Rallybio Announces In-Licensing of Potential First-In-Class Preclinical Antibody Candidate from Sanofi
Retrieved on:
Tuesday, May 10, 2022
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With our strong focus on portfolio expansion, the in-licensing of RLYB331, our first as a public company, marks a pivotal moment for Rallybio.
Key Points:
- With our strong focus on portfolio expansion, the in-licensing of RLYB331, our first as a public company, marks a pivotal moment for Rallybio.
- We believe RLYB331 is differentiated from all programs in clinical development based on its mechanism of action, with the potential to be first-in-class.
- This product candidate is a natural fit with our R&D expertise and our focus on hematological disorders.
- Rallybio plans to prosecute preclinical activities for RLYB331 including CMC, and dose-range finding and toxicity studies, which will then support transition of the asset into clinical development.