Viewing Study NCT03664635



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Last Modification Date: 2024-10-26 @ 12:53 PM
Study NCT ID: NCT03664635
Status: ACTIVE_NOT_RECRUITING
Last Update Posted: 2024-04-23
First Post: 2018-09-03

Brief Title: MB-CART201 Lymphoma
Sponsor: Miltenyi Biomedicine GmbH
Organization: Miltenyi Biomedicine GmbH

Study Overview

Official Title: A Phase III Safety Dose Finding and Feasibility Trial of MB-CART201 in Patients With Relapsed or Resistant CD20 Positive B-NHL
Status: ACTIVE_NOT_RECRUITING
Status Verified Date: 2024-04
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 trial is a phase III trial to assess safety dose finding and feasibility of ex vivo generated MB-CART201 cells in patients with relapsed or refractory CD20 positive B-NHL
Detailed Description: MB-CART201 consists of autologous Anti-CD20 Chimeric Antigen Receptor CAR transduced CD4 CD8 enriched T cells targeting CD20-positive tumor cells in Non-Hodgkin-Lymphoma NHL

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