The study purpose is to evaluate the safety, tolerability, and preliminary efficacy of the addition of INC280, trametinib, ribociclib, gefitinib, or LXH254 to EGF816 in adult patients with advanced Epidermal growth factor receptor- mutant (EGFR-mutant) non-small cell lung cancer (NSCLC).
This is a Phase Ib, open label, non-randomized dose escalation study of EGF816 in combination with ribociclib, trametinib, or LXH254, followed by dose expansion of EGF816 in combination with ribociclib, trametinib, LXH254, INC280, or gefitinib in adult patients with advanced EGFR-mutant NSCLC. During the dose escalation part, patients were assigned to the addition of trametinib, ribociclib, or LXH254 to EGF816. Following determination of the recommended dose for the combination of EGF816 + trametinib, EGF816 + ribociclib, and EGF816 + LXH254, patients could be enrolled to the dose expansion arms of each of these combinations. Patients could also be assigned to EGF816 + INC280. The planned arm EGF816 + gefitinib in dose expansion was not opened for enrollment.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
105
Novartis Investigative Site
Toronto, Ontario, Canada
Novartis Investigative Site
Cologne, North Rhine-Westphalia, Germany
Novartis Investigative Site
Essen, Germany
Number of patients with adverse events and serious adverse events
Assess safety and tolerability including incidence of dose limiting toxicities, adverse events, and serious adverse events.
Time frame: Every day until study end, approximately 4 years
Number of participants with DLTs in the first cycle of combination (Dose escalation only)
A Dose-Limiting Toxicity (DLT) is defined as an adverse event or abnormal laboratory value of Common Terminology Criteria for Adverse Events (CTCAE) grade ≥ 3 assessed as unrelated to disease, disease progression, inter-current illness or concomitant medications that occurs within the first 28 days of combination treatment during the dose escalation part of the study. Other clinically significant toxicities may be considered to be DLTs, even if not CTCAE grade 3 or higher.
Time frame: 28 days
Number of participants with dose interruptions and reductions
Assessment of tolerability. For patients who do not tolerate the protocol-specified dosing schedule, dose adjustments may be permitted in order to allow patients to continue the study treatment.
Time frame: From first dose until study ends, approximately 4 years
Dose intensity of study drugs
Dose intensity is computed as the ratio of actual cumulative dose received to actual duration of exposure.
Time frame: From first dose until study ends, approximately 4 years
ORR2
Modified objective response rate (ORR2) per RECIST v1.1 (taking as baseline the most recent assessment prior to initiating combination)
Time frame: Every 8-12 weeks until study ends, approximately 4 years
ORR
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Study Drug
Study Drug
Study Drug
Novartis Investigative Site
Hong Kong, Hong Kong
Novartis Investigative Site
Ancona, AN, Italy
Novartis Investigative Site
Milan, MI, Italy
Novartis Investigative Site
Rozzano, MI, Italy
Novartis Investigative Site
Singapore, Singapore
Novartis Investigative Site
Singapore, Singapore
Novartis Investigative Site
Tainan, Taiwan
...and 1 more locations
Overall response rate (ORR) per RECIST v1.1
Time frame: Every 8-12 weeks until study ends, approximately 4 years
PFS
Time from the date of first dose of study treatment to the date of first documented disease progression (per RECIST v1.1) or death due to any cause
Time frame: Every 8-12 weeks until study ends, approximately 4 years
DCR
Proportion of patients with best overall response of CR, PR, or SD
Time frame: Every 8-12 weeks until study ends, approximately 4 years
DOR
Time from first documented response (PR or CR) to the date of first documented disease progression or death due to any cause
Time frame: Every 8-12 weeks until study ends, approximately 4 years
Time to response
Time to response is the time between start of treatment until first documented response per RECIST v1.1.
Time frame: Every 8-12 weeks until study ends, approximately 4 years
Area under the plasma concentration-time curve (AUC) of study drugs
Pharmacokinetic (PK) parameters calculated based on the plasma concentrations versus time profiles by using non-compartmental methods.
Time frame: From pre-dose up to 8 hours post-dose on Day 15 of Cycle 1. One cycle=28 days.
Maximum observed plasma concentration (Cmax) of study drugs
PK parameters calculated based on the plasma concentrations versus time profiles by using non-compartmental methods.
Time frame: From pre-dose up to 8 hours post-dose on Day 15 of Cycle 1. One cycle=28 days.