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A clinical trial to determine efficacy, safety and tolerability of imatinib delivered by IkT-001Pro in patients with WHO Class I PAH

Trial Profile

A clinical trial to determine efficacy, safety and tolerability of imatinib delivered by IkT-001Pro in patients with WHO Class I PAH

Status: Planning
Phase of Trial: Phase I

Latest Information Update: 15 May 2024

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At a glance

  • Drugs IKT 001PRO (Primary)
  • Indications Pulmonary arterial hypertension
  • Focus Adverse reactions; Therapeutic Use

Most Recent Events

  • 09 May 2024 According to an Inhibhikase Therapeutics media release, today announced that the Company has received final meeting minutes from its recent pre-IND meeting with the Division of Cardiology and Nephrology of the U.S. Food and Drug Administration (FDA) for IkT-001Pro as a candidate treatment for Pulmonary Arterial Hypertension (PAH). Following review of the final meeting minutes, company is preparing the Investigational New Drug (IND) application.
  • 08 Apr 2024 New trial record
  • 03 Apr 2024 According to an Inhibhikase Therapeutics media release, company plans a Pre-IND meeting with the FDA to discuss cardiopulmonary applications including Pulmonary arterial hypertension of IkT 001Pro in April 2024. The meeting will be held on April 5, 2024, with meeting results to be reported following receipt of the formal meeting minutes.

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