Amylyx Pharma Q3 net loss bigger than expected

By Reuters News


Overview

  • U.S. biopharma's Q3 loss per share was in line with analyst expectations

  • Net loss and operating income for Q3 missed analyst estimates

  • Company reported positive Phase 3 LUCIDITY trial results for avexitide in post-bariatric hypoglycemia


Outlook

  • Company expects to submit NDA for avexitide by end-2026

  • Amylyx preparing for potential avexitide launch in 2027, if approved

  • Amylyx targets IND filing for AMX0318 in 2027


Result Drivers

  • CLINICAL TRIAL RESULTS - Positive topline results from Phase 3 LUCIDITY trial of avexitide in post-bariatric hypoglycemia drove activity in the quarter

  • R&D SPENDING - Higher R&D expenses driven by costs related to Phase 3 LUCIDITY trial and avexitide programs

  • COMMERCIAL PREPARATION - Increased SG&A expenses due to hiring and pre-commercialization activities ahead of potential avexitide launch


Company press release:


Key Details

Metric

Beat/Miss

Actual

Consensus Estimate

Q3 Loss Per Share

Meet

$0.38

$0.38 (10 Analysts)

Q3 Net Loss

Miss

$45.49 mln

$43.70 mln (10 Analysts)

Q3 Operating Income

Miss

-$49.66 mln

-$46.22 mln (10 Analysts)

Q3 Operating Expenses

$49.66 mln


Analyst Coverage

  • The current average analyst rating on the shares is "strong buy" and the breakdown of recommendations is 11 "strong buy" or "buy", 1 "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 Amylyx Pharmaceuticals, Inc. is $42.00, about 42.9% above its November 4 closing price of $29.40


Reuters Recommended Reads

  • Nov 4 - Kailera Therapeutics Q3 net loss widens on higher R&D costs

  • Nov 4 - Summit Therapeutics reports Q3 loss on higher R&D spending

  • Nov 3 - Rhythm Pharma Q3 net loss narrower than estimated on IMCIVREE demand


For questions concerning the data in this report, contact Estimates.Support@lseg.com. For any other questions or feedback, contact reuters.support@thomsonreuters.com.


(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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