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Denali Therapeutics Inc.

24.92

-0.0300-0.12%

Post-market: 24.920.00000.00%19:30 EDT

Volume:680.99K

Turnover:16.96M

Market Cap:3.98B

PE:-8.79

High:25.37

Open:25.25

Low:24.60

Close:24.95

52wk High:27.30

52wk Low:12.58

Shares:159.85M

Float Shares:151.07M

Volume Ratio:0.67

T/O Rate:0.45%

Dividend:- -

Dividend Rate:- -

EPS(TTM):-2.8353

EPS(LYR):-2.9700

ROE:-54.93%

ROA:-29.15%

PB:4.77

PE(LYR):-8.39

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Overview Company News Filings

Denali regains full rights to DNL593 after Takeda ends collaboration

Denali Therapeutics Regains Full Rights to Investigational Therapy Dnl593 (Ptv:Pgrn) for Grn-Related Frontotemporal Dementia (Ftd-Grn)

THOMSON REUTERS

Denali Therapeutics Inc - to Continue Clinical Development of Dnl593 Using Transportvehicle Technology

THOMSON REUTERS

Denali Therapeutics Inc - Results From Phase 1/2 Study in Ftd-Grn Expected by End of 2026

THOMSON REUTERS

FDA grants accelerated approval to Denali’s tividenofusp alfa

Denali Therapeutics Inc - Receives $200 Mln in Gross Proceeds on March 27, 2026 - SEC Filing

THOMSON REUTERS

Is Denali Therapeutics’ (DNLI) First Brain-Penetrant Biologic Redefining Its Platform Value Proposition?

Simply Wall St.

Stifel Nicolaus Sticks to Its Buy Rating for Denali Therapeutics (DNLI)

Wedbush Remains a Buy on Denali Therapeutics (DNLI)

US FDA Approves Avlayah To Treat Neurologic Manifestations Of Hunter Syndrome

BUZZ-Denali Therapeutics climbs after US FDA approves co's genetic disorder therapy

US FDA approves Denali's genetic disorder therapy for children

Denali Therapeutics granted FDA approval of AVLAYAH for treatment of MPS II

Denali Therapeutics gains FDA accelerated approval for AVLAYAH in Hunter syndrome; CSF heparan sulfate drops 91% by week 24

Denali Therapeutics Announces U.S. FDA Approval of Avlayah™ (Tividenofusp Alfa-Eknm) for Treatment of Hunter Syndrome (Mps Ii)

THOMSON REUTERS

Denali Therapeutics Inc - Avlayah to Be Available in U.S. Shortly After Approval, Administered Once Weekly

THOMSON REUTERS

Denali Therapeutics Inc - Awarded Rare Pediatric Disease Priority Review Voucher With FDA Approval

THOMSON REUTERS

Denali Therapeutics Shares up 4.4%; US FDA Approves Co's Genetic Disorder Therapy

THOMSON REUTERS

US FDA - Approves Avlayah to Treat Neurologic Manifestations of Hunter Syndrome

THOMSON REUTERS

Wedbush Remains a Buy on Denali Therapeutics (DNLI)

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4669881","title":"Denali regains full rights to DNL593 after Takeda ends collaboration","url":"https://stock-news.laohu8.com/highlight/detail?id=2624669881","media":"Reuters","labels":["corporation","event"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2624669881?lang=en_us&edition=fundamental","pubTime":"2026-04-04 01:35","pubTimestamp":1775237738,"startTime":"0","endTime":"0","summary":"Denali regained full rights and control of investigational therapy DNL593 for GRN-related frontotemporal dementia following Takeda decision to terminate collaboration.Termination was driven by strategic considerations, not by efficacy or safety data.Denali plans to continue clinical development of DNL593 independently.Phase 1/2 study enrollment completed with 40 participants; results expected by end of 2026.Disclaimer: This news brief was created by Public Technologies  using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. 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