Advanced Solid Tumor Clinical Trials
115 studies are recruiting for advanced solid tumor 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
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Phase 1 Study of Intratumoral Administration of VAX014 With Expansion in Combination With a Checkpoint Inhibitor in Subjects With Advanced Solid Tumors
The purpose of this research study is to evaluate the safety, tolerability and activity of VAX014 for intratumoral injections (VAX014) as a single agent as well as in combination with Investigator's choice of nivolumab or pembrolizumab in patients with advanced solid tumors. VAX014 is a targeted on…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of Arizona Cancer Center, Tucson, Arizona
- Locations
- 8 in total
- Run by
- Vaxiion Therapeutics
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A Study of BGB-B455 in Adults With Advanced or Metastatic Solid Tumors
The goal of this clinical trial is to learn if BGB-B455 can treat advanced or metastatic solid tumors expressing claudin 6 (CLDN6), a protein that is found on some tumors. The main questions it aims to answer are: * What is the recommended dosing for BGB-B455? * What medical problems do participant…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Adventhealth, Celebration, Florida
- Locations
- 11 in total
- Run by
- BeOne Medicines
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A Study of Tulmimetostat DZR123 (CPI-0209) in Patients With Advanced Solid Tumors and Lymphomas
The purpose of this open-label, first-in-human (FIH) trial is to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and preliminary antitumor activity of DZR123 (Tulmimetostat, CPI-0209), both as monotherapy and in combination with enzalutamide, in patients with advanced solid t…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Winship Cancer Institute of Emory University, Atlanta, Georgia
- Locations
- 80 in total
- Run by
- Novartis Pharmaceuticals
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Safety, Pharmacokinetics, and Efficacy of AI-081, a Bispecific Antibody for PD-1 And VEGF in Advanced Solid Tumors
BIPAVE-001 is a Phase 1-2 study for evaluating the safety, pharmacokinetics (PK), and efficacy of AI-081 in solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of Alabama at Birmingham, Birmingham, Alabama
- Locations
- 21 in total
- Run by
- OncoC4, Inc.
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Metformin Combined With Chemotherapy and/or Immunotherapy in Solid Malignancies
The goal of this clinical trial is to evaluate the safety of Metformin alone and in combination with chemotherapy or immunotherapy in patients with solid tumor cancers. The main questions it aims to answer are: * what are the toxicities of metformin at multiple dose levels * what is the maximum tol…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Karmanos Cancer Institute at McLaren Bay Region, Bay City, Michigan
- Locations
- 10 in total
- Run by
- Barbara Ann Karmanos Cancer Institute
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Study of Orally Administered MOMA-313 in Participants With Advanced or Metastatic Solid Tumors
This Phase 1, multi-center, open-label, dose escalation and dose optimization study is designed to assess the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PDx), and preliminary clinical activity of MOMA-313 administered orally as a single agent or combination therapy in patients w…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Investigative Site #108, Goodyear, Arizona
- Locations
- 18 in total
- Run by
- MOMA Therapeutics
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Study of Orally Administered MOMA-341 in Participants With Advanced or Metastatic Solid Tumors
This Phase 1, multi-center, open-label, dose escalation and dose optimization study is designed to assess the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PDx), and preliminary clinical activity of MOMA-341 administered orally as a single agent or combination therapy in patients w…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Investigative Site #132, Phoenix, Arizona
- Locations
- 15 in total
- Run by
- MOMA Therapeutics
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A Study of CHS-114 (Tagmokitug) in Combination With Toripalimab and/or Other Treatments in Participants With Advanced Solid Tumors
The main purpose of this study is to evaluate the safety and preliminary efficacy of CHS-114 in combination with toripalimab and/or other standard of care (SOC) compound(s) in participants with advanced or metastatic solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- City of Hope, Duarte, California
- Locations
- 30 in total
- Run by
- Coherus Oncology, Inc.
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A First-in-Human (FIH) Study of BG-C137, an Anti-Fibroblast Growth Factor Receptor 2b (FGFR2b) Antibody Drug Conjugate, in Participants With Advanced Solid Tumors
The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics, and preliminary antitumor activity of BG-C137 alone and in combination with anticancer agents in participants with advanced solid tumors. The study will be conducted in two phases: Phase 1a (…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Usc Norris Comprehensive Cancer Center (Nccc), Los Angeles, California
- Locations
- 52 in total
- Run by
- BeOne Medicines
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A Study of PYX-201 in Advanced Solid Tumors
The primary objectives of this study are to determine the recommended dose(s) of PYX-201 for participants with recurrent/metastatic (R/M) solid tumors, and to determine the objective response rate (ORR) in participants treated with PYX-201 as a single agent.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- HonorHealth Research Institute, Scottsdale, Arizona
- Locations
- 29 in total
- Run by
- Pyxis Oncology, Inc
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SNV1521 in Participants With Advanced Solid Tumors
This study is testing a new medicine, SNV1521, for people with advanced cancers. The researchers want to find out if SNV1521 is safe, well-tolerated, and effective in treating solid tumors. They are investigating different doses in order to find the most effective and safe one. They are also invest…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Smilow Cancer Hospital at Yale New Haven, New Haven, Connecticut
- Locations
- 25 in total
- Run by
- Synnovation Therapeutics, Inc.
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Safety, Pharmacokinetics (PK), and Efficacy of ONC 841 in Advanced Solid Tumors
This is a Phase I/II open label study of intravenous (IV) infusion of ONC-841 as a single agent or in combination in patients with advanced/metastatic solid tumors. The study will evaluate seven dose levels of ONC-841. The Phase 1 part is dose escalation with 7 dose levels of ONC-841 and the dose e…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of California at Davis Cancer Center, Sacramento, California
- Locations
- 8 in total
- Run by
- OncoC4, Inc.
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A Study of XB628 Alone and in Combination With Zanzalintinib in Participants With Recurrent Advanced or Metastatic Solid Tumors
This study consists of a Dose-Escalation stage and a Dose Expansion stage. The primary purpose of the dose escalation stage is to determine the maximum tolerated dose (MTD) and/or recommended dosage(s) for expansion (RDE[s]); and the dose expansion stage is to evaluate the preliminary antitumor act…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Exelixis Clinical Site #5, San Francisco, California
- Locations
- 11 in total
- Run by
- Exelixis
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XTX301 in Patients With Advanced Solid Tumors
This is a first-in-human, multicenter, Phase 1/2, open-label study designed to evaluate the safety and tolerability of XTX301 as monotherapy in patients with advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of California, Davis Comprehensive Cancer Center, Sacramento, California
- Locations
- 12 in total
- Run by
- Xilio Development, Inc.
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A Study of YL201 in Patients With Advanced Solid Tumors
This is a phase 1, multicenter, nonrandomized, open-label, first-in-human study of YL201 conducted in China and the United States. The study will include 2 parts: a dose escalation part (Part 1) followed by a dose expansion part (Part 2). Part 1 will estimate the MTD/RED(s) in dose escalation cohor…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- 002, Fair Oaks, California
- Locations
- 45 in total
- Run by
- MediLink Therapeutics (Suzhou) Co., Ltd.
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BAL0891 in Patients With Advanced Solid Tumors or Relapsed or Refractory Acute Myeloid Leukemia
This study is a multiple cohort, multicenter, open-label Phase 1 study with dose-escalation substudies investigating intravenous (IV) BAL0891 as monotherapy, and in combination with tislelizumab or paclitaxel, to determine the safety and tolerability of increasing doses of BAL0891 in patients with …
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Yale New Haven Hospital, New Haven, Connecticut
- Locations
- 17 in total
- Run by
- SillaJen, Inc.
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A First-in-human Study of PARP1 Selective Inhibitor, IMP1734, in Participants With Advanced Solid Tumors
This study investigates the safety and tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of EIK1003 in participants with advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 to 89
- Site
- The University of Arizona Cancer Center, Tucson, Arizona
- Locations
- 57 in total
- Run by
- Eikon Therapeutics
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First-in-Human Study of PLX-61639 in Locally Advanced or Metastatic Solid Tumors
A multicenter, single-arm, first-in-human study to investigate the safety, pharmacokinetics, and preliminary antitumor activity of PLX-61639 in participants with locally advanced or metastatic, relapsed/refractory, SMARCA4-deficient solid tumors who are intolerant of or have failed available, appro…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Research Site, Scottsdale, Arizona
- Locations
- 10 in total
- Run by
- Plexium, Inc.
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Study of CX-5461 in Patients With Solid Tumours and BRCA1/2, PALB2 or Homologous Recombination Deficiency (HRD) Mutation
This is an open-label, multi-center, phase 1b study designed to determine a tolerable dose of CX-5461 administered by IV infusion on Day 1 and Day 8 of a 28-day cycle in patients with selected solid tumours and associated mutations for future Phase II trials. The safety and tolerability of CX-5461,…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of California, Los Angeles, Santa Monica, California
- Locations
- 8 in total
- Run by
- Senhwa Biosciences, Inc.
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Hyperpolarized 13C MRI as a Biomarker in Advanced Solid Tumors
This is a single center prospective imaging study investigating the utility of hyperpolarized 13C-pyruvate +/-13C,15N-Urea/ metabolic MR imaging. The current protocol will serve as a companion imaging biomarker study paired with standard of care (SOC) therapeutics, as well as investigational therap…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of California, San Francisco, San Francisco, California
- Run by
- Robert Bok, MD, PhD
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A Study to Evaluate PEEL-224 in Patients With Advanced Solid Tumors
This is a first-in-human, dose escalation, repeat-dose, multi-center, open-label study evaluating safety, tolerability, PK, and preliminary antitumor activity of PEEL-224 in patients with advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- HonorHealth Research Institiute, Scottsdale, Arizona
- Locations
- 8 in total
- Run by
- Peel Therapeutics Inc
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Safety, Pharmacokinetics, and Clinical Activity of LP-284 in Adult Patients With Relapsed or Refractory Lymphomas and Solid Tumors
The goal of this clinical trial is to evaluate the safety and tolerability of escalating doses of LP-284 and to determine the maximum tolerated dose (MTD) and the recommended Phase 2 dose (RP2D) in patients with relapsed or refractory (R/R) lymphomas and solid tumors. The secondary objectives are t…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- START Mountain Region, West Valley City, Utah
- Run by
- Lantern Pharma Inc.
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Study in Advanced Solid Tumor Patients
The study will be conducted in 2 phases: Phase 1: Dose-escalation and Dose Level Expansion, Phase 1 will determine the maximum tolerated dose (MTD) and/or recommended dose for expansion (RDE). Phase 2: Tumor-Specific Expansions with Dose Optimization, Phase 2 will further evaluate CLIO-8221 in tumo…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Sarah Cannon Research Institute 335 24th Avenue North, Suite 400, Nashville, Tennessee
- Locations
- 11 in total
- Run by
- Callio Therapeutics
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GTB-5550 in Advanced Solid Tumors
This is a first-in-human Phase 1a/1b trial of a B7-H3-targeted natural killer (NK) cell engager, referred to as a TriSpecific Killer Engager (TriKE), for the treatment of select solid tumor cancers. To be considered for the study, a patient must be 18 years or older, have histologically or cytologi…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Masonic Cancer Center at University of Minnesota, Minneapolis, Minnesota
- Run by
- Masonic Cancer Center, University of Minnesota
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A Study of Oral 7HP349 (Alintegimod) in Combination With Ipilimumab Followed by Nivolumab Monotherapy
This study is an open-label Phase Ib (Part A) dose escalation followed by a blinded, randomized, multi cohort Phase 2a (Part B) comparison of combination vs. reference regimens. Currently study will only be enrolling the Phase 1b and the Phase 2a protocol requirements will be added to the study nea…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of Colorado Cancer Center, Aurora, Colorado
- Locations
- 5 in total
- Run by
- 7 Hills Pharma, LLC
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.