TYSABRI Long Term Re-Dosing Study
An Open-label, Multicenter, Extension Study to Evaluate the Safety and Tolerability of Natalizumab Following Re-Initiation of Dosing in Multiple Sclerosis Subjects Who Have Completed Study C-1801 or C-1802 and a Dosing Suspension Safety Evaluation
What it found
The trial ended early for another reason (see below).
What was tested
Treatment tested
- Natalizumab
Integrin alpha-4/beta-1 inhibitor|Integrin alpha-4/beta-7 inhibitor
What it measured
Main measures
Initial Treatment Period:
Other measures (1)
Not available
Who could take part
Relapsing MS
Show the full criteria
Inclusion criteria
Inclusion: 1) must give informed consent and provide all athorizations required by local law Exclusion: 1) considered by the Investigator to be immunocompromised, based on medical history, physical examination, or laboratory testing (results from the Dosing Suspension Safety Evaluation from Study C-1808 may be used), or due to prior immunosuppressive treatment
Exclusion criteria
Not separately supplied in the registry.
As registered. Criteria can change, so ask the trial team or your neurologist.
About this trial
In the sponsor's words
Initial Treatment Period:
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History
Started
Oct 2005