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An Open Label, Adaptive Design Evaluation, Crossover Study of the Safety, Pharmacokinetics and Pharmacodynamics of Various RECCE327 Intravenous Dose and Infusion Rate

Trial Profile

An Open Label, Adaptive Design Evaluation, Crossover Study of the Safety, Pharmacokinetics and Pharmacodynamics of Various RECCE327 Intravenous Dose and Infusion Rate

Status: Recruiting
Phase of Trial: Phase I/II

Latest Information Update: 02 Jul 2024

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At a glance

  • Drugs RECCE 327 (Primary)
  • Indications Sepsis; Urinary tract infections
  • Focus Adverse reactions; Pharmacokinetics
  • Sponsors Recce Pharmaceuticals

Most Recent Events

  • 28 Jun 2024 Results from the trial at the highest dose, 4,000mg, of R327 published in the Recce Pharmaceuticals Media Release
  • 12 Jun 2024 According to a Recce Pharmaceuticals media release, an Independent Safety Committee will review and evaluate the comprehensive data from the 6-subject cohort, with preliminary results expected in the near weeks.
  • 12 Jun 2024 According to a Recce Pharmaceuticals media release, dosing of an additional cohort has been completed. Six additional participants intravenously dosed with RECCE 327 (R327) at 4,000mg over 20 minutes-highest dosage to date in this trial.

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