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Adiposity

2
Pipeline Programs
4
Companies
3
Clinical Trials
0
Approved Products

Pipeline by Development Stage

Preclinical
Phase 1
Phase 1/2
Phase 2
Phase 2/3
Phase 3
On Market
0
0
0
0
0
0
2
Early DiscoveryClinical DevelopmentMarket

Competitive Landscape

4 companies ranked by most advanced pipeline stage

Fitzpatrick Company
Fitzpatrick CompanyON - Waterloo
1 program
1
Injectable sodium deoxycholatePhase 4
AbbVie
AbbVieNORTH CHICAGO, IL
1 program
1
Injectable sodium deoxycholatePhase 41 trial
Active Trials
NCT03361176Completed30Est. Dec 2018
Erbe
ErbeGermany - Tübingen
1 program
Hybrid Argonplasma coagulationN/A1 trial
Active Trials
NCT05574777Active Not Recruiting13Est. Mar 2026
Human BioSciences
Human BioSciencesWV - Martinsburg
1 program
Maternal Lipids and Offspring Adiposity at 5-7 YearsN/A1 trial
Active Trials
NCT03317522Completed1,224Est. Mar 2012

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
AbbVieInjectable sodium deoxycholate
ErbeHybrid Argonplasma coagulation
Human BioSciencesMaternal Lipids and Offspring Adiposity at 5-7 Years

Clinical Trials (3)

Total enrollment: 1,267 patients across 3 trials

NCT03361176AbbVieInjectable sodium deoxycholate

Kybella With Triamcinolone

Start: Mar 2018Est. completion: Dec 201830 patients
Phase 4Completed
NCT05574777ErbeHybrid Argonplasma coagulation

Endoscopic Gastric Mucosal Ablation (GMA) of Class III Obesity

Start: Apr 2023Est. completion: Mar 202613 patients
N/AActive Not Recruiting
NCT03317522Human BioSciencesMaternal Lipids and Offspring Adiposity at 5-7 Years

Maternal Lipids and Offspring Adiposity at 5-7 Years

Start: Jan 2001Est. completion: Mar 20121,224 patients
N/ACompleted

Phase Legend

PreclinicalLab & animal studies
Phase 1Safety & dosing
Phase 2Efficacy testing
Phase 3Large-scale trials
On MarketApproved & available

Key Insights

4 companies competing in this space

The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.