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Completed Phase 1Phase 2 Interventional Results available

Study to Evaluate the Safety & Tolerability of MRT5005 Administered by Nebulization in Adults With Cystic Fibrosis

ClinicalTrials.gov ID: NCT03375047

Public ClinicalTrials.gov record NCT03375047. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jun 26, 2026, 12:20 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 1/2, Randomized, Double-Blinded, Placebo-Controlled, Combined Single and Multiple Ascending Dose Study Evaluating the Safety, Tolerability, and Biological Activity of MRT5005 Administered by Nebulization to Adult Subjects With Cystic Fibrosis

Study identification

NCT ID
NCT03375047
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Sanofi
Industry
Enrollment
42 participants

Conditions and interventions

Interventions

  • MRT5005 Drug
  • Normal saline Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 9, 2018
Primary completion
Mar 14, 2022
Completion
Mar 14, 2022
Last update posted
Feb 8, 2026

2018 – 2022

United States locations

U.S. sites
16
U.S. states
14
U.S. cities
16
Facility City State ZIP Site status
University of Alabama at Birmingham Birmingham Alabama 35233
National Jewish Health Denver Colorado 80206
University of Florida Gainesville Florida 32610
Northwestern University Chicago Illinois 60611
University of Indiana Indianapolis Indiana 46202
Maine Medical Center Portland Maine 04102
Johns Hopkins University Baltimore Maryland 21287
University of Michigan Ann Arbor Michigan 48109
University of Cincinnati Cincinnati Ohio 45267
University Hospitals Cleveland Ohio 44106
Nationwide Children's Hospital Columbus Ohio 43205
Oregon Health and Sciences University Portland Oregon 97239
University of Pennsylvania Philadelphia Pennsylvania 19104
New Orleans Center for Clinical Research Knoxville Tennessee 37920
University of Utah Salt Lake City Utah 84132
Virginia Commonwealth University Richmond Virginia 23298

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03375047, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 8, 2026 · Synced Jun 26, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03375047 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →