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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
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A Feasibility Phase II Study in the Treatment of Resected Cholangiocarcinoma, Gallbladder, Pancreatic and Ampullary Cancers

Phase 2
Completed
Conditions
Gallbladder Cancer
Cholangiocarcinoma Cancer
Ampullary Cancer
Pancreatic Cancer
Interventions
First Posted Date
2008-04-17
Last Posted Date
2015-05-27
Lead Sponsor
Washington University School of Medicine
Target Recruit Count
50
Registration Number
NCT00660699
Locations
🇺🇸

Washington University School of Medicine, St. Louis, Missouri, United States

Efficacy Study of Chemotherapy to Treat Ovarian Cancer Recurrence by Prolonging the Platinum Free Interval

Phase 3
Active, not recruiting
Conditions
Ovarian Cancer
Interventions
First Posted Date
2008-04-14
Last Posted Date
2023-11-13
Lead Sponsor
National Cancer Institute, Naples
Target Recruit Count
215
Registration Number
NCT00657878
Locations
🇮🇹

Universita Cattolica del Sacro Cuore, Roma, Italy

🇮🇹

Ospedale Mazzoni, Ascoli Piceno, Italy

🇮🇹

Ospedale Senatore Antonio Perrino, Brindisi, Italy

and more 35 locations

Antiangiogenic Peptide Vaccine Therapy With Gemcitabine in Treating Patient With Pancreatic Cancer (Phase1/2)

Phase 1
Completed
Conditions
Pancreatic Cancer
Interventions
Biological: VEGFR1-1084, VEGFR2-169
Drug: Gemcitabine
First Posted Date
2008-04-10
Last Posted Date
2013-03-14
Lead Sponsor
Fukushima Medical University
Target Recruit Count
17
Registration Number
NCT00655785
Locations
🇯🇵

Fukushima Medical University Hospital, Fukushima, Japan

Ph2 Gem/Nov/Rituxan Rel/Ref MantleCell

Phase 2
Completed
Conditions
Relapsed or Refractory Mantle Cell Lymphoma (MCL)
Interventions
First Posted Date
2008-04-10
Last Posted Date
2016-11-03
Lead Sponsor
US Oncology Research
Target Recruit Count
16
Registration Number
NCT00656084

Lower Dose Chemotherapy Given More Frequent With Avastin to Treat Advanced Non-Squamous Non-Small Cell Lung Cancer

Phase 2
Completed
Conditions
Non-Small Cell Lung Cancer
Interventions
First Posted Date
2008-04-10
Last Posted Date
2017-07-17
Lead Sponsor
University of Alabama at Birmingham
Target Recruit Count
39
Registration Number
NCT00655850
Locations
🇺🇸

University of Alabama at Birmingham, Birmingham, Alabama, United States

Trial to Define the Safety and Tolerability of SGN-40, Rituximab, and Gemcitabine in Patients With DLBCL

Phase 1
Completed
Conditions
Lymphoma, Large B-Cell, Diffuse
Lymphoma, Non-Hodgkin
Interventions
First Posted Date
2008-04-10
Last Posted Date
2014-12-18
Lead Sponsor
Seagen Inc.
Target Recruit Count
33
Registration Number
NCT00655837
Locations
🇺🇸

Oncology Specialists, Park Ridge, Illinois, United States

🇺🇸

University of Alabama at Birmingham, Birmingham, Alabama, United States

🇺🇸

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

and more 6 locations

A Dose-Escalation to Rash Study of Tarceva (Erlotinib) Plus Gemcitabine in Patients With Metastatic Pancreatic Cancer

Phase 2
Completed
Conditions
Pancreatic Cancer
Interventions
Drug: Erlotinib, escalating dose
Drug: Erlotinib, standard dose
Drug: Gemcitabine
First Posted Date
2008-04-03
Last Posted Date
2015-02-11
Lead Sponsor
Hoffmann-La Roche
Target Recruit Count
467
Registration Number
NCT00652366

A Phase I Dose Escalation Study of SGN-35 Alone and in Combination With Gemcitabine for CD30-Positive Malignancies

Phase 1
Terminated
Conditions
Disease, Hodgkin
Lymphoma, Large-Cell, Anaplastic
Lymphoma, Non-Hodgkin
Interventions
Drug: SGN-35
Drug: gemcitabine
First Posted Date
2008-04-01
Last Posted Date
2014-12-18
Lead Sponsor
Seagen Inc.
Target Recruit Count
44
Registration Number
NCT00649584
Locations
🇺🇸

Stanford University Medical Center, Palo Alto, California, United States

🇺🇸

University of Miami, Miami, Florida, United States

🇺🇸

University of Alabama at Birmingham, Birmingham, Alabama, United States

and more 2 locations

Randomized Controlled Trial of Gemcitabine Combined With 125I Brachytherapy

Phase 3
Completed
Conditions
Locally Advanced Pancreatic Cancer
Interventions
Other: 125I brachytherapy PLUS gemcitabine
Drug: gemcitabine
First Posted Date
2008-03-27
Last Posted Date
2008-03-27
Lead Sponsor
Huazhong University of Science and Technology
Target Recruit Count
120
Registration Number
NCT00644618
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