I-Mab prioritizes claudin for research

 

• Givastomig: a Claudin 18.2 ("CLDN18.2") x 4-1BB bispecific antibody, will be the lead clinical program following the Company's portfolio prioritization
• The Company has completed enrollment of a dose escalation study of givastomig in combination with nivolumab plus chemotherapy, and data is expected in the early second half of 2025; a 40-patient dose expansion study is now underway with data expected in early 2026
• Cash balance of $184.4 million (as of September 30, 2024), expected to support operations into 2027, complemented by a strengthened U.S.-based leadership team and streamlined operating model

https://www.prnewswire.com/news-releases/i-mab-announces-portfolio-prioritization-of-givastomig-cldn18-2-x-4-1bb-bispecific-antibody-as-lead-clinical-program-302342671.html