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A Randomized, Single-blind, Placebo-Controlled Phase I Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single Ascending Doses of Subcutaneously Administered RBD4059 in Healthy Subjects

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Trial Profile

A Randomized, Single-blind, Placebo-Controlled Phase I Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single Ascending Doses of Subcutaneously Administered RBD4059 in Healthy Subjects

Status: Active, no longer recruiting
Phase of Trial: Phase I

Latest Information Update: 06 Dec 2024

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At a glance

  • Drugs RBD-4059 (Primary)
  • Indications Thromboembolism
  • Focus Adverse reactions; First in man
  • Sponsors Suzhou Ribo Life Science

    • Most Recent Events

    • 03 Dec 2024 Planned End Date changed from 1 Dec 2024 to 1 Dec 2025.
    • 03 Dec 2024 Planned primary completion date changed from 1 Oct 2024 to 1 Dec 2025.
    • 03 Dec 2024 Status changed from recruiting to active, no longer recruiting.

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