Viewing Study NCT06601504



Ignite Creation Date: 2024-10-26 @ 3:40 PM
Last Modification Date: 2024-10-26 @ 3:40 PM
Study NCT ID: NCT06601504
Status: NOT_YET_RECRUITING
Last Update Posted: None
First Post: 2024-09-08

Brief Title: Study of HMPL-760 Puls R-GemOx Versus Placebo Plus R-GemOx in RelapsedRefractory DLBCL
Sponsor: None
Organization: None

Study Overview

Official Title: A Phase II Randomized Controlled Study to Evaluate the Efficacy Safety and Pharmacokinetics of HMPL-760 Plus R-GemOx Versus Placebo Plus R-GemOx in Patients with RelapsedRefractory Diffuse Large B-Cell LymphomaRR DLBCL
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-09
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The goal of this study is to evaluate the efficacy of HMPL-760 in combination with R-GemOx versus placebo in combination with R-GemOx in patients with RelapsedRefractory Diffuse Large B-Cell Lymphoma RR DLBCL
Detailed Description: A Phase II Randomized Controlled Study to Evaluate the Efficacy Safety and Pharmacokinetics of HMPL-760 in Combination with R-GemOx versus Placebo in Combination with R-GemOx in Patients with RelapsedRefractory Diffuse Large B-Cell Lymphoma RR DLBCL The study phases include screening period treatment period safety observation period PFS follow-up period and OS follow-up period

Study Oversight

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