Viewing Study NCT05113069


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Study NCT ID: NCT05113069
Status: UNKNOWN
Last Update Posted: 2023-12-06
First Post: 2021-11-05
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: A Study of SHR-A1912 for Injection in Patients With B Cell Lymphomas
Sponsor: Shanghai Hengrui Pharmaceutical Co., Ltd.
Organization:

Study Overview

Official Title: A Phase I Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Efficacy of SHR-A1912 for Injection as Monotherapy in Patients With B-cell Lymphoma
Status: UNKNOWN
Status Verified Date: 2023-11
Last Known Status: ENROLLING_BY_INVITATION
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: To assess the safety and tolerability of SHR-A1912 in patients with B cell lymphoma, to determine the dose-limiting toxicity (DLT), maximum tolerated dose (MTD), and recommended phase II dose (RP2D) of SHR-A1912.
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?: