Clinical trial
A Double-Blind, Randomized, Crossover Study to Evaluate the Clinical Efficacy and Safety of Oral Tizanidine HCl (12 mg) Versus Novel Sublingual Tizanidine HCl (12 mg) for the Treatment of Spasticity in MS Patients
NCT00358293 is registered in ClinicalTrials.gov with Teva GTC as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Double-Blind, Randomized, Crossover Study to Evaluate the Clinical Efficacy and Safety of Oral Tizanidine HCl (12 mg) Versus Novel Sublingual Tizanidine HCl (12 mg) for the Treatment of Spasticity in MS Patients
- Lead sponsor
- Teva GTC
- Phase
- Phase 1/2
- Overall status
- Completed
- Start date
- December 31, 2006
- Completion date
- February 28, 2007
- Enrollment
- 20
- Sites
- 1
Conditions
As the registry lists them; a condition with its own page is linked.