Viewing Study NCT03232177



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Last Modification Date: 2024-10-26 @ 12:28 PM
Study NCT ID: NCT03232177
Status: COMPLETED
Last Update Posted: 2021-07-21
First Post: 2017-07-11

Brief Title: Anagre Cap in Patients With High-Risk Essential Thrombocythemia
Sponsor: Yuhan Corporation
Organization: Yuhan Corporation

Study Overview

Official Title: A Multicenter Open-label Clinical Study for Efficacy and Safety Evaluation of Anagrelide in Patients With Treatment-naïve High-risk Essential Thrombocythemia as a Primary Treatment
Status: COMPLETED
Status Verified Date: 2021-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This study is to evaluate the efficacy and safety according to incremental dosing for 8 weeks and duration of administration for 1 year in patients with high-risk essential thrombocythemia
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None