ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

Open-Label and Single-Arm Study of MYOBLOC® in the Treatment of Troublesome Sialorrhea in Adults

ClinicalTrials.gov ID: NCT02610868

Public ClinicalTrials.gov record NCT02610868. 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 19, 2026, 11:10 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

A Phase 3, Long-Term, Open-Label and Single-Arm Study of MYOBLOC® in the Treatment of Troublesome Sialorrhea in Adult Subjects

Study identification

NCT ID
NCT02610868
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

Drug

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
Sep 30, 2015
Primary completion
May 31, 2017
Completion
May 31, 2017
Last update posted
Apr 20, 2026

2015 – 2017

United States locations

U.S. sites
26
U.S. states
17
U.S. cities
25
Facility City State ZIP Site status
Not listed Phoenix Arizona 85013
Not listed Scottsdale Arizona 85258
Not listed Scottsdale Arizona 85259
Not listed Loma Linda California 92354
Not listed Los Angeles California 90033
Not listed Aurora Colorado 80045
Not listed Atlantis Florida 33462
Not listed Boca Raton Florida 33486
Not listed Orlando Florida 32806
Not listed Port Charlotte Florida 33980
Not listed Atlanta Georgia 30329
Not listed Kansas City Kansas 66160
Not listed Overland Park Kansas 66211
Not listed Elkridge Maryland 21075
Not listed Farmington Hills Michigan 48334
Not listed St Louis Missouri 63110
Not listed Las Vegas Nevada 89145
Not listed Edison New Jersey 08818
Not listed Centerville Ohio 45459
Not listed Tulsa Oklahoma 74136
Not listed Greenville South Carolina 29615
Not listed Cordova Tennessee 38018
Not listed San Antonio Texas 78229
Not listed Kirkland Washington 98034
Not listed Spokane Washington 99202
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 9 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02610868, 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 19, 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 NCT02610868 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →