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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
-

Veliparib, Cisplatin, and Gemcitabine Hydrochloride in Treating Patients With Advanced Biliary, Pancreatic, Urothelial, or Non-Small Cell Lung Cancer

Phase 1
Terminated
Conditions
Advanced Adult Primary Liver Cancer
Localized Unresectable Adult Primary Liver Cancer
Metastatic Transitional Cell Cancer of the Renal Pelvis and Ureter
Regional Transitional Cell Cancer of the Renal Pelvis and Ureter
Stage III Bladder Cancer
Stage III Pancreatic Cancer
Stage IIIA Non-small Cell Lung Cancer
Stage IIIB Non-small Cell Lung Cancer
Stage IV Bladder Cancer
Stage IV Non-small Cell Lung Cancer
Interventions
Drug: gemcitabine hydrochloride
Drug: veliparib
Other: diagnostic laboratory biomarker analysis
Other: pharmacological study
Drug: cisplatin
First Posted Date
2011-01-25
Last Posted Date
2013-07-02
Lead Sponsor
National Cancer Institute (NCI)
Target Recruit Count
44
Registration Number
NCT01282333
Locations
🇺🇸

University of Pittsburgh, Pittsburgh, Pennsylvania, United States

🇺🇸

Penn State Milton S Hershey Medical Center, Hershey, Pennsylvania, United States

🇺🇸

Dana-Farber Cancer Institute, Boston, Massachusetts, United States

Tissue Pharmacokinetics of Intraoperative Gemcitabine in Resectable Adenocarcinoma of the Pancreas

Early Phase 1
Terminated
Conditions
Pancreatic Cancer
Interventions
First Posted Date
2011-01-13
Last Posted Date
2019-05-02
Lead Sponsor
M.D. Anderson Cancer Center
Target Recruit Count
18
Registration Number
NCT01276613
Locations
🇺🇸

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

Trial of Gemcitabine With or Without Bavituximab in Patients With Previously Untreated Stage IV Pancreatic Cancer

Phase 2
Completed
Conditions
Metastatic Pancreatic Cancer
Interventions
Biological: bavituximab
Drug: Gemcitabine
First Posted Date
2011-01-10
Last Posted Date
2017-04-19
Lead Sponsor
Peregrine Pharmaceuticals
Target Recruit Count
70
Registration Number
NCT01272791
Locations
🇺🇸

Northeast Georgia Medical Center, Gainesville, Georgia, United States

🇺🇸

Vasicek Cancer Center at Scott & White Memorial Hospital, Temple, Texas, United States

🇺🇦

Municipal Institution "Cherkasy Regional Oncology Dispensary" of Cherkasy Regional Council, Cherkasy, Ukraine

and more 16 locations

HLA-A*0201 Restricted Peptide Vaccine Therapy With Gemcitabine With Gemcitabine in Patient Pancreatic Cancer (Phase1)

Phase 1
Conditions
Pancreatic Cancer
Interventions
Biological: VEGFR1, VEGFR2
Drug: Gemcitabine
First Posted Date
2010-12-24
Last Posted Date
2010-12-24
Lead Sponsor
Fukushima Medical University
Target Recruit Count
6
Registration Number
NCT01266720
Locations
🇯🇵

Fukushima Medical University Hospital, Fukushima, Japan

Gemcitabine and Cisplatin as Neoadjuvant Chemotherapy in Patients With High-Grade Upper Tract Urothelial Carcinoma

Phase 2
Active, not recruiting
Conditions
Urothelial Carcinoma
Interventions
First Posted Date
2010-12-16
Last Posted Date
2025-01-07
Lead Sponsor
Memorial Sloan Kettering Cancer Center
Target Recruit Count
57
Registration Number
NCT01261728
Locations
🇺🇸

Memorial Sloan Kettering Bergen, Montvale, New Jersey, United States

🇺🇸

Memorial Sloan Kettering Westchester, Harrison, New York, United States

🇺🇸

Hartford Hospital (Data Collection Only), Hartford, Connecticut, United States

and more 6 locations

A Phase I Dose Escalation Trial of Afatinib Plus Gemcitabine or Plus Docetaxel

Completed
Conditions
Neoplasms
Interventions
First Posted Date
2010-12-02
Last Posted Date
2016-05-30
Lead Sponsor
Boehringer Ingelheim
Target Recruit Count
94
Registration Number
NCT01251653
Locations
🇫🇷

1200.93.33002 Boehringer Ingelheim Investigational Site, Dijon, France

🇫🇷

1200.93.33001 Boehringer Ingelheim Investigational Site, Saint-Herblain cedex, France

🇫🇷

1200.93.33003 Boehringer Ingelheim Investigational Site, Toulouse, France

ABC-04 a Study of Cisplatin, Gemcitabine and Selumetinib in Patients With Advanced Biliary Tract Cancer

Phase 1
Completed
Conditions
Biliary Tract Neoplasms
Cholangiocarcinoma
Gallbladder Neoplasms
Interventions
First Posted Date
2010-11-17
Last Posted Date
2016-05-13
Lead Sponsor
University College, London
Target Recruit Count
13
Registration Number
NCT01242605
Locations
🇬🇧

University College London Hospital, London, United Kingdom

🇬🇧

Hammersmith Hospital, London, United Kingdom

🇬🇧

The Christie Hospital, Manchester, United Kingdom

A Phase II Study to Assess the Efficacy and Safety of Preoperative Chemo With Radiation Therapy for Patients With Borderline Unresectable Adenocarcinoma of the Pancreas

Phase 2
Terminated
Conditions
Pancreatic Cancer
Interventions
Drug: Gemcitabine
Radiation: Radiation therapy
Procedure: pancreaticoduodenectomy
First Posted Date
2010-11-15
Last Posted Date
2019-12-10
Lead Sponsor
University of Arkansas
Target Recruit Count
10
Registration Number
NCT01240304
Locations
🇺🇸

University of Arkansas for Medical Sciences, Little Rock, Arkansas, United States

High-Dose Gemcitabine, Busulfan and Melphalan With Hematopoietic-Cell Support for Patients With Poor-Risk Myeloma

Phase 2
Completed
Conditions
Myeloma
Interventions
First Posted Date
2010-11-10
Last Posted Date
2020-05-05
Lead Sponsor
M.D. Anderson Cancer Center
Target Recruit Count
75
Registration Number
NCT01237951
Locations
🇺🇸

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

Study of GSK1120212 Plus Gemcitabine vs Placebo Plus Gemcitabine in Metastatic Pancreatic Cancer

Phase 2
Completed
Conditions
Cancer
Interventions
First Posted Date
2010-11-01
Last Posted Date
2013-09-26
Lead Sponsor
GlaxoSmithKline
Target Recruit Count
160
Registration Number
NCT01231581
Locations
🇨🇳

GSK Investigational Site, Taipei, Taiwan

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