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A Phase I , Single Arm, Dose Escalation Study to Evaluate Tolerability, Safety, Pharmacokinetics and Preliminary Efficacy of HL-085 Plus Docetaxel in Patients With KRAS Mutant NSCLC

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Trial Profile

A Phase I , Single Arm, Dose Escalation Study to Evaluate Tolerability, Safety, Pharmacokinetics and Preliminary Efficacy of HL-085 Plus Docetaxel in Patients With KRAS Mutant NSCLC

Status: Discontinued
Phase of Trial: Phase I

Latest Information Update: 13 Dec 2021

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At a glance

  • Drugs Docetaxel (Primary) ; Tunlametinib (Primary)
  • Indications Non-small cell lung cancer
  • Focus Adverse reactions
  • Sponsors Kechow Pharma

    • Most Recent Events

    • 29 Nov 2021 Status changed from not yet recruiting to discontinued.
    • 15 Dec 2020 Planned End Date changed from 1 Aug 2021 to 1 Dec 2022.
    • 15 Dec 2020 Planned primary completion date changed from 1 Aug 2020 to 1 Dec 2022.

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