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ACTIVE NOT RECRUITING
NCT07008378
PHASE1

A Study to Evaluate the Safety, Tolerability, Cellular Kinetics, and Pharmacodynamics of P-CD19CD20-ALLO1 in Participants With Multiple Sclerosis

Sponsor: Genentech, Inc.

View on ClinicalTrials.gov

Summary

This study aims to explore the safety, tolerability, cellular kinetics, and pharmacodynamics of P-CD19CD20-ALLO1 in participants with progressive multiple sclerosis (PMS) and relapsing multiple sclerosis (RMS).

Official title: A Phase I, Multicenter, Open-Label Study to Evaluate the Safety, Tolerability, Cellular Kinetics, and Pharmacodynamics of P-CD19CD20-ALLO1 in Patients With Multiple Sclerosis

Key Details

Gender

All

Age Range

18 Years - 60 Years

Study Type

INTERVENTIONAL

Enrollment

60

Start Date

2025-10-15

Completion Date

2032-08-31

Last Updated

2026-04-21

Healthy Volunteers

No

Interventions

BIOLOGICAL

P-CD19CD20-ALLO1 Cells

P-CD19CD20-ALLO1 Cells will be administered intravenously as per the schedule specified in the protocol.

DRUG

Cyclophosphamide

Cyclophosphamide will be administered intravenously.

DRUG

Fludarabine

Fludarabine will be administered intravenously.

Locations (5)

UCI Sue & Bill Gross Stem Cell Research Center

Irvine, California, United States

UCSD Altman Clinical and Translational Research Institute

La Jolla, California, United States

Washington University School of Medicine

St Louis, Missouri, United States

Rutgers University- Robert Wood Johnson Medical School

New Brunswick, New Jersey, United States

Multiple Sclerosis Comprehensive Care Center at Northwell Health

New York, New York, United States