Plain-English translation of NCT06429930 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
Phase 1 — Testing in a small group (usually 20–80 people) to find a safe dose and watch for side effects.
This trial is testing a new inhaled medication called L608, which is a special formulation of a drug called iloprost designed to treat pulmonary arterial hypertension (a condition where blood pressure in the lungs becomes dangerously high). This Phase 1 study is enrolling healthy adults to find out if the medication is safe and how the body processes it, before it can be tested in patients who actually have the disease.
The current treatment for pulmonary arterial hypertension requires frequent dosing and can cause unwanted side effects like low blood pressure. This new formulation is designed to reduce how often patients need to take the medication and minimize those troubling side effects.
You likely qualify if…
You likely don't qualify if…
If you qualify, you will be randomly assigned to receive either the new medication or a placebo (a fake treatment) through inhalation. You will be one of about 32 healthy volunteers in the study, with most visits happening in New Zealand. The study uses a step-by-step approach, gradually testing higher doses to watch for safety. You will need to avoid caffeine, certain foods, alcohol, and strenuous exercise at specific times, and attend visits where researchers will check your vital signs, lung function, and blood levels.
AI-generated summary from trial data · Jun 19, 2026 · Not medical advice
New Zealand
Phase
Safety & dosing
Sponsor
Pharmosa Biopharm Inc.
Collaborators
Novotech (Australia) Pty Limited
Enrollment target
~40 participants
Started
April 2025
Primary completion
December 2026
Age range
18 Years – 65 Years
Last updated on clinicaltrials.gov in July 2026.
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Central contact
Pei Kan, PhD
Pharmosa Biopharm Inc.
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