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A Safety and Efficacy Study of OnabotulinumtoxinA in Upper Facial Rhytides

NCT02261493 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 787

Last updated 2017-07-25

Study results available
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Summary

This is a safety and efficacy study of onabotulinumtoxinA in subjects with upper facial rhytides (forehead lines, glabellar lines, lateral canthal lines \[crow's feet lines\]).

Conditions

  • Facial Rhytides
  • Glabellar Rhytides

Interventions

BIOLOGICAL

OnabotulinumtoxinA

OnabotulinumtoxinA injected into the protocol-specified areas. Subjects will receive at least 1 and up to 3 treatments.

DRUG

Normal Saline

Placebo (normal saline) injected into the protocol-specified areas on Day 1.

Sponsors & Collaborators

  • Allergan

    lead INDUSTRY

Principal Investigators

  • Medical Director · Allergan

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-10-27
Primary Completion
2015-06-03
Completion
2016-04-20
FDA Drug
Yes

Countries

  • United States
  • Belgium
  • Germany
  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02261493 on ClinicalTrials.gov