Changeflow GovPing Pharma & Drug Safety Allogeneic CD19/BCMA CAR-T B cell autoimmune trial
Routine Notice Added Final

Allogeneic CD19/BCMA CAR-T B cell autoimmune trial

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Summary

ClinicalTrials.gov registered a Phase 1/2 clinical trial (NCT07507201) evaluating allogeneic CD19/BCMA CAR-T cell therapy for B cell autoimmune diseases. The dose-escalation study will assess safety, tolerability, and preliminary efficacy in autoimmune patients. Registration includes eligibility criteria, study design, and investigator contact information.

What changed

A new clinical trial registration was added to ClinicalTrials.gov for an allogeneic CAR-T cell therapy study targeting both CD19 and BCMA antigens for B cell-mediated autoimmune diseases. The trial is registered as Phase 1/2 with dose-escalation design. NCT07507201 documents participant eligibility criteria, primary endpoints focused on safety and dose-limiting toxicity, and contact details for the principal investigator.

This is an informational registration entry that does not impose compliance obligations. Clinical investigators and sponsors conducting similar cell therapy research may wish to review the protocol for competitive landscape awareness. Patients seeking enrollment opportunities can reference this trial through ClinicalTrials.gov.

Archived snapshot

Apr 3, 2026

GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.

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Last updated

Classification

Agency
NLM
Published
July 3rd, 2025
Instrument
Notice
Legal weight
Non-binding
Stage
Final
Change scope
Minor
Document ID
NCT07507201

Who this affects

Applies to
Clinical investigators Healthcare providers Patients
Industry sector
3254 Pharmaceutical Manufacturing 6211 Healthcare Providers
Activity scope
Clinical Trial Registration
Geographic scope
United States US

Taxonomy

Primary area
Healthcare
Operational domain
Clinical Operations
Topics
Pharmaceuticals Medical Devices

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