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NASDAQ:APRE

Aprea Therapeutics Q2 2026 Earnings Report

Aprea Therapeutics logo
$0.73 0.00 (-0.62%)
Closing price 09/22/2026 04:00 PM Eastern
Extended Trading
$0.73 +0.00 (+0.22%)
As of 04:24 AM Eastern
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Aprea Therapeutics EPS Results

Actual EPS
-$0.07
Consensus EPS
-$0.18
Beat/Miss
Beat by +$0.11
One Year Ago EPS
N/A

Aprea Therapeutics Revenue Results

Actual Revenue
N/A
Expected Revenue
$0.25 million
Beat/Miss
N/A
YoY Revenue Growth
N/A

Aprea Therapeutics Announcement Details

Quarter
Q2 2026
Time
Before Market Opens
Conference Call Date
Wednesday, August 12, 2026
Conference Call Time
8:30AM ET

Upcoming Earnings

Aprea Therapeutics' Q3 2026 earnings is estimated for Wednesday, November 11, 2026, based on past reporting schedules, with a conference call scheduled on Monday, November 9, 2026 at 9:30 AM ET. Check back for transcripts, audio, and key financial metrics as they become available.

Aprea Therapeutics Earnings Headlines

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About Aprea Therapeutics

Aprea Therapeutics (NASDAQ:APRE) is a clinical-stage biopharmaceutical company focused on developing therapies for cancer. The company’s research centers on restoring the function of mutated p53, a tumor-suppressor protein that is altered in many cancers and plays an important role in regulating cell growth and programmed cell death.

Aprea’s pipeline has included eprenetapopt (APR-246), an investigational therapy designed to reactivate mutant p53, as well as next-generation p53-reactivating compounds such as APR-548. These programs have been investigated for hematologic malignancies, including myelodysplastic syndromes and acute myeloid leukemia. The company’s products remain investigational and are subject to clinical and regulatory development.

Founded in 2002, Aprea has conducted research and clinical development activities in the United States and internationally, including through studies involving patients with blood cancers. As a development-stage biotechnology company, its operations and prospects depend primarily on advancing its drug candidates through clinical testing and obtaining regulatory approval.

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