Pemetrexed

Generic Name
Pemetrexed
Brand Names
Alimta, Ciambra, Pemfexy, Pemrydi Rtu, Pemetrexed Fresenius Kabi, Pemetrexed Baxter, Pemetrexed Krka, Pemetrexed medac, Pemetrexed Accord, Pemetrexed Sandoz, Armisarte (previously Pemetrexed Actavis)
Drug Type
Small Molecule
Chemical Formula
C20H21N5O6
CAS Number
137281-23-3
Unique Ingredient Identifier
04Q9AIZ7NO
Background

Pemetrexed is a chemotherapy drug that is manufactured and marketed by Eli Lilly and Company under the brand name Alimta. It is indicated for use in combination with cisplatin for the treatment of patients with malignant pleural mesothelioma whose disease is either unresectable or who are otherwise not candidates for curative surgery. Its use in non-small ce...

Indication

Pemetrexed is indicated for the treatment of the following conditions:

Non-squamous non-small cell lung cancer (NSCLC)

Malignant pleural mesothelioma

Associated Conditions
Metastatic Cervical Cancer, Metastatic Non-squamous Non Small Cell Lung Cancer, Metastatic Urothelial Carcinoma (UC), Ovarian Cancer, Locally advanced nonsquamous non-small cell lung cancer, Recurrent, metastatic Non-squamous Non-small-cell Lung Cancer (NSQ NSCLC), Unresectable Malignant Pleural Mesothelioma (MPM), Unresectable Thymoma
Associated Therapies
Monotherapy

A Trial for Patients With Advanced/Recurrent Cervical Cancer

First Posted Date
2005-09-19
Last Posted Date
2009-11-20
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
29
Registration Number
NCT00190983
Locations
🇺🇸

Gynecologic Oncology Group 215-854-0770, Philadelphia, Pennsylvania, United States

A Study of Pemetrexed and Cyclophosphamide Given Every 21 Days in Advanced Breast Cancer Patients

Phase 1
Completed
Conditions
Interventions
First Posted Date
2005-09-19
Last Posted Date
2009-11-20
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
103
Registration Number
NCT00190671
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 ph, Saint Petersburg, Russian Federation

A Study of Pemetrexed in the Treatment of Patients With Advanced Metastatic Cancer of the Liver

Phase 2
Completed
Conditions
First Posted Date
2005-09-19
Last Posted Date
2007-11-20
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
41
Registration Number
NCT00191412
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, Denver, Colorado, United States

A Trial for Patients With Gestational Trophoblastic Disease

First Posted Date
2005-09-19
Last Posted Date
2007-08-09
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
50
Registration Number
NCT00190918
Locations
🇺🇸

Gynecologic Oncology Group 215-854-0770, Philadelphia, Pennsylvania, United States

Molecular Profiling in Lung Cancer Patients

First Posted Date
2005-09-19
Last Posted Date
2011-10-21
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
30
Registration Number
NCT00191308
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., Warsaw, Poland

Phase I Open-Label, Dose Escalation Study To Determine The Maximum Tolerated Dose And To Evaluate The Safety Profile Of Lenalidomide (Revlimid®, CC-5013) With Pemetrexed In Subjects With Advanced Non-Small Cell Lung Cancer

Phase 1
Terminated
Conditions
First Posted Date
2005-09-16
Last Posted Date
2005-11-07
Lead Sponsor
Celgene Corporation
Target Recruit Count
40
Registration Number
NCT00179699
Locations
🇺🇸

MD Anderson - Orlando, Orlando, Florida, United States

🇺🇸

Washington University, St. Louis, Missouri, United States

🇺🇸

North Shore Hem/Onc Associates, East Setauket, New York, United States

and more 2 locations

Preoperative Treatment of Breast Cancer With Two Different Sequential Treatment Regimens

First Posted Date
2005-09-08
Last Posted Date
2012-03-21
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
257
Registration Number
NCT00149214
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., Valencia, Spain

Effects of Matuzumab in Combination With Pemetrexed for the Treatment of Advanced Lung Cancer

First Posted Date
2005-05-27
Last Posted Date
2018-04-06
Lead Sponsor
EMD Serono
Target Recruit Count
150
Registration Number
NCT00111839
Locations
🇺🇸

University of Southern California/Norris Cancer Center, Los Angeles, California, United States

🇺🇸

Peachtree Hematology and Oncology, Atlanta, Georgia, United States

🇺🇸

Georgia Cancer Specialists, Tucker, Georgia, United States

and more 40 locations

Study of Pemetrexed in the Treatment of Patients With Ovarian Cancer Who Have Failed Prior Platinum-Based Chemotherapy

First Posted Date
2005-04-25
Last Posted Date
2007-05-17
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
100
Registration Number
NCT00109096
Locations
🇪🇸

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri 9 AM to 5 PM Eastern time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Valencia, Spain

🇬🇧

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., Sutton, United Kingdom

Pemetrexed as the First Treatment in Advanced or Metastatic Breast Cancer

First Posted Date
2005-03-21
Last Posted Date
2009-06-01
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
37
Registration Number
NCT00106002
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., Dallas, Texas, United States

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