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
-

Ph2 Nab-paclitaxel With Gemcitabine to Determine Efficacy in Advanced Non-squamous NSCLC.

Phase 2
Withdrawn
Conditions
Non-small Cell Lung Cancer
Interventions
First Posted Date
2015-04-01
Last Posted Date
2017-11-06
Lead Sponsor
West Virginia University
Registration Number
NCT02405910
Locations
🇺🇸

West Virginia University Hospitals - Mary Babb Randolph Cancer Center, Morgantown, West Virginia, United States

A Phase 2 Study of MM-141 Plus Nab-paclitaxel and Gemcitabine in Front-line Metastatic Pancreatic Cancer

Phase 2
Completed
Conditions
Pancreatic Cancer
Interventions
Drug: Placebo
Drug: MM-141
Drug: Gemcitabine
Drug: Nab-Paclitaxel
First Posted Date
2015-03-26
Last Posted Date
2018-09-18
Lead Sponsor
Merrimack Pharmaceuticals
Target Recruit Count
88
Registration Number
NCT02399137
Locations
🇺🇸

Reliant Medical Group, Inc., Worcester, Massachusetts, United States

🇺🇸

Banner MD Anderson Cancer Ctr., Gilbert, Arizona, United States

🇺🇸

UCLA School of Medicine, Los Angeles, California, United States

and more 62 locations

A Study of Nimotuzumab Combinated With Gemcitabine in K-RAS Wild-type Locally Advanced and Metastatic Pancreatic Cancer

Phase 3
Completed
Conditions
Pancreatic Cancer
Interventions
First Posted Date
2015-03-20
Last Posted Date
2024-04-04
Lead Sponsor
Biotech Pharmaceutical Co., Ltd.
Target Recruit Count
90
Registration Number
NCT02395016
Locations
🇨🇳

Beijing Cancer Hospital, Beijing, Beijing, China

🇨🇳

First Affiliated Hospital of Bengbu Medical College, Bengbu, Anhui, China

🇨🇳

Second Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China

and more 22 locations

Open-Label, Dose-Escalation Study of Pemigatinib in Subjects With Advanced Malignancies - (FIGHT-101)

Phase 1
Terminated
Conditions
UC
MPN
Lung Cancer
Solid Tumor
Gastric Cancer
Urothelial Cancer
Endometrial Cancer
Multiple Myeloma
Myeloproliferative Neoplasms
Breast Cancer
Interventions
First Posted Date
2015-03-19
Last Posted Date
2023-01-06
Lead Sponsor
Incyte Corporation
Target Recruit Count
201
Registration Number
NCT02393248
Locations
🇺🇸

Ohio State University - Wexner Medical Center, Columbus, Ohio, United States

🇺🇸

South Texas Accelerated Research Therapeutics, San Antonio, Texas, United States

🇺🇸

University of Michigan Health System, Ann Arbor, Michigan, United States

and more 17 locations

Study of DKN-01 and Gemcitabine/Cisplatin in Patients With Carcinoma to Primary to the Intra- or Extra-Hepatic Biliary System or Gallbladder

Phase 1
Completed
Conditions
Carcinoma of Intrahepatic and Extra-hepatic Biliary System
Carcinoma of Gallbladder
Bile Duct Cancer
Cholangiocarcinoma
Interventions
First Posted Date
2015-03-03
Last Posted Date
2018-09-10
Lead Sponsor
Leap Therapeutics, Inc.
Target Recruit Count
51
Registration Number
NCT02375880
Locations
🇺🇸

University of Southern California, Los Angeles, California, United States

🇺🇸

Massachusetts General Hospital, Boston, Massachusetts, United States

🇺🇸

Dana Farber Cancer Institute, Boston, Massachusetts, United States

and more 6 locations

Safety Study of SEA-CD40 in Cancer Patients

Phase 1
Terminated
Conditions
Neoplasms, Squamous Cell
Non-Small Cell Lung Cancer
Non-Small Cell Lung Cancer Metastatic
Melanoma
Squamous Cell Carcinoma of the Head and Neck
Squamous Cell Neoplasm
Pancreatic Adenocarcinoma
Carcinoma, Squamous Cell
Lymphoma, Large B-Cell, Diffuse
Non-small Cell Carcinoma
Interventions
Drug: Intravenous (IV) SEA-CD40
Drug: Subcutaneous (SC) SEA-CD40
Drug: Pembrolizumab
Drug: Gemcitabine
Drug: Nab-paclitaxel
First Posted Date
2015-03-03
Last Posted Date
2023-05-01
Lead Sponsor
Seagen Inc.
Target Recruit Count
159
Registration Number
NCT02376699
Locations
🇺🇸

University of Chicago Medical Center, Chicago, Illinois, United States

🇺🇸

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

🇺🇸

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

and more 16 locations

Neoadjuvant Pembrolizumab in Combination With Gemcitabine Therapy in Cis-eligible/Ineligible UC Subjects

Phase 1
Active, not recruiting
Conditions
Urothelial Carcinoma
Bladder Cancer
Interventions
First Posted Date
2015-02-19
Last Posted Date
2024-02-20
Lead Sponsor
Jason R. Brown
Target Recruit Count
83
Registration Number
NCT02365766
Locations
🇺🇸

Indiana University Melvin and Bren Simon Cancer Center, Indianapolis, Indiana, United States

🇺🇸

Community Regional Cancer Care, Indianapolis, Indiana, United States

🇺🇸

IU Health Central Indiana Cancer Center, Indianapolis, Indiana, United States

and more 6 locations

Efficacy and Safety Study of P-Gemox vs.EPOCH as First-line Chemotherapy to Treat NK/T-cell Lymphoma With Early Stage

First Posted Date
2015-02-09
Last Posted Date
2018-05-09
Lead Sponsor
Sun Yat-sen University
Target Recruit Count
50
Registration Number
NCT02359162
Locations
🇨🇳

Sun Yat-sen University Cancer Center, GuangZhou, Guangdong, China

Italian Multicenter Study Comparing FOLFOXIRI Versus Gemcitabine as Adjuvant Treatment for Resected Pancreatic Cancer

Phase 3
Conditions
Pancreatic Cancer
Interventions
Drug: FOLFOXIRI
Drug: Gemcitabine
First Posted Date
2015-02-04
Last Posted Date
2015-02-04
Lead Sponsor
Azienda Ospedaliero, Universitaria Pisana
Target Recruit Count
310
Registration Number
NCT02355119
Locations
🇮🇹

Azienda Ospedaliero-Universitaria Pisana, Pisa, PI, Italy

A Global Study to Assess the Effects of MEDI4736 (Durvalumab), Given as Monotherapy or in Combination With Tremelimumab Determined by PD-L1 Expression Versus Standard of Care in Patients With Locally Advanced or Metastatic Non Small Cell Lung Cancer

Phase 3
Completed
Conditions
Non - Small Cell Lung Cancer NSCLC
Interventions
Drug: MEDI4736 (durvalumab)
Drug: Vinorelbine
Drug: MEDI4736 (durvalumab) in combination with tremelimumab (anti-CTLA4)
Drug: tremelimumab (anti-CTLA4)
Drug: Gemcitabine
Drug: Erlotinib
First Posted Date
2015-02-02
Last Posted Date
2024-07-26
Lead Sponsor
AstraZeneca
Target Recruit Count
597
Registration Number
NCT02352948
Locations
🇬🇧

Research Site, Wolverhampton, United Kingdom

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