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Recruiting Phase 2 Interventional

Study of AGN-151607-DP to Assess Adverse Events and Change in Disease Activity in Adult Participants With Upper Limb Essential Tremor

ClinicalTrials.gov ID: NCT07673107

Public ClinicalTrials.gov record NCT07673107. 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 Oct 22, 2026, 6:09 PM 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 2b Multicenter, Randomized, Double-Blind, Placebo-Controlled Study With an Open-Label Period to Evaluate the Efficacy and Safety of AGN-151607-DP (USAN: gemibotulinumtoxinA) for the Treatment of Upper Limb Essential Tremor in Adults

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Upper limb essential tremor (UL ET) is a movement disorder characterized by postural and/or kinetic tremor. It can cause difficulty with everyday tasks such as writing, pouring, and eating. This study will assess if AGN-151607-DP is safe and effective by assessing adverse events and change in disease activity in adult participants with UL ET. AGN-151607-DP is an investigational drug being developed to treat UL ET. Participants will be randomly placed in treatment groups to receive either AGN151607-DP or matching placebo. Approximately 94 adult participants with upper limb essential tremor will be enrolled in approximately 40 sites in the United States/Canada. Participants will receive intramuscular injections of AGN-151607-DP or matching placebo. Duration of the study is approximately 72 weeks. The effect of the treatment will be checked by completion of questionnaires and side effects will be monitored by medical assessments.

Study identification

NCT ID
NCT07673107
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
AbbVie
Industry
Enrollment
94 participants

Conditions and interventions

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
Jun 23, 2026 (Actual)
Primary completion
Nov 2028 (Estimated)
Completion
Nov 2028 (Estimated)
Last update posted
Oct 22, 2026

2026 – 2028

United States locations

U.S. sites
18
U.S. states
11
U.S. cities
18
Facility City State ZIP Site status
The Neurology Center of Southern California - Carlsbad /ID# 278194 Carlsbad California 92011 Recruiting
Neuro Pain Research Center /ID# 277899 Fresno California 93710 Recruiting
Neurology Center Of North Orange County /ID# 278490 Fullerton California 92835 Recruiting
New England Institute for Clinical Research /ID# 277315 Stamford Connecticut 06905 Recruiting
Parkinson'S Disease & Movement Disorders Center Of Boca Raton /ID# 277079 Boca Raton Florida 33486 Recruiting
Charter Research - Winter Park /ID# 277875 Orlando Florida 32803-1839 Recruiting
Emerald Coast Neurology /ID# 277898 Pensacola Florida 32504-8649 Recruiting
Kansas Institute of Research /ID# 277068 Overland Park Kansas 66211-1358 Recruiting
Dent Neurologic Institute - Amherst /ID# 277242 Amherst New York 14226 Recruiting
True North Neurology /ID# 278118 Commack New York 11725 Recruiting
Neurology - Triad /ID# 277088 Winston-Salem North Carolina 27103 Recruiting
Veracity Neuroscience /ID# 277081 Memphis Tennessee 38157 Recruiting
Texas Neurology /ID# 277067 Dallas Texas 75206-5202 Recruiting
Lone Star Neurology /ID# 278266 Frisco Texas 75035 Recruiting
Houston Methodist Hospital /ID# 277326 Houston Texas 77030 Recruiting
University of Virginia /ID# 278191 Charlottesville Virginia 22908 Recruiting
Inland Northwest Research /ID# 277077 Spokane Washington 99202 Recruiting
Center For Neurological Disorders /ID# 277048 Greenfield Wisconsin 53228 Recruiting

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 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07673107, 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 Oct 22, 2026 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT07673107 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →