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Clinical Trial Summary

This is a Phase 1, randomized, double-blind, placebo-controlled multiple-ascending dose (MAD) study designed to evaluate the safety, tolerability, and pharmacokinetics (PK) of PHP-303 in otherwise healthy overweight or obese volunteer subjects. Within each ascending dose cohort, subjects will be randomized in a 4:1 ratio to receive PHP-303 or placebo. The primary objective is to establish the safety and tolerability and maximum tolerated dose (MTD) of orally-administered PHP-303.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Otherwise Healthy Overweight or Obese
  • Overweight

NCT number NCT03775278
Study type Interventional
Source pH Pharma
Contact
Status Completed
Phase Phase 1
Start date December 17, 2018
Completion date April 7, 2020