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A Study to Evaluate the Efficacy, Safety, and Tolerability of BMS-986278 in Participants With Idiopathic Pulmonary Fibrosis
NCT06003426 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to evaluate the efficacy, safety, and tolerability of BMS-986278 in participants with Idiopathic Pulmonary Fibrosis.
Conditions Studied
Interventions
- DRUG BMS-986278
- DRUG BMS-986278 Placebo
Study Locations (20)
California
- Local Institution - 0396 — La Jolla
- Local Institution - 0193 — Los Angeles
- Local Institution - 0398 — Los Angeles
- Local Institution - 0389 — Orange
- Local Institution - 0405 — Sacramento
- Local Institution - 0185 — San Francisco
- Local Institution - 0186 — Stanford
Florida
- Local Institution - 0101 — Brandon
- Local Institution - 0436 — Clearwater
- Local Institution - 0425 — DeBary
- Local Institution - 0079 — Gainesville
- Local Institution - 0352 — Hialeah
- Local Institution - 0370 — Kissimmee
Colorado
- Local Institution - 0363 — Aurora
- Local Institution - 0194 — Denver
Alabama
- Local Institution - 0189 — Birmingham
Arizona
- Local Institution - 0361 — Phoenix
Connecticut
- Local Institution - 0175 — New Haven
Delaware
- Local Institution - 0151 — Newark
District of Columbia
- Local Institution - 0367 — Washington D.C.
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,255 participants |
| Start Date | 2023-09-14 |
| Est. Completion | 2026-10-26 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06003426
The ClinicalTrials.gov registry entry for NCT06003426 describes a study currently listed as active not recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 1,255 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Bristol-Myers Squibb, which has 504 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Idiopathic Pulmonary Fibrosis appearing as the primary indexed condition, and to 2 interventions — of which BMS-986278 is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06003426 reports 20 study locations spanning 8 distinct geographic areas — top geographies include California, Florida, Colorado. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06003426 about?
NCT06003426 is a clinical study titled "A Study to Evaluate the Efficacy, Safety, and Tolerability of BMS-986278 in Participants With Idiopathic Pulmonary Fibrosis". The purpose of this study is to evaluate the efficacy, safety, and tolerability of BMS-986278 in participants with Idiopathic Pulmonary Fibrosis.
What is the current status of trial NCT06003426?
This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 1,255 participants. The study started on 2023-09-14. Estimated completion is 2026-10-26.
What conditions does trial NCT06003426 study?
This clinical trial studies the following conditions: Idiopathic Pulmonary Fibrosis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06003426?
The interventions under investigation include: BMS-986278 (DRUG), BMS-986278 Placebo (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06003426?
This trial is sponsored by Bristol-Myers Squibb, which has 504 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06003426 being conducted?
This trial has 20 study locations across Alabama, Arizona, California, Colorado, Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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