PK and ECG Determinations Following 8 Weeks of HyBryte Treatment for Cutaneous T-Cell Lymphoma
Trial details
- Registry ID
- NCT05380635
- Phase
- Phase 2
Company identity has not yet been verified
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Research sample: selected versions from May 2023 onward plus a preceding baseline where available. Only selected fields were retained; endpoint measures were truncated to 300 characters. This is not complete trial or sponsor history. Daily snapshots begin when collection starts.
| Trial | Sponsor | Phase | Status | Primary completion |
|---|---|---|---|---|
| PK and ECG Determinations Following 8 Weeks of HyBryte Treatment for Cutaneous T-Cell LymphomaNCT05380635 | Soligenix | Phase 2 | Completed | 2022-08-16Actual |
| Topical SGX302 for Mild-to-Moderate PsoriasisNCT05442190 | Soligenix | Phase 2 | Completed | 2025-10-22Actual |
| HyBryte (Synthetic Hypericin) Versus Valchlor (Mechlorethamine) in the Treatment of CTCLNCT06149247 | Soligenix | Phase 2 | Completed | 2024-05-31Actual |
| Dusquetide for the Treatment of Behcet's DiseaseNCT06386744 | Soligenix | Phase 2 | Completed | 2025-05-23Actual |
| Confirmatory Study of Topical HyBryte™ vs. Placebo for the Treatment of CTCLNCT06470451 | Soligenix | Phase 3 | Terminated | 2026-05-22Actual |
NCT06470451 · Soligenix
Estimated
Actual
80 participants (planned)
70 participants (actual)
Estimated
Actual
Jul 2026
22 May 2026
Recruiting
Terminated
NCT05442190 · Soligenix
Estimated
Actual
47 participants (planned)
15 participants (actual)
Estimated
Actual
Oct 2025
22 Oct 2025
Recruiting
Completed