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Clinical Trials/NCT03301896
NCT03301896
Terminated
Phase 1

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

Novartis Pharmaceuticals3 sites in 2 countries45 target enrollmentJanuary 31, 2018
ConditionsSolid Tumors
InterventionsLHC165PDR001
DrugsLHC165

Overview

Phase
Phase 1
Intervention
LHC165
Conditions
Solid Tumors
Sponsor
Novartis Pharmaceuticals
Enrollment
45
Locations
3
Primary Endpoint
Escalation and Expansion: Incidence and severity of Adverse Events (AEs) and Serious Adverse Events (SAEs), including changes in laboratory parameters, vital signs, electrocardiograms (ECGs)
Status
Terminated
Last Updated
last year

Overview

Brief Summary

The purpose of this trial was to explore the clinical utility of two investigational agents in patients with advanced cancer.

This was a multi-center, open-label Phase I/Ib study. The primary objectives of the trial were:

  • To characterize the safety and tolerability of intratumoral LHC165 in patients with solid tumors as a single agent and in combination with PDR001
  • To determine and evaluate the maximum tolerated dose (MTD)/recommended dose (RD) for LHC165 as a single agent and in combination with PDR001

Detailed Description

This was a multi-center, open-label Phase I/Ib study. The study consisted of four dose escalation parts and two dose expansion parts testing LHC165 as a single agent or LHC165 in combination with PDR001. The dose escalation parts estimated the Maximum Tolerated Dose (MTD) and/or Recommended Dose for Expansion (RDE) and were planned to test two different dosing schedules for LHC165 single agent (Group A and B) and LHC165 in combination with PDR001 (Group C and D). The dose expansion parts of the study were planned to use the MTD/RDE for each the LHC165 single agent (Group E) and LHC165 in combination with PDR001 (Group F), determined in the respective dose escalation parts to assess the activity, safety and tolerability of LHC165 as a single agent or LHC165 in combination with PDR001 in patients with specific types of solid tumors. The study was terminated due to business reasons. Groups B, D and E were not opened for enrollment.

Registry
clinicaltrials.gov
Start Date
January 31, 2018
End Date
June 30, 2022
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Written informed consent must be obtained prior to any procedures unless considered standard of care.
  • Adult men and women (≥ 18 years of age) with histologically confirmed diagnosis of metastatic and/or advanced solid tumors not amenable to curative treatment by surgery.
  • Patients must be willing and able to comply with the protocol for the duration of the study including undergoing treatment and scheduled visits and examinations including follow up.
  • Dose escalation: Patients with accessible tumors and with measurable disease as determined by RECIST 1.1 and have progressed despite standard treatment or are intolerant of standard treatment, or for whom no standard treatment exists.
  • Dose expansion: Patients with advanced/metastatic solid tumors: HNSCC, melanoma, accessible tumors and visceral tumors (LHC165 combination with PDR001 only). Patients must have measurable disease as determined by RECIST 1.1 and have progressed despite standard treatment or are intolerant to standard treatment, or for whom no standard treatment exists• Patients must have at least two sites of disease amenable to biopsy.
  • Patient has an Eastern Cooperative Oncology Group (ECOG) performance status 0-2.

Exclusion Criteria

  • Presence of symptomatic or uncontrolled central nervous system (CNS) metastases requiring local CNS-directed treatment.
  • Patients diagnosed with hematological malignancies.
  • Patients with prior stem cell transplants.
  • Patients previously treated with TLR-7/8 agonist treatment.
  • History of primary immunodeficiency
  • Patients who discontinued prior anti-PD-1/PD-L1 therapy due to an anti-PD-1/PD-L1-related toxicity.
  • Malignant disease, other than that being treated in this study

Arms & Interventions

LHC165 single agent

LHC165 intratumoral injection given alone

Intervention: LHC165

LHC165 in combination with PDR001

LHC165 intratumoral injection given with PDR001 infusion

Intervention: LHC165

LHC165 in combination with PDR001

LHC165 intratumoral injection given with PDR001 infusion

Intervention: PDR001

Outcomes

Primary Outcomes

Escalation and Expansion: Incidence and severity of Adverse Events (AEs) and Serious Adverse Events (SAEs), including changes in laboratory parameters, vital signs, electrocardiograms (ECGs)

Time Frame: 24 months

Escalation: Incidence of Dose-limiting Toxicities (DLTs) in Cycle 1

Time Frame: day 28

Dose Limiting Toxicity Evaluation Period

Secondary Outcomes

  • Duration of Response (DOR) per RECIST 1.1 and iRECIST(24 months)
  • Best Overall Response (BOR) per RECIST 1.1 and iRECIST(24 months)
  • Serum concentration profiles of PDR001 in combination with LHC165 and derived PK parameters: Tmax(24 months)
  • Disease Control Rate (DCR) per RECIST 1.1 and iRECIST(24 months)
  • Serum concentration profiles of LHC165 as a single agent: Cmax(24 months)
  • Serum concentration profiles of LHC165 in combination with PDR001 and derived PK parameters: Cmax(24 months)
  • Serum concentration profiles of LHC165 in combination with PDR001 and derived PK parameters: AUC(24 months)
  • Progression-Free Survival (PFS) per RECIST 1.1 and iRECIST(24 months)
  • Objective Response Rate (ORR) per RECIST 1.1 and iRECIST(24 months)
  • Serum concentration profiles of PDR001 in combination with LHC165 and derived PK parameters: Cmax(24 months)
  • Serum concentration profiles of LHC165 as a single agent: AUC(24 months)
  • Serum concentration profiles of PDR001 in combination with LHC165 and derived PK parameters: AUC(24 months)
  • Presence and titer of anti-PDR001 antibodies(24 months)
  • Change from baseline in tumor infiltrating lymphocytes in injected and distal tumor specimens(24 months)
  • Serum concentration profiles of LHC165 as a single agent: Tmax(24 months)
  • Serum concentration profiles of LHC165 in combination with PDR001 and derived PK parameters: Tmax(24 months)

Study Sites (3)

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