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Soligenix Advances Targeted CTCL Therapy HyBryte™ to Address Critical Treatment Gaps

By Editorial Staff

TL;DR

Soligenix's HyBryte therapy offers a competitive edge by providing a safer, targeted treatment for early-stage CTCL with proven efficacy, potentially capturing a niche market.

HyBryte works as a visible light-activated photodynamic therapy that selectively targets malignant T-cells in the skin while minimizing damage to surrounding healthy tissue.

This therapy improves patient outcomes by offering a safer, effective treatment for a difficult-to-diagnose cancer, enhancing quality of life for those with rare diseases.

HyBryte uses synthetic hypericin activated by red-yellow light, a novel approach that avoids the long-term risks of traditional ultraviolet phototherapies for CTCL.

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Soligenix Advances Targeted CTCL Therapy HyBryte™ to Address Critical Treatment Gaps

Soligenix Inc. (NASDAQ: SNGX) is advancing a novel therapeutic approach for cutaneous T-cell lymphoma through its development of HyBryte™, also known as synthetic hypericin. CTCL is recognized by clinicians as one of the most difficult cancers to diagnose accurately in its early stages, creating significant challenges within the diagnostic and treatment landscape.

HyBryte is a visible light-activated photodynamic therapy designed specifically for the treatment of early-stage CTCL. Unlike traditional ultraviolet-based phototherapies, which can carry long-term safety risks with cumulative exposure, HyBryte is activated by visible light in the red-yellow spectrum. This mechanism allows for targeted treatment of malignant T-cells in the skin while minimizing damage to surrounding healthy tissue, addressing a critical gap in current treatment options.

Clinical data reported by Soligenix indicate that HyBryte has demonstrated statistically significant efficacy in reducing CTCL lesions in patients with early-stage disease. The company's Specialized BioTherapeutics business segment is developing and moving toward potential commercialization of HyBryte, with regulatory approvals being sought worldwide following successful completion of the second Phase 3 study. For further information about the company's development programs, visit https://www.Soligenix.com.

Soligenix is a late-stage biopharmaceutical company focused on developing and commercializing products to treat rare diseases where there is an unmet medical need. Beyond HyBryte, the company's development programs in this business segment include expansion of synthetic hypericin into psoriasis, its first-in-class innate defense regulator technology dusquetide for the treatment of inflammatory diseases including oral mucositis in head and neck cancer, and additional applications in Behçet's disease.

The company's Public Health Solutions business segment includes development programs for RiVax®, its ricin toxin vaccine candidate, as well as vaccine programs targeting filoviruses such as Marburg and Ebola, and CiVax™, the company's vaccine candidate for the prevention of COVID-19. These programs incorporate the company's proprietary heat stabilization platform technology known as ThermoVax® and have been supported with government grants and contract funding from the National Institute of Allergy and Infectious Diseases, the Defense Threat Reduction Agency, and the Biomedical Advanced Research and Development Authority.

The advancement of HyBryte represents a significant development in oncology treatment, particularly for rare diseases that have historically received limited therapeutic innovation. For investors and industry observers, the latest news and updates relating to SNGX are available through specialized financial communications platforms. The development of targeted therapies like HyBryte that minimize damage to healthy tissue while effectively treating malignant cells could establish new standards for cancer treatment approaches across multiple indications.

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Editorial Staff

Editorial Staff

@editorial-staff

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