Viewing Study NCT04237233


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Study NCT ID: NCT04237233
Status: UNKNOWN
Last Update Posted: 2022-09-16
First Post: 2019-12-31
Is Gene Therapy: True
Has Adverse Events: False

Brief Title: Intense Monitoring Study on Tyvyt
Sponsor: Innovent Biologics (Suzhou) Co. Ltd.
Organization:

Study Overview

Official Title: Intense Monitoring Study on Sintilimab Injection (Tyvyt®)
Status: UNKNOWN
Status Verified Date: 2022-09
Last Known Status: RECRUITING
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: The study is a multi-center, prospective, non-interventional and observational study, and will collect data on the safety and efficacy of Tyvyt® in the treatment of Chinese patients with relapsed or refractory classical Hodgkin's lymphoma.
Detailed Description: None

Study Oversight

Has Oversight DMC: False
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?: