Obesity

  • STATUS
    Recruiting
  • sponsor
    VIVUS LLC
Updated on 18 April 2022
diabetes
hypertension
type 2 diabetes mellitus
dyslipidemia

Summary

A Multicenter, Randomized, Double-Blind Study to Compare the Effectsof VI-0521, Phentermine, and Placebo on Ambulatory Blood Pressure inOverweight or Obese Subjects

Description

  • Condition: Obesity
  • Clinical Trial Identifier: N/A
  • Sponsor: VIVUS LLC 
Looking for participants within a 50 mile radius of the study site.

Details
Condition Obesity
Clinical Study IdentifierTX290691
SponsorVIVUS LLC
Last Modified on18 April 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

Overweight or obese adult males and females 18-75 years of age with a BMI ≥ 27 kg/m2
Medical diagnosis of at least 1 weight-related comorbidity (i.e., hypertension, dyslipidemia, type 2 diabetes mellitus or prediabetes, or obstructive sleep apnea)

Exclusion Criteria

Known allergy or hypersensitivity to phentermine or topiramate, any prior use of a combination of phentermine and topiramate for weight loss or use of phentermine or topiramate for any indication within the past 3 months
Obesity of a known genetic or endocrine origin
Previous bariatric surgery or other non-surgical weight loss procedure
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What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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