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A Phase I, Open-Label, Multi-Center Dose Escalation Study to Evaluate Safety, Pharmacokinetics and Preliminary Efficacy of HL-085 in Patients With Advanced Solid Tumors

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Trial Profile

A Phase I, Open-Label, Multi-Center Dose Escalation Study to Evaluate Safety, Pharmacokinetics and Preliminary Efficacy of HL-085 in Patients With Advanced Solid Tumors

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 16 Feb 2023

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At a glance

  • Drugs Tunlametinib (Primary)
  • Indications Solid tumours
  • Focus Adverse reactions; Pharmacokinetics
  • Sponsors Kechow Pharma

    • Most Recent Events

    • 10 Feb 2023 Status changed from recruiting to completed.
    • 11 Feb 2021 Status changed from not yet recruiting to recruiting.
    • 30 Dec 2020 New trial record

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