MARKET

DAWN

DAWN

Day One Biopharmaceuticals, Inc.
NASDAQ
16.64
+1.26
+8.19%
After Hours: 17.07 +0.43 +2.58% 19:59 04/23 EDT
OPEN
15.58
PREV CLOSE
15.38
HIGH
17.39
LOW
15.11
VOLUME
6.70M
TURNOVER
0
52 WEEK HIGH
17.85
52 WEEK LOW
9.67
MARKET CAP
1.45B
P/E (TTM)
-7.0264
1D
5D
1M
3M
1Y
5Y
Buy Rating Affirmed for Day One Biopharmaceuticals Following FDA Approval of Ojemda
TipRanks · 10h ago
Day One's OJEMDA Receives U.S. FDA Accelerated Approval For Relapsed Or Refractory BRAF-Altered Pediatric Low-Grade Glioma
First and only FDA-approved type II RAF inhibitor for patients with relapsed or refractory pLGG harboring a BRAF fusion or rearrangement. Day One receives rare pediatric disease priority review voucher. Conference call and webcast to be April 24, 8:30 a.m. Eastern Time.
Benzinga · 12h ago
DAY ONE’S OJEMDA™ (TOVORAFENIB) RECEIVES US FDA ACCELERATED APPROVAL FOR RELAPSED OR REFRACTORY BRAF-ALTERED PEDIATRIC LOW-GRADE GLIOMA (PLGG), THE MOST COMMON FORM OF CHILDHOOD BRAIN TUMOR
Reuters · 12h ago
Day One Biopharmaceuticals Drug Tovorafenib Gets FDA Accelerated Approval
Day One Biopharmaceuticals' drug tovorafenib gets accelerated approval from the FDA. The drug is approved for patients with relapsed or refractory pediatric low-grade glioma. The company's shares rose 10%, to $16.90.
Dow Jones · 13h ago
Buy Rating on Day One Biopharmaceuticals Amid FDA Approval and Strong Market Prospects
TipRanks · 13h ago
BUZZ-Day One Biopharma gains on FDA's accelerated nod for brain tumor treatment
Shares of Day One Biopharmaceuticals rise 10.2% to $16.94. FDA granted accelerated approval to DAWN's monotherapy for brain tumor treatment. The therapy will require confirmatory trials to receive traditional approval. YTD stock up 16%.
Reuters · 13h ago
SHARES OF DAY ONE BIOPHARMACEUTICALS RISE ABOUT 10% AS FDA GRANTS ACCELERATED APPROVAL FOR BRAIN TUMOR THERAPY
Reuters · 13h ago
BRIEF-FDA Grants Accelerated Approval To Tovorafenib For Patient With Relapsed Or Refractory Braf-Altered Pediatric Low-Grade Glioma
FDA Grants Accelerated Approval To Tovorafenib For Patient With Relapsed Or Refractory Braf-Altered Pediatric Low-Grade Glioma. FDA says drug can be used to treat patients with relapsed or refractory cancer.
Reuters · 13h ago
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About DAWN
Day One Biopharmaceuticals, Inc. is a clinical-stage biopharmaceutical company focused on developing and commercializing targeted therapies for people of all ages with life-threatening diseases. The Company partners with clinical oncologists, families, and scientists to identify, acquire, and develop cancer treatments. Its product candidates include tovorafenib, pimasertib and the VRK1 program. The Company’s lead product candidate, tovorafenib, is an investigational, oral, brain-penetrant, highly selective type II RAF kinase inhibitor. The Company’s pipeline also includes pimasertib, an investigational, oral, highly selective small molecule inhibitor of mitogen-activated protein kinases 1 and 2 (MEK-1/-2). It has initiated an open-label, multicenter, phase Ib/IIa umbrella master trial, or FIRELIGHT-1, of tovorafenib as a monotherapy or in combination, which consists of two substudies. Substudy 1 is a phase IIa trial of tovorafenib as a monotherapy in patients 12 years and older.

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