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Phase I Study to Evaluate the Safety ,Tolerability, and Pharmacokinetics of HRS-4642 in Patients With Advanced Solid Tumors Harboring KRAS G12D Mutation

Trial Profile

Phase I Study to Evaluate the Safety ,Tolerability, and Pharmacokinetics of HRS-4642 in Patients With Advanced Solid Tumors Harboring KRAS G12D Mutation

Status: Recruiting
Phase of Trial: Phase I

Latest Information Update: 09 Nov 2023

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At a glance

  • Drugs HRS 4642 (Primary)
  • Indications Adenocarcinoma; Appendiceal cancer; Colorectal cancer; Lung cancer; Ovarian cancer; Pancreatic cancer; Solid tumours
  • Focus Adverse reactions; First in man
  • Sponsors Jiangsu Hengrui Medicine Co.
  • Most Recent Events

    • 09 Nov 2023 Last checked against ClinicalTrials.gov: US National Institutes of Health record.
    • 24 Oct 2023 Preliminary (n=18, At data cutoff on Aug 4, 2023) results of the dose escalation part assessing safety and efficacy of HRS-4642 in patients with advanced KRAS G12D mutant solid tumors, presented at the 48th European Society for Medical Oncology Congress.
    • 21 Oct 2022 Status changed from not yet recruiting to recruiting.

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