Study of safety of CSJ117 in participants with moderate to severe uncontrolled asthma
- Conditions
- Asthma
- Registration Number
- JPRN-jRCT2031210301
- Lead Sponsor
- Yamada Hiroyuki
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- All
- Target Recruitment
- 60
1. Participants completing the Treatment period of prior study and continuing with this study must have completed the Treatment period of prior study.
2. Participants completing the Treatment period and Follow-up period of prior study and continuing with this study must have completed the Treatment period of prior study and Follow-up period of the core study.
1. Participants prematurely discontinued irrespective of the reason from the prior study.
2. Participants who were enrolled into prior study and developed a significant and/or permanent health condition during the prior study that would have excluded them from participation in that study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method umber of treatment emergent adverse events (AEs) and serious adverse events (SAEs)
- Secondary Outcome Measures
Name Time Method