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.
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.
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
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
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
Investigational Site Number 840004, Philadelphia, Pennsylvania, United States
Investigational Site Number 840005, Cincinnati, Ohio, United States
Investigational Site Number 840001, Nashville, Tennessee, United States
Cancer Therapy & Research Center at UTHSCSA, San Antonio, Texas, United States
Montefiore Medical Center, New York, New York, United States
Fondazione San Raffaele del Monte Tabor, Milan, Italy
Istituto Europeo Oncologico, Milan, Italy
Istituto Nazionale per la ricerca sul cancro, Genoa, Italy
Huntsman Cancer Institute, Salt Lake City, Utah, United States
ImClone Investigational Site, Preston, United Kingdom
ImClone Investigational site, Zagreb, Croatia
University of Miami, Miami, Florida, United States
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