Soligenix Announces Positive Phase 3 FLASH Study Demonstrates Increased Efficacy with Continued Treatment in Patients with Cutaneous T-Cell Lymphoma
Soligenix, Inc. (SNGX)
NASDAQ:AMEX Investor Relations:
soligenix.com/investors
Company Research
Source: PR Newswire
PRINCETON, N.J., April 30, 2020 /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 continued treatment with SGX301 (synthetic hypericin) twice weekly for 12 weeks increased the positive response rate to 40% (pSoligenix previously announced positive top-line results when the study achieved statistical significance (p=0.04) in its primary endpoint over the first 6 week double-blind treatment cycle (referred to as Cycle 1) (available here). The study enrolled 169 patients randomized 2:1 to receive either SGX301 or placebo in Cycle 1. After the subsequent additional 6-week treatment in the open-label Cycle 2, the response rate in patients receiving a total of 12 weeks treatment increased two and a half-fold. Treatment responses for each cycle were assessed at Week 8 (after 6 weeks of
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News
- Cutaneous T-cell Lymphoma Market Landscape Report 2024: Comprehensive Insights About 25+ Companies and 30+ Pipeline Drugs [Yahoo! Finance]Yahoo! Finance
- Soligenix Announces Formation of European Medical Advisory Board for Cutaneous T-Cell Lymphoma [Yahoo! Finance]Yahoo! Finance
- Soligenix Announces Formation of European Medical Advisory Board for Cutaneous T-Cell LymphomaPR Newswire
- Soligenix to Present at November 21st Virtual Investor Summit Microcap Event [Yahoo! Finance]Yahoo! Finance
- Soligenix to Present at November 21st Virtual Investor Summit Microcap EventAccesswire
SNGX
Sec Filings
- 11/8/24 - Form 424B3
- 11/8/24 - Form 424B3
- 11/8/24 - Form 424B3
- SNGX's page on the SEC website