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A Single-center, Double-blind, Placebo-controlled, Dose-escalation Phase I Clinical Study to Evaluate the Safety and Tolerability of BPR-30221616 Injection in Healthy Subjects

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Trial Profile

A Single-center, Double-blind, Placebo-controlled, Dose-escalation Phase I Clinical Study to Evaluate the Safety and Tolerability of BPR-30221616 Injection in Healthy Subjects

Status: Recruiting
Phase of Trial: Phase I

Latest Information Update: 20 Feb 2025

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At a glance

  • Drugs BPR 30221616 (Primary) ; Sodium chloride
  • Indications Transthyretin-related hereditary amyloidosis
  • Focus Adverse reactions
  • Sponsors Chengdu Brilliant Pharmaceutical

Most Recent Events

  • 12 Feb 2025 Status changed from not yet recruiting to recruiting.
  • 10 Jan 2025 New trial record

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