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A pivotal global multicenter, randomized, double-blind, placebo-controlled study of YOLT-203 for the treatment of Primary Hyperoxaluria Type 1 (PH1)

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Trial Profile

A pivotal global multicenter, randomized, double-blind, placebo-controlled study of YOLT-203 for the treatment of Primary Hyperoxaluria Type 1 (PH1)

Status: Planning
Phase of Trial: Phase III

Latest Information Update: 17 Dec 2025

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At a glance

  • Drugs YOLT-203 (Primary)
  • Indications Primary hyperoxaluria type 1
  • Focus Registrational; Therapeutic Use

Most Recent Events

  • 17 Dec 2025 New trial record
  • 18 Nov 2025 According to a YolTech Therapeutics media release, company announced that the U.S. Food and Drug Administration (FDA) has cleared the companys Investigational New Drug (IND) application for YOLT-203, an in vivo gene-editing therapy for the treatment of Primary Hyperoxaluria Type 1 (PH1).

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