Safety, Efficacy and Pharmacokinetics of C21 in Subjects With IPF
Trial details
- Registry ID
- NCT04533022
- Phase
- Phase 2
Company identity has not yet been verified
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Research sample: selected versions from May 2023 onward plus a preceding baseline where available. Only selected fields were retained; endpoint measures were truncated to 300 characters. This is not complete trial or sponsor history. Daily snapshots begin when collection starts.
| Trial | Sponsor | Phase | Status | Primary completion |
|---|---|---|---|---|
| Safety, Efficacy and Pharmacokinetics of C21 in Subjects With IPFNCT04533022 | Vicore Pharma AB | Phase 2 | Completed | 2024-03-30Actual |
| A Trial to Investigate Recovery From COVID-19 With C21 in Adult SubjectsNCT04880642 | Vicore Pharma AB | Phase 3 | Completed | 2022-04-25Actual |
| A Trial to Evaluate Efficacy and Safety of Buloxibutid in People With Idiopathic Pulmonary Fibrosis.NCT06588686 | Vicore Pharma AB | Phase 2 | Active not recruiting | 2027-05Estimated |
NCT06588686 · Vicore Pharma AB
Estimated
Actual
360 participants (planned)
378 participants (actual)
NCT06588686 · Vicore Pharma AB
Recruiting
Active not recruiting
NCT06588686 · Vicore Pharma AB
Feb 2027
May 2027
NCT06588686 · Vicore Pharma AB
270 participants (planned)
360 participants (planned)