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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.
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

Full criteria on ClinicalTrials.gov

Sites (37)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Antrim Area Hospital
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AntrimUnited KingdomUnknown status
MAC Clinical Research
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BarnsleyUnited KingdomUnknown status
Heartlands Hospital
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BirminghamUnited KingdomUnknown status
Royal Papworth Hospital
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CambridgeUnited KingdomUnknown status
Castle Hill Hospital
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CottinghamUnited KingdomUnknown status
Royal Infirmary of Edinburgh
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EdinburghUnited KingdomUnknown status
Royal Devon and Exeter Hospital
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ExeterUnited KingdomUnknown status
Churchill Hospital
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HeadingtonUnited KingdomUnknown status
MAC Clinical Research
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LeedsUnited KingdomUnknown status
Guy's Hospital
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LondonUnited KingdomUnknown status
Altnagelvin Area Hospital
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LondonderryUnited KingdomUnknown status
MAC Clinical Research
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ManchesterUnited KingdomUnknown status
Nottingham City Hospital
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NottinghamUnited KingdomUnknown status
Perth Royal Infirmary
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PerthUnited KingdomUnknown status
MAC Clinical Research
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PrescotUnited KingdomUnknown status
Royal Berkshire Hospital
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ReadingUnited KingdomUnknown status
Southampton General Hospital
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SouthamptonUnited KingdomUnknown status
Zuyderland Medical Centre
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HeerlenNetherlandsUnknown status
Sint Antonius Hospital
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NieuwegeinNetherlandsUnknown status
Erasmus University Medical Centre
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RotterdamNetherlandsUnknown status
Isala Ziekenhuis
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ZwolleNetherlandsUnknown status
University of Michigan
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Ann ArborUnited StatesUnknown status
Medical University of South Carolina
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CharlestonUnited StatesUnknown status
American Health Research
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CharlotteUnited StatesUnknown status
University of Virginia Health System
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CharlottesvilleUnited StatesUnknown status
Baylor University
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DallasUnited StatesUnknown status
National Jewish Health
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DenverUnited StatesUnknown status
PulmonIx, LLC
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GreensboroUnited StatesUnknown status
University of Southern California
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Los AngelesUnited StatesUnknown status
Loyola University Chicago
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MaywoodUnited StatesUnknown status
Vanderbilt University Medical Center
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NashvilleUnited StatesUnknown status
Temple University
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PhiladelphiaUnited StatesUnknown status
Mayo Clinic
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RochesterUnited StatesUnknown status
University of Utah
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Salt Lake CityUnited StatesUnknown status
University of California
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San FranciscoUnited StatesUnknown status
Jadestone Clinical Research, LLC
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Silver SpringUnited StatesUnknown status
Clear Lake Health
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WebsterUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.