Aptose Initiates TUSCANY Phase 1/2 Study for Newly Diagnosed AML Patients to Receive Tuspetinib-based Triplet Therapy
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Aptose Biosciences has initiated the TUSCANY Phase 1/2 study to evaluate a triplet therapy for newly diagnosed AML patients. The study involves tuspetinib, venetoclax, and azacitidine, and is being conducted at select US sites. An update on the study's execution is expected during ASH 2024.
November 20, 2024 | 12:45 pm
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Aptose Biosciences has started the TUSCANY Phase 1/2 study for a new triplet therapy for AML, potentially expanding its market reach. Updates are expected at ASH 2024.
The initiation of the TUSCANY study by Aptose Biosciences is a significant step in developing a new treatment for AML, which could potentially expand the company's market reach if successful. The study's promising safety and activity profile, along with the upcoming update at ASH 2024, could positively influence investor sentiment and the stock price in the short term.
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