Sellas Teases Biomarker-Driven Efficacy Of AML Drug With Phase IIa Results

The company remained tight-lipped on the biomarker driving high response rates for its CDK9 inhibitor SLS009 from a Phase II trial, as a Phase III interim analysis for its AML cancer vaccine galinpepimut-S draws near.

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SELLAS Life Sciences Group, Inc. is in a strong position in acute myeloid leukemia (AML) with positive data from a Phase IIa study of SLS009 and the completion of enrollment in its Phase III trial of the cancer vaccine galinpepimut-S (GPS).

The company announced 26 March topline data from the Phase IIa study of SLS009, a CDK9 inhibitor that Sellas in-licensed from GenFleet Therapeutics, in combination with AbbVie Inc./Roche Holding AG’s Venclexta (venetoclax) and Bristol Myers Squibb Company’s Vidaza (azacitidine)

Key Takeaways
  • Sellas announced positive topline results for the Phase IIa trial of SLS009, its CDK9 inhibitor for acute myeloid leukemia.

  • In addition to a high overall response rate, the study showed a 100% response rate among patients with certain undisclosed biomarkers receiving the optimal 30mg dose

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