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Safety, Tolerability, and Pharmacokinetics of HRS-3802 Monotherapy in Patients With Malignant Solid Tumors: a Single-arm, Open, Multicenter Phase I Study

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Trial Profile

Safety, Tolerability, and Pharmacokinetics of HRS-3802 Monotherapy in Patients With Malignant Solid Tumors: a Single-arm, Open, Multicenter Phase I Study

Status: Recruiting
Phase of Trial: Phase I

Latest Information Update: 20 Feb 2025

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At a glance

  • Drugs HRS 3802 (Primary)
  • Indications Solid tumours
  • Focus Adverse reactions
  • Sponsors Shandong Suncadia Medicine
  • Most Recent Events

    • 13 Feb 2025 Status changed from not yet recruiting to recruiting.
    • 04 Feb 2025 According to a Jiangsu Hengrui Medicine Co. media release, the clinical trial application for HRS-3802 sustained-release tablets, which was accepted on September 18, 2018, has been approved by the Food and Drug Administration ("FDA") of China and the "Notice of Approval for Clinical Trial of Drugs" for HRS-3802 sustained-release tablets, has been issued.
    • 20 Jan 2025 New trial record

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