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
-

Phase III of RRM1 & ERCC1 Directed Customized Chemotherapy for the Treatment of Patients With NSCLC

First Posted Date
2007-07-11
Last Posted Date
2014-07-09
Lead Sponsor
H. Lee Moffitt Cancer Center and Research Institute
Target Recruit Count
275
Registration Number
NCT00499109
Locations
🇺🇸

Leesburg Regional Medical Center, Leesburg, Florida, United States

🇺🇸

Center for Cancer Care & Research/Watson, Lakeland, Florida, United States

🇺🇸

Johns Hopkins Sidney Kimmell Comprehensive Cancer Center, Baltimore, Maryland, United States

and more 6 locations

Phase III of Gemcitabine Vs TS-1 Vs Gemcitabine Plus TS-1 in Pancreatic Cancer

First Posted Date
2007-07-09
Last Posted Date
2012-11-02
Lead Sponsor
Taiho Pharmaceutical Co., Ltd.
Target Recruit Count
834
Registration Number
NCT00498225
Locations
🇨🇳

Chang Gung Memorial Hospital, Kaohsiung, No.123, Ta-Pei Rd., Niao-Sung Hsiang, Kaohsiung Hsien, Taiwan

🇨🇳

Chung-Ho Memorial Hospital, Kaohsiung Medical University, No.100, Tzyou 1st Rd., Kaohsiung, Taiwan

🇯🇵

National Cancer Center Hospital, Tokyo, Japan

and more 9 locations

Capecitabine, Gemcitabine, and Bevacizumab in Combination for Patients With Sarcomatoid Renal Cell Carcinoma

First Posted Date
2007-07-04
Last Posted Date
2017-07-19
Lead Sponsor
M.D. Anderson Cancer Center
Target Recruit Count
34
Registration Number
NCT00496587
Locations
🇺🇸

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

1st or 2nd Line MBC (Metastatic Breast Cancer) With Previous Avastin (Bevacizumab) Therapy

First Posted Date
2007-06-28
Last Posted Date
2014-05-20
Lead Sponsor
Accelerated Community Oncology Research Network
Target Recruit Count
160
Registration Number
NCT00493636
Locations
🇺🇸

Compassionate Cancer Care-Fountain Valley, Fountain Valley, California, United States

🇺🇸

Hematology Oncology Associates of New York, East Syracuse, New York, United States

🇺🇸

California Cancer Care, Greenbrae, California, United States

and more 40 locations

Pemetrexed Plus Gemcitabine in Renal Cell Cancer

Phase 2
Terminated
Conditions
Interventions
First Posted Date
2007-06-25
Last Posted Date
2013-04-24
Lead Sponsor
M.D. Anderson Cancer Center
Target Recruit Count
16
Registration Number
NCT00491075
Locations
🇺🇸

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

Neoadjuvant Chemo (Gemcitabine and Cisplatin) With Radical Cystectomy or Radiotherapy in Patients With Bladder Cancer

Phase 2
Completed
Conditions
First Posted Date
2007-06-25
Last Posted Date
2007-06-25
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
2
Registration Number
NCT00490880
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., Warsaw, Poland

Trial of Perioperative Chemotherapy (Gemcitabine and Cisplatin) and Adjuvant Chemoradiotherapy (With Weekly Low Dose Gemcitabine) in Patients With Lung Cancer With Positive Nodes

Phase 2
Completed
Conditions
First Posted Date
2007-06-25
Last Posted Date
2007-06-25
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
13
Registration Number
NCT00490659
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., Lublin, Poland

Intravesical Chemotherapy Treatment of Superficial Bladder Cancer

Phase 2
Completed
Conditions
First Posted Date
2007-06-25
Last Posted Date
2007-06-25
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
8
Registration Number
NCT00491114
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., Varese, Italy

Treatment of Paclitaxel Plus Carboplatin Followed by Gemcitabine Plus Carboplatin for Patients With Epithelial Ovarian Cancer

Phase 2
Completed
Conditions
First Posted Date
2007-06-25
Last Posted Date
2007-06-25
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
7
Registration Number
NCT00490711
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., Bratislava, Slovakia

Cisplatin With Gemcitabine With Dexamethasone in Patients With Aggressive Non-Hodgkin's Lymphoma

Phase 2
Completed
Conditions
First Posted Date
2007-06-25
Last Posted Date
2007-06-25
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
10
Registration Number
NCT00491127
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., Madrid, Spain

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