Efficacy and Safety of SPARC0921 in Subjects With Spasticity
Status: | Active, not recruiting |
---|---|
Conditions: | Neurology |
Therapuetic Areas: | Neurology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 2/7/2018 |
Start Date: | September 2012 |
End Date: | March 2018 |
The purpose of this study is to assess whether SPARC0921 demonstrate efficacy and safety in
the treatment of spasticity.
the treatment of spasticity.
Inclusion Criteria:
- Men and women age 18 years and older
- Known history of spasticity due to MS prior to starting baclofen
- Able and willing to comply with the protocol, including availability for a scheduled
clinic visits
- Willingness and giving of written informed consent
Exclusion Criteria:
- In relapse or history of unstable course over the prior 30 days prior to the Screening
Visit
- Concomitant neurologic conditions causing spasticity
- Has received an investigational drug or device within 30 days that would interfere
with the study goals prior to the Screening Visit
- Unable to comply with study procedures in the opinion of the investigator
We found this trial at
56
sites
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