NCT05185089CompletedPhase 2
Efficacy and Safety Study of Orvepitant for Chronic Cough in Patients With Idiopathic Pulmonary Fibrosis
A Double-Blind, Randomised, Placebo Controlled, Two Period Cross-Over Study to Evaluate the Efficacy and Safety of Orvepitant in Chronic Cough in Patients With Idiopathic Pulmonary Fibrosis
Source: ClinicalTrials.gov · Last updated 10 Nov 2025
Brief summary (registry, in English)
ORV-PF-01 is a two way, placebo controlled, cross-over study, to evaluate the effect of two doses of orvepitant on cough in patients with IPF.
- Status (registry)
- Completed
- Phase (registry)
- Phase 2
- Study type
- Interventional
- Enrollment
- 80 (actual)
- First submitted
- 23 Dec 2021
- Start date
- 1 Aug 2022
- Primary completion date
- 5 Jun 2024
- Lead sponsor
- Nerre Therapeutics Ltd.
- Diseases
- Idiopathic pulmonary fibrosis
- NCT number
- NCT05185089
What you commit to
- Study type: Interventional · Phase 2
- Participants enrolled: 80
- From 1 Aug 2022 to the primary completion date, 5 Jun 2024
- 37 sites in 3 countries
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Recent respiratory tract infection (\<8 weeks prior to Screening)
- Recent acute exacerbation of IPF (\<8 weeks prior to Screening)
- Current smokers or ex-smokers with \<6 months' abstinence prior to Screening
Other
- Emphysema ≥50% on high-resolution computed tomography, or the extent of emphysema is greater than the extent of fibrosis according to the reported results of the most recent scan
- Mean early morning cough scale score ≥5 and rest of the day cough scale score \<5 (after rounding) during the second week of the baseline assessment period (assessed at Visit 2)
- Cough that is predominantly productive in nature and attributable to lung pathology such as chronic bronchitis or bronchiectasis
Who the study is looking for
- Diagnosis of IPF established according to the 2018 or 2022 joint ATS/ERS/JRS/ALAT Clinical Practice Guideline
- FEV1/FVC ratio ≥0.65 at the screening visit
- Haemoglobin-corrected diffusion capacity of carbon monoxide (Hb-corrected DLCO) ≥25% within 12 months of the screening visit
- Arterial oxygen saturation on room air or oxygen ≥90% at Screening
- Life expectancy of at least 12 months
- Cough that is attributed to IPF, which has not responded to anti-tussive treatment, and which has been present for at least 8 weeks prior to Screening
- Mean daily IPF Coughing Severity Scale score ≥5 (after rounding) during the second week of the baseline assessment period
Age in the registry: 40 years to - · Sex: All · Does not accept healthy volunteers
Sites (37)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Antrim Area Hospital Coordinator of this site? Confirm its status | Antrim | United Kingdom | Unknown status |
| MAC Clinical Research Coordinator of this site? Confirm its status | Barnsley | United Kingdom | Unknown status |
| Heartlands Hospital Coordinator of this site? Confirm its status | Birmingham | United Kingdom | Unknown status |
| Royal Papworth Hospital Coordinator of this site? Confirm its status | Cambridge | United Kingdom | Unknown status |
| Castle Hill Hospital Coordinator of this site? Confirm its status | Cottingham | United Kingdom | Unknown status |
| Royal Infirmary of Edinburgh Coordinator of this site? Confirm its status | Edinburgh | United Kingdom | Unknown status |
| Royal Devon and Exeter Hospital Coordinator of this site? Confirm its status | Exeter | United Kingdom | Unknown status |
| Churchill Hospital Coordinator of this site? Confirm its status | Headington | United Kingdom | Unknown status |
| MAC Clinical Research Coordinator of this site? Confirm its status | Leeds | United Kingdom | Unknown status |
| Guy's Hospital Coordinator of this site? Confirm its status | London | United Kingdom | Unknown status |
| Altnagelvin Area Hospital Coordinator of this site? Confirm its status | Londonderry | United Kingdom | Unknown status |
| MAC Clinical Research Coordinator of this site? Confirm its status | Manchester | United Kingdom | Unknown status |
| Nottingham City Hospital Coordinator of this site? Confirm its status | Nottingham | United Kingdom | Unknown status |
| Perth Royal Infirmary Coordinator of this site? Confirm its status | Perth | United Kingdom | Unknown status |
| MAC Clinical Research Coordinator of this site? Confirm its status | Prescot | United Kingdom | Unknown status |
| Royal Berkshire Hospital Coordinator of this site? Confirm its status | Reading | United Kingdom | Unknown status |
| Southampton General Hospital Coordinator of this site? Confirm its status | Southampton | United Kingdom | Unknown status |
| Zuyderland Medical Centre Coordinator of this site? Confirm its status | Heerlen | Netherlands | Unknown status |
| Sint Antonius Hospital Coordinator of this site? Confirm its status | Nieuwegein | Netherlands | Unknown status |
| Erasmus University Medical Centre Coordinator of this site? Confirm its status | Rotterdam | Netherlands | Unknown status |
| Isala Ziekenhuis Coordinator of this site? Confirm its status | Zwolle | Netherlands | Unknown status |
| University of Michigan Coordinator of this site? Confirm its status | Ann Arbor | United States | Unknown status |
| Medical University of South Carolina Coordinator of this site? Confirm its status | Charleston | United States | Unknown status |
| American Health Research Coordinator of this site? Confirm its status | Charlotte | United States | Unknown status |
| University of Virginia Health System Coordinator of this site? Confirm its status | Charlottesville | United States | Unknown status |
| Baylor University Coordinator of this site? Confirm its status | Dallas | United States | Unknown status |
| National Jewish Health Coordinator of this site? Confirm its status | Denver | United States | Unknown status |
| PulmonIx, LLC Coordinator of this site? Confirm its status | Greensboro | United States | Unknown status |
| University of Southern California Coordinator of this site? Confirm its status | Los Angeles | United States | Unknown status |
| Loyola University Chicago Coordinator of this site? Confirm its status | Maywood | United States | Unknown status |
| Vanderbilt University Medical Center Coordinator of this site? Confirm its status | Nashville | United States | Unknown status |
| Temple University Coordinator of this site? Confirm its status | Philadelphia | United States | Unknown status |
| Mayo Clinic Coordinator of this site? Confirm its status | Rochester | United States | Unknown status |
| University of Utah Coordinator of this site? Confirm its status | Salt Lake City | United States | Unknown status |
| University of California Coordinator of this site? Confirm its status | San Francisco | United States | Unknown status |
| Jadestone Clinical Research, LLC Coordinator of this site? Confirm its status | Silver Spring | United States | Unknown status |
| Clear Lake Health Coordinator of this site? Confirm its status | Webster | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.