Regulatory PathwayThe adaptive design and early unblinding points provide optionality for the timeline and potential for accelerated regulatory feedback or mid-trial modifications, a favorable design feature.
Study EnrollmentPhase 3 MIRACLE study recruitment reaches 60% of first 45 patients, underscoring unmet need in r/r AML.
Therapeutic PotentialPromising preclinical data demonstrate the potential of Moleculin Biotech's lead asset, annamycin, as a therapeutic agent for liver cancers.