A Pilot Study to Characterize the Biological Effect of a Pre-planned 12 Week Dose Interruption of Natalizumab

Status unconfirmed · Phase 4

Conditions studied: Multiple Sclerosis, Multiple Sclerosis, Relapsing-Remitting

In brief

This is an open-label study of patients with relapsing forms of MS is designed to assess the biochemical, immunological, and kinetic profiles of natalizumab being used with specific brief dosing interruption. The study will be conducted at one site in the US. Ten subjects currently treated with natalizumab will be enrolled and will be evaluated for both PK/PD and cell trafficking in blood and/or CSF during standard dosing of natalizumab and at the end of a planned 12-week dosing interruption. MS disease activity will be carefully monitored clinically and by MRI and NfL.

Key facts

Study ID

NCT04048577

Run by

Berkovich, Regina MD, PhD Inc.

People needed

10

Starts

2019-07-03

Expected to finish

2021-12-01

Last updated by the study team

2021-07-22

Who can join

Age: 21 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• To be eligible for entry into this study, candidates must meet all of the following eligibility criteria at the time of randomization:
• Screening Visit:
• Ability to understand the purpose and risks of the study and provide signed and dated informed consent and authorization to use protected health information (PHI) in accordance with national and local subject privacy regulations.
• At least 18 years old at the time of informed consent.
• Must be a patient with a relapsing form of Multiple Sclerosis enrolled in the TOUCH Prescribing Program who is not expected to discontinue Tysabri® therapy prior to completion of the requirements of this study.
• Must weigh between 50 and 110 kg, inclusive.
• Patients must be considered clinically stable and scheduled for their pre-planned annual dose interruption of 2 consecutive skipped doses.
• No evidence of disease activity with on standard (28-day interval) dosing of natalizumab.

You may not qualify if…

• Candidates will be excluded from study entry if any of the following exclusion criteria exist at the time of screening:
• Medical History
• If subject answers 'Yes" to any question on the PML questionnaire that is not resolved prior to infusion as per standard operating procedure for natalizumab infusion.
• If subject consumes alcohol within 24 hours of blood specimen collection.

Where it is running

• Regina Berkovich MD, PhD Inc. — West Hollywood, California, United States (enrolling)

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.