Overview
US biotech reported Q1 net loss widened to $19.1 mln, EPS at -$0.22
Company ended Q1 with $234 mln in cash and investments after $150 mln private placement
R&D expenses fell yr/yr due to non-recurring 2025 costs, G&A expenses increased
Outlook
Relmada expects to file NDV-01 IND and start Phase 3 RESCUE program in mid-2026
Company anticipates Sepranolone Phase 2 trial initiation in Prader-Willi syndrome in mid-2026
Relmada expects current cash to fund operations through 2029, including NDV-01 Phase 3 completion
Result Drivers
R&D EXPENSE DECREASE - Co said lower R&D expense was due to non-recurring costs for sepranolone acquisition and NDV-01 license in 2025, partially offset by increased costs for new trials and R&D personnel
G&A EXPENSE INCREASE - Higher G&A expense was mainly due to increased compensation costs, partially offset by lower stock-based compensation
Company press release: ID:nGNX4z10tW
Key Details
Metric
Beat/Miss
Actual
Consensus Estimate
Q1 EPS
-$0.22
Q1 Net Income
-$19.10 mln
Q1 Cash & Investments
$234 mln
Analyst Coverage
The current average analyst rating on the shares is "buy" and the breakdown of recommendations is 5 "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 Relmada Therapeutics Inc is $13.00, about 76.6% above its May 11 closing price of $7.36
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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.)