FDA
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Aprea Therapeutics Announces that Safety Review Committee (SRC) Endorses Dosing of Patients with ATRN-119 at 800 mg Once Daily in Ongoing ABOYA-119 Clinical Trial
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Aprea Therapeutics (APRE) Announces Private Placement Financing of up to $34.0 Million
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Aprea Therapeutics (APRE) Provides Corporate Update and Announces Development Plans for 2024
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Aprea Therapeutics Reports Fourth Quarter and Full Year 2021 Financial Results and Provides Update on Business Operations
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Aprea Therapeutics Presents Primary Analysis from Phase 2 Trial of Eprenetapopt + Azacitidine for Post-Transplant Maintenance Therapy in TP53 Mutant MDS and AML at the 2021 American Society of Hematol
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Aprea Therapeutics to Present Data from Clinical Trials Evaluating Eprenetapopt at 63rd American Society of Hematology Annual Meeting
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Aprea Therapeutics Reports Second Quarter 2021 Financial Results and Provides Update on Business Operations
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