Advanced Solid Tumor Clinical Trials
122 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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Study of STK-012 Alone and With Other Treatments in Patients With Advanced Lung Cancer and Other Cancers
This is a phase 1/2, multicenter, open-label study. The phase 1 portion is a dose escalation and expansion study of STK-012 as monotherapy and in combination therapy in patients with selected advanced solid tumors. The phase 2 portion is a randomized study of STK-012 in combination with standard of…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of Arizona Cancer Center, Tucson, Arizona
- Locations
- 47 in total
- Run by
- Synthekine
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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 Phase 1 Study of BMS-986500 as Monotherapy or Combination Therapy in Advanced Solid Tumors
The purpose of this study is to assess BMS-986500 as monotherapy in advanced solid tumors and as combination therapy in CDK4/6 inhibitor pre-treated advanced breast cancer.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of Alabama at Birmingham, Birmingham, Alabama
- Locations
- 21 in total
- Run by
- Bristol-Myers Squibb
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A Phase 1 Clinical Study of NXP900 in Subjects With Advanced Cancers
This is a multi-center, first-in-human, open label, dose escalation (Part A) and expansion (Part B) Phase 1 study in subjects with advanced solid tumors and in subjects with solid tumors with selected genetic alterations that are either direct (YES1 amplification) or dependent (Hippo Pathway altera…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Mayo Clinic, Phoenix, Arizona
- Locations
- 15 in total
- Run by
- Nuvectis Pharma, 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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FORTRAS: A Study of MSK-TCR5 in People With Solid Tumor Cancers
The purpose of this study is to test the safety of MSK-TCR5 in participants with advance solid tumor cancer that has a KRAS, HRAS, or NRAS G12D mutation.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Memorial Sloan Kettering at Basking Ridge (Limited Protocol Activities), Basking Ridge, New Jersey
- Locations
- 7 in total
- Run by
- Memorial Sloan Kettering Cancer Center
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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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Dose-Escalation and Dose-Expansion Study of BSI-082 Monotherapy and Combined Therapy in Patients With Advanced or Metastatic Solid Tumors
This is a study that will enroll patients with cancer who have tumors that may have spread. The patients will know what medication they are being given. There will be 2 parts to the study. For the first part of the study only one medication will be taken, and the dose changed to a higher dose over …
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of Texas Health Science Center at San Antonio, San Antonio, Texas
- Run by
- Lei Zheng
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Study of Ifinatamab Deruxtecan (DS-7300a, I-DXd) in Participants With Advanced Solid Malignant Tumors
This is a single group study of participants with advanced solid tumors who have not been cured by other treatments. It is the first time the drug will be used in humans, and will be in two parts. The primary purpose of the parts are: * Dose Escalation Part: To evaluate the safety and tolerability …
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Sarah Cannon Research Institute at HealthONE, Denver, Colorado
- Locations
- 28 in total
- Run by
- Daiichi Sankyo
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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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Pemigatinib + Afatinib in Advanced Refractory Solid Tumors
This study is researching whether the combination of Afatinib and Pemigatinib is safe and effective in FGFR altered unresectable or metastatic advanced solid tumors. The study is also trying to discover the highest doses of the study drugs that can be administered without causing any intolerable si…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Massachusetts General Hospital, Boston, Massachusetts
- Run by
- Massachusetts General Hospital
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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 With NKT3964 for Adults With Advanced/Metastatic Solid Tumors
The goal of the Dose Escalation phase of the study is to evaluate the safety, tolerability, pharmacokinetics (PK) and preliminary anti-tumor activity to determine the preliminary recommended dose for expansion (RDE) of NKT3964 in adults with advanced or metastatic solid tumors. The goal of the Expa…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of Arkansas Medical School, Little Rock, Arkansas
- Locations
- 19 in total
- Run by
- NiKang Therapeutics, 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.