IMPROVE-PAH | Clinical Research Studies Listing

Recruiting

99 years or below

All

Phase N/A

484 participants needed

Brief description of study

The goal of this study is to evaluate the efficacy and safety of IKT-001 treatment versus placebo in addition to background pulmonary arterial hypertension (PAH) therapy in adults with World Health Organization (WHO) Group 1 PAH. This is a 2-part randomized double blind placebo-controlled trial with a 24-week treatment period that consists of 6 outpatient visits, and the 24-week Extended DBPC.

Eligibility of study

You may be eligible for this study if you meet the following criteria:

Conditions: Medical Research
Age: 99 years or below
Gender: All

TBD

Updated on 29 Sep 2026. Study ID: 26-7166

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