Plain-English translation of NCT07035990 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 is an early-stage safety study testing combined with two complementary medications ( and ) that are being developed to treat cystic fibrosis. Researchers want to understand how the medication works in the body and whether it causes any side effects when healthy people take it. This helps determine if the treatment is safe enough to test in people with cystic fibrosis.
Cystic fibrosis is a serious genetic disease that damages the lungs and digestive system. Researchers are developing these new medications to address the underlying problems in CF, and this study is the first step to make sure the treatment is safe before testing it in patients who actually have the disease.
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You would receive either the new medication combination or a placebo (inactive pill) multiple times over several weeks. The study involves regular clinic visits where researchers check your blood pressure, heart rhythm, and blood work to monitor safety. Some participants will receive one combination of medications, while others receive a different combination, and some will receive placebo instead—neither you nor the researchers will know which group you're in during the study.
AI-generated summary from trial data · Jun 3, 2026 · Not medical advice
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