Multiple Sclerosis (MS) Clinical Trials

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AttackMS: Natalizumab for the Treatment of People With Inflammatory Demyelination Suggestive of Multiple Sclerosis, or Definite Multiple Sclerosis, at First Presentation

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Multiple Sclerosis (MS) is a chronic inflammatory \& degenerative disease of the central nervous system (CNS) Recent data from the MS Base registry demonstrated an average delay of 152 - 215 days between first presentation and the diagnosis of MS, and more than one year until Disease Modifying Treatment (DMT) begins. Evidence suggests that shutting down inflammation using highly effective DMTs early after diagnosis leads to better long term clinical outcomes The AttackMS trial will test the effect of starting a highly-effective DMT licensed for MS, Tyruko® (Natalizumab 300mg), within a short time - 14 days - after symptom onset.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 55
Healthy Volunteers: f
View:

• Participant has provided informed consent.

• Age 18-55 years

• Participant with CIS or MS at first presentation.

• Participants show two or more lesions on T2 weighted MRI suggestive of demyelination.

• Participant is willing and able to comply with clinical visits and procedures outlined in the study protocol.

Locations
Other Locations
United Kingdom
Royal London Hospital
NOT_YET_RECRUITING
London
St George's Hospital
RECRUITING
London
Contact Information
Primary
Klaus Schmierer
k.schmierer@qmul.ac.uk
+44 20 7882 6246
Backup
Julia Elizabeth Phillips
attackms@qmul.ac.uk
Time Frame
Start Date: 2022-12-01
Estimated Completion Date: 2027-10-31
Participants
Target number of participants: 40
Treatments
Active_comparator: Tyruko® 300mg
Tyruko® 300mg, administered via intravenous infusion in a 4 week cycle, for a total of 6 cycles
Placebo_comparator: Placebo
Placebo, administered via intravenous infusion in a 4 week cycle, for 3 cycles, followed by Tyruko® 300mg, administered via intravenous infusion for a total of 3 cycles
Related Therapeutic Areas
Sponsors
Collaborators: UCL Queen Square Institute of Neurology, Barts & The London NHS Trust, Biogen, Moorfields Eye Hospital NHS Foundation Trust
Leads: Queen Mary University of London

This content was sourced from clinicaltrials.gov