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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 Gemcitabine With or Without MSC1936369B in Pancreatic Cancer

Phase 1
Completed
Conditions
Pancreatic Adenocarcinoma
Interventions
First Posted Date
2009-11-19
Last Posted Date
2017-07-13
Lead Sponsor
EMD Serono
Target Recruit Count
141
Registration Number
NCT01016483
Locations
🇺🇸

For Recruiting Locations in the United States, please Contact U.S. Medical Information, Rockland, Massachusetts, United States

🇩🇪

For Recruiting Locations outside the United States, Please contact the Merck KGaA Communication Center, Darmstadt, Germany

A Study of the Safety and Pharmacokinetics of AGS-8M4 Given in Combination With Chemotherapy in Women With Ovarian Cancer

Phase 1
Terminated
Conditions
Carcinoma
Ovarian Cancer
Ovarian Diseases
Ovarian Neoplasms
Interventions
First Posted Date
2009-11-18
Last Posted Date
2013-02-27
Lead Sponsor
Astellas Pharma Inc
Target Recruit Count
4
Registration Number
NCT01016054

Erlotinib, Gemcitabine and Nab-Paclitaxel in Advanced Pancreatic Cancer

Phase 1
Completed
Conditions
Advanced Pancreatic Cancer
Interventions
First Posted Date
2009-11-10
Last Posted Date
2024-11-21
Lead Sponsor
OSI Pharmaceuticals
Target Recruit Count
19
Registration Number
NCT01010945
Locations
🇺🇸

University of Colorado Cancer Center, Aurora, Colorado, United States

🇺🇸

Desert Comprehensive Cancer Center, Palm Springs, California, United States

🇺🇸

University of North Carolina, Chapel Hill, North Carolina, United States

and more 2 locations

A Study Comparing Two Different Chemotherapy Types in Chinese Patients With Advanced Non Small Cell Lung Cancer

Phase 3
Completed
Conditions
Non Small Cell Lung Cancer
Interventions
First Posted Date
2009-11-01
Last Posted Date
2013-12-13
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
256
Registration Number
NCT01005680
Locations
🇨🇳

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Sichuan, China

Dose-Escalation, Safety, Pharmacokinetics Study of Cabazitaxel With Gemcitabine In Patients With Solid Tumor

Phase 1
Terminated
Conditions
Neoplasms, Malignant
Interventions
First Posted Date
2009-10-26
Last Posted Date
2013-09-11
Lead Sponsor
Sanofi
Target Recruit Count
19
Registration Number
NCT01001221
Locations
🇺🇸

Investigational Site Number 840004, Philadelphia, Pennsylvania, United States

🇺🇸

Investigational Site Number 840005, Cincinnati, Ohio, United States

🇺🇸

Investigational Site Number 840001, Nashville, Tennessee, United States

and more 1 locations

A Study of REOLYSIN® in Combination With Gemcitabine in Patients With Advanced Pancreatic Adenocarcinoma

Phase 2
Completed
Conditions
Metastatic Pancreatic Adenocarcinoma
First Posted Date
2009-10-20
Last Posted Date
2015-04-10
Lead Sponsor
Oncolytics Biotech
Target Recruit Count
34
Registration Number
NCT00998322
Locations
🇺🇸

Cancer Therapy & Research Center at UTHSCSA, San Antonio, Texas, United States

🇺🇸

Montefiore Medical Center, New York, New York, United States

NGR-hTNF in Combination With Standard Chemotherapy to Treat Patients With Advanced Non-small Cell Lung Cancer

Phase 2
Completed
Conditions
Non-small Cell Lung Cancer
Interventions
First Posted Date
2009-10-14
Last Posted Date
2018-09-27
Lead Sponsor
AGC Biologics S.p.A.
Target Recruit Count
121
Registration Number
NCT00994097
Locations
🇮🇹

Fondazione San Raffaele del Monte Tabor, Milan, Italy

🇮🇹

Istituto Europeo Oncologico, Milan, Italy

🇮🇹

Istituto Nazionale per la ricerca sul cancro, Genoa, Italy

and more 1 locations

Chemoradiation +Gemcitabine +Continuous 5-FU (Fluorouracil) Followed by High Dose Brachytherapy/Stereotactic Radiation Boost in Locally Advanced Intra/Extrahepatic Cholangiocarcinoma

Phase 2
Terminated
Conditions
Cancer
Interventions
Drug: Fluorouracil (5-FU)
Radiation: Brachytherapy or SBRT (Stereotactic body radiation therapy)
Drug: Gemcitabine
First Posted Date
2009-09-24
Last Posted Date
2015-08-19
Lead Sponsor
University of Utah
Target Recruit Count
1
Registration Number
NCT00983541
Locations
🇺🇸

Huntsman Cancer Institute, Salt Lake City, Utah, United States

First-line Treatment of Participants With Stage IV Squamous Non-Small Cell Lung Cancer With Necitumumab and Gemcitabine-Cisplatin

Phase 3
Completed
Conditions
Non Small Cell Lung Cancer
Interventions
Biological: Necitumumab
Drug: Gemcitabine
Drug: Cisplatin
First Posted Date
2009-09-22
Last Posted Date
2024-08-02
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
1093
Registration Number
NCT00981058
Locations
🇬🇧

ImClone Investigational Site, Preston, United Kingdom

🇭🇷

ImClone Investigational site, Zagreb, Croatia

A Study of Combination of Gemcitabine, Oxaliplatin (GEMOX)-Sorafenib in Patients With Advanced Biliary Tract Cancer

Phase 1
Terminated
Conditions
Cholangiocarcinoma
Biliary Tract Cancer
Gallbladder Cancer
Interventions
First Posted Date
2009-08-10
Last Posted Date
2018-01-03
Lead Sponsor
University of Miami
Target Recruit Count
9
Registration Number
NCT00955721
Locations
🇺🇸

University of Miami, Miami, Florida, United States

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