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Trial ID IM027-1016  |   NCT07441408

Long-term Extension Study to Evaluate Safety and Tolerability of Admilparant in Participants With Pulmonary Fibrosis

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Summary

  • Phase 3
  • Male and Female Gender icon
  • N/A
    Age Range
  • 92
    Locations
  • BMS Not Yet Recruiting Study icon
    Not Yet Recruiting

Overview

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)).

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Key Eligibility Criteria

Inclusion Criteria

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:
  • Participants must have completed participation in either IM027068 or IM0271015 (defined as receiving study intervention (IMP) until completion of EOT visit).

    Exclusion Criteria

    Exclusion Criteria Icon
    :
    • Clinically significant AE that resulted in discontinuation or interruption of IMP (Investigational Medicinal Product) in IM027068 or IM0271015 without reinitiation of IMP.
      1. Exhibit symptoms of heart failure at rest.
        1. History of lung reduction surgery or lung transplant. Note: Being on the transplantation list is allowed.
          1. Participants with known PAH (Pulmonary Arterial Hypertension) who has been on single drug therapy that now requires multi-drug therapy.
            Additional Information *
            • Other protocol-defined Inclusion/Exclusion criteria apply.

              Treatment Options

              Study Arms

              ASSIGNED INTERVENTION

              Study Arms

              Experimental: BMS-986278 Arm

              ASSIGNED INTERVENTION
              • Drug: BMS-986278
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