BM201
/ InnoBM Pharma
- LARVOL DELTA
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September 17, 2024
Clinical efficacy, safety, and PK/PD from the first in human study of BM201, a TLR7/8 agonist
(ESMO Asia 2024)
- P1 | "Conclusions BM201 has a favorable safety profile and has shown encouraging anti-tumor activity in the dose escalation phase. Follow-up is still ongoing."
Clinical • P1 data • PK/PD data • Oncology • Sarcoma • Soft Tissue Sarcoma • Solid Tumor
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