Study of Safety and Efficacy of DKY709 Alone or in Combination With PDR001 in Patients With Advanced Solid Tumors.
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.
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These are broad labels—not an eligibility decision.
Checked against the public recordLast updated Oct 19, 2026 · Source: ClinicalTrials.gov
The study is underway but is not accepting new participants.
Interventional
Locations may change over time.
Study sponsor
What this study is about
- Purpose
- Treatment
- Study type
- Interventional
- Phase
- Phase 1
- Sponsor
- Novartis Pharmaceuticals
- Interventions being studied
- Drug: DKY709; Drug: PDR001
How this study is categorized
These labels come from structured fields and exact terms in the public record.
Who may be able to participate
The sponsor separates these requirements into two groups. You do not need to interpret them alone—use them to guide a conversation with the study team.
- 1. Signed informed consent must be obtained prior to participation in the study. 2. Patients must be ≥18 years of age at the time of informed consent form (ICF) signature. 3. 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 4. In expansion: patient with measurable disease as determined by RECIST version 1.1, 5. 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
- NPC 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 6. ECOG Performance Status ≤ 1 7. 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.
- 1. 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. 2. History of severe hypersensitivity reactions to any ingredient of study drug(s) or other mAbs and/or their excipients. 3. 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 4. 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
Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.
U.S. locations
- Massachusetts General HospitalBoston, Massachusetts
- Dana Farber Cancer InstituteBoston, Massachusetts
- Tennessee OncologyNashville, Tennessee
- Novartis Investigative SiteDresden, Saxony
- Novartis Investigative SiteEssen
- Novartis Investigative SiteHong Kong
- Novartis Investigative SiteChuo Ku, Tokyo
- Novartis Investigative SiteBarcelona
- Novartis Investigative SiteTaipei
Source and freshness
Processed from ClinicalTrials.gov. Last public update: Oct 19, 2026. Always confirm current availability with the study team.