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 3

  1. A First-In Human (FIH) Study to Find Out How Well REGN10597 Medicine Given Alone or in Combination With Cemiplimab Works in Adult Participants Who Have Cancer With Tumors That Have Spread in Their Body

    This study is researching an experimental drug called REGN10597 alone or in combination with another drug called cemiplimab (called "study drug(s)"). The study is focused on patients with certain solid tumors that are in an advanced stage. The aim of the study is to see how safe, tolerable, and eff…

    Stage
    Phase 1
    Ages
    18 and older
    Site
    USC Norris Comprehensive Cancer Center, Los Angeles, California
    Locations
    11 in total
    Run by
    Regeneron Pharmaceuticals
  2. 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
    UCSF - Helen Diller Family Cancer Center, San Francisco, California
    Locations
    7 in total
    Run by
    MacroGenics
  3. A First-in-Human Study of CKD-703 in Advanced Solid Tumors and Non-Small Cell Lung Cancer

    This is a Phase 1/2a open-label multicenter study to evaluate the safety, efficacy, and pharmacokinetics of CKD-703 in Advanced c-Met Expressing Solid Tumors, and in MET-Amplified and c-Met Overexpressing Non-Small Cell Lung Cancer. CKD-703 is composed of a c-Met-targeting monoclonal antibody (mAb)…

    Stage
    Phase 1
    Ages
    19 and older
    Site
    Gabrail Cancer Center, Ohio City, Ohio
    Run by
    Chong Kun Dang Pharmaceutical
  4. 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
    Stanford Cancer Center, Palo Alto, California
    Locations
    6 in total
    Run by
    Gilead Sciences
  5. 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
    Honor Health, Scottsdale, Arizona
    Locations
    7 in total
    Run by
    Tagworks Pharmaceuticals BV
  6. EIK1005-002: A Clinical Research Study Evaluating EIK1005, a Werner Helicase Inhibitor, as Monotherapy and in Combination With Pembrolizumab in Participants With Advanced Solid Tumors Including Microsatellite Instability High (MSI-H) Tumors

    The goal of this clinical trial is to determine the most effective dose of EIK1005 that a person can take safely. Additionally, this study will test how well EIK1005 is tolerated alone and in combination with pembrolizumab in treating patients with advanced cancer.

    Stage
    Phase 1
    Ages
    18 and older
    Site
    University of Texas MD Anderson Cancer Center, Houston, Texas
    Locations
    10 in total
    Run by
    Eikon Therapeutics
  7. A First-in-Human (FIH) Study to Evaluate the Safety and Tolerability of VVD-159642 in Participants With Advanced Solid Tumors

    A FIH study to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and preliminary anti-tumor activity of VVD-159642, a rat sarcoma viral oncogene-phosphatidylinositol 3-kinase alpha (RAS-PI3Kα) inhibitor, as a single agent and in combination with either sotorasib or tr…

    Stage
    Phase 1
    Ages
    18 and older
    Site
    START Mid West, Grand Rapids, Michigan
    Locations
    9 in total
    Run by
    Vividion Therapeutics, Inc.
  8. 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
    The Angeles Clinic and Research Institute, A Cedars-Sinai Affiliate, Los Angeles, California
    Locations
    12 in total
    Run by
    Pikavation Therapeutics, Inc.
  9. Study to Evaluate the Pharmacokinetics and Safety of Pralatrexate in Patients With Advanced Solid Tumor or Hematological Malignancy and Either Normal Hepatic Function or Mild, Moderate, or Severe Hepatic Impairment

    This purpose of this study is to help to evaluate the pharmacokinetic (PK) profile of pralatrexate when administered to patients with various degrees of hepatic impairment and to evaluate the safety and establish the dosing recommendations for pralatrexate administered once weekly for 6 weeks of ev…

    Stage
    Phase 1
    Ages
    18 and older
    Site
    Northwestern University - Feinberg School of Medicine, Chicago, Illinois
    Locations
    4 in total
    Run by
    Acrotech Biopharma Inc.
  10. A Study of BMS-986482 Alone or as Combination Therapy in Participants With Advanced Solid Tumors

    The purpose of this study is to test the safety and efficacy of BMS-986482 alone and as combination therapy in participants with advanced solid tumors.

    Stage
    Phase 1
    Ages
    18 and older
    Site
    University of California, Irvine (UCI) Health - UC Irvine Medical Center, Irvine, California
    Locations
    21 in total
    Run by
    Bristol-Myers Squibb
  11. Phase 1/2a Study to Assess the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of WEF-001 as Monotherapy in Advanced KRAS-Mutant Solid Tumours.

    This is a study designed to assess the safety, tolerability, pharmacokinetics and preliminary efficacy of WEF-001 as monotherapy in patients with Advanced KRAS-mutant solid tumours.

    Stage
    Phase 1
    Ages
    18 and older
    Site
    NEXT Oncology Dallas, Dallas, Texas
    Locations
    4 in total
    Run by
    Auricula Biosciences Inc.
  12. A Study of ASKG915 in Patients With Selected Advanced Solid Tumors.

    The study is a dose-escalation and dose-expansion study to evaluate the safety, tolerability, and pharmacokinetics of ASKG915 as a single agent or in combination with standard of care (SOC) in patients with selected types of advanced solid tumors.

    Stage
    Phase 1
    Ages
    18 and older
    Site
    Columbia University Irving Medical Center, New York, New York
    Locations
    4 in total
    Run by
    AskGene Pharma, Inc.
  13. JAB-23E73 in Adult Participants With Advanced Solid Tumors With KRAS Alteration

    This study is to evaluate the safety and tolerability of pan-KRAS inhibitor JAB-23E73 in adult participants with advanced solid tumors

    Stage
    Phase 1
    Ages
    18 and older
    Site
    Mayo Clinic, Rochester, Minnesota
    Locations
    4 in total
    Run by
    Jacobio Pharmaceuticals Co., Ltd.
  14. A Clinical Study of YL205 in Patients With Advanced Solid Tumors

    This study is a multicenter, open-label, phase I/II study of YL205 in China to evaluate the safety, tolerability, PK characteristics and preliminary efficacy of YL205 in the following selected patients with advanced solid tumors.

    Stage
    Phase 1
    Ages
    18 and older
    Site
    Sarah Cannon Research Institute (SCRI)- Denver, Denver, Colorado
    Locations
    43 in total
    Run by
    MediLink Therapeutics (Suzhou) Co., Ltd.
  15. BTM-3566 in Advanced Solid Tumors

    The goal of this clinical trial is to learn about what doses of BTM-356 are safe to use in adults with advanced cancers in solid tumors. It will also learn about how effective different doses of BTM-3566 are in treating cancer. The main questions it aims to answer are: What adverse events and toxic…

    Stage
    Phase 1
    Ages
    18 and older
    Site
    NEXT Houston, Houston, Texas
    Locations
    2 in total
    Run by
    Bantam Pharmaceuticals
  16. PAS-004 in Patients With Advanced Solid Tumors

    The main purpose of this clinical trial is to test PAS-004 in people with advanced solid tumors with rat sarcoma virus (RAS), neurofibromatosis type I (NF1), or rapidly accelerated fibrosarcoma (RAF) mutations. The main questions it aims to answer are: * How well participants are able tolerate diff…

    Stage
    Phase 1
    Ages
    18 and older
    Site
    MBAL Sveta Sofia, Sofia,
    Locations
    7 in total
    Run by
    Pasithea Therapeutics Corp.
  17. A Phase 1/2a Study of DB-1311/BNT324 in Advanced/Metastatic Solid Tumors

    This is a dose-escalation and dose-expansion Phase 1/2a trial to evaluate the safety and tolerability of DB-1311/BNT324 in subjects with advanced solid tumors.

    Stage
    Phase 1
    Ages
    18 and older
    Site
    Research Site 111, Tucson, Arizona
    Locations
    107 in total
    Run by
    DualityBio Inc.
  18. 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
    Cedars Sinai Medical Center, Los Angeles, California
    Locations
    8 in total
    Run by
    LigaChem Biosciences, Inc.
  19. 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
    Sarah Cannon Research Institute at HealthOne, Denver, Colorado
    Locations
    10 in total
    Run by
    Eikon Therapeutics
  20. To Evaluate the Efficacy, Safety, Tolerability and Pharmacokinetic Profile of ABN401 in Patients With Advanced Solid Tumors Harboring c-MET Dysregulation

    ABN401-003 is a Phase 2 clinical study to assess efficacy, safety, tolerability and pharmacokinetic profile of ABN401 (vabametkib) in specific populations of advance solid tumors with c-MET alterations as monotherapy.

    Stage
    Phase 2
    Ages
    18 and older
    Site
    Cancer Care of North Florida, PA (Lake City Cancer Care, LLC) - Medical Oncology, Lake City, Florida
    Locations
    24 in total
    Run by
    Abion Inc
  21. Pan-RAS Inhibitor YL-17231 in Patients With Advanced Solid Tumors Harboring Mutations in KRAS, HRAS, or NRAS

    This study will evaluate the safety, tolerability, drug levels, pharmacodynamic effects, and clinical activity of YL 17231 in patients with advanced solid tumors harboring mutations in KRAS, HRAS, or NRAS.

    Stage
    Phase 1
    Ages
    18 and older
    Site
    The Lindner Center for Research & Education at The Christ Hospital, Cincinnati, Ohio
    Locations
    3 in total
    Run by
    Shanghai YingLi Pharmaceutical Co. Ltd.
  22. Dose Escalation and Expansion Study Evaluating ODC-IL2 in Adult Patients With Advanced or Metastatic Solid Tumors

    This is a first-in-human, Phase I, multicenter, open-label, dose escalation study with dose expansion to evaluate the safety and antitumor activity of ODC-IL2 in patients with advanced or metastatic solid tumors. ODC-IL2 is a conditionally activated IL-2 prodrug and will be administered as a single…

    Stage
    Phase 1
    Ages
    18 and older
    Site
    HonorHealth, Scottsdale, Arizona
    Run by
    Trutino Biosciences Inc.

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.