Micromet scores multiple development deals

Publication
Article
Oncology NEWS InternationalOncology NEWS International Vol 18 No 12
Volume 18
Issue 12

Micromet and Sanofi-aventis announced a global collaboration and license agreement to develop a BiTE antibody against a carcinoma cell antigen. Micromet will be responsible for the discovery, research, and development of the BiTE antibody through the completion of phase I clinical trials and under a joint steering committee’s supervision. Sanofi-aventis will have full responsibility for additional as well as worldwide commercialization of the BiTE antibody.

Micromet and Sanofi-aventis announced a global collaboration and license agreement to develop a BiTE antibody against a carcinoma cell antigen. Micromet will be responsible for the discovery, research, and development of the BiTE antibody through the completion of phase I clinical trials and under a joint steering committee’s supervision. Sanofi-aventis will have full responsibility for additional as well as worldwide commercialization of the BiTE antibody.

Sanofi-Aventis agreed to pay Micromet an upfront cash payment of approximately $12 million following signing of the agreement. Micromet is eligible for development and regulatory milestone payments of up to approximately $241 million plus performance-based sales milestones of up to approximately $224 million, and royalties on worldwide product sales.

In other Micromet news, the firm signed an agreement with MedImmune to buy out the rights to blinatumomab (MT-103) in North America and to terminate a 2003 collaboration agreement. As a result, Micromet will control global rights to develop and commercialize blinatumomab.

Finally, Bayer Schering Pharma AG has exercised its option under the option, collaboration, and license agreement with Micromet, to develop a new BiTE antibody for the treatment of solid tumors.

Micromet will be responsible for the preclinical development of the BiTE antibody and will collaborate with Bayer through the completion of phase I clinical trials. Bayer Schering Pharma will then assume full control of the further development and commercialization of the BiTE antibody.

Recent Videos
Data from the SPOTLIGHT and GLOW trials reveal that zolbetuximab increased survival in patients with CLDN18.2-positive gastric or GEJ adenocarcinoma.
The incorporation of zolbetuximab in addition to chemotherapy has shown benefit in patients with Claudin 18.2–positive gastric cancers in clinical trials.
Michael J. Hall, MD, MS, FASCO, discusses the need to reduce barriers to care for those with Li-Fraumeni syndrome, including those who live in rural areas.
Patrick Oh, MD, highlights next steps for further research in treating patients with systemic therapy in addition to radiotherapy for early-stage NSCLC.
The ability of metformin to disrupt mitochondrial metabolism may help mitigate the risk of cancer in patients with Li-Fraumeni syndrome.
Related Content