Purpose

This is a randomized, double-blind, placebo-controlled study to measure the reduction in mucus plug score at 24 weeks of treatment with SAR445399 compared with placebo in adult participants aged 18 to 80 years with non-cystic fibrosis bronchiectasis (NCFB).

Condition

Eligibility

Eligible Ages
Between 18 Years and 80 Years
Eligible Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Participants must be 18 to 80 years of age inclusive, at the time of signing the informed consent - Clinical history consistent with NCFB, such as chronic productive cough and/or recurrent respiratory infections - Documented evidence of at least 2 PEx defined as episodes requiring a physician-prescribed course of antibiotics (oral and/or IV) for ≥5 days for signs and symptoms of respiratory infection within the 12 months prior to the Screening Visit - Radiologic evidence of bronchiectasis, confirmed by a chest HRCT - A minimum MPS of 4 (out of maximum 18) on chest HRCT performed before Baseline Visit - Current sputum production with a documented history of chronic expectoration lasting ≥3 months within the previous 12 months - Participants must have a post-bronchodilator FEV1 ≥30% of predicted normal value

Exclusion Criteria

  • A primary diagnosis of smoking-related COPD or asthma as determined by the Investigator. Participants with comorbid smoking-related COPD may be included if bronchiectasis is confirmed as their primary diagnosis and is the predominant cause of their respiratory symptoms - Diagnosis of ABPA or any of the allergic bronchopulmonary mycoses - Active NTM lung infection or incomplete NTM treatment course - Bronchiectasis due to any of the following: CF, CVID, AAT or PCD - History of significant hemoptysis (requiring medical intervention and/or requiring blood transfusion) - Current tobacco smokers - Known or suspected immunosuppression, including history of invasive opportunistic infections (eg., histoplasmosis, listeriosis, coccidioidomycosis, pneumocystosis, aspergillosis), despite infection resolution, or otherwise recurrent infections of abnormal frequency, or prolonged infections suggesting an immune-compromised status, as judged by the Investigator - Participants with active autoimmune disease or participants using immunosuppressive therapy for autoimmune disease, including but not limited to connective tissue diseases (eg., systemic lupus erythematosus, scleroderma, polymyositis, dermatomyositis, mixed connective tissue disease), rheumatoid arthritis, inflammatory bowel disease, multiple sclerosis, Hashimoto's thyroiditis, Graves' disease, primary biliary cirrhosis, and psoriasis vulgaris The above information is not intended to contain all considerations relevant to a participant's potential participation in a clinical trial.

Study Design

Phase
Phase 2
Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary Purpose
Treatment
Masking
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Masking Description
[Specify Complex Masking]

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Arm A
Participants will receive SAR445399
  • Biological: SAR445399
    Pharmaceutical form: solution for injection Route of administration: injection
Placebo Comparator
Arm B
Participants will receive placebo
  • Biological: Placebo
    Pharmaceutical form: solution for injection Route of administration: injection

Recruiting Locations

Advanced Pulmonary Research Institute- Site Number : 8400001
Loxahatchee Groves, Florida 33470

More Details

Status
Recruiting
Sponsor
Sanofi

Study Contact

Trial Transparency email recommended (Toll free for US & Canada)
800-633-1610
Contact-US@sanofi.com

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.