ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

Efficacy and Safety Study of MYOBLOC® in the Treatment of Sialorrhea in Adult Subjects

ClinicalTrials.gov ID: NCT01994109

Public ClinicalTrials.gov record NCT01994109. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 16, 2026, 9:25 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Phase 3, Multicenter, Double-Blind, Placebo-Controlled, Single-Treatment Efficacy and Safety Study of MYOBLOC® Followed by Open-Label, Multiple-Treatment With MYOBLOC® in the Treatment of Troublesome Sialorrhea in Adult Subjects

Study identification

NCT ID
NCT01994109
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Solstice Neurosciences, LLC, a subsidiary of US WorldMeds, LLC
Industry
Enrollment
187 participants

Conditions and interventions

Conditions

Interventions

  • MYOBLOC Drug
  • PLACEBO Other

Drug · Other

Eligibility (public fields only)

Age range
18 Years to 85 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 31, 2013
Primary completion
Dec 31, 2015
Completion
Dec 31, 2016
Last update posted
Apr 20, 2026

2013 – 2017

United States locations

U.S. sites
24
U.S. states
17
U.S. cities
24
Facility City State ZIP Site status
Not listed Loma Linda California 92354
Not listed Los Angeles California 90033
Not listed National City California 91950
Not listed Aurora Colorado 80045
Not listed Washington D.C. District of Columbia 20007
Not listed Boca Raton Florida 33486
Not listed Port Charlotte Florida 33980
Not listed Carmel Indiana 46032
Not listed Baltimore Maryland 21287
Not listed Elkridge Maryland 21075
Not listed Detroit Michigan 48334
Not listed St Louis Missouri 63110
Not listed Edison New Jersey 08818
Not listed Albany New York 12208
Not listed New York New York 10003
Not listed Cincinnati Ohio 45219
Not listed Tulsa Oklahoma 74136
Not listed Port Royal South Carolina 29935
Not listed Cordova Tennessee 38018
Not listed Houston Texas 77030
Not listed San Antonio Texas 78229
Not listed Salt Lake City Utah 84132
Not listed Kirkland Washington 98034
Not listed Tacoma Washington 98409

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 10 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01994109, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 20, 2026 · Synced May 16, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01994109 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →