MARKET

APRE

APRE

Aprea Therapeutics, Inc.
NASDAQ
3.960
+0.100
+2.59%
After Hours: 3.960 0 0.00% 16:00 07/26 EDT
OPEN
3.840
PREV CLOSE
3.860
HIGH
3.960
LOW
3.800
VOLUME
3.76K
TURNOVER
0
52 WEEK HIGH
8.85
52 WEEK LOW
2.830
MARKET CAP
21.50M
P/E (TTM)
-1.1921
1D
5D
1M
3M
1Y
5Y
1D
Weekly Report: what happened at APRE last week (0715-0719)?
Weekly Report · 4d ago
Weekly Report: what happened at APRE last week (0708-0712)?
Weekly Report · 07/15 10:43
Weekly Report: what happened at APRE last week (0701-0705)?
Weekly Report · 07/08 10:44
Weekly Report: what happened at APRE last week (0624-0628)?
Weekly Report · 07/01 10:45
Buy Rating on Aprea Therapeutics: Outshining Competitors with Selective and Potent WEE1 Inhibitor APR-1051
TipRanks · 06/27 19:35
Aprea Therapeutics Price Target Maintained With a $20.00/Share by HC Wainwright & Co.
Dow Jones · 06/24 17:45
HC Wainwright & Co. Reiterates Buy on Aprea Therapeutics, Maintains $20 Price Target
Benzinga · 06/24 17:34
Buy Rating Affirmed for Aprea Therapeutics on APR-1051’s Promising Safety and Efficacy Profile
TipRanks · 06/24 16:25
More
About APRE
Aprea Therapeutics, Inc. is a clinical-stage biopharmaceutical company focused on precision oncology through synthetic lethality. The Company's advanced synthetic lethality product candidate is ATRN-119, a clinical-stage small molecule inhibitor of ataxia telangiectasia and Rad3-related (ATR) a kinase that plays a critical role in DNA damage response (DDR). ATR and Checkpoint Kinase 1 are critical DDR kinases that prevent the collapse of replication forks into DNA double-strand breaks. It has completed all IND enabling studies for its oral, small molecule WEE1 inhibitor, APR-1051, and received United States Food and Drug Administration (FDA) clearance of its IND. It has an early-stage program that is in the lead optimization stage, for an undisclosed DDR target. The Company is evaluating potential combination opportunities within its pipeline, including research on the combination of ATRN-119 and APR-1051 that is supported by a Phase II SBIR grant from the National Cancer Institute.

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