC), Stage IIIA Non Small Cell Lung Cancer, Stage IIIB Non-Small Cell Lung Cancer, Stage IV Non-small Cell Lung Cancer (NSCLC), Stage 4 Pancreatic adenocarcinoma
Associated Therapies
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Trial of Paclitaxel, Gemcitabine and Cisplatin in Patients With Relapsing Germ Cell Cancer

First Posted Date
2007-09-19
Last Posted Date
2017-10-03
Lead Sponsor
Rigshospitalet, Denmark
Target Recruit Count
8
Registration Number
NCT00531687
Locations
🇩🇰

Department of Oncology 5073, Rigshospitalet, Copenhagen, Denmark

Study With Gemcitabine and RTA 402 for Patients With Unresectable Pancreatic Cancer

First Posted Date
2007-09-14
Last Posted Date
2024-02-02
Lead Sponsor
Reata, a wholly owned subsidiary of Biogen
Target Recruit Count
33
Registration Number
NCT00529113
Locations
🇺🇸

Central Indiana Cancer Centers (US Oncology), Indianapolis, Indiana, United States

🇺🇸

Rocky Mountain Cancer Center (US Oncology), Denver, Colorado, United States

🇺🇸

Cancer Centers of Florida (US Oncology), Ocoee, Florida, United States

and more 2 locations

CAPPA-2: Cisplatin Added to Gemcitabine in Poor Performance Advanced NSCLC Patients

Phase 3
Terminated
Conditions
Interventions
First Posted Date
2007-09-10
Last Posted Date
2017-03-28
Lead Sponsor
National Cancer Institute, Naples
Target Recruit Count
57
Registration Number
NCT00526643
Locations
🇮🇹

Istituto Scientifico S. Raffaele, Milano, MI, Italy

🇮🇹

Istituto Oncologico di Bari, U.O. di Oncologia Medica e Sperimentale, Bari, BA, Italy

🇮🇹

Azienda Ospedaliera C. Poma, Mantova, MN, Italy

and more 12 locations

Open-label Study of CS-1008 for Subjects With Untreated and Unresectable Pancreatic Cancer

First Posted Date
2007-08-27
Last Posted Date
2021-04-08
Lead Sponsor
Daiichi Sankyo
Target Recruit Count
65
Registration Number
NCT00521404
Locations
🇺🇸

Georgia Cancer Specialists, Tucker, Georgia, United States

A Study of Tarceva (Erlotinib) and Gemcitabine in Treatment-Naive Patients With Advanced Non-Small Cell Lung Cancer.

First Posted Date
2007-08-17
Last Posted Date
2016-05-16
Lead Sponsor
Hoffmann-La Roche
Target Recruit Count
17
Registration Number
NCT00518011

Study to Assess the Safety & Tolerability of a PARP Inhibitor in Combination With Gemcitabine in Pancreatic Cancer

First Posted Date
2007-08-14
Last Posted Date
2013-12-20
Lead Sponsor
AstraZeneca
Target Recruit Count
68
Registration Number
NCT00515866
Locations
🇬🇧

Research Site, Oxford, United Kingdom

GEM vs GEM+TS-1 for Advanced Pancreatic Cancer

Phase 2
Completed
Conditions
Interventions
First Posted Date
2007-08-09
Last Posted Date
2011-06-28
Lead Sponsor
Japan Clinical Cancer Research Organization
Target Recruit Count
110
Registration Number
NCT00514163
Locations
🇯🇵

Cancer Institute Ariake Hospital, Tokyo, Japan

PVAG-14 Pilot for Intermediate Stages Hodgkin Lymphoma

First Posted Date
2007-08-08
Last Posted Date
2015-12-03
Lead Sponsor
University of Cologne
Registration Number
NCT00512980
Locations
🇩🇪

University of Cologne, Cologne, Germany

Abraxane, Avastin, and Gemcitabine as First-Line Therapy for Patients With Metastatic Breast Cancer

Phase 2
Completed
Conditions
Interventions
First Posted Date
2007-07-19
Last Posted Date
2017-05-12
Lead Sponsor
University of Miami
Target Recruit Count
30
Registration Number
NCT00503906
Locations
🇺🇸

University of Miami, Miami, Florida, United States

Doxil, Gemcitabine, and Velcade (PS341) in Advanced Cancer Patients

Phase 1
Completed
Conditions
Interventions
First Posted Date
2007-07-12
Last Posted Date
2013-02-13
Lead Sponsor
M.D. Anderson Cancer Center
Target Recruit Count
134
Registration Number
NCT00500422
Locations
🇺🇸

UT MD Anderson Cancer Center, Houston, Texas, United States

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