Evaluation of Safety and Efficacy of Deoxycholic Acid Injection (ATX-101) in the Reduction of Submental Fat

Moderate or Severe Submental Fullness Clinical Trial

Official title:

Phase 3, Multicenter, Randomized, Double-blind, Placebo-controlled Study of ATX-101 (Sodium Deoxycholate Injection) Versus Placebo for the Reduction of Localized Subcutaneous Fat in the Submental Area

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01305577
• Other study ID #: ATX-101-10-16
• Secondary ID: 2010-020690-17
• Status: Completed
• Phase: Phase 3
• First received: February 10, 2011
• Last updated: June 17, 2015
• Start date: December 2010
• Est. completion date: January 2012

Study information

• Verified date: June 2015
• Source: Kythera Biopharmaceuticals
• Contact: n/a
• Is FDA regulated: No
• Health authority: United Kingdom: Medicines and Healthcare Products Regulatory Agency
• Study type: Interventional

Clinical Trial Summary

To evaluate the safety and efficacy of deoxycholic acid injection in the reduction of submental fat (fat below the chin).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 363
• Est. completion date: January 2012
• Est. primary completion date: January 2012
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

1. Submental fat graded by the investigator as 2 or 3 using the Clinician-Reported Submental Fat Rating Scale (CR-SMFRS) as determined on Visit 2.

2. Dissatisfaction with the submental area rated by the subject as 0, 1, 2, or 3 using the Subject Self Rating Scale (SSRS).

3. Males and nonpregnant, nonlactating females between 18 and 65 years of age, inclusive on the day of randomization. Females of childbearing potential must have a negative human chorionic gonadotropin (hCG) test result within 28 days before randomization and agree to practice medically acceptable birth control during the course of the study. Medically acceptable birth control includes: surgical sterilization, hormonal contraceptives, barrier methods or an intrauterine device (IUD).

4. History of stable body weight, in the judgment of the investigator, for at least 6 months before randomization. No significant change, in the judgment of the investigator, in diet or exercise practices for at least 6 months before randomization and agreement to not change diet or exercise practices during the course of the study.

5. Expected to comply with and understand the visit schedule and all protocol-specified tests and procedures.

6. Medically able to undergo the administration of study material determined by clinical evaluations made within 56 days before and laboratory tests obtained within 28 days before randomization for which the investigator identified no clinically significant abnormality.

7. Signed informed consent obtained before any study-specific procedure is performed.

Exclusion Criteria:

1. History of any intervention to treat submental fat (e.g., liposuction, surgery, or lipolytic agents) or trauma associated with the chin or neck areas, which in the judgment of the investigator may affect evaluation of safety or efficacy of treatment.

2. Loose skin in the neck or chin area for which reduction in submental fat may, in the judgment of the investigator, result in an aesthetically unacceptable outcome or a score of 4 on the Skin Laxity Rating Scale (SLRS).

3. Prominent platysmal bands at rest or other anatomical features that, in the judgment of the investigator, may interfere with the evaluation of submental fat or result in an aesthetically unacceptable outcome.

4. Evidence of any cause of enlargement in the submental area (e.g., thyroid enlargement or cervical adenopathy) other than localized submental fat.

5. Body mass index (BMI) greater than 30.

6. Currently on or considering starting a weight reduction regimen.

7. Any medical condition (e.g., respiratory, cardiovascular, hepatic, neurological disease, uncontrolled hypertension, or thyroid dysfunction) that would interfere with assessment of safety or efficacy or compromise the subject's ability to undergo study procedures or provide informed consent.

8. Treatment with radio frequency, laser procedures, chemical peels, or dermal fillers in the neck or chin area within 12 months before randomization, or botulinum toxin injections in the neck or chin area within 6 months before randomization.

9. History of sensitivity to any components of the study material or to topical or local anesthetics (e.g., lidocaine, benzocaine, or novocaine).

10. Previous randomization into this study or previous treatment with ATX-101.

11. Treatment with an investigational device or agent within 30 days of randomization.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Moderate or Severe Submental Fullness

Intervention

Drug:
• Deoxycholic acid injection

• Placebo
Phosphate buffered saline placebo for injection

Locations

Country	Name	City	State
Belgium	Investigational Site	Oudenaarde	Minderbroederstaraat
France	Investigational Site	Arras
France	Investigational Site	Cannes
France	Investigational Site	Nice
France	Investigational Site	Pantin
France	Investigational Site	Paris
France	Investigational Site	Paris
Germany	Investigational Site	Augsburg
Germany	Investigational Site	Augsburg
Germany	Investigational Site	Berlin
Germany	Investigational Site	Darmstadt
Germany	Investigational Site	Frankfurt/Main
Germany	Investigational Site	Landau
Germany	Investigational Site	Ludwigshafen
Germany	Investigational Site	München
Germany	Investigational Site	Northeim
Germany	Investigational Site	Potsdam
Germany	Investigational Site	Starnberg
Germany	Investigational Site	Wuppertal
Spain	Investigational Site	Barcelona
Spain	Investigational Site	Barcelona
Spain	Investigational Site	Barcelona
Spain	Investigational Site	Barcelona
United Kingdom	Investigational Site	Cheltenham
United Kingdom	Investigational Site	London
United Kingdom	Investigational Site	Northampton
United Kingdom	Investigational Site	Nottingham
United Kingdom	Investigational Site	Nottingham
United Kingdom	Investigational Site	Plymouth
United Kingdom	Investigational Site	Salford	Manchester

Sponsors (2)

Lead Sponsor	Collaborator
Kythera Biopharmaceuticals	Bayer

Countries where clinical trial is conducted

Belgium,  France,  Germany,  Spain,  United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Percentage of Participants With a Clinician-Reported Submental Fat Rating Scale (CR-SMFRS) 1-grade Response	A CR-SMFRS response is defined as at least a 1-point improvement (i.e. 1-point reduction) from Baseline 12 weeks after the last treatment.; The CR-SMFRS 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.	Baseline and 12 weeks after last treatment (up to 24 weeks after first dose)	No
Primary	Percentage of Participants With a Subject Self Rating Scale (SSRS) Response	A SSRS response is defined as an SSRS score that is 4 or greater 12 weeks after the last treatment.; The SSRS assesses participant's 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.	Baseline and 12 weeks after last treatment (up to 24 weeks after first dose)	No
Secondary	Percentage of Participants With a CR-SMFRS 2-grade Response	A CR-SMFRS 2-grade response is defined as at least a 2-point improvement (i.e. 2-point reduction) from Baseline 12 weeks after the last treatment.; The CR-SMFRS 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.	Baseline and 12 weeks after last treatment (up to 24 weeks after first dose)	No
Secondary	Change From Baseline in CR-SMFRS Scores	The CR-SMFRS 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 12 weeks after last treatment (up to 24 weeks after first dose)	No
Secondary	Change From Baseline in SSRS Scores	The SSRS assesses participant's 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.	Baseline and 12 weeks after last treatment (up to 24 weeks after first dose)	No
Secondary	Change From Baseline in Submental Fat Thickness	Submental thickness was measured using caliper devices.	Baseline and 12 weeks after last treatment (up to 24 weeks after first dose)	No
Secondary	Change From Baseline in Patient-reported Submental Fat Rating Scale (PR-SMFRS)	The PR-SMFRS is based on the participant's response to the question "How much fat do you currently have under your chin?" answered on a 5-point ordinal scale (0-4) with 0 = no chin fat at all, 1 = a slight amount of chin fat, 2 = a moderate amount of chin fat, 3 = a large amount of chin fat, and 4 = a very large amount of chin fat. Improvement is defined as any decrease in score and worsened as any increase in score.	Baseline and 12 weeks after last treatment (up to 24 weeks after first dose)	No
Secondary	Change From Baseline in Patient-Reported Submental Fat Impact Scale (PR-SMFIS)	The PR-SMFIS assesses the impact of submental fat on self-perception of 6 characteristics related to the appearance of submental fullness as evaluated by the participant. Each item is rated on an 11-point numeric scale from 0 to 10.	Baseline and 12 weeks after last treatment (up to 24 weeks after first dose)	No
Secondary	Change From Baseline in Self-rating of Attractiveness	Self-rating of attractiveness assesses aspects of appearance from the participant's perspective by a series of 6 questions: How attractive do you think your overall appearance (chin/neck, eyes, nose, mouth, entire face) is/are?" Each question was answered on a scale from 1 to 9 where 1 = Not at all attractive, 5 = Neither attractive nor unattractive and 9 = Extremely attractive.; A positive change from Baseline indicates improvement.	Baseline and 12 weeks after last treatment (up to 24 weeks after first dose)	No
Secondary	Change From Baseline in Derriford Appearance Scale 24 (DAS24)		Baseline and 12 weeks after last treatment (up to 24 weeks after first dose)	No
Secondary	Change From Baseline in Body Image Quality of Life Inventory (BIQLI)		Baseline and 12 weeks after last treatment (up to 24 weeks after first dose)	No