Moleculin Biotech reports interim MIRACLE trial data showing higher remission rates in relapsed/refractory AML

• Moleculin Biotech highlighted interim results already presented from its pivotal MIRACLE study of Annamycin in relapsed or refractory AML.
• The update showed patients receiving Annamycin were more likely to reach remission than those on the control regimen.
• Enrollment is expected to reach 90 patients in September 2026, setting up an unblinded efficacy readout in December 2026 to February 2027.
• Part B is expected to start in the first half of 2027 once the company selects an optimal dose from Part A results.
• The company reported no cardiotoxicity signals to date, supporting a safety profile that could aid positioning if efficacy holds.

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