CompletedPhase 1NCT05513950
A Study to Investigate the Safety, Tolerability, and Pharmacokinetics of Monoclonal Antibody (mAb) in Patients With IPF (SAD).
Studying Idiopathic pulmonary fibrosis
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Chiesi Farmaceutici S.p.A.
- Principal Investigator
- Lisa SpencerLiverpool University Hospitals NHS Foundation Trust
- Intervention
- CHF10067 starting dose -- 1000mg (Cohort A)(biological)
- Enrollment
- 52 enrolled
- Eligibility
- 40 years · All sexes
- Timeline
- 2023 – 2024
Study locations (9)
- PHI University Clinic of Pulmonology and Allergology, Skopje, North Macedonia
- Medical Center of Limited Liability Company "Arensia Exploratory Medicine", department of Clinical Trials, Kyiv, Ukraine
- Queen Elizabeth Hospital - NIHR Birmingham Clinical Research Facility - University Hospitals Birmingham NHS Foundation Trust, Birmingham, United Kingdom
- Royal Papworth Hospital NHSFT - Cambridge Biomedical Campus, Cambridge, United Kingdom
- University of Dundee, NHS Tayside - Ninewells Hospital & Medical School, Dundee, United Kingdom
- Interstitial Lung Disease Research - NHS Lothian - Royal Infirmary of Edinburgh,, Edinburgh, United Kingdom
- Liverpool Clinical Research Facility - Liverpool University Hospital Foundation Trust, Liverpool, United Kingdom
- Medicines Evaluation Unit - The Langley Building, Manchester, United Kingdom
- University Hospital Southampton - Department of Respiratory Medicine, Southampton, United Kingdom
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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