This is a Trial Designed to Evaluate the Combination of Nerandomilast With Mycophenolate Across a Wide Variety of Pulmonary Fibrosis Subtypes, With the Aim of Providing Clinicians With Assurance That This is an Appropriate Therapeutic Combination.
- Sponsor
- University of British Columbia
- Study ID
- NCT07570888
- Phase
- PHASE4
- Status
- Not Yet Recruiting
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Conditions
- Interstitial Lung Disease (ILD)
- Pulmonary Fibrosis
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Nerandomilast 18 mg - adult formulation — DRUGParticipant who are already treated with mycophenolate and have pulmonary fibrosis will receive also treatment with nerandomilast.
Study Details
This is a trial designed to evaluate the combination of nerandomilast with mycophenolate across a wide variety of pulmonary fibrosis subtypes, with the aim of providing clinicians with assurance that this is an appropriate therapeutic combination.
Key Dates
- Start date
- Jun 30, 2026
- Status verified
- Mar 2026
- Primary completion
- Jun 30, 2027
- Completion
- Jul 31, 2027
Study Design
- Enrollment
- 120 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Participants already receiving treatment with mycophenolate
Primary Outcome Measure
Determine the persistency of nerandomilast at 4 months when used in combination with mycophenolate in patients with pulmonary fibrosis [ Time Frame: Four months ]
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