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NOT YET RECRUITING
NCT07472413
PHASE3

Alternate Pre-med in Anti-Cluster of Differentiation 20 (CD20) Pilot Project

Sponsor: University of Miami

View on ClinicalTrials.gov

Summary

The purpose of this study is to assess and compare how well multiple sclerosis (MS) patients tolerate cetirizine versus diphenhydramine as a pre-medication before receiving anti-CD20 infusion therapy of ocrelizumab, ublituximab or rituximab. The study will also compare the safety of cetirizine versus diphenhydramine as a pre-medication for preventing infusion reactions in MS patients receiving anti-CD20 infusion therapy.

Official title: Cetirizine Versus Diphenhydramine as a Pre-medication: Tolerability and Safety in Patients With MS Receiving Anti-Cluster of Differentiation 20 (CD20) Infusion Therapy

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

60

Start Date

2026-07-01

Completion Date

2028-07-01

Last Updated

2026-03-16

Healthy Volunteers

No

Interventions

DRUG

Cetirizine

Participants will receive a single oral dose of cetirizine 10 mg administered 30-60 minutes before the scheduled standard-of-care anti-CD20 infusion at each visit.

DRUG

Diphenhydramine

Participants will receive a single oral dose of diphenhydramine 50 mg administered 30-60 minutes before the scheduled standard-of-care anti-CD20 infusion at each visit.

Locations (1)

UHealth Boca Raton

Boca Raton, Florida, United States