Switzerland's MoonLake Q3 net loss widens as R&D costs rise

By Reuters News


Overview

  • Switzerland biotech posted Q3 net loss as R&D expenses rose on milestone license fees

  • Company submitted Biologics License Application for sonelokimab to FDA for hidradenitis suppurativa

  • MoonLake ended Q3 with $498.5 mln in cash, expects runway to mid-2028


Outlook

  • Company expects FDA decision on sonelokimab BLA filing acceptance by end of Nov 2026

  • MoonLake anticipates potential US commercial launch of sonelokimab in H2 2027, if approved


Result Drivers

  • R&D EXPENSES - Co said expenses increased mainly due to milestone license fees tied to regulatory milestone associated with the expected acceptance of the Company's BLA submission


Company press release:


Key Details

Metric

Beat/Miss

Actual

Consensus Estimate

Q3 Loss Per Share

$0.93

Q3 Net Loss

$79.55 mln


Analyst Coverage

  • The current average analyst rating on the shares is "buy" and the breakdown of recommendations is 12 "strong buy" or "buy", 2 "hold" and 2 "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 MoonLake Immunotherapeutics is $30.00, about 156.4% above its November 3 closing price of $11.70


Reuters Recommended Reads

  • Nov 3 - Switzerland's Oculis Q3 net loss widens as expenses rise

  • Nov 2 - Switzerland's CRISPR Therapeutics Q3 CASGEVY revenue jumps 30% sequentially

  • Nov 2 - FDA to review uniQure's Huntington's gene therapy, decision due on May 2027


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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