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A single dose, randomised, 2-period, 2-sequence, crossover, comparative bioavailability study between 4 x 60 mg R107 tablets administered orally and 0.5mg/kg ketamine IV infusion over 40 minutes in healthy male and female participants under fasting conditions.

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Trial Profile

A single dose, randomised, 2-period, 2-sequence, crossover, comparative bioavailability study between 4 x 60 mg R107 tablets administered orally and 0.5mg/kg ketamine IV infusion over 40 minutes in healthy male and female participants under fasting conditions.

Status: Not yet recruiting
Phase of Trial: Phase I

Latest Information Update: 27 Oct 2021

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At a glance

  • Drugs Ketamine (Primary) ; Ketamine (Primary)
  • Indications Major depressive disorder
  • Focus Pharmacokinetics

Most Recent Events

  • 26 Oct 2021 Planned initiation date changed from 18 Jul 2018 to 1 Mar 2022.
  • 13 Jul 2018 New trial record

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