Evaluate Safety & Efficacy of a Single Treatment Cycle of EB-001 in

Clinical Trial Description

This study of EB-001 to measure safety and efficacy in GL. Single doses of EB- 001 administered through IM injection into procerus at midline and the medial and lateral corrugators will be assessed in healthy subjects with glabellar frown lines. ;

Study Design

See also
	Status	Clinical Trial	Phase
	Completed	`NCT04247074` - Treatment of Moderate to Severe Lateral Canthal Lines and Glabellar Lines Alone or in Combination	Phase 3

See also

Status

Clinical Trial

Phase

Completed

NCT04247074 - Treatment of Moderate to Severe Lateral Canthal Lines and Glabellar Lines Alone or in Combination

Phase 3

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT02939326
Study type	Interventional
Source	Bonti, Inc.
Contact
Status	Completed
Phase	Phase 2
Start date	December 2016
Completion date	July 12, 2017

Evaluate Safety and Efficacy of a Single Treatment Cycle of EB-001 in Subjects With Glabellar Frown Lines

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms