- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00618722
Phase 1-2 Study of Deoxycholic Acid Injection (ATX-101) for the Reduction of Submental Fat (ATX-101)
Phase 1-2, Multicenter, Randomized, Placebo-Controlled, Parallel-Group Study of the Safety and Efficacy of ATX-101 (Sodium Deoxycholate for Injection) for the Reduction of Subcutaneous Fat in the Submental Area
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Phase 2
- Phase 1
Contacts and Locations
Study Locations
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Carina Heights, Australia
- Investigational Site
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Gold Coast, Australia
- Investigational Site
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Toorak, Australia
- Investigational Site
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Niagara Falls, Canada
- Investigational Site
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Ontario
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Oakville, Ontario, Canada
- Investigational Site
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London, United Kingdom
- Investigational Site
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Submental fat (SMF) that was considered undesirable by the subject and graded by the investigator as 2 or 3 using the SMF rating scale
- Good general health
- Signed informed consent
Exclusion Criteria:
- History of any treatment in the neck or chin area
- Loose skin or prominent platysmal bands in the neck or chin area
- Recent treatment with anticoagulants
- Presence of clinically significant health problems
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
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Experimental: Deoxycholic Acid Injection 1 mg/cm²
Participants received 0.5% deoxycholic acid administered in 0.2 mL injections, up to 4.8 mL (1 mg/cm²) per treatment session at intervals of approximately 1 month for up to a maximum of 4 treatments.
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Other Names:
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Experimental: Deoxycholic acid Injection 2 mg/cm²
Participants received 1.0% deoxycholic acid administered in 0.2 mL injections, up to 4.8 mL (2 mg/cm²) per treatment session at intervals of approximately 1 month for up to a maximum of 4 treatments.
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Other Names:
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Experimental: Deoxycholic acid Injection 4 mg/cm²
Participants received 2.0% deoxycholic acid administered in 0.2 mL injections, up to 4.8 mL (4 mg/cm²) per treatment session at intervals of approximately 1 month for up to a maximum of 4 treatments.
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Other Names:
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Placebo Comparator: Placebo
Participants received placebo administered in 0.2 mL injections, up to 4.8 mL per treatment session at intervals of approximately 1 month for up to a maximum of 4 treatments.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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Number of Participants With Adverse Events
Time Frame: From the first dose of study drug until 12 weeks after the last dose (up to 24 weeks after first treatment).
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The investigator determined the relationship of each adverse event to the administration of study drug. Severity of adverse events was determined using the following scale:
A serious AE (SAE) was defined as an event that may constitute a significant medical hazard or side-effect, regardless of the investigator or sponsor's opinion regarding relatedness to study material. Serious events included, but were not limited to, any event that:
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From the first dose of study drug until 12 weeks after the last dose (up to 24 weeks after first treatment).
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Number of Participants With Clinically Significant Changes From Baseline in Laboratory Values, Weight, Vital Signs, and Physical Examinations
Time Frame: From the first dose of study drug until 12 weeks after the last dose (up to 24 weeks after first treatment).
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From the first dose of study drug until 12 weeks after the last dose (up to 24 weeks after first treatment).
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change From Baseline in Submental Fat (SMF) Rating Scale Score
Time Frame: Baseline and 4 weeks after last treatment (up to 16 weeks after first dose)
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The SMF rating scale score is based on the investigator's clinical evaluation of the participant, where submental fullness is scored on a 5-point ordinal scale (0-4) with 0 = absent, 1 = mild, 2 = moderate, 3 = severe, and 4 = extreme. A negative change from Baseline indicates improvement. |
Baseline and 4 weeks after last treatment (up to 16 weeks after first dose)
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Change From Baseline in Subject Satisfaction With Appearance Rating Scale
Time Frame: Baseline and 4 weeks after last treatment (up to 16 weeks after first dose)
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The Subject Satisfaction with Appearance Rating Scale assesses participants' satisfaction with their appearance in association with the face and chin on a 7-point scale from 0 to 6 where 0 = Extremely dissatisfied, 1 = Dissatisfied, 2 = Slightly dissatisfied, 3 = Neither satisfied nor dissatisfied, 4 = Slightly satisfied, 5 = Satisfied and 6 = Extremely satisfied.
A positive change from Baseline indicates improvement.
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Baseline and 4 weeks after last treatment (up to 16 weeks after first dose)
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Percentage of Participants With a Response in the Subject Global Improvement Rating
Time Frame: 4 weeks after last treatment (up to 16 weeks after first dose)
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Participants were asked to rate their total improvement or worsening in the appearance and physical feeling of their chin and neck area since before they received study treatment, whether or not they believed it was due to study treatment or to any other cause. 0 = Very much worse, 1 = Much worse, 2 = Minimally worse, 3 = No change, 4 = Minimally improved, 5 = Much improved, 6 = Very much improved. Response is defined as any improvement, ie, a global improvement rating of 4, 5, or 6. |
4 weeks after last treatment (up to 16 weeks after first dose)
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Change From Baseline in Skin Laxity Rating
Time Frame: Baseline and Week 4, Week 8, Week 12, Week 16 (4 weeks after last treatment) and Week 24 (12 weeks after last treatment)
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Skin laxity assessment was based on clinical evaluation and palpation of the submental area on the following scale: 1 = no laxity; 2 = minimal laxity; 3 = moderate laxity; 4 = very lax. A negative change from Baseline indicates improvement. |
Baseline and Week 4, Week 8, Week 12, Week 16 (4 weeks after last treatment) and Week 24 (12 weeks after last treatment)
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Change From Baseline in the Cervicomental Angle
Time Frame: Baseline and 4 weeks after last treatment (up to 16 weeks after first dose)
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The cervicomental angle was measured using a profile view photograph obtained at each visit.
A goniometer was used to determine the angle.
Cervicomental angle measurements less than 80 degrees are excluded, due to error in measurement.
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Baseline and 4 weeks after last treatment (up to 16 weeks after first dose)
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Collaborators and Investigators
Sponsor
Investigators
- Study Director: Frederick Beddingfield, MD. PhD, Kythera Biopharmaceuticals, Inc.
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ATX-101-06-03
- 2007-000146-13 (EudraCT Number)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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