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®

NCT05898984

Phase 1 Completed 69 enrolled Chiesi Farmaceutici S.p.A. SGS S.A. · collab
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

EvaluationDrugModalityDoseRoute
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

Indications