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A Phase 1 (First in Human) Randomized, Double-blind, Placebo-controlled SAD, MAD Study With an Adaptive Dose Design to Evaluate the Safety, Tolerability, and Pharmacokinetics of REM0046127 in Healthy Subjects

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A Phase 1 (First in Human) Randomized, Double-blind, Placebo-controlled SAD, MAD Study With an Adaptive Dose Design to Evaluate the Safety, Tolerability, and Pharmacokinetics of REM0046127 in Healthy Subjects

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 24 May 2022

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At a glance

  • Drugs REM 0046127 (Primary)
  • Indications Alzheimer's disease
  • Focus Adverse reactions; First in man; Pharmacokinetics
  • Sponsors reMYND

    • Most Recent Events

    • 18 May 2022 Status changed from recruiting to completed.
    • 14 Oct 2021 Planned End Date changed from 30 Oct 2021 to 30 May 2022.
    • 14 Oct 2021 Planned primary completion date changed from 29 Sep 2021 to 29 Mar 2022.

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