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Soligenix Advances HyBryte Therapy for Early-Stage Cutaneous T-Cell Lymphoma Treatment

By Burstable Editorial Team

TL;DR

Soligenix's HyBryte therapy offers investors a strategic advantage by targeting the challenging early-stage CTCL market with a novel, visible light-activated treatment showing significant clinical efficacy.

HyBryte works as a photodynamic therapy using synthetic hypericin activated by visible red-yellow light to target malignant T-cells in skin while minimizing damage to healthy tissue.

This therapy improves patient outcomes by providing a safer, targeted treatment for early-stage CTCL, reducing long-term risks and addressing a critical gap in rare disease care.

Soligenix's visible light therapy represents an innovative shift from traditional ultraviolet treatments, using synthetic hypericin to precisely target cancer cells with minimal collateral damage.

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Soligenix Advances HyBryte Therapy for Early-Stage Cutaneous T-Cell Lymphoma Treatment

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. Cutaneous T-cell lymphoma is recognized by clinicians as one of the most difficult cancers to diagnose accurately in its early stages, creating significant challenges for patients and healthcare providers within a challenging diagnostic and treatment landscape.

HyBryte represents a visible light-activated photodynamic therapy designed specifically for the treatment of early-stage CTCL. Unlike traditional ultraviolet-based phototherapies that 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, potentially addressing critical safety concerns associated with existing therapies.

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 as a novel photodynamic therapy utilizing safe visible light. With successful completion of the second Phase 3 study, regulatory approvals will be sought to support potential commercialization worldwide.

Soligenix is a late-stage biopharmaceutical company focused on developing and commercializing products to treat rare diseases where there is an unmet medical need. The company's development programs in this business segment also include expansion of synthetic hypericin into psoriasis, the company's 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 maintains a Public Health Solutions business segment that 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. The development of Soligenix's vaccine programs incorporates the use of its proprietary heat stabilization platform technology known as ThermoVax. This business segment has 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.

For further information about the company's developments, visit https://www.Soligenix.com. Additional news and updates relating to SNGX are available through specialized financial communications platforms that provide wire-grade press release syndication for public companies and the investment community.

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Burstable Editorial Team

Burstable Editorial Team

@burstable

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