drugset / Trial / NCT03375047

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

NCT03375047 ↗

Phase 1/2 Completed 42 enrolled Sanofi
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This Phase 1/2, first-in-human study evaluated the safety and tolerability of single and multiple escalating doses of MRT5005 administered by nebulization to the respiratory tract of adult subjects with cystic fibrosis (CF).

Timeline

Start
2018-05-10
Primary completion
2022-03-15
Completion
2022-03-15

Drugs

EvaluationDrugModalityDoseRoute
Subject MRT5005 Unknown 4 mg Inhaled
Subject MRT5005 Unknown 8 mg Inhaled
Subject MRT5005 Unknown 12 mg Inhaled
Subject MRT5005 Unknown 16 mg Inhaled
Subject MRT5005 Unknown 20 mg Inhaled
Subject MRT5005 Unknown 24 mg Inhaled

Indications