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

Genentech, Inc.
NCT IDNCT07008378ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1

Target enrollment

60

Study length

about 6.9 years

Ages

18–60

Locations

1 site in MO

What this study is about

This trial is testing a treatment called P-CD19CD20-ALLO1 for people with multiple sclerosis. The goal is to see how safe and well the treatment works, including how it affects cells in the body and its effects on the disease.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Receive P-CD19CD20-ALLO1 Cells
  • 2.Take Cyclophosphamide
  • 3.Take Fludarabine

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Injection / IV

How treatment is administered

Treatment Assignment
Standard assignment

Assignment is predetermined by the study protocol.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug classes

cyclophosphamide (Alkylating chemotherapy; crosslinks DNA strands), fludarabine

Drug routes

infusion

Endpoints

Primary: Number of Participants With Adverse Events (AEs), Number of Participants With Dose-limiting Toxicity (DLTs) at Each Dose Level of P-CD19CD20-ALLO1

Body systems

Neurology