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Aprea Therapeutics, Inc. news in 2020

Aprea Therapeutics, Inc.'s news releases, calls and decks from 2020, newest first.

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Aprea Therapeutics Announces Results of Primary Endpoint from Phase 3 Trial of Eprenetapopt in TP53 Mutant Myelodysplastic Syndromes (MDS)

December 27, 2020

Aprea Therapeutics Receives FDA Fast Track Designation for Eprenetapopt in the Treatment of TP53 Mutant Acute Myeloid Leukemia (AML)

November 29, 2020

Aprea Therapeutics Reports Third Quarter 2020 Financial Results and Provides Update on Business Operations

November 4, 2020

Aprea Therapeutics Launches Disease Awareness Website for Healthcare Professionals, p53reactivation.com

October 13, 2020

Aprea Therapeutics Receives OK from FDA to Initiate Phase 1 Clinical Studies for Next-Generation Mutant p53 Reactivator, APR-548

October 6, 2020

Aprea Therapeutics Appoints Michael A. Kelly to Board of Directors

September 28, 2020

Aprea Therapeutics Promotes Gregory S. Wessels to Chief Commercial Officer and Announces Governance Changes

September 17, 2020

Aprea Therapeutics Reports Second Quarter 2020 Financial Results and Provides Update on Business Operations

August 10, 2020

Aprea Therapeutics Announces Expansion of Clinical Trial Evaluating Eprenetapopt for the Front-Line Treatment of TP53 Mutant Acute Myeloid Leukemia (AML)

July 15, 2020

Aprea Therapeutics Appoints Fouad Namouni, M.D. and Richard Peters, M.D., Ph.D. to Board of Directors

June 28, 2020

Aprea Therapeutics Completes Full Enrollment of Phase 3 Clinical Trial in TP53 Mutant Myelodysplastic Syndromes (MDS)

June 2, 2020

Aprea Therapeutics Reports First Quarter 2020 Financial Results and Provides Update on Business Operations

May 14, 2020

Aprea Therapeutics Launches New Corporate Website - www.aprea.com

April 5, 2020

Aprea Therapeutics Reports Fourth Quarter and Full Year 2019 Financial Results and Provides Corporate Update

March 25, 2020

Aprea Therapeutics Appoints Gregory S. Wessels as Vice President, Commercial

February 12, 2020

Aprea Therapeutics Receives FDA Breakthrough Therapy Designation for APR-246 in Combination with Azacitidine for the Treatment of Myelodysplastic Syndromes (MDS) with a TP53 Mutation

January 29, 2020

Decks in 2020