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Aprea Therapeutics Inc

APRE
î˜đ
āļ”āļđāđāļœāļ™āļ āļđāļĄāļīāđ‚āļ”āļĒāļĨāļ°āđ€āļ­āļĩāļĒāļ”
1.370USD
-0.030-2.14%
āļ›āļīāļ” 11/04, 16:00ETāļĢāļēāļ„āļēāļĨāđˆāļēāļŠāđ‰āļē 15 āļ™āļēāļ—āļĩ
7.88MāļĄāļđāļĨāļ„āđˆāļēāļ•āļĨāļēāļ”
āļ‚āļēāļ”āļ—āļļāļ™P/E TTM
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Intraday
1m
30m
1h
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W
M
D

āļ§āļąāļ™āļ™āļĩāđ‰

-2.14%

5 āļ§āļąāļ™

-3.52%

1 āđ€āļ”āļ·āļ­āļ™

-8.67%

6 āđ€āļ”āļ·āļ­āļ™

-25.94%

āļ•āđ‰āļ™āļ›āļĩāļˆāļ™āļ–āļķāļ‡āļ›āļąāļˆāļˆāļļāļšāļąāļ™

-58.36%

1 āļ›āļĩ

-65.51%

āļ”āļđāđāļœāļ™āļ āļđāļĄāļīāđ‚āļ”āļĒāļĨāļ°āđ€āļ­āļĩāļĒāļ”

āļ„āļ°āđāļ™āļ™āļŦāļļāđ‰āļ™ TradingKey āļ‚āļ­āļ‡ Aprea Therapeutics Inc

āļŠāļāļļāļĨāđ€āļ‡āļīāļ™: USD āļ­āļąāļ›āđ€āļ”āļ•āđ€āļĄāļ·āđˆāļ­: 2025-11-04

āļ‚āđ‰āļ­āļĄāļđāļĨāđ€āļŠāļīāļ‡āļĨāļķāļ

āļ›āļąāļˆāļˆāļąāļĒāļžāļ·āđ‰āļ™āļāļēāļ™āļ‚āļ­āļ‡āļšāļĢāļīāļĐāļąāļ—āļ„āđˆāļ­āļ™āļ‚āđ‰āļēāļ‡ āđāļ‚āđ‡āļ‡āđāļāļĢāđˆāļ‡āļĄāļēāļāļĄāļđāļĨāļ„āđˆāļēāļ›āļĢāļ°āđ€āļĄāļīāļ™āļ‚āļ­āļ‡āļšāļĢāļīāļĐāļąāļ—āļ™āļĩāđ‰āļ–āļ·āļ­āļ§āđˆāļē āļĄāļđāļĨāļ„āđˆāļēāļĒāļļāļ•āļīāļ˜āļĢāļĢāļĄāđāļĨāļ°āļāļēāļĢāļĒāļ­āļĄāļĢāļąāļšāļˆāļēāļāļŠāļ–āļēāļšāļąāļ™āļ–āļ·āļ­āļ§āđˆāļē āļŠāļđāļ‡āļĄāļēāļāļ•āļĨāļ­āļ”āļŠāđˆāļ§āļ‡ 30 āļ§āļąāļ™āļ—āļĩāđˆāļœāđˆāļēāļ™āļĄāļē āļ™āļąāļāļ§āļīāđ€āļ„āļĢāļēāļ°āļŦāđŒāļŦāļĨāļēāļĒāļĢāļēāļĒāđ„āļ”āđ‰āđƒāļŦāđ‰āđ€āļĢāļ•āļ•āļīāđ‰āļ‡āļšāļĢāļīāļĐāļąāļ—āļ™āļĩāđ‰āđ€āļ›āđ‡āļ™ āđāļ™āļ°āļ™āļģāđƒāļŦāđ‰āļ‹āļ·āđ‰āļ­āļ­āļĒāđˆāļēāļ‡āļĒāļīāđˆāļ‡āđāļĄāđ‰āļ§āđˆāļēāļœāļĨāļāļēāļĢāļ”āļģāđ€āļ™āļīāļ™āļ‡āļēāļ™āđƒāļ™āļ•āļĨāļēāļ”āļŦāļļāđ‰āļ™āļˆāļ°āļ­āļĒāļđāđˆāđƒāļ™āļĢāļ°āļ”āļąāļšāļ›āļēāļ™āļāļĨāļēāļ‡ āđāļ•āđˆāļšāļĢāļīāļĐāļąāļ—āļĄāļĩāļ—āļąāđ‰āļ‡āļ›āļąāļˆāļˆāļąāļĒāļžāļ·āđ‰āļ™āļāļēāļ™āđāļĨāļ°āļŠāļąāļāļāļēāļ“āļ—āļēāļ‡āđ€āļ—āļ„āļ™āļīāļ„āļ—āļĩāđˆāđāļ‚āđ‡āļ‡āđāļāļĢāđˆāļ‡āļĢāļēāļ„āļēāļŦāļļāđ‰āļ™āļāļģāļĨāļąāļ‡āđ€āļ„āļĨāļ·āđˆāļ­āļ™āđ„āļŦāļ§āđƒāļ™āļāļĢāļ­āļšāđāļ„āļšāļĢāļ°āļŦāļ§āđˆāļēāļ‡āđāļ™āļ§āļĢāļąāļšāđāļĨāļ°āđāļ™āļ§āļ•āđ‰āļēāļ™ āļ—āļģāđƒāļŦāđ‰āđ€āļŦāļĄāļēāļ°āļŠāļģāļŦāļĢāļąāļšāļāļēāļĢāđ€āļ—āļĢāļ”āđāļšāļšāļŠāļ§āļīāļ‡āđƒāļ™āļāļĢāļ­āļšāļĢāļēāļ„āļē

āļ„āļ°āđāļ™āļ™āļ‚āļ­āļ‡ Aprea Therapeutics Inc

āļ‚āđ‰āļ­āļĄāļđāļĨāļ—āļĩāđˆāđ€āļāļĩāđˆāļĒāļ§āļ‚āđ‰āļ­āļ‡

āļ­āļąāļ™āļ”āļąāļšāđƒāļ™āļ­āļļāļ•āļŠāļēāļŦāļāļĢāļĢāļĄ
106 / 407
āļ­āļąāļ™āļ”āļąāļšāļĢāļ§āļĄ
223 / 4616
āļ­āļļāļ•āļŠāļēāļŦāļāļĢāļĢāļĄ
āđ€āļ—āļ„āđ‚āļ™āđ‚āļĨāļĒāļĩāļŠāļĩāļ§āļ āļēāļžāđāļĨāļ°āļāļēāļĢāļ§āļīāļˆāļąāļĒāļ—āļēāļ‡āļāļēāļĢāđāļžāļ—āļĒāđŒ

āđāļ™āļ§āļ•āđ‰āļēāļ™ & āđāļ™āļ§āļĢāļąāļš

āđ„āļĄāđˆāļĄāļĩāļ‚āđ‰āļ­āļĄāļđāļĨ

āđāļœāļ™āļ āļđāļĄāļīāđ€āļĢāļ”āļēāļĢāđŒ

āļĢāļēāļ„āļēāļ›āļąāļˆāļˆāļļāļšāļąāļ™
āļ„āļĢāļąāđ‰āļ‡āļāđˆāļ­āļ™

āļĢāļēāļ„āļēāđ€āļ›āđ‰āļēāļŦāļĄāļēāļĒāļ™āļąāļāļ§āļīāđ€āļ„āļĢāļēāļ°āļŦāđŒ

āļ­āđ‰āļēāļ‡āļ­āļīāļ‡āļˆāļēāļāļ™āļąāļāļ§āļīāđ€āļ„āļĢāļēāļ°āļŦāđŒāļ—āļąāđ‰āļ‡āļŦāļĄāļ” 2 āļ„āļ™
āđāļ™āļ°āļ™āļģāđƒāļŦāđ‰āļ‹āļ·āđ‰āļ­āļ—āļąāļ™āļ—āļĩ
āļ„āļ°āđāļ™āļ™āļ›āļąāļˆāļˆāļļāļšāļąāļ™
10.500
āļĢāļēāļ„āļēāđ€āļ›āđ‰āļēāļŦāļĄāļēāļĒ
+650.00%
āđ‚āļ­āļāļēāļŠāđƒāļ™āļāļēāļĢāđ€āļ•āļīāļšāđ‚āļ•āļ‚āļ­āļ‡āļĢāļēāļ„āļē
āļ„āļģāļŠāļĩāđ‰āđāļˆāļ‡: āļāļēāļĢāļˆāļąāļ”āļ­āļąāļ™āļ”āļąāļšāđāļĨāļ°āļĢāļēāļ„āļēāđ€āļ›āđ‰āļēāļŦāļĄāļēāļĒāđ‚āļ”āļĒāļ™āļąāļāļ§āļīāđ€āļ„āļĢāļēāļ°āļŦāđŒāļˆāļąāļ”āļ—āļģāđ‚āļ”āļĒ LSEG āđ€āļžāļ·āđˆāļ­āļ§āļąāļ•āļ–āļļāļ›āļĢāļ°āļŠāļ‡āļ„āđŒāđƒāļ™āļāļēāļĢāđƒāļŦāđ‰āļ‚āđ‰āļ­āļĄāļđāļĨāđ€āļ—āđˆāļēāļ™āļąāđ‰āļ™ āđāļĨāļ°āđ„āļĄāđˆāļ–āļ·āļ­āđ€āļ›āđ‡āļ™āļ„āļģāđāļ™āļ°āļ™āļģāđƒāļ™āļāļēāļĢāļĨāļ‡āļ—āļļāļ™

āļˆāļļāļ”āđ€āļ”āđˆāļ™āļ‚āļ­āļ‡ Aprea Therapeutics Inc

āļˆāļļāļ”āđāļ‚āđ‡āļ‡āļ„āļ§āļēāļĄāđ€āļŠāļĩāđˆāļĒāļ‡
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.
āļāļģāļĨāļąāļ‡āđ€āļ•āļīāļšāđ‚āļ•
āļšāļĢāļīāļĐāļąāļ—āļ­āļĒāļđāđˆāđƒāļ™āļŠāđˆāļ§āļ‡āļāļēāļĢāđ€āļ•āļīāļšāđ‚āļ• āđ‚āļ”āļĒāļĄāļĩāļĢāļēāļĒāđ„āļ”āđ‰āļĢāļ§āļĄāļ›āļĢāļ°āļˆāļģāļ›āļĩāļĨāđˆāļēāļŠāļļāļ”āļ­āļĒāļđāđˆāļ—āļĩāđˆ USD 1.50M
āļĄāļđāļĨāļ„āđˆāļēāļĒāļļāļ•āļīāļ˜āļĢāļĢāļĄ
PE āļĨāđˆāļēāļŠāļļāļ”āļ‚āļ­āļ‡āļšāļĢāļīāļĐāļąāļ—āļ­āļĒāļđāđˆāļ—āļĩāđˆ -0.60 āļ‹āļķāđˆāļ‡āļ­āļĒāļđāđˆāđƒāļ™āļŠāđˆāļ§āļ‡āđ€āļ›āļ­āļĢāđŒāđ€āļ‹āđ‡āļ™āđ„āļ—āļĨāđŒāļ›āļēāļ™āļāļĨāļēāļ‡āļ‚āļ­āļ‡āļĢāļ­āļš 3 āļ›āļĩ
āļāļēāļĢāļ‚āļēāļĒāđ‚āļ”āļĒāļŠāļ–āļēāļšāļąāļ™
āļāļēāļĢāļ–āļ·āļ­āļ„āļĢāļ­āļ‡āļĨāđˆāļēāļŠāļļāļ”āđ‚āļ”āļĒāļŠāļ–āļēāļšāļąāļ™āļ­āļĒāļđāđˆāļ—āļĩāđˆ 1.82M āļŦāļļāđ‰āļ™ āļĨāļ”āļĨāļ‡ 27.31% āđāļšāļšāđ„āļ•āļĢāļĄāļēāļŠāļ•āđˆāļ­āđ„āļ•āļĢāļĄāļēāļŠ
āļ–āļ·āļ­āļ„āļĢāļ­āļ‡āđ‚āļ”āļĒ The Vanguard
āļ™āļąāļāļĨāļ‡āļ—āļļāļ™āļŠāļ·āđˆāļ­āļ”āļąāļ‡ The Vanguard āļ–āļ·āļ­āļŦāļļāđ‰āļ™āļ•āļąāļ§āļ™āļĩāđ‰āļ­āļĒāļđāđˆāļˆāļģāļ™āļ§āļ™ 173.84K āļŦāļļāđ‰āļ™

Aprea Therapeutics Inc āļ‚āđˆāļēāļ§āļŠāļēāļĢ

āļˆāļ°āļĄāļĩāļ‚āđˆāļēāļ§āļŠāļēāļĢāđ€āļžāļīāđˆāļĄāđ€āļ•āļīāļĄāđ€āļĢāđ‡āļ§āđ† āļ™āļĩāđ‰ āđ‚āļ›āļĢāļ”āļ•āļīāļ”āļ•āļēāļĄ...

āļ•āļąāļ§āļŠāļĩāđ‰āļ§āļąāļ”āļ—āļēāļ‡āļāļēāļĢāđ€āļ‡āļīāļ™î˜

EPS

āđ„āļĄāđˆāļĄāļĩāļ‚āđ‰āļ­āļĄāļđāļĨ

āļĢāļēāļĒāđ„āļ”āđ‰āļĢāļ§āļĄ

āđ„āļĄāđˆāļĄāļĩāļ‚āđ‰āļ­āļĄāļđāļĨ

āļ‚āđ‰āļ­āļĄāļđāļĨ Aprea Therapeutics Inc

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.
āļŠāļąāļāļĨāļąāļāļĐāļ“āđŒāļĒāđˆāļ­āļ‚āļ­āļ‡āļŦāļļāđ‰āļ™APRE
āļšāļĢāļīāļĐāļąāļ—Aprea Therapeutics Inc
āļ‹āļĩāļ­āļĩāđ‚āļ­Dr. Oren Gilad, Ph.D.
āđ€āļ§āđ‡āļšāđ„āļ‹āļ•āđŒhttps://www.aprea.com/
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