3 results
Approved WMOCompleted
To investigate the clinical feasibility of the TW22.
Approved WMOPending
Main Phase:To demonstrate the superiority of medium-dose BDP/FF/GB pMDI compared to high-dose BDP/FF pMDI in terms of the proportion of subjects exhibiting on average NPAL over 26 weeks of treatment in the study sub-population with PAL at screening…
Approved WMOPending
• To evaluate the efficacy of treatment• To evaluate the safety of treatment