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APRE
NASDAQ Life Sciences

Aprea Therapeutics Reports Second Unconfirmed Partial Response for WEE1 Inhibitor APR-1051 in Phase 1 Study

Arie Shkolnikov · Analysis by Wiseek AI
More coverage: Biotech Stocks · Healthcare
Sentiment info
Positive
Importance info
8
Price
$0.7
Mkt Cap
$4.196M
52W Low
$0.548
52W High
$3.715
52W Position info
28% above low
Off High info
81% below high
Rel. Volume info
0.1× avg
Market data snapshot near publication time

APRE sits 28% above its 52-week low of $0.548 on light trading volume (0.1× avg).

Summary

Aprea Therapeutics reported a second unconfirmed partial response for its WEE1 inhibitor, APR-1051, in a Phase 1 study, showing significant tumor shrinkage and biomarker reduction with good tolerability.


Key Events · Product Development and Regulatory · APRE

  • Second Unconfirmed Partial Response Achieved

    A patient with advanced endometrial cancer in the Phase 1 ACESOT-1051 study achieved a second unconfirmed partial response (uPR) at the 220 mg dose level.

  • Significant Tumor Shrinkage and Biomarker Reduction

    The responding patient showed a 50% reduction in target lesion measurements and an 87% decline in the CA-125 tumor biomarker, from 362 U/mL to 47 U/mL.

  • Favorable Safety Profile

    The patient experienced only Grade 1 treatment-emergent adverse events and continues treatment, supporting a potentially improved therapeutic index for APR-1051.

  • Genomically Guided Patient Selection

    Both patients with uPRs to date harbored PPP2R1A mutations, reinforcing the mechanistic thesis of targeting WEE1 for this specific patient population.


Analysis · APRE · Life Sciences

Aprea Therapeutics announced a second unconfirmed partial response (uPR) in its Phase 1 ACESOT-1051 study for its WEE1 inhibitor, APR-1051. This positive clinical update is highly significant for the micro-cap biopharmaceutical company, especially following a recent Nasdaq deficiency letter and a dilutive private placement. The observed 50% tumor shrinkage and substantial 87% reduction in the CA-125 biomarker, coupled with a favorable safety profile (only Grade 1 adverse events), provide further evidence of APR-1051's biological activity and therapeutic potential in advanced endometrial cancer patients with PPP2R1A mutations. This reinforces the company's development strategy and could help improve investor sentiment and address concerns about its financial and compliance status. Investors should monitor the confirmation of these responses and the further update expected in Q2 2026.

At the time of this filing, APRE was trading at $0.70 on NASDAQ in the Life Sciences sector, with a market capitalization of approximately $4.2M. The 52-week trading range was $0.55 to $3.72. This filing was assessed with positive market sentiment and an importance score of 8 out of 10.

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APRE - Latest Insights

APRE
Jul 23, 2026, 4:05 PM EDT
Filing Type: 8-K
Importance Score:
8
Price at Filing: $0.631
Real-time Price: $0.6047 info
Change: -$0.0263 (-4%) info
Market Cap: $7.599M info
APRE
Jun 17, 2026, 4:15 PM EDT
Filing Type: 8-K
Importance Score:
8
Price at Filing: $0.7798
Real-time Price: $0.6047 info
Change: -$0.1751 (-22%) info
Market Cap: $7.599M info
APRE
Jun 01, 2026, 8:00 AM EDT
Source: GlobeNewswire
Importance Score:
8
Price at Filing: $0.9076
Real-time Price: $0.6047 info
Change: -$0.3029 (-33%) info
Market Cap: $7.599M info
APRE
May 14, 2026, 3:54 AM EDT
Source: Wiseek News
Importance Score:
8
Price at Filing: $0.880
Real-time Price: $0.6047 info
Change: -$0.2753 (-31%) info
Market Cap: $7.599M info
APRE
May 13, 2026, 6:46 AM EDT
Filing Type: 10-Q
Importance Score:
8
Price at Filing: $0.870
Real-time Price: $0.6047 info
Change: -$0.2653 (-30%) info
Market Cap: $7.599M info