HOOKIPA Pharma Receives FDA Clearance for IND Application for HB-700, a Novel KRAS-Mutated Cancer Vaccine

HOOKIPA Pharma Inc. (HOOK) has received clearance from the FDA for its Investigational New Drug (IND) application for HB-700, a novel arenaviral therapeutic vaccine for the treatment of KRAS-mutated cancers. The HB-700 program is designed to treat KRAS-mutated lung, colorectal, pancreatic, and other cancers by targeting the five most prevalent KRAS mutations in these disease indications: G12D, G12V, G12R, G12C, and G13D. The company says the program can benefit more patients than single mutation inhibitors. The IND submission achieves a final $10 million milestone payment from Roche Holdings AG (RHHBY). Effective April 25, 2024, the company will regain full control of the associated intellectual property portfolio and have full collaboration and licensing rights for the HB-700 program. The company will publish preclinical data in an abstract at the American Society for Clinical Oncology (ASCO) 2024 Annual Meeting.

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