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Overview
* US biotech firm's Q4 net loss widened, driven by higher R&D expenses for nomlabofusp
* Company completed $115 mln public offering in Feb 2026, extending cash runway into Q2 2027
* FDA granted Breakthrough Therapy Designation for nomlabofusp in adults and children with FA
Outlook
* Larimar plans to report topline open label study data in Q2 2026
* Company expects to initiate screening for global Phase 3 study in Q2 2026
* Larimar targets BLA submission seeking accelerated approval in June 2026; U.S. launch first-half 2027, if approved
Result Drivers
* NOMLABOFUSP MANUFACTURING COSTS - Higher Q4 R&D expenses were mainly due to increased nomlabofusp manufacturing costs, including process qualification and scale up activities
* CLINICAL AND REGULATORY SPENDING - Additional increases came from higher costs for ongoing clinical studies, consulting fees for quality, clinical, and regulatory activities, and personnel expenses
* LOWER INTEREST INCOME - Decrease in other income was mainly due to lower interest yields and lower average investable cash balances
Company press release: ID:nGNXbPqYrY
Key Details
Metric Beat/Mis Actual Consensu
s s
Estimate
Q4 EPS -$0.73
Q4 Net -$62.50
Income mln
Q4 -$64.02
Income mln
From
Operatio
ns
Q4 $64.02
Operatin mln
g
Expenses
Analyst Coverage
* The current average analyst rating on the shares is "strong buy" and the breakdown of recommendations is 11 "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 Larimar Therapeutics Inc is $16.00, about 272.1% above its March 18 closing price of $4.30
For questions concerning the data in this report, contact Estimates.Support@lseg.com. For any other questions or feedback, contact .
(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.)