New pill aims to slow lung scarring in IPF patients
NCT ID NCT06747923
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests an experimental drug called SB17170 in 30 adults with moderate to severe idiopathic pulmonary fibrosis (IPF), a disease that scars the lungs and makes breathing hard. Participants take either the drug or a placebo daily for 12 weeks. The main goal is to see if the drug improves lung function, measured by how much air they can exhale.
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
- Active substance
- SB17170 (an experimental oral drug)
- What this could lead to
- If successful, this could point toward a new treatment option to slow lung function decline in people with idiopathic pulmonary fibrosis.
- What could go wrong
- This is an early Phase 2a trial with only 30 participants, so results may not apply broadly. The drug may not improve lung function or could cause 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
-
Ajou University Hospital
NOT_YET_RECRUITINGSuwon, South Korea
-
Chung-Ang University Gwangmyeong Hospital
RECRUITINGGwangmyeong, South Korea
-
Myong Ji Hospital
RECRUITINGGoyang, South Korea
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Seoul Asan Hospital
NOT_YET_RECRUITINGSeoul, South Korea
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The Catholic Univ. of Korea Seoul St. Mary's Hospital
NOT_YET_RECRUITINGSeoul, South Korea
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can a new pill slow lung scarring in IPF?
- Beyond the lungs: the hidden emotional toll of IPF medications
- Can umbilical cord stem cells ease a scarring lung disease?
- Spotting hidden blood clots in scarred lungs: a study hunts for clues
- Can a new daily pill slow lung scarring in IPF?
- What makes someone stop a lung fibrosis drug? a study asks patients directly