jRCT2031210566CompletedNot Applicable
Follow ups of patients in AK1830 Phase II Studies
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Enrollment
- 10
- Primary Endpoint
- -
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
- Allocation
- Single Arm Study
- Intervention Model
- Single Assignment
- Primary Purpose
- Other
- Masking
- Open(masking Not Used)
Eligibility Criteria
- Ages
- No limit to No limit (—)
- Sex
- All
Inclusion Criteria
- •Patients who provided written informed consent to participate in the clinical study and who met all of the following criteria
- •[1] Patients who participated in the AK1830 Phase II Study and were deemed to require follow up.
- •[2] Patients who fully understand the contents of the study and are capable of providing informed consent
Exclusion Criteria
- •Patients who met any of the following criteria are to be excluded.
- •[1] Patients who have received their long-term safety outcomes in the AK1830 Phase II Study
- •[2] Patients deemed by the investigator or sub-investigator to be unsuitable for study participation
Outcomes
Primary Outcomes
-
image evaluations
Secondary Outcomes
No secondary outcomes reported
Investigators
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