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Extension Study in Japanese PV and ET Patients

Phase 3
Recruiting
Conditions
Polycuthemia Vera and Essential Thrombocythemia
Myeloproliferative 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
Inclusion Criteria

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

Exclusion Criteria

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
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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