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Soligenix Inc. Reports Promising Phase 3 Progress for HyBryte(TM) in CTCL Treatment

By Advos

TL;DR

Soligenix's HyBryte(TM) shows a 75% reduction in disease severity in early trials, positioning it as a potential leader in CTCL treatment by 2026.

HyBryte(TM), a light-activated topical therapy, targets early-stage mycosis fungoides in CTCL patients, with phase 3 trial results expected in late 2026.

Soligenix's HyBryte(TM) offers hope for CTCL patients, promising a significant improvement in quality of life through innovative, targeted treatment options.

Discover how Soligenix's HyBryte(TM) is revolutionizing CTCL treatment with a 75% efficacy rate in early trials, a breakthrough in rare disease therapy.

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Soligenix Inc. Reports Promising Phase 3 Progress for HyBryte(TM) in CTCL Treatment

Soligenix Inc. (NASDAQ: SNGX) recently provided an update on the progress of its Phase 3 trial for HyBryte(TM), a novel treatment for cutaneous T-cell lymphoma (CTCL), during an investment webinar. The company highlighted interim results from an investigator-initiated study at the University of Pennsylvania, where 75% of the first eight patients completing 18 weeks of treatment showed a greater than 50% reduction in disease severity. This development is significant as CTCL, a rare non-Hodgkin’s lymphoma, affects a considerable number of patients with limited treatment options available.

HyBryte(TM), Soligenix's lead asset, is a topical therapy activated by visible light, designed to target early-stage mycosis fungoides, which constitutes nearly 90% of CTCL cases. The therapy's mechanism offers a promising alternative to current treatments, which often come with significant side effects. With top-line results from the Phase 3 trial expected in the second half of 2026, the medical community and patients alike are keenly watching for potential advancements in CTCL treatment options.

The webinar, led by Dr. Christopher Schaber and Dr. Christopher Pullion, underscored Soligenix's commitment to addressing rare diseases and unmet medical needs. The positive interim results not only bolster the case for HyBryte(TM)'s efficacy but also highlight the importance of continued investment in rare disease research. For more information on the trial, visit https://ibn.fm/dz7eO.

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Advos

Advos

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