MetaVia Q3 net loss widens on higher R&D costs
Overview
Biotechnology firm's Q3 net loss widened yr/yr on higher R&D and administrative expenses
Company reported positive interim Phase 1 data for DA-1726 in liver-related cardiometabolic diseases
MetaVia appointed Sarah Browne, M.D., as Chief Medical Officer to lead clinical development
Outlook
MetaVia targets initiation of a 48-week Phase 2 study for DA-1726 in MetALD and ALD in H2 2027
Company expects full data from DA-1726 Phase 1 Parts 3A and 3B in Q1 2027
MetaVia plans to begin Phase 2a proof-of-concept study for vanoglipel in combination with resmetirom in H1 2027
Result Drivers
R&D SPENDING - Higher Q3 R&D expenses were mainly due to increased direct costs for DA-1726 product development
CLINICAL DATA - Positive interim Phase 1 data for DA-1726 showed reductions in liver fat, body weight, and uric acid, supporting further development in liver-related diseases
Company press release:
Key Details
Metric | Beat/Miss | Actual | Consensus Estimate |
Q3 Loss Per Basic Share | $0.69 |
Analyst Coverage
The current average analyst rating on the shares is "buy" and the breakdown of recommendations is 2 "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 MetaVia Inc is $20.00, about 1,438.5% above its November 12 closing price of $1.30
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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.)