A Study to Investigate the Safety, Tolerability, and Pharmacokinetics of Monoclonal Antibody (mAb) in Patients With IPF


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The purpose of this study is to assess the safety of CHF10067 (the study drug) and any side effects that might be associated with it. In addition, the study will evaluate how much of the study drug gets into the bloodstream and how long the body takes to remove it. The body's immune response to the study drug will also be evaluated. The study may also evaluate the effect of the study drug on the level of a certain protein in the body.

Chiesi is conducting this study on patients affected by idiopathic pulmonary fibrosis (IPF, a lung disease).

Chiesi is doing this study to establish the doses suitable for future studies.

Study Overview

Start Date
January 25, 2023
Completion Date
June 25, 2024
Date Posted
August 24, 2022
Accepts Healthy Volunteers?


Full Address
PHI University Clinic of Pulmonology and Allergology
Skopje 1000, North Macedonia

Medical Center of Limited Liability Company "Arensia Exploratory Medicine", department of Clinical Trials
Kyiv 01135, Ukraine

Queen Elizabeth Hospital - NIHR Birmingham Clinical Research Facility - University Hospitals Birmingham NHS Foundation Trust
Birmingham B15 2TH, United Kingdom

Royal Papworth Hospital NHSFT - Cambridge Biomedical Campus
Cambridge CB2 0AY, United Kingdom

University of Dundee, NHS Tayside - Ninewells Hospital & Medical School
Dundee DD1 9SY, United Kingdom

Interstitial Lung Disease Research - NHS Lothian - Royal Infirmary of Edinburgh,
Edinburgh EH16 4SA, United Kingdom

Liverpool Clinical Research Facility - Liverpool University Hospital Foundation Trust
Liverpool L7 8XP, United Kingdom

Medicines Evaluation Unit - The Langley Building
Manchester M23 9QZ, United Kingdom

University Hospital Southampton - Department of Respiratory Medicine
Southampton, United Kingdom


Minimum Age (years)
Eligibility Criteria
Inclusion Criteria:

Subject's written informed consent obtained prior to any study-related procedure.
Males or females, of any race, aged ≥ 40 years of age.
Body weight ≥ 45 kg.
Diagnosis of IPF as defined by current American Thoracic Society/European Respiratory Society/Japanese Respiratory Society/Latin American Thoracic Association guidelines. Diagnosis of IPF must be within the past 5 years prior to enrolment, and in the opinion of the Investigator, has been stable for at least 3 months.
Subjects not receiving any IPF treatment (including subjects with previous use of antifibrotic treatment that has been stopped for at least 2 weeks prior to screening) or receiving well-tolerated standard of care approved treatments at a stable dose for at least 8 weeks prior to screening (nintedanib or pirfenidone) and it is anticipated the dose will remain unchanged throughout the study.
Forced vital capacity (FVC) ≥ 50% of predicted and ratio of forced expiratory volume in the first second (FEV1)/FVC ≥ 0.7 at screening.
Diffusing capacity of the lung for carbon monoxide (DLCO; corrected for haemoglobin) ≥ 35% at screening.
Able to understand the study procedures and the risks involved.
Male and Female subjects following contraceptive requirements detailed in the study protocol.

Exclusion Criteria:

History of lower respiratory tract infection within 4 weeks prior to screening and up to Day 1 of the study.
History of acute exacerbation of IPF within 3 months prior to screening and up to Day 1 of the study
Active diagnosis of lung cancer or a history of lung cancer.
Active cancer or a history of cancer (other than lung cancer) with less than 5 years disease free survival time (whether or not there is evidence of local recurrence or metastases).
Infiltrative lung disease other than IPF
Subjects exhibiting unhealed wounds or foot ulcers or have known history of wound healing complications.
Chronic heart failure categorized as New York Heart Association Class II, III, or IV; clinical diagnosis of cor pulmonale requiring specific treatment; or severe pulmonary hypertension
Currently receiving, or have received, a systemic corticosteroid, immunosuppressant, cytotoxic therapy, vasodilator therapy for pulmonary hypertension, or unapproved or investigational treatment for IPF within 4 weeks prior to screening or prior to randomization.
Coronavirus disease-2019 (COVID-19) vaccine at least 7 days before dosing. Any systemic symptoms (e.g. myalgia, fever, chills, fatigue, etc.) after COVID-19 vaccine should subside at least 2 days before the Day 1 visit.
Documented COVID-19 diagnosis within the last 4 weeks or which has not resolved within 7 days prior to screening or before treatment.
Known intolerance and/or hypersensitivity to any of the excipients contained in the formulation or any other substance used in the study.
History of allergic or anaphylactic reaction to human, humanised, chimeric, immunoglobulins (Igs), or murine monoclonal antibodies.
Clinically relevant abnormal laboratory values (clinical chemistry and haematology) at screening suggesting an unknown disease and requiring further clinical investigation or which may impact the safety of the subject or the evaluation of the study results according to Investigator judgement. .
Pregnant or lactating women.

Study Contact Info

Study Contact Name
Chiesi Clinical Trial Info
Study Contact Email
Study Contact Phone

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Other Details

FDA Regulated Drug?
FDA Regulated Device?
Detailed Description
The principal aim of this study is to obtain safety and tolerability data when CHF10067 is administered intravenously as single ascending doses to subjects with IPF. This information, together with the pharmacokinetic (PK) and immunogenicity data, will help establish the doses suitable for future studies in subjects. The effect of CHF10067 on TG2 levels will also be investigated as an exploratory endpoint.

A sequential group, single ascending dose design has been chosen for safety reasons because CHF10067 is in the early stages of clinical development and no data in the IPF population has been collected so far. In addition, sentinel dosing will be used so that in each cohort 2 subjects (1 CHF10067 and 1 placebo) will be dosed at least 24 hours before the remaining 6 subjects.

The study will be double-blind and placebo-controlled to avoid bias in the collection and evaluation of data during its conduct. Placebo has been chosen as the comparison treatment to assess whether any observed effects are treatment-related or simply reflect the study conditions.
NCTid (if applicable)