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Aptose Announces Positive CSRC Approval to Dose Escalate to 120 mg of Tuspetinib in Phase 1/2 Tuscany Trial of Frontline AML
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Aptose Selected for Oral Presentation of Data from TUSCANY Phase 1/2 Clinical Trial of Tuspetinib Triplet Therapy in Newly Diagnosed AML at EHA2025
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Aptose Provides Clinical Update for the Tuspetinib-based Triple Drug Frontline Therapy in Newly Diagnosed AML Patients from the Phase 1/2 TUSCANY Trial