Advanced Solid Tumors Clinical Trials in Boston, Massachusetts
25 studies are recruiting for advanced solid tumors in Boston, Massachusetts 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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Study of RMC-5127 in Patients With Advanced KRAS G12V-Mutant Solid Tumors
The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics (PK), and preliminary antitumor activity of RMC-5127 as a monotherapy and in combination with either daraxonrasib or cetuximab in adults with KRAS G12V-mutant solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Dana-Farber Cancer Institute, Boston, Massachusetts
- Locations
- 9 in total
- Run by
- Revolution Medicines, Inc.
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First in Human Study of TUB-030 in Patients With Advanced Solid Tumors
The goal of this clinical trial is to learn if the drug TUB-030 works to treat solid cancer in adults. The study will also explore the safety of TUB-030. The main questions it aims to answer are: To determine the safety and tolerability of TUB-030 To determine the maximum tolerated dose of TUB-030 …
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Massachusetts General Hospital, Boston, Massachusetts
- Locations
- 20 in total
- Run by
- Tubulis GmbH
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A Study to Learn More About How Well Treatment With Sevabertinib (BAY 2927088) Tablets Works and How Safe it is in Participants Who Have a Solid Tumor With Mutations of the Human Epidermal Growth Factor Receptor 2 (HER2)
Researchers are looking for a better way to treat people who have solid tumors with HER2-activating mutations. Before a treatment can be approved for people to take, researchers do clinical trials to better understand its safety and how it works. In this trial, the researchers want to learn how wel…
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- Dana-Farber Cancer Institute - Oncology Department, Boston, Massachusetts
- Locations
- 54 in total
- Run by
- Bayer
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Phase 1/2 Study of PYX-201 in Combination With Pembrolizumab in Advanced Solid Tumors
The primary objective of this study is to determine the recommended Phase 2 doses (RP2D(s)) and maximum tolerated dose (MTD) of PYX-201 in combination with pembrolizumab for participants with advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Massachusetts General Hospital, Boston, Massachusetts
- Locations
- 22 in total
- Run by
- Pyxis Oncology, Inc
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A Phase I Study of SIM0505 in Participants With Advanced Solid Tumors
This is an open-label, multicenter phase 1 study to evaluate the safety, Tolerability, Pharmacokinetics and Preliminary Antitumor Activity of SIM0505 in Adult Participants with Advanced Solid Tumors
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Dana-Farber Cancer Institute, Boston, Massachusetts
- Locations
- 17 in total
- Run by
- NextCure, Inc.
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Study of GS-0201 Alone and in Combination in Participants With Advanced Solid Tumors
The main goal of this first in human (FIH) study is to learn about the safety and dosing of GS-0201 when given alone or in combination with sacituzumab govitecan (SG) in participants with advanced solid tumors. The primary objectives of this study are to: * To assess the safety and tolerability of …
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Dana-Farber Cancer Institute, Boston, Massachusetts
- Locations
- 8 in total
- Run by
- Gilead Sciences
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A Study of OTP-01, a Dual Paratopic PD-1/VEGFR2 Antibody, in Patients With Advanced Solid Tumors
The main goals of this clinical trial are to find out what the best dose of the study drug, OTP-01, is for patients with solid tumors through understanding how it is tolerated and any side effects that it may cause. The trial will also see if OTP-01 causes tumors to shrink and how the body processe…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Dana-Farber Cancer Institute, Boston, Massachusetts
- Locations
- 14 in total
- Run by
- Ottimo Pharma Limited
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A Study of PHST001 in Advanced Solid Tumors
This is a multi-center, first-in-human (FIH), open-label, Phase 1a/1b dose escalation and dose expansion study to assess the safety, PK, pharmacodynamics, and antitumor activity of PHST001 monotherapy (Phase 1a) or in combination with chemotherapy (Phase 1b) in adult participants with advanced rela…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Dana Farber Cancer Institute, Boston, Massachusetts
- Locations
- 20 in total
- Run by
- Pheast Therapeutics
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A Study of a Selective T Cell Receptor (TCR) Targeting, Bifunctional Antibody-fusion Molecule STAR0602 in Participants With Advanced Solid Tumors
This is an open label, multicenter, phase 1/2 study to assess the safety/tolerability and preliminary clinical activity of STAR0602 as a single agent and in combination with chemotherapy administered intravenously in participants with advanced solid tumors that are antigen-rich.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Massachusetts General Hospital Cancer Center, Boston, Massachusetts
- Locations
- 19 in total
- Run by
- Marengo Therapeutics, Inc.
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A Study of PHN-012 in Patients With Advanced Solid Tumors
This first-in-human study will evaluate safety, tolerability, anti-tumor activity, immunogenicity, pharmacokinetics and pharmacodynamics of PHN-012, a novel antibody-drug conjugate (ADC), in patients with advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- PHN-012-001 Site, Boston, Massachusetts
- Locations
- 26 in total
- Run by
- Pheon Therapeutics
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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
- Mass General Cancer Center, Boston, Massachusetts
- Locations
- 16 in total
- Run by
- Tyra Biosciences, Inc
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A Study to Evaluate Claudin 18.2-Directed ADC LCB02A in Advanced Solid Tumors
This is a Phase 1/2 open label study consisting of dose escalation cohorts (Phase 1) followed by expansion cohorts (Phase 2). The Phase 1 dose escalation population includes subjects with advanced solid tumors that are refractory to standard of care therapy or for whom no standard of care options a…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Mass General Hospital, Boston, Massachusetts
- Locations
- 8 in total
- Run by
- LigaChem Biosciences, Inc.
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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
- Dana Farber Cancer Institute, Boston, Massachusetts
- Locations
- 39 in total
- Run by
- Incyte Corporation
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Study of mRNA-4359 Administered Alone and in Combination With Immune Checkpoint Blockade in Participants With Advanced Solid Tumors
The primary goal of this study is to assess the safety and tolerability of mRNA-4359 administered alone and in combination with pembrolizumab or ipilimumab and nivolumab.
- Stage
- Phase 1
- Ages
- 12 and older
- Site
- Massachusetts General Hospital, Boston, Massachusetts
- Locations
- 39 in total
- Run by
- ModernaTX, Inc.
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Phase 1/2 Study of ETX-636 in Participants With Advanced Solid Tumors
Phase 1/2, open-label study of ETX-636 in participants with advanced solid tumors
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Beth Israel Deaconess Medical Center, Boston, Massachusetts
- Locations
- 15 in total
- Run by
- Ensem Therapeutics
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A Study to Learn About Study Medicine ALTA3263 in Adults With Advanced Solid Tumors With KRAS Mutations
The purpose of this study is to characterize the safety and tolerability of ALTA3263 in adults with advanced solid tumors with KRAS mutations.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Research Site, Boston, Massachusetts
- Locations
- 12 in total
- Run by
- Alterome Therapeutics, Inc.
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Study of RMC-9805 in Participants With KRAS G12D-Mutant Solid Tumors
This study is to evaluate the safety and tolerability of RMC-9805 as monotherapy and in combination with RMC-6236 in adults with KRAS G12D-mutant solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Massachusetts General Hospital, Boston, Massachusetts
- Locations
- 17 in total
- Run by
- Revolution Medicines, Inc.
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A Phase 1/1B Study of ST-01156, a Small Molecule RBM39 Degrader, in Patients With Advanced Solid Malignancies
A Phase 1/1B Study of ST-01156 in Patients with Advanced Solid Malignancies
- Stage
- Phase 1
- Ages
- 16 and older
- Site
- Mass General Brigham Cancer Institute, Boston, Massachusetts
- Locations
- 6 in total
- Run by
- SEED Therapeutics, Inc.
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Study of RMC-6236 in Patients With Advanced Solid Tumors Harboring Specific Mutations in RAS
Evaluate the safety and tolerability of RMC-6236 in adults with specific RAS mutant advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Dana Farber Cancer Institute, Boston, Massachusetts
- Locations
- 21 in total
- Run by
- Revolution Medicines, Inc.
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A Study of MGC028 in Participants With Advanced Solid Tumors
The goal of this clinical trial is to characterize the safety, tolerability, dose-limiting toxicities (DLT), and maximum tolerated dose (MTD) or maximum administered dose of MGC028 (if no MTD is defined). The study will enroll adult participants with relapsed or refractory, unresectable, locally ad…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Mass General Brigham, Boston, Massachusetts
- Locations
- 7 in total
- Run by
- MacroGenics
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Study of GS-2121 Given Alone or in Combination in Adults With Advanced Solid Tumors
The main goal of this first-in-human (FIH) study is to learn about the safety and dosing of GS-2121 when given alone or in combination with zimberelimab (ZIM) in participants with advanced solid tumors. The primary objectives of this study are: * To assess the safety and tolerability of GS-2121 as …
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Beth Israel Deaconess Medical Center, Boston, Massachusetts
- Locations
- 6 in total
- Run by
- Gilead Sciences
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Study Evaluating the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of TGW101 in Participants With Advanced Solid Tumors
The primary objectives of this study are to evaluate the safety and tolerability of TGW101 and determine the recommended dosing regimen(s) for further study. The secondary objectives are to assess pharmacokinetics and preliminary antitumor activity.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Massachusetts General Hospital, Boston, Massachusetts
- Locations
- 7 in total
- Run by
- Tagworks Pharmaceuticals BV
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SNV4818 in Participants With Advanced Solid Tumors
This study is testing a new medicine, SNV4818, for people with advanced cancers. The researchers want to find out if SNV4818 is safe, well-tolerated, and effective in treating solid tumors. They are investigating different doses in order to find the safest and most effective one.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Massachusetts General Hospital, Boston, Massachusetts
- Locations
- 12 in total
- Run by
- Pikavation Therapeutics, Inc.
-
A Study to Evaluate TROP2 ADC LCB84 Single Agent and in Combination With an Anti-PD-1 Ab in Advanced Solid Tumors
This is a first-in-human, Phase 1/2 study to evaluate LCB84, a TROP2-directed antibody-drug conjugate, alone and in combination with an anti-PD-1 Ab, in dose escalation (Phase 1) followed by dose expansion (Phase 2). The study population in dose escalation (Phase 1) consists of patients with advanc…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Dana Farber Cancer Institute, Boston, Massachusetts
- Locations
- 8 in total
- Run by
- LigaChem Biosciences, Inc.
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A Study of PARP1 Selective Inhibitor, EIK1004 (IMP1707) in Participants With Advanced Solid Tumors.
This study will evaluate the safety, tolerability, and preliminary efficacy of EIK1004 (IMP1707) in participants with recurrent advanced/metastatic breast cancer, ovarian cancer, metastatic castrate resistant prostate cancer (mCRPC) and pancreatic cancer with deleterious/suspected deleterious mutat…
- Stage
- Phase 1
- Ages
- 18 to 89
- Site
- Beth Israel Deaconess Medical Center, Boston, Massachusetts
- Locations
- 10 in total
- Run by
- Eikon Therapeutics
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.