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
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Phase 3 Trial of 90Y-Clivatuzumab Tetraxetan & Gemcitabine vs Placebo & Gemcitabine in Metastatic Pancreatic Cancer

Phase 3
Terminated
Conditions
Metastatic Pancreatic Cancer
Pancreatic Cancer
Interventions
Drug: IMMU-107
Drug: placebo
Drug: Gemcitabine
First Posted Date
2013-10-08
Last Posted Date
2021-08-16
Lead Sponsor
Gilead Sciences
Target Recruit Count
334
Registration Number
NCT01956812
Locations
🇺🇸

University of Maryland Medical Center, Baltimore, Maryland, United States

🇺🇸

University of Pennsylvania Abramson Cancer Center, Philadelphia, Pennsylvania, United States

🇺🇸

University of Pittsburgh Medical Center/Hillman Cancer Center, Pittsburgh, Pennsylvania, United States

and more 60 locations

A Clinical Study in Three-arm of Lurbinectedin (PM01183) Alone or in Combination With Gemcitabine and a Control Arm With Docetaxel as Second Line Treatment in Non-Small Cell Lung Cancer (NSCLC) Patients

Phase 2
Completed
Conditions
Non-Small Cell Lung Cancer (NSCLC)
Interventions
First Posted Date
2013-09-26
Last Posted Date
2019-09-24
Lead Sponsor
PharmaMar
Target Recruit Count
69
Registration Number
NCT01951157

Selumetinib (AZD6244, ARRY-142886) J-BTC Phase 1 Study

Phase 1
Terminated
Conditions
Inoperable Locally Advanced or Metastatic Biliary Tract Cancer
Interventions
First Posted Date
2013-09-25
Last Posted Date
2016-05-13
Lead Sponsor
AstraZeneca
Target Recruit Count
6
Registration Number
NCT01949870
Locations
🇯🇵

AZD6244 PhI Japanese Gem/, Chuo Ku, Tokyo, Japan

Phase Ib/II Trials of RAD001 in Triple Negative Metastatic Breast Cancer

Phase 1
Terminated
Conditions
Metastatic Breast Cancer
Interventions
First Posted Date
2013-09-11
Last Posted Date
2017-10-03
Lead Sponsor
National Cancer Center, Korea
Target Recruit Count
23
Registration Number
NCT01939418
Locations
🇰🇷

National cancer center, Goyangsi, Gyeonggido, Korea, Republic of

Hepatic Arterial Infusion With Floxuridine and Dexamethasone in Combination With Gemcitabine as Adjuvant Treatment After Resection of Intrahepatic Cholangiocarcinoma

Phase 1
Completed
Conditions
Intrahepatic Cholangiocarcinoma
Peripheral Cholangiocarcinoma
Cholangiocellular Carcinoma) (ICC)
Cholangiolar Carcinoma
Interventions
Procedure: Liver resection and placement of hepatic artery infusion pump
Drug: FLOXURIDINE
Drug: DEXAMETHASONE
Drug: GEMCITABINE
First Posted Date
2013-09-10
Last Posted Date
2020-09-11
Lead Sponsor
Memorial Sloan Kettering Cancer Center
Target Recruit Count
8
Registration Number
NCT01938729
Locations
🇺🇸

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

🇺🇸

Memorial Sloan Kettering Cancer Center at Basking Ridge, Basking Ridge, New Jersey, United States

🇺🇸

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

and more 2 locations

Gemcitabine Pharmacokinetics After Preoperative Chemoradiation Therapy

Not Applicable
Terminated
Conditions
Pancreatic Cancer
Interventions
First Posted Date
2013-09-10
Last Posted Date
2020-11-05
Lead Sponsor
M.D. Anderson Cancer Center
Target Recruit Count
12
Registration Number
NCT01938716
Locations
🇺🇸

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

(PGA) for Platinum-resistant/Refractory, Paclitaxel-Pretreated Recurrent Ovarian and Peritoneal Carcinoma

Phase 2
Terminated
Conditions
Ovarian Carcinoma
Fallopian Tube Carcinoma
Peritoneal Carcinoma
Interventions
First Posted Date
2013-09-06
Last Posted Date
2018-02-20
Lead Sponsor
Western Regional Medical Center
Target Recruit Count
7
Registration Number
NCT01936974
Locations
🇺🇸

Western Regional Medical Center, Goodyear, Arizona, United States

Azacitidine and Entinostat Before Chemotherapy in Treating Patients With Advanced Non-small Cell Lung Cancer

Phase 2
Terminated
Conditions
Recurrent Non-Small Cell Lung Carcinoma
Stage IV Non-Small Cell Lung Cancer
Stage IIIA Non-Small Cell Lung Cancer
Stage IIIB Non-Small Cell Lung Cancer
Interventions
First Posted Date
2013-09-05
Last Posted Date
2018-07-27
Lead Sponsor
National Cancer Institute (NCI)
Target Recruit Count
17
Registration Number
NCT01935947
Locations
🇺🇸

USC Norris Oncology/Hematology-Newport Beach, Newport Beach, California, United States

🇺🇸

Medical University of South Carolina, Charleston, South Carolina, United States

🇺🇸

Johns Hopkins Bayview Medical Center, Baltimore, Maryland, United States

and more 2 locations

Phase I Trial of LCL161 and Gemcitabine Plus Nab-Paclitaxel in Metastatic Pancreatic Cancer

Phase 1
Conditions
Metastatic Pancreatic Cancer
Interventions
First Posted Date
2013-09-04
Last Posted Date
2015-11-10
Lead Sponsor
US Oncology Research
Target Recruit Count
24
Registration Number
NCT01934634
Locations
🇺🇸

2 Sites, incl Tyler, TX and Dallas, TX, Texas, United States

An Open-Label Study of a Novel JAK-inhibitor, INCB047986, Given in Patients With Advanced Malignancies

Phase 1
Terminated
Conditions
Metastatic Cancer
Hodgkin's Lymphoma
Pancreatic Cancer
Breast Cancer
UC (Ureter and Urethera)
Solid Tumor
NHL (Non-Hodgkin Lymphoma)
Advanced Cancer
Interventions
First Posted Date
2013-08-28
Last Posted Date
2018-01-17
Lead Sponsor
Incyte Corporation
Target Recruit Count
5
Registration Number
NCT01929941
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