Extension Study in Japanese PV and ET Patients
- Conditions
- Polycuthemia Vera and Essential ThrombocythemiaMyeloproliferative nemoplasms
- Registration Number
- JPRN-jRCT2031200269
- Lead Sponsor
- Kawase Hiroaki
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 67
1. Patients who have completed the 52-week P1101 treatment duration in Study A19-201 and are considered by the investigator or subinvestigator to be eligible for participation in this study
2. Patients who have completed the follow-up/end-of-study visit in Study P1101 ET and are considered by the investigator or subinvestigator to be eligible for participation in this study
3. Patients who have given written informed consent to participate in this study
1. Patients who are considered by the investigator or subinvestigator to be ineligible for continued treatment with P1101 or switch from anagrelide to P1101
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method