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
-

Perioperative Therapy for Resectable and Borderline-Resectable Pancreatic Adenocarcinoma With Molecular Correlates

Phase 2
Active, not recruiting
Conditions
Pancreas Ductal Adenocarcinoma
Pancreatic Cancer
Pancreatic Adenocarcinoma
Interventions
First Posted Date
2016-03-30
Last Posted Date
2024-06-28
Lead Sponsor
Academic Thoracic Oncology Medical Investigators Consortium
Target Recruit Count
48
Registration Number
NCT02723331
Locations
🇺🇸

Mayo Clinic Hospital, Scottsdale, Arizona, United States

🇺🇸

University of Colorado Cancer Center, Aurora, Colorado, United States

🇺🇸

New York University, New York, New York, United States

and more 1 locations

STUDY 15 - Comparing Gemcitabine/Carboplatin and Hydroxychloroquine Versus Carboplatin/Etoposide Therapy Alone in Small Cell Lung Cancer (SCLC)

Phase 2
Terminated
Conditions
Small Cell Lung Cancer
Interventions
First Posted Date
2016-03-30
Last Posted Date
2021-03-18
Lead Sponsor
University College, London
Target Recruit Count
72
Registration Number
NCT02722369
Locations
🇬🇧

UCLH, London, United Kingdom

🇬🇧

The Christie, Manchester, United Kingdom

🇬🇧

East and North Herts NHS Foundation Trust, Northwood, United Kingdom

and more 10 locations

A Study of PEGylated Recombinant Human Hyaluronidase in Combination With Nab-Paclitaxel Plus Gemcitabine Compared With Placebo Plus Nab-Paclitaxel and Gemcitabine in Participants With Hyaluronan-High Stage IV Previously Untreated Pancreatic Ductal Adenocarcinoma

Phase 3
Terminated
Conditions
Pancreatic Ductal Carcinoma
Interventions
First Posted Date
2016-03-22
Last Posted Date
2020-07-14
Lead Sponsor
Halozyme Therapeutics
Target Recruit Count
492
Registration Number
NCT02715804
Locations
🇺🇸

Allegheny General Hospital, Pittsburgh, Pennsylvania, United States

🇺🇸

Beth Israel Deaconess Medical Center, Boston, Massachusetts, United States

🇺🇸

Baylor College of Medicine - Baylor Clinic, Houston, Texas, United States

and more 213 locations

A Study of the Safety and Efficacy of Atezolizumab Administered in Combination With Bevacizumab and/or Other Treatments in Participants With Solid Tumors

First Posted Date
2016-03-22
Last Posted Date
2021-07-09
Lead Sponsor
Hoffmann-La Roche
Target Recruit Count
243
Registration Number
NCT02715531
Locations
🇺🇸

Stanford Cancer Institute; Hematology, Palo Alto, California, United States

🇺🇸

Georgetown University Medical Center, Washington, District of Columbia, United States

🇺🇸

Columbia University Medical Center, New York, New York, United States

and more 27 locations

A Study of Ramucirumab (LY3009806) or Merestinib (LY2801653) in Advanced or Metastatic Biliary Tract Cancer

Phase 2
Active, not recruiting
Conditions
Biliary Tract Cancer
Metastatic Cancer
Advanced Cancer
Interventions
First Posted Date
2016-03-17
Last Posted Date
2024-10-17
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
309
Registration Number
NCT02711553
Locations
🇺🇸

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

🇺🇸

UCSF Medical Center at Mission Bay, San Francisco, California, United States

🇺🇸

Georgetown University Medical Center, Washington, District of Columbia, United States

and more 76 locations

Open-Label Safety and Tolerability Study of INCB057643 in Subjects With Advanced Malignancies

Phase 1
Terminated
Conditions
Solid Tumors
Interventions
First Posted Date
2016-03-17
Last Posted Date
2022-04-28
Lead Sponsor
Incyte Corporation
Target Recruit Count
137
Registration Number
NCT02711137
Locations
🇺🇸

Yale University, New Haven, Connecticut, United States

🇺🇸

Hematology - Oncology Associates of Treasure Coast, Port Saint Lucie, Florida, United States

🇺🇸

The Methodist Hospital, Houston, Texas, United States

and more 15 locations

Study To Establish Maximum Tolerated Dose (MTD) of Cyberknife in Patients With Un-Resectable Pancreas Cancer (TL002)

Phase 1
Terminated
Conditions
Pancreatic Cancer
Pancreatic Adenocarcinoma
Adenocarcinoma of the Pancreas
Pancreas Adenocarcinoma
Pancreas Cancer
Interventions
First Posted Date
2016-03-14
Last Posted Date
2019-07-30
Lead Sponsor
The Cooper Health System
Target Recruit Count
30
Registration Number
NCT02707328
Locations
🇺🇸

MD Anderson Cancer Center at Cooper, Camden, New Jersey, United States

A Study of Pre-Operative Cyberknife in Patients With Potentially Resectable Pancreas Cancer

Early Phase 1
Conditions
Pancreatic Cancer
Adenocarcinoma of the Pancreas
Pancreas Adenocarcinoma
Pancreas Cancer
Pancreatic Adenocarcinoma
Interventions
Drug: Gemcitabine
Radiation: Stereotactic Radiosurgery
First Posted Date
2016-03-14
Last Posted Date
2016-03-14
Lead Sponsor
The Cooper Health System
Target Recruit Count
15
Registration Number
NCT02707315
Locations
🇺🇸

MD Anderson Cancer Center at Cooper, Camden, New Jersey, United States

LOAd703 Oncolytic Virus Therapy for Pancreatic Cancer

Phase 1
Recruiting
Conditions
Pancreatic Cancer
Interventions
Genetic: delolimogene mupadenorepvec
Drug: gemcitabine
Drug: nab-paclitaxel
Biological: atezolizumab
First Posted Date
2016-03-10
Last Posted Date
2024-02-01
Lead Sponsor
Lokon Pharma AB
Target Recruit Count
55
Registration Number
NCT02705196
Locations
🇺🇸

Baylor College of Medicine, Houston, Texas, United States

🇺🇸

Baylor St Luke's Medical Center, Houston, Texas, United States

PEG-ASP, Etoposide and Gemcitabine for Natural Killer/T Lymphoma

Phase 2
Recruiting
Conditions
Treatment Refusal
Interventions
Drug: Gemcitabine
Drug: etoposide
Drug: Pegaspargase
Radiation: involved-field radiotherapy
First Posted Date
2016-03-10
Last Posted Date
2023-06-18
Lead Sponsor
Sun Yat-sen University
Target Recruit Count
35
Registration Number
NCT02705508
Locations
🇨🇳

Sun Yat-sen University Cancer Center, Guangzhou, Please Select, China

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