← Eichor
Study identifier: NCT06747923 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

SB17170 Phase 2 Trial in IPF Patients

Condition: IPF · Idiopathic Pulmonary Fibrosis · Idiopathic Pulmonary Fibrosis (IPF)  ·  Sponsor: SPARK Biopharma

PhasePhase 2
Planned participants30
Who can joinAll sexes, 40 Years to no upper limit
Healthy volunteersNo

About this study

This clinical trial is a 2:2:1 randomized, double-blind, placebo-controlled, parallel group, exploratory phase II trial. The main objective of this trial is to compare and evaluate change in FVC compared to placebo by administering SB17170 to moderate to severe patients with IPF. This clinical trial treatment involves administering SB17170 or placebo for 12 weeks.

This description comes directly from the study's public registry record.

Talk to the study team

Seong Yun Bang  ·  +82-2-887-8032  ·  sybang@sparkbio.co.kr

Yu Jin Choi  ·  +82-2-887-9972  ·  yjchoi@sparkbio.co.kr

Always discuss trial participation with your own doctor first.

Locations (5)

Myong Ji HospitalGoyang, South KoreaRecruiting
Chung-Ang University Gwangmyeong HospitalGwangmyeong, South KoreaRecruiting
Seoul Asan HospitalSeoul, South KoreaNot Yet Recruiting
The Catholic Univ. of Korea Seoul St. Mary's HospitalSeoul, South KoreaNot Yet Recruiting
Ajou University HospitalSuwon, South KoreaNot Yet Recruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06747923