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_RECRUITING

    Suwon, South Korea

  • Chung-Ang University Gwangmyeong Hospital

    RECRUITING

    Gwangmyeong, South Korea

  • Myong Ji Hospital

    RECRUITING

    Goyang, South Korea

  • Seoul Asan Hospital

    NOT_YET_RECRUITING

    Seoul, South Korea

  • The Catholic Univ. of Korea Seoul St. Mary's Hospital

    NOT_YET_RECRUITING

    Seoul, South Korea

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