Overview
US rare disease drug developer's Q4 net loss widened yr/yr as expenses rose
General and administrative expenses increased due to workforce expansion and commercial planning
Company achieved key regulatory milestones for MOLBREEVI in US and Europe
Outlook
Savara expects FDA PDUFA decision on MOLBREEVI by August 22, 2026
Result Drivers
REGULATORY COSTS - Higher research and development expenses were primarily due to regulatory affairs and quality assurance activities related to the MOLBREEVI BLA submission
COMMERCIAL PLANNING - General and administrative expenses rose due to workforce expansion and commercial activities ahead of potential MOLBREEVI launch
Company press release: ID:nBw2mblyra
Key Details
Metric | Beat/Miss | Actual | Consensus Estimate |
Q4 EPS |
| -$0.13 |
|
Q4 Net Income |
| -$32.24 mln |
|
Q4 Income from Operations |
| -$33.42 mln |
|
Q4 Operating Expenses |
| $33.42 mln |
|
Analyst Coverage
The current average analyst rating on the shares is "buy" and the breakdown of recommendations is 8 "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 Savara Inc is $10.25, about 92.7% above its March 12 closing price of $5.32
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