Soligenix Shares Gain On HyBrytes Data From Blood Cancer Study

Soligenix Inc SNGX announced the results of its Phase 3 FLASH study evaluating HyBryte (synthetic hypericin) for cutaneous T-cell lymphoma (CTCL) had been published in the Journal of the American Medical Association (JAMA) Dermatology.
"The peer-reviewed publication of these data in JAMA Dermatology is a testament and further validation to the importance of the findings for the scientific and CTCL disease communities," stated Ellen Kim, the Lead Principal Investigator for Phase 3 FLASH study.
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The published findings demonstrate that HyBryte statistically significantly reduced lesion size, with the treatment response further improving over successive 6-week treatment cycles.
After the first 6-week treatment window, 16% of patients responded. This response rate continued to increase significantly to 49% through 18 weeks of treatment versus patients with 6-week hypericin or placebo.
Throughout the study, HyBryte was safe and well-tolerated. HyBryte was observed to perform similarly against both patch and thicker plaque lesions characteristic of CTCL.
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