CompletedPHASE2, PHASE3NCT00125203
Study of Myobloc in the Treatment of Sialorrhea (Drooling) in Patients With Amyotrophic Lateral Sclerosis (ALS)
Studying Amyotrophic lateral sclerosis
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- The University of Texas Health Science Center at San Antonio
- Principal Investigator
- Carlayne E Jackson, MDThe University of Texas Health Science Center at San Antonio
- Intervention
- Botulinum toxin type B (Myobloc)(drug)
- Enrollment
- 20 enrolled
- Eligibility
- 21-85 years · All sexes
- Timeline
- 2003 – 2007
Study locations (2)
- University of Kansas Medical Center/Neurology, 1008 Wescoe, Kansas City, Kansas, United States
- Carolinas MDA Neuromuscular/ALS Center; Carolinas Medical System; 1540 Garden Terrace, Charlotte, North Carolina, United States
Collaborators
ALS Association · University of Kansas · Carolinas MDA Neuromuscular/ALS Center-Carolinas Medical System
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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