Solid Tumors Clinical Trials in New York, New York
20 studies are recruiting for solid tumors 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.
Search these by distance from you
Studies now recruiting
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Long-term Safety and Efficacy Extension Study for Participants With Advanced Tumors Who Are Currently on Treatment or in Follow-up in a Pembrolizumab (MK-3475) Study (MK-3475-587/KEYNOTE-587)
The purpose of this study is to evaluate the long-term safety and efficacy of pembrolizumab (MK-3475) in participants from previous Merck pembrolizumab-based parent studies who transition into this extension study. This study will consist of three phases: 1) First Course Phase, 2) Survival Follow-u…
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- Laura and Isaac Perlmutter Cancer Center at NYU Langone Health ( Site 0032), New York, New York
- Locations
- 782 in total
- Run by
- Merck Sharp & Dohme LLC
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A Study of BMS-986504 Monotherapy and in Combination With Other Agents in Participants With Advanced and/or Metastatic Solid Tumors With Homozygous MTAP Deletion (MountainTAP-5)
This is an open-label, multicenter Phase 2 study evaluating BMS-986504 in participants with advanced and/or metastatic solid tumors that have MTAP deletion. The study includes a monotherapy component and a combination component in which BMS-986504 is given with other anti-cancer agents. The trial w…
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- Memorial Sloan Kettering Cancer Center, New York, New York
- Locations
- 58 in total
- Run by
- Bristol-Myers Squibb
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A Study to Evaluate INCA036873 in Participants With Advanced Solid Tumors and Hematological Malignancies
A study to evaluate the safety and tolerability of INCA036873 in participants with advanced solid tumors and hematological malignancies.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Memorial Sloan Kettering Cancer Center, New York, New York
- Locations
- 22 in total
- Run by
- Incyte Corporation
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A Study to Evaluate Chemotherapy With or Without INCB161734 in Previously Untreated, KRAS G12D-Mutated Metastatic Pancreatic Ductal Adenocarcinoma
The purpose of this study is to evaluate the efficacy and safety of standard chemotherapy with or without INCB161734 in participants with metastatic pancreatic ductal adenocarcinoma (PDAC).
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- Investigative Site US031, New York, New York
- Locations
- 229 in total
- Run by
- Incyte Corporation
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Study of ORIC-114 in Patients With Advanced Solid Tumors Harboring an EGFR or HER2 Alteration
The purpose of this study is to establish the recommended Phase 2 dose (RP2D) and/or maximum tolerated dose (MTD), safety, pharmacokinetics (PK), pharmacodynamics (PD), and antitumor activity of ORIC-114 as a Single Agent or in Combination with Chemotherapy when administered to patients with advanc…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- NYU Langone Health Perlmutter Cancer Center, New York, New York
- Locations
- 42 in total
- Run by
- ORIC Pharmaceuticals
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First-in-Human Trial of DS-2243a in Participants With Advanced Solid Tumors
This 2-part study will evaluate safety, tolerability, and clinical efficacy of DS-2243a as a treatment for participants with advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- David H. Koch Center for Cancer Care at Memorial Sloan Kettering Cancer Center, New York, New York
- Locations
- 7 in total
- Run by
- Daiichi Sankyo
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A Phase 1 Study of AB521 Monotherapy and Combination Therapies in Renal Cell Carcinoma and Other Solid Tumors
The purpose of this study is to evaluate the safety and tolerability of: * casdatifan when taken alone in participants with advanced solid tumor malignancies and clear cell renal cell carcinoma (ccRCC) during the dose escalation stage; and * casdatifan monotherapy and casdatifan in combination with…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Research Site, New York, New York
- Locations
- 25 in total
- Run by
- Arcus Biosciences, Inc.
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A Study of ZL-1310 in Participants With Selected Solid Tumors
A Phase 1b/2, Open-label, Multi-center Study of ZL-1310 in Participants With Selected Solid Tumors
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Memorial Sloan-Kettering Cancer Center, New York, New York
- Locations
- 23 in total
- Run by
- Zai Lab (Shanghai) Co., Ltd.
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Safety and Preliminary Anti-Tumor Activity of TYRA-430 in Advanced Hepatocellular Carcinoma and Other Solid Tumors With Activating FGF/FGFR Pathway Aberrations
A Phase 1 study to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamic (PD), and preliminary antitumor activity of TYRA-430 in cancers with FGF/FGFR pathway aberrations, including locally advanced/metastatic hepatocellular carcinoma and other advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Columbia University Irving Medical Center, New York, New York
- Locations
- 16 in total
- Run by
- Tyra Biosciences, Inc
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A Study to Assess the Efficacy and Safety of FORE8394 in Participants With Cancer Harboring BRAF Alterations
The objective of this Master Protocol is to evaluate the efficacy and safety of plixorafenib in participants with BRAF altered (BRAF V600E or BRAF fusions) locally advanced or metastatic solid tumors, or recurrent or progressive primary central nervous system (CNS) tumors, including rare BRAF V600E…
- Stage
- Phase 2
- Ages
- 8 and older
- Site
- Columbia University Irving Medical Center, New York, New York
- Locations
- 70 in total
- Run by
- Fore Biotherapeutics
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A Study to Evaluate the Safety of INCA33890 in Participants With Advanced or Metastatic Solid Tumors
To evaluate the safety, tolerability, and DLTs and determine the MTD and/or RDE(s) of INCA33890 in participants with select advanced or metastatic solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Laura and Isaac Perlmutter Cancer Center, New York, New York
- Locations
- 39 in total
- Run by
- Incyte Corporation
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Phase 1a/b Study of ZL-6201 Safety, PK, and Preliminary Efficacy in Sarcoma and Selected Tumors
The purpose of this study is to evaluate the safety and tolerability of investigational study drug ZL-6201 for treating sarcoma and solid tumors cancer.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Zai Lab Site 02002, New York, New York
- Locations
- 8 in total
- Run by
- Zai Lab (Shanghai) Co., Ltd.
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A Study to Evaluate INCB161734 in Participants With Advanced or Metastatic Solid Tumors With KRAS G12D Mutation
This study is conducted to determine the safety and tolerability of INCB161734 as a single agent or in combination with other anticancer therapies.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Weill Cornell Medicine, New York, New York
- Locations
- 34 in total
- Run by
- Incyte Corporation
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Genomic Profiling in Cancer Patients
The purpose of this study is to determine whether certain genes in cancer may be abnormal. When a gene is abnormal this is called a mutation. Most mutations in cancer cells are not inherited (passed down from parents) but happen after birth in the cancer itself. Most cancers have many mutations. So…
- Stage
- Not phased
- Ages
- Any age
- Site
- Metropolitan Hospital Center, New York, New York
- Locations
- 18 in total
- Run by
- Memorial Sloan Kettering Cancer Center
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A Study to Evaluate the Safety,Tolerability, Pharmacokinetics and Clinical Activity of Mocertatug Rezetecan for Injection in Participants With Advanced Solid Tumors (BEHOLD-1)
The goal of this study is to assess the safety and tolerability of Mocertatug Rezetecan . The study will also see how the levels of Mo-Rez change over time at different dose amount
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- GSK Investigational Site, New York, New York
- Locations
- 65 in total
- Run by
- GlaxoSmithKline
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DB-1311 in Combination With BNT327 or DB-1305 in Advanced/Metastatic Solid Tumors
A Phase II, Multicenter, Open-Label Trial of DB-1311 in combination with BNT327 or DB-1305 in Participants with Advanced/Metastatic Solid Tumors
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- USA04-0, New York, New York
- Locations
- 37 in total
- Run by
- DualityBio Inc.
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QTX3034 in Patients With KRAS G12D Mutation
Phase 1 study to determine the safety and tolerability of QTX3034 as a single agent or in combination with cetuximab.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- NYU Langone Health, New York, New York
- Locations
- 14 in total
- Run by
- Quanta Therapeutics
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ORIC-114 in Combination With Subcutaneous Amivantamab in Patients With EGFR Exon20 Insertion Mutant NSCLC
The purpose of this study is to establish the recommended phase 2 dose (RP2D), safety, pharmacokinetics (PK), pharmacodynamics (PD), and preliminary antitumor activity of ORIC-114 in combination with subcutaneous (SC) amivantamab in patients with advanced or metastatic NSCLC harboring an EGFR exon …
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- NYU Langone Health, New York, New York
- Locations
- 4 in total
- Run by
- ORIC Pharmaceuticals
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The FLOTILLA Study: Providing Continued Access to The Study Medicines Encorafenib and Binimetinib for Participants in Prior Clinical Trials
The purpose of this clinical trial (called the FLOTILLA study) is to give continued access to the study medicines, as well as safety follow-up, for participants in prior clinical trials of encorafenib and/or binimetinib. All participants who took part in earlier encorafenib and/or binimetinib studi…
- Stage
- Phase 4
- Ages
- 18 and older
- Site
- Rockefeller Outpatient Pavilion (53rd Street), New York, New York
- Locations
- 67 in total
- Run by
- Pfizer
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Study of IBI3020 Treatment in Participants With Late-Stage Solid Tumors
The main purpose of this study is to evaluate the safety and tolerability of IBI3020 and to determine the maximum tolerated dose (MTD) and/or the recommended dose for expansion (RP2D) of IBI3020.
- Stage
- Phase 1
- Ages
- 18 to 75
- Site
- Montefiore Cancer Center, New York, New York
- Locations
- 9 in total
- Run by
- Innovent Biopharmaceutical Technology (Hangzhou) Co., LTD.
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.