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 and Cisplatin in Patients With Inoperable Biliary Tract Carcinomas

Phase 2
Completed
Conditions
First Posted Date
2007-06-22
Last Posted Date
2007-06-22
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
39
Registration Number
NCT00490399
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., Seoul, Korea, Republic of

Trial Comparing 3 and 4 Week Regimen of Gemcitabine and Cisplatin in Patients With Lung Cancer

Phase 2
Completed
Conditions
First Posted Date
2007-06-22
Last Posted Date
2007-06-22
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
100
Registration Number
NCT00489996
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., Shanghai, China

Trial of Pemetrexed or Pemetrexed With Gemcitabine for Patients With Advanced Lung Cancer Who Are Not Eligible for Platinum-Based Chemotherapy and Have Not Previously Been Treated With Chemotherapy

Phase 2
Completed
Conditions
First Posted Date
2007-06-22
Last Posted Date
2007-06-22
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
91
Registration Number
NCT00489983
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., London, United Kingdom

Phase III Trial of Gemcitabine, Curcumin and Celebrex in Patients With Advance or Inoperable Pancreatic Cancer

Phase 3
Conditions
First Posted Date
2007-06-14
Last Posted Date
2007-06-14
Lead Sponsor
Tel-Aviv Sourasky Medical Center
Registration Number
NCT00486460
Locations
🇮🇱

Sourasky Medical Center, Tel Aviv, Israel

A Phase I Trial of Capecitabine in Combination With Gemcitabine and Erlotinib for Advanced Pancreatic Cancer

First Posted Date
2007-05-31
Last Posted Date
2012-11-08
Lead Sponsor
H. Lee Moffitt Cancer Center and Research Institute
Target Recruit Count
20
Registration Number
NCT00480584
Locations
🇺🇸

H. Lee Moffitt Cancer Center & Research Institute, Tampa, Florida, United States

Gemcitabine/Vinorelbine Versus Gemcitabine/Cisplatin Versus Gemcitabine/Capecitabine in Metastatic Breast Cancer

Phase 2
Completed
Conditions
First Posted Date
2007-05-31
Last Posted Date
2010-10-28
Lead Sponsor
Ludwig-Maximilians - University of Munich
Target Recruit Count
141
Registration Number
NCT00480597

Bortezomib With Gemcitabine/Doxorubicin in Patients With Urothelial Cancer and Other Solid Tumors

Phase 1
Active, not recruiting
Conditions
Interventions
First Posted Date
2007-05-25
Last Posted Date
2024-10-26
Lead Sponsor
M.D. Anderson Cancer Center
Target Recruit Count
80
Registration Number
NCT00479128
Locations
🇺🇸

University of Texas MD Anderson Cancer Center, Houston, Texas, United States

Post-transplant Autologous Cytokine-induced Killer (CIK) Cells for Treatment of High Risk Hematologic Malignancies

First Posted Date
2007-05-22
Last Posted Date
2017-01-11
Lead Sponsor
Sally Arai
Target Recruit Count
22
Registration Number
NCT00477035
Locations
🇺🇸

Stanford University School of Medicine, Stanford, California, United States

A Phase II Safety and Tolerability Study of Bevacizumab When Added to Single-agent Chemotherapy to Treat Patient With Breast Cancer Metastatic to Brain

First Posted Date
2007-05-22
Last Posted Date
2013-07-17
Lead Sponsor
Duke University
Target Recruit Count
16
Registration Number
NCT00476827
Locations
🇺🇸

Duke University Medical Center, Durham, North Carolina, United States

🇺🇸

Palm Beach Cancer Center Institute, West Palm Beach, Florida, United States

🇺🇸

Presbyterian Health Care, Charlotte, North Carolina, United States

and more 1 locations

A Study of XL844 Administered as a Single Agent and in Combination With Gemcitabine in Adults With Advanced Malignancies

Phase 1
Terminated
Conditions
Interventions
First Posted Date
2007-05-21
Last Posted Date
2015-08-21
Lead Sponsor
Exelixis
Target Recruit Count
28
Registration Number
NCT00475917
Locations
🇺🇸

Memorial Sloan-Kettering Cancer Center, New York, New York, United States

🇺🇸

M.D. Anderson Cancer Center, Houston, Texas, United States

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