Home BMS's $1 Billion Bet on Next-Gen ADC Reaches Key Clinical Milestone

BMS's $1 Billion Bet on Next-Gen ADC Reaches Key Clinical Milestone

May 23, 2025 09:54 CST Updated 09:55
Tubulis

Developer of Drug Conjugates

Bristol-Myers Squibb

Biopharmaceutical and Nutritional Product R&D and Sales

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Recently, GermanyTubulis GmbH announced a collaboration withThe first project of Bristol-Myers Squibb (BMS) collaboration has entered the clinical development stage, marking an important milestone in the ongoing collaborative development of next-generation antibody-drug conjugate (ADC) candidates for cancer treatment.


The two companies signed a cooperation agreement in April 2023.BMS with$22.75 Million Upfront Payment, acquiring Tubulis' proprietary P5 conjugates and Tubutecan platform, aiming to combine BMS' deep oncology and clinical development expertise with Tubulis' unique ADC design approach to develop versatile and customizable ADC drugs for cancer treatment.The total amount may exceed 1 billion US dollars, plus a tiered royalty on net product sales.

Dr. Dominik Schumacher

Tubulis CEO and co-founder Dominik Schumacher, Ph.D., stated,Within just one year, we have advanced three tubutecan-based ADC candidates into clinical trials, including our wholly owned programs TUB-030 and TUB-040, and we will continue to demonstrate the versatility and translational potential of our technology in delivering more effective cancer treatments.


Tubulis’ P5 and Tubutecans help generate ultra-stable ADCs, which have the potential to actively reduce unwanted target-independent toxicity and are optimized for the delivery of potent topoisomerase-1 inhibitors.

After BMS selects the antibody target, Tubulis will provide its linker payload to the company, creating a uniquely matched ADC for each antibody. Bristol-Myers Squibb Company will be solely responsible for the development, manufacturing, and commercialization of the resulting ADC candidates.

Tubulis Pipeline

December 2024,Gilead and TubulisAlso signed an exclusive option and license agreement to discover and develop ADCs targeting solid tumor antigens. According to the agreement,Tubulis to Receive $20 Million Upfront Payment and Additional $30 Million Option Exercise Fee if Gilead Exercises Its Option.In addition, Tubulis will be eligible to receiveTotaling up to $415 millionDevelopment and commercialization milestone payments, as well as tiered royalties in the mid-single-digit to low-double-digit range on sales of marketed products resulting from the collaboration.

References:

https://tubulis.com/







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