Advanced Solid Tumors Clinical Trials
72 studies are recruiting for advanced solid tumors in the United States 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, page 2
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A Study to Investigate the Effects of Multiple Doses of Rezatapopt on the Pharmacokinetics of Metformin, Rosuvastatin, Repaglinide, and Midazolam in Patients With Advanced Solid Tumors Harboring a TP53 Y220C Mutation.
This study aims to evaluate the effects of rezatapopt on the pharmacokinetics of metformin, rosuvastatin, repaglinide, and midazolam in patients with advanced solid tumors harboring a TP53 Y220C mutation.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- HealthOne Denver, Denver, Colorado
- Locations
- 5 in total
- Run by
- PMV Pharmaceuticals, Inc
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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
- AdventHealth Celebration, Celebration, Florida
- Locations
- 19 in total
- Run by
- Marengo Therapeutics, Inc.
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A Study of mRNA-4106 or mRNA-4200 Administered Alone or in Combination With Anti-Cancer Agents in Participants With Solid Tumors
The purpose of this study is to assess the safety and tolerability of mRNA-4106 monotherapy and of mRNA-4200 in combination with checkpoint inhibitor therapy in participants with solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- START Midwest, Grand Rapids, Michigan
- Locations
- 4 in total
- Run by
- ModernaTX, 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, Los Angeles, California
- Locations
- 26 in total
- Run by
- Pheon Therapeutics
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Study of RAS(ON) Inhibitors in Combination With Ivonescimab in Patients With Solid Tumors
The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics (PK), and preliminary antitumor activity of RAS(ON) inhibitors in combination with ivonescimab in adults with advanced or metastatic solid tumors with a RAS mutation.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- USC Norris Comprehensive Cancer Center, Los Angeles, California
- Locations
- 9 in total
- Run by
- Revolution Medicines, Inc.
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Study of GS-2426 in Participants With Advanced Solid Tumors
The goal of this clinical study is to learn more about the study drug GS-2426, and how safe and tolerable it is in participants with advanced methylthioadenosine phosphorylase (MTAP)-deleted solid tumors. The primary objective of this study is to evaluate the safety and tolerability of GS-2426 in p…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- START Midwest, Grand Rapids, Michigan
- Locations
- 4 in total
- Run by
- Gilead Sciences
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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
- USC Norris Comprehensive Cancer Center, Los Angeles, California
- Locations
- 16 in total
- Run by
- Tyra Biosciences, Inc
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A Study to Test the Safety and Tolerability of SBO-154 in Patients With Advanced Solid Tumors.
This is a Phase 1 study of SBO-154 in patients with advanced cancers who are unable to tolerate or have not previously responded to standard therapy available in the country. The study involves multiple doses and takes place at several centers.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Honorhealth Research Institute, Scottsdale, Arizona
- Locations
- 16 in total
- Run by
- Sun Pharma Advanced Research Company Limited
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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
- START New York - Long Island, Lake Success, New York
- Locations
- 8 in total
- Run by
- LigaChem Biosciences, Inc.
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A Study of ASP1002 in Adults for Treatment of Solid Tumors
ASP1002 is being studied in people with tumors that have spread to nearby tissue (locally advanced) that cannot be removed by surgery (unresectable) or tumors that have spread to other parts of the body (metastatic). Claudin 4 protein, or CLDN4, is a protein found on tumors in different parts of th…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Yale University Cancer Center, New Haven, Connecticut
- Locations
- 15 in total
- Run by
- Astellas Pharma Global Development, 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
- The Angeles Clinic and Research Institute, Los Angeles, California
- Locations
- 39 in total
- Run by
- Incyte Corporation
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A Clinical Trial to Evaluate the Safety, Tolerability and Clinical Efficacy of M3T01 Monotherapy and in Combination With Pembrolizumab and Other Systemic Therapies
Phase 1 first-in-human, open-label, dose-escalation (3 + 3), dose-expansion clinical trial to evaluate the safety, tolerability and preliminary clinical efficacy of M3T01 (fully human IgG4/kappa monoclonal antibody targeting FasL) in subjects with metastatic or unresectable solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Providence Portland Cancer Institute - Franz Clinic, Portland, Oregon
- Run by
- Providence Health & Services
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A Rollover Study Evaluating Sotorasib With or Without Panitumumab in Participants With KRAS p.G12C Mutation
The primary objective of the study is to evaluate the safety and tolerability of the continuation of sotorasib with or without panitumumab and/or other anti-cancer therapies in participants continuing to derive benefit in Amgen-sponsored protocols.
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- Florida Cancer Specialists - Fort Myers, Fort Myers, Florida
- Locations
- 11 in total
- Run by
- Amgen
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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
- The Angeles Clinic and Research Institute, Los Angeles, California
- Locations
- 39 in total
- Run by
- ModernaTX, Inc.
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A Study of Safety, Tolerability and Preliminary Efficacy of NTS071 in Subjects With Advanced Solid Tumors Harboring a TP53 Y220C Mutation
This study is to evaluate the safety, tolerability, PK, and preliminary efficacy of NTS071 in adults with TP53 Y220C-mutated solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Next Oncology, San Antonio, Texas
- Locations
- 2 in total
- Run by
- Nutshell Therapeutics (Shanghai) Co., LTD.
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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
- Hoag Memorial Hospital Presbyterian, Newport Beach, California
- 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, Orlando, Florida
- Locations
- 12 in total
- Run by
- Alterome Therapeutics, Inc.
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An Open-label Dose Escalation/Expansion Trial to Evaluate the Safety and Anti-tumor Activity of TEV-56278 Alone or in Combination With Pembrolizumab in Participants With Advanced or Metastatic Solid Tumors
The primary objectives of this trial are to: * Characterize the safety and tolerability of TEV-56278 * Determine the Recommended Phase 2 Dose (RP2D) * Evaluate antitumor activity of TEV-56278 (Part 2 only) * Determine the safety and tolerability of TEV-56278 in combination with pembrolizumab * Dete…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Teva Investigational Site 12017, Los Angeles, California
- Locations
- 12 in total
- Run by
- Teva Branded Pharmaceutical Products R&D LLC
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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
- University of California, Davis Comprehensive Cancer Center, Sacramento, California
- 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
- The City of Hope National Medical Center, Duarte, California
- Locations
- 6 in total
- Run by
- SEED Therapeutics, Inc.
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A TRIAL TO EVALUATE THE SAFETY, TOLERABILITY, PHARMACOKINETICS, AND EFFICACY OF SHR-A1904 IN SUBJECTS WITH ADVANCED SOLID TUMORS
The study (dose escalation/expansion) is being conducted to assess the safety and tolerability of SHR-A1904 in subjects with advanced solid tumors, and to determine maximum tolerated dose (MTD) and/or recommended phase II dose (RP2D), to assess preliminary efficacy of SHR-A1904, pharmacokinetic (PK…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Dong-A University Hospital, Busan,
- Locations
- 28 in total
- Run by
- Jiangsu HengRui Medicine Co., Ltd.
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A Study to Evaluate the Safety, Tolerability, Pharmacokinetics (PK), and Antitumor Activity of ALK201 in Participants With Advanced Solid Tumors
This is a first-in-human (FIH), open-label, multicenter dose escalation and expansion study of ALK201. The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics (PK), and antitumor activity of ALK201 as a monotherapy in adult participants with Advanced Solid Tumors. The st…
- Stage
- Phase 1
- Ages
- 18 to 75
- Site
- Denver Drug Development Unit, Denver, Colorado
- Locations
- 38 in total
- Run by
- Shanghai Allink Biotherapeutics Co., Ltd.
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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
- UC Irvine/Chao Family Comprehensive Cancer Center, Orange, California
- Locations
- 21 in total
- Run by
- Revolution Medicines, Inc.
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A First-in-Human (FIH) Study to Evaluate the Safety and Tolerability of VVD-130037 in Participants With Advanced Solid Tumors
A FIH dose escalation and dose expansion study to evaluate VVD-130037 in participants with advanced solid tumors as a single agent, and in combination with docetaxel, paclitaxel, or pembrolizumab.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Mayo Clinic Jacksonville, Jacksonville, Florida
- Locations
- 26 in total
- Run by
- Vividion Therapeutics, Inc.
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Study of DT-7012 as a Single Agent and in Combination With an Immune Checkpoint Inhibitor in Participants With Advanced Solid Tumors
This is a phase 1/2, dose-escalation, clinical study to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics and efficacy of DT-7012 (an anti-CCR8 monoclonal antibody) as a single agent and in combination with an immune checkpoint inhibitor in adult participants with selected advan…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Macquarie University Clinical Trial Unit, North Ryde, New South Wales
- Locations
- 9 in total
- Run by
- Domain Therapeutics Australia Pty 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.