Rare disease drug developer Egetis Q3 revenue rises on EMCITATE sales
Overview
Sweden rare disease drug developer's Q3 net revenue rose 24% at CER, driven by EMCITATE sales
Company posted a wider Q3 net loss
FDA approved EMCITATE for MCT8 deficiency in the U.S. during the quarter
Outlook
Company prioritizes successful U.S. launch of EMCITATE in 2026
Company aims to optimize pricing and reimbursement and continue EMCITATE rollout in Europe
Egetis plans to finalize tiratricol development plan for RTH-beta in 2026
Result Drivers
FDA APPROVAL - EMCITATE received U.S. FDA approval for MCT8 deficiency, marking a key milestone for the company
COMMERCIAL LAUNCH PREPARATIONS - Co said extensive preparations enabled rapid U.S. launch of EMCITATE and early physician uptake
GERMANY SALES - Most Q3 EMCITATE sales came from Germany, where national reimbursement is in place
Company press release:
Key Details
Metric | Beat/Miss | Actual | Consensus Estimate |
9M Revenue | SEK 52.30 mln | ||
9M Adjusted Loss Per Share | SEK 0.80 | ||
9M Net Loss | SEK 350.40 mln |
Analyst Coverage
The current average analyst rating on the shares is "buy" and the breakdown of recommendations is 4 "strong buy" or "buy", no "hold" and 1 "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 Egetis Therapeutics AB (publ) is SEK18.00, about 80.2% above its November 4 closing price of SEK9.99
Reuters Recommended Reads
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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.)