Study of Immunotherapy (Sasanlimab) in Combination With Targeted Therapies in People With Advanced Non-small Cell Lung Cancer (NSCLC) (Landscape 1011 Study)
Phase 1b/Phase 2 Umbrella Study; open-label, multi-center, parallel group study. Sasanlimab (a PD-1 antagonist monoclonal antibody) will be combined with a different targeted therapy in each sub-study. Phase1b of each sub-study will evaluate the safety of the combination and select the dose for the Phase 2 portion. Phase 2 of each sub-study will evaluate the anti-tumor activity of the combination. Sub-Study A is active, not recruiting, ongoing participants are still receiving treatment in Phase 1, Phase 2 will not be initiated. Sub-study B is complete. All participants have discontinued treatment and any additional follow up required by protocol.
Checked against the public recordLast updated Jan 9, 2026 · Source: ClinicalTrials.gov
What this study is about
- Purpose
- Treatment
- Study type
- Interventional
- Phase
- Phase 1 / Phase 2
- Sponsor
- Pfizer
- Interventions being studied
- Drug: Sasanlimab Prefilled syringe; Drug: Encorafenib; Drug: Binimetinib; Drug: Sasanlimab; Drug: Axitinib; Drug: SEA-TGT
How this study is categorized
These labels come from structured fields and exact terms in the public record.
Who may be able to participate
Inclusion Criteria Umbrella Phase 1b \& 2: * Histologically or cytologically confirmed locally advanced/metastatic (Stage IIIB-IV) NSCLC. * At least one measurable lesion per RECIST v1.1 at Screening. * ECOG Performance Status 0 or 1. * Resolved acute effects of any prior therapy to baseline severity or CTCAE Grade ≤1. * Adequate hepatic, renal, and bone marrow function. Additional Inclusion Criteria for Sub-Study A Phase 1b \&2: -BRAFV600E mutation in tumor tissue or plasma as determined by a local laboratory PCR or NGS assay and documented in a local pathology report. Additional Inclusion Criteria for Sub-Study A Phase 1b only: -Any line of therapy for locally advanced/metastatic NSCLC. Additional Inclusion Criteria for Sub-Study A Phase 2 only: -Previously untreated for locally advanced/metastatic NSCLC Additional Inclusion Criteria for Sub-Study B Phase 1b only:: -Any line of therapy for locally advanced/metastatic NSCLC. Additional Inclusion Criteria for Sub-Study B Phase 2 only: * Previously untreated for locally advanced/metastatic NSCLC (Arms B1 \& B2), or * One or 2 prior lines of therapy for advanced/metastatic NSCLC (Arm B3), including immune checkpoint inhibitor treatment + chemotherapy, and have progressed during or after that therapy. * PD-L1 TPS ≥1% Exclusion Criteria Umbrella Phase 1b \&2: * Active or prior autoimmune disease that might deteriorate when receiving an immunostimulatory agent. * Active non-infectious pneumonitis, pulmonary fibrosis, or known history of immune-mediated pneumonitis. * Active infection requiring systemic therapy. * Clinically significant cardiovascular disease. * Other malignancy within 2 years of first dose, with exceptions. * Symptomatic brain metastasis, with exceptions. Additional Exclusion Criteria for Sub-Study A Phase 1b\&2: * EGFR mutation, ALK fusion oncogene, or ROS1 rearrangement. * Prior treatment with any BRAF inhibitor or MEK inhibitor. Additional Exclusion Criteria for Sub-Study A Phase 2 only: -Prior therapy with anti-PD-1, anti-PD-L1, or anti-PD-L2 agents. Additional Exclusion Criteria for Sub-Study B Phase 1b\&2: -Documentation of any tumor-driving molecular alteration (eg, BRAF, EGFR, ALK) Additional Exclusion Criteria for Sub-Study B Phase 2 only: * Prior therapy with anti-PD-1, anti-PD-L1, or anti-PD-L2 agents.(Arms B1 \& B2) * Confirmed progressive disease on 1st or 2nd imaging tumor assessment after initiation of therapy for advanced/metastatic NSCLC.
Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.
U.S. locations
- City of Hope Investigational Drug Services (IDS)Duarte, California
- City of HopeDuarte, California
- UCSD Medical Center - EncinitasEncinitas, California
- California Cancer Associates for Research and Excellence, Inc (cCARE)Fresno, California
- The Oncology Institute of Hope and InnovationGlendale, California
- Koman Family Outpatient PavilionLa Jolla, California
- Sulpizio Cardiovascular Center at UC San Diego HealthLa Jolla, California
- UC San Diego Medical Center - La Jolla (Jacobs Medical Center / Thornton Pavilion)La Jolla, California
- UC San Diego Moores Cancer Center - Investigational Drug ServicesLa Jolla, California
- UCSD Perlman Medical OfficesLa Jolla, California
- UC San Diego Moores Cancer CenterLa Jolla, California
- The Oncology Institute of Hope and InnovationLong Beach, California
Source and freshness
Processed from ClinicalTrials.gov. Last public update: Jan 9, 2026. Always confirm current availability with the study team.