drugset / Trial / NCT05898984
Clinical Study to Evaluate the Safety, Tolerability and the Concentration of the BDP (Beclomethasone Dipropionate), Active Metabolite of BDP, FF( Formoterol Fumarate) and GB (Glycopyrronium Bromide), After Inhalation of CHF 5993 at Two Different Doses and QVAR®
RandomizedCrossoverOpen-labelBasic science
Summary
The study is being conducted to compare the pharmacokinetic (PK) of BDP (and its main active metabolite B17MP), FF, and GB between CHF 5993 BDP/FF/GB 200/6/12.5 µg pMDI and CHF 5993 BDP/FF/GB 100/6/12.5 µg pMDI (pressurized Metered Dose Inhaler), to assess the proportionality of systemic exposure to BDP and B17MP (17-Monoproprionate), and the systemic exposure to FF and GB with increasing doses of BDP. The study includes a QVAR REDIHALER® arm too.
Timeline
- Start
- 2023-04-24
- Primary completion
- 2023-07-14
- Completion
- 2023-07-14
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Formoterol | Other / unclassified | 6 ug | Inhaled |
| Subject | Glycopyrronium | Unknown | 12.5 ug | Inhaled |
| Comparator | beclomethasone dipropionate | Other / unclassified | 80 ug | Inhaled |
| Comparator | beclomethasone dipropionate | Other / unclassified | 100 ug | Inhaled |
| Comparator | beclomethasone dipropionate | Other / unclassified | 200 ug | Inhaled |