drugset / Trial / NCT03375047
Study to Evaluate the Safety & Tolerability of MRT5005 Administered by Nebulization in Adults With Cystic Fibrosis
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |