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Condition / disease
Location
Status: Recruiting

A Phase 2 Study of PTX 100 in Patients With Relapsed/Refractory CTCL

This is an open-label, phase 2 randomized study to evaluate the efficacy, safety, pharmacokinetics (PK) and pharmadynamics (PD), of PTX-100 monotherapy at 500 or 1000 mg/m2 in patients with relapsed/refractory Cutaneous T-Cell Lymphoma (CTCL). PTX-100 will be administered by IV infusion over 60 minutes on days 1 to 5 of a 14-day cycle for 4 cycles, then 21 day cycle thereafter. Subjects will be treated or followed up, if subjects discontinue treatment, for up to 18 months.

Participants needed: 115
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Prescient Therapeutics, Ltd.Updated: Apr 29, 2026Locations: 15
Eligibility criteria

Adult patient ≥18 years of age at the time of signing the informed consent. [+20]

Patients with known central nervous system involvement. [+2]