NCT07441408 Admilparant Pulmonary Fibrosis Clinical Landscape Report 2026: Design, Endpoints, Sponsor and Readout Outlook
Turn a newly registered trial into a decision-ready clinical landscape. This report examines NCT07441408 using PatSnap Clinical Trials MCP for protocol design and endpoint evidence, with Drug & Asset MCP and Company & Deal Intelligence MCP used as the companion asset and sponsor enrichment workflow. Explore PatSnap MCP Servers to reproduce the research sequence inside an AI workflow.
MCP evidence snapshot: 17 August 2026. Trial records, recruitment status and projected dates can change after the snapshot and should be rechecked before operational decisions.
Why NCT07441408 is a hot trial to watch
Pulmonary Fibrosis is being segmented by mechanism, treatment setting, geography and endpoint architecture. NCT07441408 is notable because it evaluates Admilparant in a Phase 3 design sponsored by Bristol Myers Squibb Co.. The main development question is whether the protocol can translate its rationale into a clinically interpretable and operationally credible readout.
Trial landscape snapshot
| Field | Indexed detail |
|---|---|
| Registration | NCT07441408 |
| Official title | Long-term Extension Study to Evaluate Safety and Tolerability of Admilparant in Participants With Pulmonary Fibrosis |
| Phase / status | Phase 3 / Not yet recruiting |
| Intervention | Admilparant |
| Sponsor | Bristol Myers Squibb Co. |
| Geography | United States, Portugal, Greece, South Korea, Netherlands, Ireland, China, Brazil, France, Chile, Colombia, Argentina, Japan, United Kingdom, Spain, India, Canada, Belgium, Taiwan Province, Finland, Denmark, Mexico, Italy, Israel, Australia, Peru, Germany |
| Enrollment | [object Object] |
| Primary endpoint | Number of Participants With Treatment Emergent Adverse Events (TEAEs) |
| Endpoint time frame | Up to Week 100 |
| Primary completion / readout proxy | [object Object] |
Protocol design and endpoint interpretation
The purpose of this study is to evaluate the long-term safety and tolerability of Admilparant in participants who completed participation in parent studies IM027-068 (for idiopathic pulmonary fibrosis (IPF)) and IM027-1015 (for progressive pulmonary fibrosis (PPF)).
Allocation is N/A, masking is None (Open Label), and the intervention model is Single Group Assignment. Planned enrollment of [object Object] participants across United States, Portugal, Greece, South Korea, Netherlands, Ireland, China, Brazil, France, Chile, Colombia, Argentina, Japan, United Kingdom, Spain, India, Canada, Belgium, Taiwan Province, Finland, Denmark, Mexico, Italy, Israel, Australia, Peru, Germany shapes statistical precision, execution risk and external validity. Interpretation should account for baseline risk, prior therapy, assessment schedule, missing-data handling and clinical relevance—not only statistical significance.
- Number of Participants With Treatment Emergent Adverse Events (TEAEs) (Up to Week 100)
- Number of Participants With Serious Adverse Events (SAEs) (Up to Week 100)
- Number of Participants With AEs leading to Discontinuation (Up to Week 100)
- Number of Participants With AEs leading to Deaths (Up to Week 100)
Readout outlook and evidence gap
The current protocol points to [object Object] as the best available readout proxy. Because this is an active or newly posted study, a trial-specific result citation is not included until a normalized clinical-trial-result record becomes available. That gap is itself operationally important: teams should monitor first result indexing, conference abstracts, protocol amendments and changes to the primary-completion date.
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Asset and sponsor context
Drug & Asset MCP profile: Admilparant is indexed as No normalized modality returned, with target No normalized target returned, mechanism No normalized mechanism returned, and global highest development status No normalized global status returned.
Company & Deal Intelligence MCP profile: Bristol Myers Squibb Co. is resolved to a normalized organization record in United States. The organization workflow adds identity, location, portfolio and partnering context where available.
The sponsor profile matters because scientific rationale alone does not determine development value. Manufacturing readiness, portfolio fit, geographic reach, partnering capacity and the ability to fund confirmatory development can determine whether a positive signal becomes a competitive asset.
White space around this program
- Sharper patient selection: prospective biomarker or phenotype definitions that identify who is most likely to benefit.
- Clinically interpretable endpoints: outcomes connecting activity with function, symptoms, survival or treatment burden.
- Comparator relevance: evidence against the most decision-relevant contemporary standard of care.
- Broader external validity: evidence across additional geographies, demographic groups and real-world settings.
- Operational differentiation: a development path that closes the readout gap without sacrificing safety or durability.
What to monitor next
Monitor recruitment, enrollment changes, protocol amendments, endpoint hierarchy, primary-completion timing, first result indexing, asset ownership and sponsor partnerships. A change in endpoint, population or ownership can alter the probability of success before a headline data release.
Bottom line
NCT07441408 provides a focused lens on Pulmonary Fibrosis development. Its value will be determined by whether Admilparant can convert the current Phase 3 design into evidence that is clinically meaningful, operationally credible and differentiated from competing programs.
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