Spanish biotechnology firm PharmaMar, a part of the Zeltia Group, has initiated a Phase I/II study of Irvalec, a synthetic depsipeptide, with Roche's Tarceva (erlotinib) in non-small cell lung cancer.
The study will determine the safety and tolerability of the drug and will establish dose-limiting toxicity, as well as the recommended dose. Recruitment will last 18 months, the firm noted.
Irvalec, which is derived from the PharmaMar development program of marine-origin compounds, is a new drug with antiproliferative activity against a wide range of tumors, including breast, colon, pancreas, lung and prostate.
This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.
Login to your accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed
Chairman, Sanofi Aventis UK
| Headless Content Management with Blaze