NCT03891953Active, not recruitingPhase 1
A Phase I/Ib, Open-label, Multi-center, Study of DKY709 as a Single Agent and in Combination With PDR001 in Patients With Advanced Solid Tumors
Conditions
Interventions
Drugs
Trial Snapshot
- Phase
- Phase 1
- Status
- Active, not recruiting
- Sponsor
- Novartis Pharmaceuticals
- Enrollment
- 98
- Locations
- 4
- Primary Endpoint
- incidence of Dose Limiting Toxicities (DLTs)
Study Overview
Brief Summary
This is a phase I/Ib, open label study. The escalation portion will characterize the safety and tolerability of DKY709 and DKY709 in combination with PDR001 in subjects with NSCLC or melanoma who have received prior anti-PD-1/PD-L1 therapy, or subjects with NPC. After the determination of the MTD/RD for a particular treatment arm, dose expansion will further assess safety, tolerability, PK/PD, and anti-tumor activity of each regimen at the MTD/RD.
Study Design
- Study Type
- Interventional
- Allocation
- Non Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to 100 Years (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Signed informed consent must be obtained prior to participation in the study.
- •Patients must be ≥18 years of age at the time of informed consent form (ICF) signature.
- •Patients with advanced/metastatic cancer who have progressed despite having received standard therapy in the metastatic setting or are intolerant to standard therapy, and for whom no effective standard therapy is available
- •In expansion: patient with measurable disease as determined by RECIST version 1.1,
- •Dose escalation, patients must fit into one of the following groups:
- •NSCLC, previously treated with an anti-PD-1/PD-L1 therapy
- •Cutaneous Melanoma, previously treated with an anti-PD-1/PD-L1 therapy
- •Dose expansion part, patients must fit into one of the following groups:
- •NSCLC with historic documentation of PD-L1 ≥ 1%. Patients must have progressive disease after having experienced at least 4 months of investigator-assessed disease stability or response on prior anti-PD-L1-containing therapy
- •Cutaneous Melanoma, previously treated with anit-PD-1/PD-L1 therapy. Patients should have documented progression following anti-PD-1/PD-L1 therapy.
- •NPC, naive to anti-PD-1/PD-L1 therapy
- •mssCRC, naive to anti-PD-1/PD-L1 therapy
- •TNBC, naive to anti-PD-1/PD-L1 therapy
- •ECOG Performance Status ≤ 1
- •Patients must have a site of disease amenable to core needle biopsy, and be a candidate for tumor biopsy according to the treating institution's guidelines. Patients must be willing to undergo a new tumor biopsy at baseline, and during therapy on the study. Exceptions may be considered after documented discussion with Novartis.
Exclusion Criteria
- •Presence of symptomatic central nervous system (CNS) metastases, or CNS metastases that require local CNS-directed therapy (such as radiotherapy or surgery), or increasing doses of corticosteroids within 2 weeks prior to study entry. Patients with treated brain metastases should be neurologically stable for at least 4 weeks prior to study entry and off steroids for at least 2 weeks before administration of any study treatment.
- •History of severe hypersensitivity reactions to any ingredient of study drug(s) or other mAbs and/or their excipients.
- •Patient with out of range laboratory values defined as:
- •Creatinine clearance (calculated using Cockcroft-Gault formula, or measured) < 40 mL/min
- •Total bilirubin > 1.5 x ULN, except for patients with Gilbert's syndrome who are excluded if total bilirubin > 3.0 x ULN or direct bilirubin > 1.5 x ULN
- •Alanine aminotransferase (ALT) > 3 x ULN, except for patients that have tumor involvement of the liver, who are excluded if ALT > 5 x ULN
- •Aspartate aminotransferase (AST) > 3 x ULN, except for patients that have tumor involvement of the liver, who are excluded if AST > 5 x ULN
- •Absolute neutrophil count (ANC) < 1.0 x 109/L
- •Platelet count < 75 x 109/L (growth factor or transfusion support may not be used to meet entry criterion)
- •Hemoglobin (Hgb) < 8 g/dL (growth factor or transfusion support may not be used to meet entry criterion)
- •Magnesium, calcium or phosphate abnormality CTCAE > grade 1
- •Potassium abnormality CTCAE ≥ grade 1; supplementation to meet eligibility criteria is acceptable
- •Clinically significant cardiac disease or impaired cardiac function, including any of the following:
- •Clinically significant and/or uncontrolled heart disease such as congestive heart failure requiring treatment (NYHA grade ≥ 2), uncontrolled hypertension or clinically significant arrhythmia
- •On screening: QTcF > 450 msec (male), or > 460 msec (female)
- •QTc not assessable
- •Congenital long QT syndrome
- •History of familial long QT syndrome or known family history of as Torsades de Pointes
- •Acute myocardial infarction or unstable angina pectoris < 3 months prior to study entry
Arms & Interventions
DKY709
Experimental
DKY709 monotherapy
Intervention: DKY709 (Drug)
DKY709 + PDR001
Experimental
Combination therapy with DKY709 and PDR001
Intervention: DKY709 (Drug)
DKY709 + PDR001
Experimental
Combination therapy with DKY709 and PDR001
Intervention: PDR001 (Drug)
Outcomes
Primary Outcomes
incidence of Dose Limiting Toxicities (DLTs)
Time Frame: 1 Month
The incidence of DLTs during the first cycle of treatment with single agent DKY709 or the combination of DKY709 with PDR001.
Safety of DKY709 single agent treatment or DKY709 in combination with PDR001.
Time Frame: 24 months
Incidence and severity of AEs and SAEs
Tolerability of DKY709 single agent treatment or DKY709 in combination with PDR001.
Time Frame: 24 months
Incidence and severity of AEs and SAEs
Secondary Outcomes
- Tmax of DKY709 and PDR001(24 months)
- Half-life of DKY709 and PDR001(24 months)
- AUC of DKY709 and PDR001(24 months)
- Progression Free Survival (PFS)(24 months)
- Cmax of DKY709 and PDR001(24 months)
- Best Overall Response (BOR)(24 months)
- Duration of Response (DOR)(24 months)
- Time to Progression (TTP)(24 months)
Investigators
Novartis Pharma Arzneimittel GmbH
Scientific
Novartis Pharma AG
Study Sites (4)
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