Soligenix Receives Positive Opinion from the European Medicines Agency on the Request for Orphan Drug Designation for SGX945 for the Treatment of Behçet's Disease [Yahoo! Finance]
Soligenix, Inc. (SNGX)
NASDAQ:AMEX Investor Relations:
soligenix.com/investors
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Source: Yahoo! Finance
PRINCETON, N.J. Feb. 26, 2026 /PRNewswire/ -- Soligenix, Inc. (Nasdaq: SNGX) (Soligenix or the Company), a late-stage biopharmaceutical company focused on developing and commercializing products to treat rare diseases where there is an unmet medical need, announced today that the European Medicines Agency (EMA) Committee for Orphan Medicinal Products (COMP) provided a positive recommendation on the Company's request for orphan drug designation for dusquetide (the active pharmaceutical ingredient in SGX945) for the treatment of Behçet's Disease, following review of the recently published Phase 2a clinical results demonstrating biological efficacy and safety in patients with Behçet's Disease The next step in the process will be ratification of the positive opinion by the European Commission. SGX945 has previously been granted both orphan drug and fast track designations from the US Food and Drug Administration (FDA) for the treatment of Behçet's Disease. (PRNewsfoto/Soligenix, Inc.)
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News
- Soligenix Receives Positive Opinion from the European Medicines Agency on the Request for Orphan Drug Designation for SGX945 for the Treatment of Behçet's DiseasePR Newswire
- Soligenix to Present at BIO Investment & Growth Summit [Yahoo! Finance]Yahoo! Finance
- Soligenix to Present at BIO Investment & Growth SummitPR Newswire
- Soligenix Details Recent Progress and Upcoming MilestonesPR Newswire
- Soligenix (NASDAQ:SNGX) had its "sell (e+)" rating reaffirmed by analysts at <a style="font-weight:bold" href="https://weissratings.com/">Weiss Ratings</a>.MarketBeat
SNGX
Sec Filings
- 2/17/26 - Form SCHEDULE
- 2/12/26 - Form 8-K
- 1/23/26 - Form 424B5
- SNGX's page on the SEC website