Solid Tumors Clinical Trials
45 studies are recruiting for 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 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
- Precision NextGen Oncology & Research Center, Beverly Hills, California
- 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
- The Angeles Clinic and Research Institute, Los Angeles, California
- 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 02003, Los Angeles, California
- 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
- Mayo Clinic Hospital, Phoenix, Arizona
- Locations
- 34 in total
- Run by
- Incyte Corporation
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Phase II Biomarker Study of BND-22 in Combination With Cemiplimab in Solid Tumors
To study possible biomarkers that may be related to how SAR444881 works (either alone or when combined with cemiplimab) in participants with solid tumors.
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- Md Anderson Cancer Center, Houston, Texas
- Run by
- M.D. Anderson 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, Birmingham, Alabama
- Locations
- 65 in total
- Run by
- GlaxoSmithKline
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JAB-30355 in Patients With Advanced Solid Tumors Harboring TP53 Y220C Mutation
This study is to evaluate the efficacy and safety of JAB-30355 in adult participants with advanced solid tumors harboring TP53 Y220C mutation.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Research Site, Denver, Colorado
- Locations
- 15 in total
- Run by
- Jacobio Pharmaceuticals Co., Ltd.
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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
- UCLA Hematology/Oncology, Los Angeles, California
- 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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A Study of HS-20110 in Participants With Advanced Solid Tumors
This is an open-label, multicenter study to evaluate the safety and tolerability of HS-20110 in participants with advanced solid malignant tumors
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- BRCR Medical Center INC, Tamarac, Florida
- Locations
- 8 in total
- Run by
- Hansoh BioMedical R&D Company
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Mayo Clinic Radiotherapy Patient Outcomes Registry and Biobanking Study
To collect and analyze specimens that will correlate with clinical outcomes such as acute and late toxicities, quality of life, local control, and survival of patients treated with photon/proton therapy.
- Stage
- Not phased
- Ages
- Any age
- Site
- Mayo Clinic, Rochester, Minnesota
- Run by
- Mayo Clinic
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PumaRx Registry Trial
This study is a multicenter, observational, post-marketing, registry study designed to track the safety and performance of the RenovoCath® device and assess survival outcomes in patients diagnosed with solid tumors who are treated with localized intra-arterial (IA) delivery of therapeutic agents to…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Baptist Health South Florida, Coral Gables, Florida
- Locations
- 3 in total
- Run by
- RenovoRx
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S-531011 as Monotherapy and in Combination With an Immune Checkpoint Inhibitor in Advanced or Metastatic Solid Tumors
The primary objective of Part A is to evaluate the safety and tolerability of S-531011 and to determine the maximum tolerated dose (MTD) and/or recommended Phase 2 dose (RP2D) of S-531011 with or without pembrolizumab. The primary objective of Parts B and C is to evaluate the antitumor activity of …
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of Florida Health, Gainesville, Florida
- Locations
- 8 in total
- Run by
- Shionogi
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A Study of XB371 Administered in Participants With Locally Advanced or Metastatic Solid Tumors
The primary purpose of the study is to characterize the safety and tolerability of XB371. The dose-escalation cohorts and Part B of the expansion cohorts are non-randomized. Part A of the expansion cohorts is randomized.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Exelixis Clinical Site #5, Rogers, Arkansas
- Locations
- 9 in total
- Run by
- Exelixis
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DPTX3186 in Wnt Pathway Activated Solid Tumors
This is a first-in human clinical study of DPTX3186 in subjects with Wnt-pathway activated solid tumors where no other treatments exist. The study will evaluate safety, pharmacokinetics, and initial activity of DPTX3186, as well as explore pharmacodynamic parameters to identify potential biomarkers…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- NEXT San Antonio, San Antonio, Texas
- Locations
- 2 in total
- Run by
- Dewpoint Therapeutics
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JAB-2485 Activity in Adult Patients With Advanced Solid Tumors
This study is to evaluate the safety and tolerability of JAB-2485 monotherapy in adult participants with advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Henry Ford Health System, Detroit, Michigan
- Locations
- 8 in total
- Run by
- Jacobio Pharmaceuticals Co., Ltd.
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ABL103 in Combination With Pembrolizumab, With or Without Taxane in Advanced or Metastatic Solid Tumors
This study is to assess the safety and antitumor activity of ABL103 plus pembrolizumab, with or without taxane, in advanced or metastatic solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Seoul National University Bundang Hospital, Seongnam,
- Locations
- 6 in total
- Run by
- ABL Bio, Inc.
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CIBMTR Research Database
The primary purpose of the Research Database is to have a comprehensive source of observational data that can be used to study HSC transplantation and cellular therapies. A secondary purpose of the Research Database is to have a comprehensive source of data to study marrow toxic injuries. Objective…
- Stage
- Not phased
- Ages
- Any age
- Site
- Center for International Blood and Marrow Transplant Research, Minneapolis, Minnesota
- Locations
- 2 in total
- Run by
- Center for International Blood and Marrow Transplant Research
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APL-101 Study of Subjects With NSCLC With c-Met EXON 14 Skip Mutations and c-Met Dysregulation Advanced Solid Tumors
To assess: * efficacy of APL-101 as monotherapy for the treatment of NSCLC harboring MET Exon 14 skipping mutations, NSCLC harboring MET amplification, solid tumors harboring MET amplification, solid tumors harboring MET fusion, primary CNS tumors harboring MET alterations, solid tumors harboring w…
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- Cedars-Sinai Medical Center - Samuel Oschin Comprehensive Cancer Institute, Los Angeles, California
- Locations
- 35 in total
- Run by
- Apollomics Inc.
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A Study of ADRX-0405 in Subjects With Select Advanced Solid Tumors
The primary purpose of this study is to assess the safety, tolerability, and pharmacokinetics, and to identify the optimal dose of ADRX-0405 in patients with select advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- City of Hope, Duarte, California
- Locations
- 8 in total
- Run by
- Adcentrx 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.