New drug YOLT-202 tested in early trial for rare lung and liver disease
NCT ID NCT07193615
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This early-phase study is testing a single dose of a new drug called YOLT-202 in 18 adults with Alpha-1 antitrypsin deficiency (AATD), a genetic condition that can damage the lungs and liver. The main goal is to see if the drug is safe and to find the best dose. Participants will receive one intravenous infusion and be monitored for side effects and how the drug moves through the body.
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
- Active substance
- YOLT-202 (a single-dose intravenous drug)
- What this could lead to
- If it works, this could point toward a new treatment option for people with Alpha-1 antitrypsin deficiency, a genetic lung and liver condition.
- What could go wrong
- This is a very early, small study with only 18 participants. It is designed mainly to check safety, not effectiveness. The drug may not work or could have side effects.
This is an AI summary of the original study and may miss details. Read our disclaimer.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Ren Ji Hospital Affiliated to Shanghai Jiao Tong University
Shanghai, China
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- RNA editing drug WVE-006 enters first human safety trial
- Can a smartphone breathing game help Alpha-1 patients breathe easier?
- Gene-Editing shot aims to fix rare lung and liver disease
- Hidden gene behind breathlessness? study tests link to rare lung condition