RecruitingPhase 4NCT05919797

Weight Loss Study: Genetics and Response to Naltrexone/Bupropion

Studying Genetic obesity

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Key facts

Sponsor
Columbia University
Principal Investigator
Judith Korner, MD,PhD
Columbia University
Intervention
Naltrexone-Bupropion Combination(drug)
Enrollment
120 target
Eligibility
18-65 years · All sexes
Timeline
20232027

Study locations (1)

Collaborators

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT05919797 on ClinicalTrials.gov

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