Evaluating the Efficacy and Safety of Embella (Deoxycholic Acid, Produced by Espad Pharmed Co.) for the Treatment of Flank Fat

NCT ID: NCT07004010

Last Updated: 2026-01-21

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 30 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-08-01
• Study Completion Date: 2024-12-30

Brief Summary

Flank region fat is a factor affecting beauty that makes people feel uncomfortable about themselves. In 2015, deoxycholic acid was approved by the American FDA for treatment of flank fat. The purpose of this study is to evaluate the efficacy and safety of deoxycholic acid injection with the brand name Embella®, manufactured by Espad Pharmed Company, for treatment of this condition.

The Primary objective of this study was the proportion of participants with grade 1 or higher ("improved, much improved, very much improved") in investigator-assessed Global Aesthetic Improvement Scale (GAIS) at Week 12 Secondary objective was assessment of other efficacy parameters as well as safety of the product

Conditions

Flank Fat

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Embella (Deoxycholic acid, produced by Espad Pharmed Co.)

Group Type: EXPERIMENTAL

Deoxycholic Acid Injection

Intervention Type: DEVICE

The intervention include Deoxycholic acid, SC, 0.15 ml each injection, up to 2-4 ml in each site (2 ml at visit 1 for everyone, and 2 ml at visit 2 unless the patient does not agree)

Interventions

Deoxycholic Acid Injection

The intervention include Deoxycholic acid, SC, 0.15 ml each injection, up to 2-4 ml in each site (2 ml at visit 1 for everyone, and 2 ml at visit 2 unless the patient does not agree)

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

• Having mild to moderate flank fat assessed by the investigator and sonography and/or caliper (≥2cm thickness of the fat tissue in posterior axillary lines at the level of ASIS)
• Signing informed consent by the subject
• Ability to follow study instructions and likely to complete all required visits
• Agreement to abstain from any treatment to the flank region, including botulinum toxins, hyaluronic acid fillers, cosmetic surgery, laser/light therapy, chemical peels, etc., during the study

Exclusion Criteria

• Planning to change lifestyle within the projected duration of the trial
• History of liposuction surgery or laser lipolysis in the past 12 months or planning to have these procedures
• Significant weight reduction in the past 6 months or planning for weight reduction within the projected duration of the trial
• BMI > 30 kg/m2
• Waist circumference > 105 cm
• Uncontrolled systemic diseases
• Severe cardiovascular diseases
• Known allergy or sensitivity to the study medication or its components
• Females who are pregnant or breastfeeding, or expecting to conceive children within the projected duration of the trial
• Current enrollment in an investigational drug or device study or participation in such a study within 30 days of entry into this study and for the duration of the study.
• Previous treatment to the flanks with hyaluronic acid fillers or semi-permanent filler in the past 12 months
• Use of any permanent filler materials or silicone in the flanks
• Subjects planning a cosmetic procedure in the treatment area during the study or with prior cosmetic procedures (i.e., surgery) in the treatment area or visible scars that may affect the evaluation
• Subjects with volume deficit due to trauma, abnormalities in adipose tissue related to immune-mediated diseases such as generalized lipodystrophy (e.g., juvenile dermatomyositis), partial lipodystrophy (e.g., Barraquer-Simons syndrome), inherited disease, or HIV-related disease
• Infection or dermatoses at the injection site
• Evidence of recent alcohol or drug abuse
• Medical and/or psychiatric problems that are severe enough to interfere with the study results
• Known bleeding disorder or receiving medication that will likely increase the risk of bleeding after injection
• Having hair that would interfere with evaluation and treatment of the flank area
• Being prone to develop hypertrophic scarring
• Having a history of anaphylaxis or allergy to lidocaine (or any amide-based anesthetics), hyaluronic acid products, or Streptococcal protein
• Having porphyria
• Having an active inflammation, infection, cancerous or precancerous lesion, or unhealed wound in the flank area
• Having a condition or being in a situation that, in the investigator's opinion, may put the subject at significant risk, may confound the study results, or may interfere significantly with the subject's participation in the study

• Minimum Eligible Age: 21 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Espad Pharmed

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Razi hospital

Tehran, , Iran

Countries

Iran

Provided Documents

Document Type: Study Protocol

View Document

Document Type: Statistical Analysis Plan

View Document

Other Identifiers

EMB.ESP.KB.IV.02

Identifier Type: -

Identifier Source: org_study_id