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A Phase 1, Randomized, Double-Blind, Single-Dose, Dose Escalation Study to Determine the Safety, Tolerability, and Pharmacokinetics of CD101 Injection in Healthy Subjects

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Trial Profile

A Phase 1, Randomized, Double-Blind, Single-Dose, Dose Escalation Study to Determine the Safety, Tolerability, and Pharmacokinetics of CD101 Injection in Healthy Subjects

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 20 Aug 2021

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At a glance

  • Drugs Rezafungin (Primary)
  • Indications Aspergillosis; Candidaemia; Candidiasis
  • Focus Adverse reactions
  • Sponsors Cidara Therapeutics

    • Most Recent Events

    • 16 Aug 2021 Results of a PopPK model analysis characterizing disposition of rezafungin in plasma following IV administration using data from three clinical studies: NCT02516904, NCT02551549 and NCT02734862 published in the Antimicrobial Agents and Chemotherapy
    • 07 Oct 2018 Results assessing Pharmacokinetic-Pharmacodynamic (PK-PD) Target Attainment Analyses for dose scelection of Rezafungin in the treatment of Candid, presented at the IDWeek 2018.
    • 19 Mar 2018 Results assessing population pharmacokinetic analyses for rezafungin efficacy using pooled data from two phase 1 studies, were published in the Antimicrobial Agents and Chemotherapy.

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