A Phase I/Ib, Open-label, Multi-center Dose-escalation and Dose-expansion Study of the Safety and Tolerability of Intra-tumorally Administered LHC165 Single Agent and in Combination With PDR001 in Patients With Advanced Malignancies

Trial Profile

A Phase I/Ib, Open-label, Multi-center Dose-escalation and Dose-expansion Study of the Safety and Tolerability of Intra-tumorally Administered LHC165 Single Agent and in Combination With PDR001 in Patients With Advanced Malignancies

Not yet recruiting
Phase of Trial: Phase I

Latest Information Update: 11 Nov 2017

At a glance

  • Drugs LHC-165 (Primary) ; PDR 001 (Primary)
  • Indications Solid tumours
  • Focus Adverse reactions
  • Sponsors Novartis Pharmaceuticals
  • Most Recent Events

    • 03 Nov 2017 Planned End Date changed from 16 Jan 2021 to 7 Feb 2021.
    • 03 Nov 2017 Planned primary completion date changed from 16 Jan 2021 to 7 Feb 2021.
    • 03 Nov 2017 Planned initiation date changed from 21 Nov 2017 to 13 Dec 2017.
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