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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.