Viewing Study NCT03470233


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Study NCT ID: NCT03470233
Status: COMPLETED
Last Update Posted: 2021-09-17
First Post: 2018-02-06
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: Post Marketing Registry to Assess Usage, Safety and Effectiveness of Deltyba Tablets in Korean Patients With MDR-TB
Sponsor: Korea Otsuka Pharmaceutical Co., Ltd.
Organization:

Study Overview

Official Title: Post-marketing Registry to Assess Usage Information, Safety and Effectiveness of Deltyba® Tablets in Korean Patients With Pulmonary Multi-drug Resistant Tuberculosis (MDR-TB)
Status: COMPLETED
Status Verified Date: 2021-08
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: Deltyba Registry aims to collect the usage information of Deltyba which could be a factor of developing resistance in actual clinical settings.
Detailed Description: To collect the usage information of Deltyba in actual clinical settings for the management of resistance to Deltyba

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?: