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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

About this study

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.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Receive P-CD19CD20-ALLO1 Cells
  • 2.Take Cyclophosphamide
  • 3.Take Fludarabine
PhasePhase 1
DrugCyclophosphamide
Routeinfusion
Primary goalNumber of Participants With Adverse Events (AEs)

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low9%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

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