Non Small Cell Lung Cancer Clinical Trials in New York, New York
66 studies are recruiting for non small cell lung cancer in New York, New York right now. Each one is listed on ClinicalTrials.gov, the public registry the research teams themselves file with. TrialBoost is not a doctor, a research site, or a study sponsor: the research team decides who takes part.
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Studies now recruiting
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Clinical Study of Ivonescimab for First-line Treatment of Metastatic NSCLC Patients With High PD-L1
Clinical study of ivonescimab for first-line treatment of metastatic NSCLC patients with high PD-L1. Evaluating overall survival and progression free survival.
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- Clinical Study Site, New York, New York
- Locations
- 285 in total
- Run by
- Summit Therapeutics
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A Study of [225Ac]Ac-AKY-1189 in Patients With Solid Tumors
This is a first-in-human Phase 1b, 2-part, multicenter open-label clinical study to evaluate safety and efficacy of a Nectin-4 radiopharmaceutical ([225Ac]Ac-AKY-1189) in patients with locally advanced or metastatic solid tumors and to establish the maximum tolerated dose (MTD) or maximum administe…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Icahn School of Medicine at Mt. Sinai, New York, New York
- Locations
- 14 in total
- Run by
- Aktis Oncology, Inc.
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Beamion LUNG-3: Adjuvant Zongertinib vs Standard Treatment in People With Completely Resected Stage II-IIIB NSCLC Harboring Activating HER2 TKD Mutations
Beamion LUNG-3 study evaluates whether zongertinib, an oral HER2-targeted treatment, can improve outcomes compared with standard adjuvant treatment in adults with completely resected Stage II-IIIB non-small cell lung cancer (NSCLC) whose tumors have activating HER2 tyrosine kinase domain (TKD) muta…
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- Laura & Isaac Perlmutter Cancer Center at NYU Langone Health, New York, New York
- Locations
- 202 in total
- Run by
- Boehringer Ingelheim
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A Phase 2 Study of VS-7375 in Patients With KRAS G12D-Mutated Non-Small Cell Lung Cancer
This study will assess the safety and efficacy of VS-7375 alone and in combination with cetuximab in patients with metastatic KRAS G12D - mutated Non-Small Cell Lung Cancer
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- NYU, New York, New York
- Locations
- 13 in total
- Run by
- Verastem, Inc.
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Phase 1/2 Trial of S241656 in Selected RAS/MAPK Mutation- Positive Malignancies
BDTX-4933-101 is a first-in-human, open-label, Phase 1/2 dose escalation, dose optimization and expansion study designed to evaluate the safety and tolerability of S241656 as monotherapy and in combination with other anti-cancer therapies in participants with selected advanced malignancies. The stu…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- NYU Langone Medical Center - Perlmutter Cancer Center (NYU Cancer Institute), New York, New York
- Locations
- 49 in total
- Run by
- Institut de Recherches Internationales Servier
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A Study of BIO 300 and Thoracic Radiation Therapy in People With Non-Small Cell Lung Cancer and Interstitial Lung Disease
The purpose of this study to find out whether giving BIO 300 in combination with thoracic radiation therapy is effective in preventing pneumonitis in people with non-small cell lung cancer (NSCLC) and interstitial lung disease (ILD).
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- Memorial Sloan Kettering Cancer Center (All Protocol Activities), New York, New York
- Locations
- 7 in total
- Run by
- Memorial Sloan Kettering Cancer Center
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A Study of Tepotinib and Ivonescimab in People With Non-Small Cell Lung Cancer
The researchers are doing this study to find out whether the combination of tepotinib and ivonescimab is a safe and effective treatment for people with non-small cell lung cancer (NSCLC) that is positive for METex14 skipping. The researchers will test up to two different doses of tepotinib in combi…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Memorial Sloan Kettering Cancer Center (All Protocol Activities), New York, New York
- Locations
- 7 in total
- Run by
- Memorial Sloan Kettering Cancer Center
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The Evaluation of PC14586 in Patients With Advanced Solid Tumors Harboring a TP53 Y220C Mutation (PYNNACLE)
The Phase 2 monotherapy portion of this study is currently enrolling and will evaluate the efficacy and safety of PC14586 (INN rezatapopt) in participants with locally advanced or metastatic solid tumors harboring a TP53 Y220C mutation. The Phase 1 portion of the study will assess the safety, toler…
- Stage
- Phase 1
- Ages
- 12 and older
- Site
- Memorial Sloan Kettering, New York, New York
- Locations
- 77 in total
- Run by
- PMV Pharmaceuticals, Inc
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Using Urine Samples to Identify Lung Cancer
The researchers are doing this study to test the ability of an animal biosensor platform (ABP) to detect NSCLC. Participants in this study will either be diagnosed with NSCLC, suspected to have NSCLC, or have not been diagnosed or suspected to have NSCLC. The ABP test uses laboratory animals that a…
- Stage
- Not phased
- Ages
- 18 to 90
- Site
- Memorial Sloan Kettering Cancer Center (All Protocol Activities), New York, New York
- Locations
- 7 in total
- Run by
- Memorial Sloan Kettering Cancer Center
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ORACLE: Observation of ResiduAl Cancer With Liquid Biopsy Evaluation
The purpose of ORACLE is to demonstrate the ability of a novel ctDNA assay developed by Guardant Health to detect recurrence in individuals treated for early-stage solid tumors. It is necessary that ctDNA test results are linked to clinical outcomes in order to demonstrate clinical validity for rec…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Icahn School of Medicine at Mount Sinai, New York, New York
- Locations
- 57 in total
- Run by
- Guardant Health, Inc.
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FiH Study to Investigate Safety, PK and Efficacy of the NaPi2b ADC TUB-040 in Patients With PROC or r/r Adenocarcinoma NSCLC
The purpose of this multicenter, open label trial (NAPISTAR 1-01) is to evaluate the safety/tolerability, pharmacokinetics and preliminary efficacy of TUB-040 and to find the best dose of TUB-040 in participants with ovarian cancer and Non Small Cell Lung Cancer. TUB-040 is an antibody-drug-conjuga…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Mount Sinai, New York, New York
- Locations
- 29 in total
- Run by
- Tubulis GmbH
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A Study to Compare the Efficacy of Nivolumab and Relatlimab Plus Chemotherapy vs Pembrolizumab Plus Chemotherapy for Stage IV/Recurrent Non-squamous Non-small Cell Lung Cancer With PD-L1 Expression ≥ 1%
The purpose of this study is to compare the efficacy of Nivolumab and Relatlimab in combination with chemotherapy to Pembrolizumab with Chemotherapy in participants with stage IV or recurrent Non-squamous Non-small Cell Lung Cancer with PD-L1 expression ≥ 1%
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- Veterans Affairs New York Harbor Healthcare System, New York, New York
- Locations
- 326 in total
- Run by
- Bristol-Myers Squibb
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A Study of Multiple Therapies in Biomarker-selected Participants With Resectable Stages IB-III Non-small Cell Lung Cancer (NSCLC)
This trial will evaluate the efficacy and safety of various therapies in participants with Stage IB, IIA, IIB, IIIA, or selected IIIB resectable and untreated NSCLC tumors that meet protocol-specified biomarker criteria.
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- Laura and ISAAC Perlmutter Cancer Center at NYU Langone., New York, New York
- Locations
- 38 in total
- Run by
- Genentech, Inc.
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A Study Evaluating the Safety, Activity, and Pharmacokinetics of Divarasib as a Single Agent or in Combination With Other Anti-Cancer Therapies in Participants With Previously Untreated Advanced or Metastatic Non-Small Cell Lung Cancer With a KRAS G12C Mutation
The purpose of this study is to evaluate the safety, pharmacokinetics (PK), and activity of single-agent divarasib or combined with other anti-cancer therapies in participants with previously untreated, advanced or metastatic non-small cell lung cancer (NSCLC).
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- NYU Cancer Center, New York, New York
- Locations
- 71 in total
- Run by
- Hoffmann-La Roche
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A Study of LY4050784 in Participants With Advanced or Metastatic Solid Tumors
The main purpose of this study is to find out whether the study drug, LY4050784, is safe, tolerable and effective in participants alone or in combination with other anticancer agents. In addition, with locally advanced or metastatic solid tumors with a BRG1 (Brahma-related gene 1, also known as SMA…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Columbia University Medical Center, New York, New York
- Locations
- 33 in total
- Run by
- Eli Lilly and Company
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A Study of LY4052031 in Participants With Advanced or Metastatic Urothelial Cancer or Other Solid Tumors
The purpose of this study is to find out whether the study drug, LY4052031, is safe, tolerable and effective in participants with advanced, or metastatic solid tumors including urothelial cancer. The study is conducted in two parts - phase Ia (dose-escalation, dose-optimization) and phase Ib (dose-…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- NYU Langone Medical Center - Perlmutter Cancer Center (NYU Cancer Institute), New York, New York
- Locations
- 39 in total
- Run by
- Eli Lilly and Company
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A Study of a Selective ERBB2 Inhibitor (CGT4255), in Patients With Advanced Solid Tumors
This is an open-label, phase 1/1b study evaluating the safety, tolerability, pharmacokinetic (what the body does to the drug), pharmacodynamic (what the drug does to the body), and antitumor activity of CGT4255 in adult participants with advanced solid tumors with ERBB2 alterations or HER2 overexpr…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- NYU Langone, New York, New York
- Locations
- 15 in total
- Run by
- Cogent Biosciences, Inc.
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Solid Tumor Analysis for HLA Loss of Heterozygosity (LOH) and Apheresis for CAR T- Cell Manufacturing
Objective: To collect information on how often a solid tumor cancer might lose the Human Leukocyte Antigen (HLA) by next generation sequencing and perform apheresis to collect and store an eligible participant's own T cells for future use to make CAR T-Cell therapy for their disease treatment. Desi…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- NYU Langone Medical Center, New York, New York
- Locations
- 16 in total
- Run by
- A2 Biotherapeutics Inc.
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Open-label Study of BBO-8520 in Adult Subjects With KRASG12C Non-small Cell Lung Cancer
A first in human study to evaluate the safety and preliminary antitumor activity of BBO-8520, a KRAS G12C (ON and OFF) inhibitor, as a single agent and in combination with pembrolizumab and BBO-10203 in subjects with locally advanced and unresectable or metastatic non-small cell lung cancer with a …
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Perlmutter Cancer Center - NYU Langone Health, New York, New York
- Locations
- 38 in total
- Run by
- TheRas, Inc., d/b/a BBOT (BridgeBio Oncology Therapeutics)
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A Study to Evaluate KIN-2787 in Participants With BRAF and/or NRAS Mutation Positive Solid Tumors
The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics (PK), and preliminary efficacy of KIN-2787 in adults with BRAF/NRAS-mutated advanced or metastatic solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- NYU Langone, New York, New York
- Locations
- 48 in total
- Run by
- Pierre Fabre Medicament
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Phase 1 Study of MRTX1719 in Solid Tumors With MTAP Deletion
This is a Phase 1, open-label, multicenter, study of the safety, tolerability, PK, PD, and anti-tumor activity of MRTX1719 patients with advanced, unresectable or metastatic solid tumor malignancy with homozygous deletion of the MTAP gene.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- David H Koch, Memorial Sloan Kettering Cancer Center, New York, New York
- Locations
- 25 in total
- Run by
- Bristol-Myers Squibb
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A Study of Radiation Therapy to Treat Solid Tumor Cancer That Has Spread to Soft Tissue
The purpose of this study is to find out whether lattice radiation therapy (LRT) is an effective radiation therapy technique when compared to standard stereotactic body radiation therapy (SBRT). The study will also study how the different radiation therapy techniques (LRT and SBRT) affect how many …
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Memorial Sloan Kettering Cancer Center (All Protocol Activities), New York, New York
- Locations
- 7 in total
- Run by
- Memorial Sloan Kettering Cancer Center
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A Study of Tolododekin Alfa (ANK-101) in Combination With an Anti-PD-1/PD-L1 Antibody in Participants With Advanced Non-Small Cell Lung Cancer
A study of tolododekin alfa (also known as ANK-101) administered in combination with an anti-programmed cell death protein 1 (PD-1)/programmed cell death ligand 1 (PD-L1) antibody in participants with advanced or metastatic non-small cell lung cancer (NSCLC). Cohort A will enroll participants who h…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Icahn School of Medicine at Mount Sinai, New York, New York
- Locations
- 11 in total
- Run by
- Ankyra Therapeutics, Inc
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A Study of NT-175 in Adult Participants With Advanced Malignancies That Are Positive for HLA-A*02:01 and the TP53 R175H Mutation
Phase I Study of NT-175, an autologous T cell therapy product genetically engineered to express an HLA-A*02:01-restricted T cell receptor (TCR), targeting TP53 R175H mutant malignancies
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Research Site, New York, New York
- Locations
- 23 in total
- Run by
- AstraZeneca
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Study to Evaluate Efficacy and Safety of Firmonertinib Compared With Investigator's Choice of EGFR Inhibitor as First-Line Treatment in Participants Who Have Locally Advanced or Metastatic NSCLC With EGFR P-Loop and Alpha C-Helix Compressing (PACC) Uncommon Mutations
Global, Phase 3, randomized, multicenter, open-label study evaluating the efficacy and safety of firmonertinib at a dose level of 240 mg QD compared to investigator's choice of osimertinib (80 mg QD) or afatinib (40 mg QD) in participants who have locally advanced or metastatic NSCLC with EGFR PACC…
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- Laura & Isaac Perlmutter Cancer Center at NYU Langone Health, New York, New York
- Locations
- 118 in total
- Run by
- ArriVent BioPharma, Inc.
How to read this page. Every study here comes from ClinicalTrials.gov, the public registry that research teams are required to file with. We have summarised each one in plain language and shown where it is running. We have not changed what any study says it is doing.
What TrialBoost is. We help people find research that might suit them, and, if they ask us to, we pass their details to the research team running it. We are not a doctor, a research site, or a study sponsor, and we do not decide who takes part in anything. Joining costs nothing and you can change your mind at any point.
Paid placement. Some studies pay us when someone asks to be connected to them. Those are labelled Sponsored wherever they appear, and they only appear when they match what you were actually looking for.