Overview
Denali Q3 net loss widens to $126.9 mln from $107.2 mln last year
Operating expenses increased due to R&D and commercial launch preparations
FDA extends tividenofusp alfa review timeline to April 2026 from January
Outlook
Denali expects to launch tividenofusp alfa for Hunter syndrome after FDA review by April 2026
Company plans global Phase 3 study for DNL126 in Sanfilippo syndrome type A
Denali submitted applications to start clinical studies for Alzheimer's and Pompe diseases
Result Drivers
R&D EXPENSES - Increase in R&D expenses driven by operations at new manufacturing facility and personnel-related costs
COMMERCIAL LAUNCH PREPARATIONS - Increase in general and administrative expenses due to preparations for tividenofusp alfa commercial launch
Key Details
Metric | Beat/Miss | Actual | Consensus Estimate |
Q3 Net Income | -$126.90 mln | ||
Q3 Basic EPS | -$0.74 | ||
Q3 Operating Expenses | $137.43 mln | ||
Q3 Operating Income | -$137.43 mln |
Analyst Coverage
The current average analyst rating on the shares is "buy" and the breakdown of recommendations is 19 "strong buy" or "buy", no "hold" and no "sell" or "strong sell"
The average consensus recommendation for the biotechnology & medical research peer group is "buy"
Wall Street's median 12-month price target for Denali Therapeutics Inc is $30.00, about 50.4% above its November 5 closing price of $14.89
Press Release: ID:nGNX9zKDmR
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(This story was created using Reuters automation and AI based on LSEG and company data. It was checked and edited by a Reuters journalist prior to publication.)
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