Active, not recruitingPhase 2NCT05570058
Assess the Safety, Pharmacokinetics, Pharmacodynamics and Clinical Activity of RXC007 in Idiopathic Pulmonary Fibrosis
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
- Redx Pharma Ltd
- Principal Investigator
- Philip Molyneaux, MDRoyal Brompton & Harefield NHS Foundation Trust
- Intervention
- RXC007(drug)
- Enrollment
- 48 target
- Eligibility
- 40-80 years · All sexes
- Timeline
- 2022 – 2025
Study locations (30)
- Medical University of Vienna, Vienna, Austria
- E PNE UZ Leuven, Leuven, Belgium
- CHU De Liège, Liège, Belgium
- Pneumologicka klinika 1.LF UK a, Prague, Czechia
- Azienda Ospedaliero-Universitaria "Ospedali-Riuniti" di Ancona, Ancona, Italy
- Azienda Ospedaliero Universitaria Policlinico ''G.Rodolico-San Marco'', Catania, Italy
- Colonello D'avanzo Hospital, Foggia, Italy
- PO Vito Fazzi, Lecce, Italy
- Ospedale S. Giuseppe Milano, Milan, Italy
- Azienda Ospedaliera Universitaria of Modena, Modena, Italy
- Fondazione Policlinico Universitario A. Gemelli, Roma, Italy
- Azienda Ospedaliera Universitaria Integrata Verona, Verona, Italy
- University Clinical Centre in Gdansk, Gdansk, Poland
- Barlicki University Hospital, Lodz, Poland
- Institute of Tuberculosis and Lung Diseases in Warsaw, Warsaw, Poland
- +15 more locations on ClinicalTrials.gov
Collaborators
Simbec-Orion Group
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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