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A Phase 1a/1b Trial in Relapsed/Refractory T-cell Non-Hodgkin Lymphoma to Determine the Safety Profile, Pharmacology, and Maximum Tolerated Dose of ST-001, a Fenretinide Phospholipid Suspension (12.5 Mg/mL) for Intravenous Infusion

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Trial Profile

A Phase 1a/1b Trial in Relapsed/Refractory T-cell Non-Hodgkin Lymphoma to Determine the Safety Profile, Pharmacology, and Maximum Tolerated Dose of ST-001, a Fenretinide Phospholipid Suspension (12.5 Mg/mL) for Intravenous Infusion

Status: Recruiting
Phase of Trial: Phase I

Latest Information Update: 10 Oct 2025

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At a glance

  • Drugs Fenretinide (Primary)
  • Indications Anaplastic large cell lymphoma; Cutaneous T-cell lymphoma; Follicular lymphoma; Mycosis fungoides; Non-Hodgkin's lymphoma; Peripheral T-cell lymphoma; Sezary syndrome; Squamous cell cancer; T-cell lymphoma
  • Focus Adverse reactions; First in man
  • Sponsors SciTech Development

Most Recent Events

  • 22 Sep 2025 Planned End Date changed from 1 Nov 2025 to 1 May 2027.
  • 22 Sep 2025 Planned primary completion date changed from 1 May 2025 to 1 Dec 2026.
  • 13 Jan 2025 According to a SciTech Development media release, Patient Enrollment is Complete in Phase 1a Accelerated Trial and the trial begins detailed evaluation of clinical activity and response rates in T-cell lymphomas. and actively underway at nine renowned medical centers across the country, To determine the recommended treatment dose (RTD) to evaluate disease activity and response rates in the follow-on Phase 1b.

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