Keros Therapeutics (KROS)’ treatment of Duchenne muscular dystrophy was granted FDA orphan designation, according to a post to the agency’s site.
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Read More on KROS:
- Keros Therapeutics Reports Strong Revenue Growth
- Strategic Focus on KER-065 and Leadership Changes Justify Buy Rating for Keros Therapeutics
- Keros Therapeutics’ Workforce Cuts: Potential Savings vs. Strategic Risks
- Keros Therapeutics: Hold Rating Amid Strategic Focus on KER-065 and Pipeline Adjustments
- Keros Therapeutics to discontinue cibotercept, announces COO departure
