On November 1, 2024 AimedBio reported to have received IND clearance from the U.S. Food and Drug Administration (FDA) for AMB302.
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– AimedBio plans to initiate a Phase 1 clinical trial in both Korea and the United States, enrolling patients with solid tumors, including bladder cancer and head and neck cancer.
– First patient dosing is expected to begin in Q1 2025 in both countries.
(Press release, AimedBio, NOV 1, 2024, View Source;s_keyword=&s_where=&start=10 [SID1234656919])