m4 Award winner Tubulis enters into billion-dollar agreement with BMS
Munich/ Martinsried, Germany — Tubulis and Bristol Myers Squibb have entered into a strategic license agreement for the development of differentiated antibody-drug conjugates (ADCs). Under the terms of the license agreement, Bristol Myers Squibb will receive exclusive rights to Tubulis’ proprietary conjugation platforms for the development of a select number of highly differentiated ADCs for the treatment of solid tumors. The agreement includes an upfront payment of $22.75 million to Tubulis and potential milestone payments in excess of $1 billion for development, regulatory approval and commercialization, as well as royalties on the resulting marketed products.
Tubulis, based in Martinsried, Germany, and Bristol Myers Squibb (BMS) intend to use the strategic partnership to further advance the development of antibody-drug conjugates (ADC). BMS will gain access to Tubulis’ proprietary P5 conjugation and Tubutecan platforms to develop versatile and customizable ADCs for cancer treatment.
The Tubulis P5 and Tubutecan platforms enable the production of ultra-stable ADCs with the potential to actively reduce unwanted target-independent toxicities. At the same time, they are optimized for targeted delivery of potent topoisomerase‑1 inhibitors. Following Bristol Myers Squibb’s selection of the target, Tubulis will provide the company with its linker payloads to generate a uniquely matched ADC for each antibody.
Bristol Myers Squibb will assume sole responsibility for the development, manufacturing and commercialization of the resulting ADC candidates.
Almost exactly a year ago, m4 Award winner Tubulis had announced a major success, successfully closing a Series B financing of €60 million.
“This strategic agreement with Bristol Myers Squibb is an important validation of the potential of our approach to developing next-generation ADC-based therapeutics and our state-of-the-art ADC conjugation technologies that enable advanced ADC design to treat tumors with high unmet medical need,” said Dominik Schumacher, M.D., CEO and co-founder of Tubulis. He sees the collaboration with BMS as a significant step “in changing oncology treatment paradigms and achieving better outcomes for cancer patients.”
“ADCs play a promising role in cancer therapy, and Tubulis’ differentiated technologies offer opportunities to overcome current challenges in developing safe and effective ADC therapeutics,” said Dr. Emma Lees, senior vice president, research and early development and head of the Thematic Research Center for Mechanisms of Cancer Resistance at Bristol Myers Squibb.