The company successfully cleared FDA review for its IND application without clinical hold, enabling U.S. patient enrollment. This represents a significant milestone for the company's rheumatology program and vilamakitug development, demonstrating regulatory progress and advancement toward potential commercialization of a next-generation IL-1α antibody targeting an unmet medical need.
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Close Sep 29, 2026 · split-adjustedArticles · 30 days0English, de-duplicated
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GlobeNewswire Inc.Jun 15, 9:00 AM ET▲ Positive
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