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A Randomized, Double-Blind, Placebo-Controlled, Dose-Escalating Phase 1b Study to Assess the Safety, Pharmacodynamics and Pharmacokinetics of SHP 141, A Histone Deacetylase Inhibitor, Administered Topically Up to 28 Days to Patients With Stage IA, IB or IIA Cutaneous T-Cell Lymphoma.

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A Randomized, Double-Blind, Placebo-Controlled, Dose-Escalating Phase 1b Study to Assess the Safety, Pharmacodynamics and Pharmacokinetics of SHP 141, A Histone Deacetylase Inhibitor, Administered Topically Up to 28 Days to Patients With Stage IA, IB or IIA Cutaneous T-Cell Lymphoma.

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 03 Oct 2021

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At a glance

  • Drugs Remetinostat (Primary)
  • Indications Cutaneous T-cell lymphoma
  • Focus Adverse reactions
  • Sponsors Shape Pharmaceuticals; TetraLogic Pharmaceuticals

Most Recent Events

  • 07 Aug 2014 Status changed from active, no longer recruiting to completed as reported by ClinicalTrials.gov record.
  • 07 Apr 2014 Results have been reported in a TetraLogic Pharmaceuticals media release.
  • 13 Feb 2014 Status changed from recruiting to active, no longer recruiting according to ClinicalTrials.gov

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