Overview

ALIMTA (Pemetrexed) in Patients With Locally Advanced or Metastatic Cancer

Status:
Completed
Trial end date:
1969-12-31
Target enrollment:
Participant gender:
Summary
This is a non-randomized, phase 1, study with the primary objective of determining the toxicities and establishing the maximum tolerated dose of ALIMTA when administered as a 10 minute infusion every 21 days with folic acid or multi-vitamin supplementation therapy in lightly or heavily pre-treated patients with locally advanced or metastatic cancer.
Phase:
Phase 1
Details
Lead Sponsor:
Eli Lilly and Company
Treatments:
Folic Acid
Pemetrexed