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

  1. 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
  2. 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
  3. 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.
  4. 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
  5. 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
  6. 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
  7. 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.
  8. 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
  9. 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
  10. 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
  11. 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
  12. 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
  13. 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
  14. 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
  15. 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
  16. 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.
  17. 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.
  18. 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
  19. 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.
  20. 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.