Evaluation of Safety, Side Effects, and How the Drug, Inhaled CHF10136, Is Absorbed, Modified and Removed From the Body in Healthy Adults and Adults With Asthma

October 7, 2026 updated by: Chiesi Farmaceutici S.p.A.

A Randomised, Double-Blind, Placebo-Controlled Study to Investigate the Safety, Tolerability and Pharmacokinetics of CHF10136, Administered Via Dry Powder Inhaler, After Single Ascending Dose in Healthy Subjects, Multiple Ascending Doses in Mild Asthmatic Subjects and Followed by a Repeated Dose in One Cohort of Moderate-to-Severe Asthmatic Subjects

This study evaluates the safety and tolerability of CHF10136 administered by inhalation in healthy adults and adults with asthma. The study includes single-dose, multiple-dose, and repeated-dose treatment periods and will also characterize the pharmacokinetic profile of CHF10136.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Detailed Description

This is a first-in-human (FiH), randomized, double-blind, placebo-controlled study of CHF10136 administered via dry powder inhaler.

The study consists of three sequential parts. Part 1 is a single ascending dose evaluation in healthy adult participants. Part 2 is a multiple ascending dose evaluation in participants with mild asthma. Part 3 is a repeated-dose evaluation in participants with moderate-to-severe asthma. Dose escalation and progression between study parts will occur following review of available safety and pharmacokinetic data.

Healthy participants and participants with asthma will be enrolled and randomized to receive CHF10136 or placebo. Safety assessments, pharmacokinetic sampling, and exploratory pharmacodynamic assessments will be performed throughout the study.

Study Type

Interventional

Enrollment (Estimated)

120

Phase

  • Phase 1

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

      • Leeds, United Kingdom
        • Recruiting
        • Fortrea Leeds CRU
      • London, United Kingdom
        • Not yet recruiting
        • hVIVO
      • Manchester, United Kingdom
        • Not yet recruiting
        • MEU

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

INCLUSION CRITERIA

For PART 1 - SAD

  • Healthy male or female participant ≥18 and ≤55 years of age
  • Body mass index (BMI) ≥18 and ≤30 kg/m2 at screening and weight at least 50 kg;
  • Good physical and mental status, determined via assessment of medical history at screening and physical examination at screening and prior to randomisation;
  • Spirometry measurements within normal limits at screening and prior to randomisation based on the American Thoracic Society (ATS)/European Respiratory Society (ERS) interpretative strategies for spirometry. The forced expiratory volume in the first second (FEV1) must be >80% of predicted normal value and the FEV1/Forced Vital Capacity (FVC) ratio must be >0.7.
  • Male and Female participants willing and able to comply with study procedures

For PART 2 - MAD

  • Male or female participants ≥18 and ≤55 years of age at screening
  • BMI ≥18 and ≤32 kg/m2 at screening and weight at least 50 kg;
  • Physician-diagnosed asthma for at least 6 months and before the age of 50 years. Documented evidence of one of the confirmed variable expiratory airflow criteria, as per the GINA 2026 guidelines, is required within 10 years prior to screening.
  • Not currently receiving regular maintenance therapy for asthma, with no changes to treatment within <4 weeks prior to screening, and no exposure to ICS in the 12 weeks prior to screening including ICS reliever therapy;
  • Pre-bronchodilator FEV1 ≥70% of predicted at the screening visit and prior to randomisation;
  • Male and Female participants willing and able to comply with study procedures

For PART 3 - REPEATED DOSE

  • Male or female participants ≥18 and ≤65 years of age at screening
  • BMI ≥18 and ≤35 kg/m2 at screening and weight at least 50 kg;
  • Physician-diagnosed asthma for at least 6 months and before the age of 50 years. Documented evidence of one of the confirmed variable expiratory airflow criteria, as per the GINA 2026 guidelines, is required within 10 years prior to screening.
  • On a stable asthma treatment regimen of medium to high dose Inhaled Corticosteroids/Long-Acting Beta2-Agonists(ICS/LABA) (as defined by GINA 2026 guidelines) with no changes to treatment within 12 weeks prior to screening.
  • Pre-bronchodilator FEV1 ≥40% and ≤90% of predicted at the screening visit and prior to randomisation;
  • Asthma Control Questionnaire - 6 Items (ACQ-6) score of 0.5 to 3.0 at screening and prior to randomisation;
  • Male and Female participants willing and able to comply with study procedures

EXCLUSION CRITERIA:

For PART 1 - SAD

  • Participation in another clinical study where investigational drug was received less than 90 days or 5 half-lives prior to screening, whichever is longer;
  • Clinically relevant respiratory, cardiac, hepatic, gastrointestinal, renal, endocrine, haematologic, metabolic, neurological or psychiatric disorders that may interfere with successful completion of this protocol, according to the Investigator's judgment;
  • Clinically relevant abnormal laboratory values at screening suggesting an unknown disease and requiring further clinical investigation or which may impact the safety of the participant or the evaluation of the results of the study, according to the Investigator's judgment.
  • Positive hepatitis panel and/or positive HIV test at the screening visit.
  • Presence of any current infection, previous infection that resolved less than 7 days prior to screening or prior to randomisation or other latent or chronic infections (e.g. recurrent sinusitis, genital or ocular herpes, urinary tract infection);
  • History of malignancy within 5 years of screening (non-melanoma skin cancer is permitted if adequately treated for 12 months prior to screening);
  • Abnormal liver enzymes at screening or prior to randomisation (alanine aminotransferase [ALT] or aspartate aminotransferase [AST] or total bilirubin: >1.0 × upper limit of normal [ULN]).
  • Known intolerance and/or hypersensitivity to the Investigational Medicinal Product (IMP) or to any of the excipients contained in the formulation used in the study;
  • For females only: pregnant or lactating women, where pregnancy is defined as the state of a female after conception and until termination of the gestation.

For PART 2 - MAD

  • Participation in another clinical study where investigational drug was received less than 90 days or 5 half-lives prior to screening, whichever is longer;
  • Clinically relevant and uncontrolled respiratory disorders, including high-risk and non-persistent asthma; clinically relevant, uncontrolled, cardiac, hepatic, gastrointestinal, renal, endocrine, haematologic, metabolic, neurological or psychiatric disorders that may interfere with successful completion of this protocol, according to the Investigator's judgment;
  • History of any clinically significant respiratory disorders including but not limited to chronic obstructive pulmonary disease, idiopathic pulmonary fibrosis, alpha-1 antitrypsin deficiency, bronchiectasis, sarcoidosis, pulmonary hypertension or interstitial lung disease;
  • Clinically relevant abnormal laboratory values at screening suggesting an unknown disease and requiring further clinical investigation or which may impact the safety of the participant or the evaluation of the results of the study, according to the Investigator's judgment.
  • Positive hepatitis panel and/or positive HIV test at the screening visit.
  • Presence of any current infection, previous infection that resolved less than 7 days prior to screening or prior to randomisation or other latent or chronic infections (e.g. recurrent sinusitis, genital or ocular herpes, urinary tract infection);
  • Lower respiratory tract infection not resolved within 8 weeks prior to screening and/or randomisation, as determined by the Investigator;
  • Asthma exacerbation requiring medication or visit to the emergency department, including increase in Short-Acting Beta-Agonists (SABA) use, within 8 weeks of screening or during the study;
  • Use of inhaled or systemic corticosteroids within 12 weeks of screening or prior to randomisation;
  • Use of any asthma controller medication within 4 weeks of screening or prior to randomisation (including, but not limited to, LABA, leukotriene antagonists, xanthines, anti-cholinergics);
  • History of malignancy within 5 years of screening (non-melanoma skin cancer is permitted if adequately treated for 12 months prior to screening);
  • Abnormal liver enzymes at screening or prior to randomisation (ALT or AST or total bilirubin:>1.0 × upper limit of normal [ULN]).
  • For females only: pregnant or lactating women, where pregnancy is defined as the state of a female after conception and until termination of the gestation.

For PART 3 - REPEATED DOSE

  • Participation in another clinical study where investigational drug was received less than 90 days or 5 half-lives prior to screening, whichever is longer;
  • Clinically relevant and uncontrolled respiratory disorders, including high-risk and non-persistent asthma; clinically relevant, uncontrolled, cardiac, hepatic, gastrointestinal, renal, endocrine, haematologic, metabolic, neurological or psychiatric disorders that may interfere with successful completion of this protocol, according to the Investigator's judgment;
  • History of any clinically significant respiratory disorders including but not limited to chronic obstructive pulmonary disease, idiopathic pulmonary fibrosis, alpha-1 antitrypsin deficiency, bronchiectasis, sarcoidosis, pulmonary hypertension or interstitial lung disease;
  • Clinically relevant abnormal laboratory values at screening suggesting an unknown disease and requiring further clinical investigation or which may impact the safety of the participant or the evaluation of the results of the study, according to the Investigator's judgment.
  • Positive hepatitis panel and/or positive HIV test at the screening visit.
  • Presence of any current infection, previous infection that resolved less than 7 days prior to screening or prior to randomisation or other latent or chronic infections (e.g. recurrent sinusitis, genital or ocular herpes, urinary tract infection);
  • Asthma exacerbation or lower respiratory tract infection requiring medication or visit to the emergency department within 4 weeks prior to screening and/or prior to randomisation;
  • Use of systemic corticosteroids within 8 weeks of screening or prior to randomisation;
  • History of malignancy within 5 years of screening;
  • For females only: pregnant or lactating women, where pregnancy is defined as the state of a female after conception and until termination of the gestation;

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Sequential Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: CHF10136.

Participants receive CHF10136 administered via dry powder inhaler. Doses vary according to study cohort.

CHF10136 powder for inhalation administered orally using a Dry Powder Inhaler.

Placebo Comparator: Placebo

Participants receive placebo powder for inhalation administered via dry powder inhaler.

Matching placebo powder for inhalation administered using a Dry Powder Inhaler.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Number of Participants With Treatment-Emergent Adverse Events
Time Frame: Part 1, 2 and 3: Day - 28 to Day - 2 (Screening Visit), Day -1, Day 1, Day 2, Day 3, Day 4, and Day 8 (Follow-up Visit)

Assessment of safety through collection of treatment-emergent adverse events.

Part 1, 2 and 3: Day - 28 to Day - 2 (Screening Visit), Day -1, Day 1, Day 2, Day 3, Day 4, and Day 8 (Follow-up Visit)
Change From Baseline in Systolic Blood Pressure and Diastolic Blood Pressure
Time Frame: Part 1, 2 and 3:Day - 28 to Day - 2 (Screening Visit), Day -1, Day 1, Day 2, Day 3, Day 4, and Day 8 (Follow-up Visit)
Part 1, 2 and 3:Day - 28 to Day - 2 (Screening Visit), Day -1, Day 1, Day 2, Day 3, Day 4, and Day 8 (Follow-up Visit)
Change From Baseline in Electrocardiogram Parameters: HR (Heart Rate)
Time Frame: Part 1, 2 and 3:Day - 28 to Day - 2 (Screening Visit), Day -1, Day 1, Day 2, Day 3, Day 4, and Day 8 (Follow-up Visit)
Part 1, 2 and 3:Day - 28 to Day - 2 (Screening Visit), Day -1, Day 1, Day 2, Day 3, Day 4, and Day 8 (Follow-up Visit)
Change From Baseline in Electrocardiogram Parameters: Intervals recorded: PR, QT, QRS duration, QTcF (Fridericia corrected QT interval)
Time Frame: Part 1: Day 1 to Day 2 - Part 2 & 3: Day 1 to Day N + 1 (Day after the last treatment intake)
Part 1: Day 1 to Day 2 - Part 2 & 3: Day 1 to Day N + 1 (Day after the last treatment intake)
Change From Baseline in Clinical Laboratory Parameters
Time Frame: Part 1: Screening visit, Day -1, Day 4 and Day 8 - Part 2 & 3: Screening Visit, Day -1, Day 4 , Day 7, Day N+1 (Day after the last treatment intake), Day N+7 (Follow-up Visit)

Number of subjects with abnormal blood laboratory test results. Quantitative laboratory parameters (chemistry and haematology) will be summarised by treatment as absolute value and change from baseline using descriptive statistics.

Number of subjects with abnormal urine laboratory test results.

Part 1: Screening visit, Day -1, Day 4 and Day 8 - Part 2 & 3: Screening Visit, Day -1, Day 4 , Day 7, Day N+1 (Day after the last treatment intake), Day N+7 (Follow-up Visit)
Change From Baseline in Forced Expiratory Volume in One Second (FEV1)
Time Frame: Part 1: Screening Visit, Day 1 and Day 2 - Part 2& 3: Screening Visit, Day -1, Day 1 and Day N (the last day of treatment intake)
Part 1: Screening Visit, Day 1 and Day 2 - Part 2& 3: Screening Visit, Day -1, Day 1 and Day N (the last day of treatment intake)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Area Under the Plasma Concentration-Time Curve (AUC) for CHF10136 (parent compound) and its main metabolite.)
Time Frame: Part 1: Up to 72 hours post-dose and on Day 1 - Part 2 & 3: Day N (the last day of treatment intake )
Part 1: Up to 72 hours post-dose and on Day 1 - Part 2 & 3: Day N (the last day of treatment intake )
Maximum Observed Plasma Concentration (Cmax) of CHF10136 (parent compound) and its main metabolite.)
Time Frame: Part 1: on Day 1, up to 72 hours post-dose - Part 2 & 3: on Day 1 and Day N (the last day of treatment intake )
Part 1: on Day 1, up to 72 hours post-dose - Part 2 & 3: on Day 1 and Day N (the last day of treatment intake )
Time to Maximum Plasma Concentration (Tmax) of CHF10136 (parent compound) and its main metabolite.)
Time Frame: Part 1: on Day 1, up to 72 hours post-dose - Part 2 & 3: on Day 1 and Day N (the last day of treatment intake )
Part 1: on Day 1, up to 72 hours post-dose - Part 2 & 3: on Day 1 and Day N (the last day of treatment intake )
Terminal Half-Life (t½) of CHF10136 (parent compound) and its main metabolite.)
Time Frame: Day 1 for Part 1
Day 1 for Part 1
Apparent Clearance (CL/F) of CHF10136 (parent compound) and its main metabolite.)
Time Frame: Up to 72 hours post-dose
Up to 72 hours post-dose
Apparent Volume of Distribution (Vz/F) of CHF10136 (parent compound) and its main metabolite.)
Time Frame: Up to 72 hours post-dose
Up to 72 hours post-dose
Pharmacokinetic Parameters of the main Metabolite
Time Frame: Up to 72 hours post-dose

includes AUC

Up to 72 hours post-dose
Pharmacokinetic Parameters of the main Metabolite
Time Frame: Up to 72 hours post-dose

includes Cmax

Up to 72 hours post-dose
Pharmacokinetic Parameters of the main Metabolite
Time Frame: Up to 72 hours post-dose

include Metabolite Ratios

Up to 72 hours post-dose

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Investigators

  • Study Director: Rory Taylor, MD, Chiesi Farmaceutici S.p.A.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

October 2, 2026

Primary Completion (Estimated)

December 27, 2027

Study Completion (Estimated)

December 27, 2027

Study Registration Dates

First Submitted

September 18, 2026

First Submitted That Met QC Criteria

September 25, 2026

First Posted (Actual)

October 1, 2026

Study Record Updates

Last Update Posted (Actual)

October 13, 2026

Last Update Submitted That Met QC Criteria

October 7, 2026

Last Verified

October 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • CLI-10136AA1-01
  • 1014398 (Other Identifier: IRAS)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Chiesi clinical data sharing scope, process and data access criteria is available on the Chiesi Group website

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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