MedPath

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
-

Trial of GSK1120212 and GSK1120212 in Combination With GEM in Japanese Subjects With Solid Tumors

Phase 1
Completed
Conditions
Solid Tumours
Interventions
First Posted Date
2011-03-28
Last Posted Date
2017-11-13
Lead Sponsor
GlaxoSmithKline
Target Recruit Count
19
Registration Number
NCT01324258
Locations
🇯🇵

GSK Investigational Site, Tokyo, Japan

Ganitumab in Locally Advanced Unresectable Adenocarcinoma of the Pancreas

Phase 2
Terminated
Conditions
Unresectable
Adenocarcinoma of the Pancreas
Locally Advanced
Interventions
Drug: Gemcitabine
Drug: Placebo
Drug: AMG 479
First Posted Date
2011-03-18
Last Posted Date
2024-11-08
Lead Sponsor
NantBioScience, Inc.
Target Recruit Count
10
Registration Number
NCT01318642
Locations
🇬🇧

Guys Hospital, London, United Kingdom

🇬🇧

Research Site, Preston, United Kingdom

Gemcitabine and CT-011 for Resected Pancreatic Cancer

Phase 2
Terminated
Conditions
Pancreatic Cancer
Pancreatic Neoplasms
Pancreas Cancer
Neoplasms Pancreatic
Cancer of the Pancreas
Interventions
Biological: CT-011
Drug: Gemcitabine
First Posted Date
2011-03-11
Last Posted Date
2019-07-10
Lead Sponsor
Augusta University
Target Recruit Count
2
Registration Number
NCT01313416
Locations
🇺🇸

Georgia Regents University, Augusta, Georgia, United States

Gemcitabine, Oxaliplatin and Panitumumab in Kras/B-raf Wild-Type Biliary Track and Gallbladder Cancer

Phase 2
Completed
Conditions
Biliary Tract Cancer
Gallbladder Cancer
Interventions
First Posted Date
2011-03-04
Last Posted Date
2016-08-17
Lead Sponsor
University of Rochester
Target Recruit Count
31
Registration Number
NCT01308840
Locations
🇺🇸

Dana-Farber / Harvard Cancer Center, Boston, Massachusetts, United States

🇺🇸

University of Rochester Medical Center, Rochester, New York, United States

A Trial Comparing Gemcitabine With and Without IMM-101 in Advanced Pancreatic Cancer

Phase 2
Completed
Conditions
Advanced Pancreatic Cancer
Interventions
Biological: IMM-101
Drug: Gemcitabine
First Posted Date
2011-02-24
Last Posted Date
2021-11-10
Lead Sponsor
Immodulon Therapeutics Ltd
Target Recruit Count
110
Registration Number
NCT01303172
Locations
🇮🇪

St Vicents University Hospital, Dublin, Ireland

🇪🇸

Hospital General de Alicante, Alicante, Spain

🇪🇸

Hospital Miguel Servet, Zaragoza, Spain

and more 18 locations

C14 Study in Oncology Patients With Advanced and/or Metastatic Solid Tumors

Phase 1
Completed
Conditions
Advanced Cancer
Interventions
First Posted Date
2011-02-15
Last Posted Date
2019-01-07
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
3
Registration Number
NCT01296568
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., Bruderholz, Switzerland

Regional Chemotherapy in Locally Advanced Pancreatic Cancer: RECLAP Trial

Phase 1
Completed
Conditions
Unresectable or Borderline Resectable Pancreatic Ca
Histologically or Cytologically Confirmed Pancreatic Ca
Interventions
First Posted Date
2011-02-11
Last Posted Date
2019-11-13
Lead Sponsor
National Cancer Institute (NCI)
Target Recruit Count
7
Registration Number
NCT01294358
Locations
🇺🇸

National Institutes of Health Clinical Center, 9000 Rockville Pike, Bethesda, Maryland, United States

Phase I Study of Gemcitabine or S-1 Adjuvant Therapy After Hemihepatectomy for Biliary Tract Cancer

Phase 1
Completed
Conditions
Biliary Tract Cancer
Interventions
First Posted Date
2011-02-08
Last Posted Date
2014-10-23
Lead Sponsor
Kansai Hepatobiliary Oncology Group
Target Recruit Count
6
Registration Number
NCT01291615
Locations
🇯🇵

Osaka University, Graduate School of Medicine, Osaka, Japan

A Study of LY2801653 in Advanced Cancer

Phase 1
Completed
Conditions
Cancer
Interventions
First Posted Date
2011-01-27
Last Posted Date
2018-02-20
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
190
Registration Number
NCT01285037
Locations
🇺🇸

Arizona Cancer Center, Tucson, Arizona, United States

🇺🇸

Mount Sinai Medical Center, New York, New York, United States

🇺🇸

Fox Chase Cancer Center, Philadelphia, Pennsylvania, United States

and more 4 locations

A Safety Study in Participants With Advanced Solid Tumors

First Posted Date
2011-01-27
Last Posted Date
2019-01-10
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
234
Registration Number
NCT01284335
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., Yakima, Washington, United States

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