NCT03689972A Study to Evaluate Efficacy, Safety, and Tolerability of EID of Natalizumab (BG00002) in Participants With RRMS Switching From Treatment With Natalizumab SID in Relation to Continued SID Treatment- Followed by Extension Study Comprising SC and IV Natalizumab Administration
Please note, some trial-specific information on this page is sourced from clinicaltrials.gov.
About
Trial summary
TYPEINTERVENTIONAL
PHASE
Phase
Clinical trials are done in different phases (0-4). Each phase provides important information about the drug. If a drug does not pass a particular phase, it cannot progress to the next phase. Visit the About Clinical Trials page to learn more.
PHASE3
CONDITION
Multiple Sclerosis, Relapsing-Remitting
INTERVENTIONS
Interventions
The drug, device, or procedure being tested.
DRUG:Natalizumab
Natalizumab 300 mg IV infusion.
DRUG:Natalizumab
Natalizumab 300 mg SC injection or IV infusion.
ENROLLMENT
Enrollment
The number of participants needed to take part in this trial.
585 participants
(ACTUAL)
18 Years to 60 Years
(ADULT)
LOCATIONS107
Key dates
Key dates
When the trial is conducted - from the date the first participant is enrolled to the date of the last participants's final visit.
Results from this trial have been made available. Some information may be redacted (edited) to protect privacy, publication rights, and confidential commercial information. To review the information please visit biogentrialtransparency.com.
PDF
Clinical trial registers
Clinical trial registers, like clinicaltrials.gov, provide information about registered clinical trials.
Publishing results for completed clinical trials on clinical trial registers help us share information about our clinical research. The results we publish here are written for healthcare professionals.
Please contact a clinical trial site directly to learn more about the trial. If no contact details are available, or for general inquiries, please contact the Biogen Clinical Trial Center.
