Overview
U.S. CNS biopharma's Q1 net loss widened yr/yr on higher R&D and admin costs
Company's cash and investments rose to $1.4 bln, expected to fund operations into 2028
FDA accepted NDAs for ulixacaltamide and relutrigine; clinical pipeline advancing
Outlook
Company expects topline results from POWER1 study of vormatrigine in Q2 2026
Praxis anticipates EMERALD study topline results in broad DEEs in Q4 2026
FDA decision on ulixacaltamide NDA expected by Jan. 29, 2027; relutrigine by Sept. 27, 2026
Result Drivers
HIGHER R&D SPENDING - Praxis said increased Q1 research and development expenses were mainly due to higher costs for the Cerebrum platform, personnel, and Solidus platform
INCREASED ADMIN COSTS - General and administrative expenses rose due to higher personnel and professional expenses
Company press release: ID:nGNX8PgKR8
Key Details
Metric
Beat/Miss
Actual
Consensus Estimate
Q1 EPS
-$3.20
Q1 Net Income
-$92.56 mln
Q1 Operating Expenses
$105.86 mln
Q1 Operating Income
-$105.86 mln
Analyst Coverage
The current average analyst rating on the shares is "buy" and the breakdown of recommendations is 15 "strong buy" or "buy", 1 "hold" and 1 "sell" or "strong sell"
Wall Street's median 12-month price target for Praxis Precision Medicines Inc is $554.00, about 63.9% above its May 6 closing price of $338.07
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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.)