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Study identifier: NCT07014163 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Evaluating the Efficacy and Safety of Embella (Deoxycholic Acid, Produced by Espad Pharmed Co.) Injection in the Management of Superficial Lipomas

Condition: Lipoma  ·  Sponsor: Espad Pharmed

PhaseNA
Planned participants10
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersNo

About this study

Lipoma is a relatively common, slow-growing mesenchymal neoplasm originating from adipose tissue. Patients seek treatment for lipomas for various reasons, such as concerns about their growth and spread, aesthetic issues, or worries about the compressive effects of the lipoma. Lipomas are typically removed surgically through excision, which can have complications including bleeding, infection, scarring, and recurrence. Other mentioned treatment methods include liposuction, laser, and medicinal approaches. Purified synthetic deoxycholic acid has been introduced as the first pharmacological intervention approved by the FDA for the reduction of submental fat. Deoxycholic acid is a type of bile acid that, due to its ability to cause non-selective cell lysis and disruption of adipocyte membranes (adipocytolysis), leads to emulsification of fat in the intestine. This is an interventional (pre-post), single-arm, and open-label study to evaluate the efficacy and safety of Embella (Deoxycholic acid, produced by Espad Pharmed Co.) for the management of superficial lipomas.

This description comes directly from the study's public registry record.

Talk to the study team

Hamidreza kafi, PHD  ·  +982143473000  ·  Kafi.H@orchidpharmed.com

Kamran Balighi, Prof. Derm  ·  Kamran.Balighi@yahoo.com

Always discuss trial participation with your own doctor first.

Locations (2)

Orchid Pharmed, Medical DepartmentTehran, Tehran Province, IranCompleted
Razi hospitalTehran, IranRecruiting

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Source record: clinicaltrials.gov/study/NCT07014163