Merck Serono/Takeda Matuzumab Development In Question After Phase II Study
This article was originally published in PharmAsia News
Executive Summary
Merck Serono is reconsidering development of its monoclonal antibody matuzumab for the treatment of metastatic colorectal cancer after a Phase II study failed to meet its efficacy endpoint, the company announced Aug. 29
You may also be interested in...
Takeda Discontinues Involvement In Matuzumab After Phase II Failure
Takeda will no longer jointly pursue development of cancer monoclonal antibody matuzumab because the epidermal growth factor receptor antagonist failed to meet primary endpoints in a Phase II trial, the Osaka, Japan-based company announced Feb. 18
PharmAsia News Business Bulletin
A regular roundup of commercial stories appearing in Scrip’s sister publication PharmAsia News, whose multilingual team of regional experts provides authoritative business intelligence focused on the Asian marketplace. Full stories can be accessed by clicking on the story title (subscription required).