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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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Gemcitabine/Capecitabine Followed by SBRT in Pancreatic Adenocarcinoma

Phase 2
Completed
Conditions
Pancreatic Cancer
Interventions
Drug: Gemcitabine
Drug: Capecitabine
Radiation: Stereotactic Body Radiation Therapy (SBRT)
First Posted Date
2011-05-25
Last Posted Date
2022-03-08
Lead Sponsor
David A. Clump, MD, PhD
Target Recruit Count
35
Registration Number
NCT01360593
Locations
🇺🇸

UPMC Cancer Centers, Pittsburgh, Pennsylvania, United States

A Study Evaluating the Safety, Tolerability, and Pharmacokinetics of GDC-0425 Administered With and Without Gemcitabine in Patients With Refractory Solid Tumors or Lymphoma

Phase 1
Completed
Conditions
Solid Tumor
Interventions
First Posted Date
2011-05-25
Last Posted Date
2017-04-12
Lead Sponsor
Genentech, Inc.
Target Recruit Count
40
Registration Number
NCT01359696
Locations
🇺🇸

Sarah Cannon Cancer Center, Nashville, Tennessee, United States

🇺🇸

Karmanos Cancer Institute.., Detroit, Michigan, United States

🇫🇷

Institut Gustave Roussy; Ser. de Med. Nucleaire; Cancerologie Endo, Villejuif, France

A Drug Interaction Study to Assess the Effect of LY2603618 on the Metabolic Pathway of Desipramine

Phase 1
Completed
Conditions
Cancer
Interventions
First Posted Date
2011-05-24
Last Posted Date
2018-10-25
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
20
Registration Number
NCT01358968
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., Memphis, Tennessee, United States

Neoadjuvant Chemotherapy With Docetaxel and Gemcitabine in Locally Advanced Breast Cancer

Phase 2
Conditions
Breast Cancer Stage II
Breast Cancer Stage III
Interventions
First Posted Date
2011-05-12
Last Posted Date
2011-05-27
Lead Sponsor
Korean Breast Cancer Study Group
Target Recruit Count
99
Registration Number
NCT01352494
Locations
🇰🇷

Department of Surgery, the Catholic university of Korea, St. Vincent's hospital, Suwon, Gyeonggi-do, Korea, Republic of

Gemcitabine, Carboplatin, and Lenalidomide for Treatment of Advanced/Metastatic Urothelial Cancer and Other Solid Tumors

Phase 1
Completed
Conditions
Urethral Neoplasms
Neoplasms, Urethral
Cancer of the Urethra
Urethral Cancer
Interventions
First Posted Date
2011-05-12
Last Posted Date
2024-12-27
Lead Sponsor
National Cancer Institute (NCI)
Target Recruit Count
18
Registration Number
NCT01352962
Locations
🇺🇸

National Institutes of Health Clinical Center, Bethesda, Maryland, United States

Study of CEP-9722 in Combination With Gemcitabine and Cisplatin in Patients With Advanced Solid Tumors or Mantle Cell Lymphoma

Phase 1
Completed
Conditions
Solid Tumors or Mantle Cell Lymphoma
Interventions
First Posted Date
2011-05-02
Last Posted Date
2013-01-18
Lead Sponsor
Cephalon
Target Recruit Count
24
Registration Number
NCT01345357
Locations
🇫🇷

Teva Investigational Site 1, Nantes, France

🇫🇷

Teva Investigational Site 2, Villejuif, France

🇧🇪

Teva Investigational Site 3, Bruxelles, Belgium

A Study of LY2603618 in Combination With Gemcitabine in Participants With Solid Tumors

Phase 1
Completed
Conditions
Solid Tumors
Interventions
Drug: LY2603618
Drug: Gemcitabine
First Posted Date
2011-04-25
Last Posted Date
2019-03-01
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
17
Registration Number
NCT01341457
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., Chiba, Japan

Maintenance Gemcitabine in the Chinese Advanced Lung Cancer

Phase 4
Conditions
Non Small Cell Lung Cancer
Interventions
Drug: Gemcitabine
Drug: Best supportive care
First Posted Date
2011-04-15
Last Posted Date
2011-04-15
Lead Sponsor
Tongji University
Target Recruit Count
240
Registration Number
NCT01336192
Locations
🇨🇳

Shanghai Pulmonary Hospital Medical Oncology Department, Shanghai, Shanghai, China

Transarterial Chemoembolization vs CyberKnife for Recurrent Hepatocellular Carcinoma

Phase 3
Withdrawn
Conditions
Carcinoma, Hepatocellular
First Posted Date
2011-04-01
Last Posted Date
2012-06-11
Lead Sponsor
Albert Koong
Registration Number
NCT01327521
Locations
🇺🇸

Stanford University School of Medicine, Stanford, California, United States

A Study of ALT-801 in Combination With Cisplatin and Gemcitabine in Muscle Invasive or Metastatic Urothelial Cancer

Phase 1
Completed
Conditions
Urethra Cancer
Transitional Cell Carcinoma of Bladder
Ureter Cancer
Malignant Tumor of Renal Pelvis
Interventions
First Posted Date
2011-03-31
Last Posted Date
2024-06-25
Lead Sponsor
Altor BioScience
Target Recruit Count
68
Registration Number
NCT01326871
Locations
🇺🇸

UPMC Cancer Center, Pittsburgh, Pennsylvania, United States

🇺🇸

The University of Arizona Cancer Center, Tucson, Arizona, United States

🇺🇸

UF Health Center at Orlando Health, Orlando, Florida, United States

and more 13 locations
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