Solid Tumor Clinical Trials
104 studies are recruiting for 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 4
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NEROFE and Doxorubicin in KRAS-mutated ST2-positive Solid Tumors
The goal of this clinical trial is to learn about the safety of NEROFE and doxorubicin and how well it works in patients with advanced/unresectable or metastatic solid KRAS-mutated and ST-positive solid tumors. The main question it aims to answer is to find the recommended dose and scheduled for th…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Georgetown Lombardi Comprehensive Cancer Center, Washington D.C., District of Columbia
- Run by
- Georgetown University
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Phase I Study of Tolododekin Alfa (ANK-101) in Advanced Solid Tumors
This is a Phase 1, multicenter, open-label dose escalation study to determine the safety and tolerability of intratumoral (IT) injection of tolododekin alfa (ANK-101) in participants with advanced solid tumors who have progressed during or after receiving standard of care (SOC) therapy or who will …
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- National Cancer Institute, Bethesda, Maryland
- Locations
- 5 in total
- Run by
- Ankyra Therapeutics, Inc
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Study of TJ033721 (Givastomig) in Subjects With Advanced or Metastatic Solid Tumors
This is an open label, multi-center, multiple dose Phase 1 study to evaluate the safety, tolerability, MTD PK, and PD of TJ033721 (givastomig) in subjects with advanced or metastatic solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Stern Center for Cancer Clinical Trials and Research, Orange, California
- Locations
- 21 in total
- Run by
- I-Mab Biopharma US Limited
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SB-4826 in Adult Participants With Locally Advanced or Metastatic Solid Tumors or Non-Hodgkin Lymphomas
The goal of this clinical trial is to learn what dose of the drug SB-4826 can be given safely in patients with solid tumors and non-Hodgkin lymphomas. This drug will be used alone in patients with solid tumors, and will be used alone or in combination with rituximab in patients with non-Hodgkin lym…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of California, San Diego, La Jolla, California
- Run by
- University of California, San Diego
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Sirolimus in Combination With Metronomic Chemotherapy in Children With High-Risk Solid Tumors
The primary objective of this study is to improve the 2-year progression-free survival in children with high-risk solid tumors who are administered a maintenance regimen with continuous sirolimus administered on a backbone of metronomic chemotherapy following the completion of "standard" therapy, a…
- Stage
- Phase 2
- Ages
- 1 to 30
- Site
- Aflac Cancer & Blood Disorders Centers, Atlanta, Georgia
- Locations
- 5 in total
- Run by
- Emory University
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Binary Oncolytic Adenovirus in Combination With HER2-Specific Autologous CAR VST, Advanced HER2 Positive Solid Tumors
This study is a first in human Phase 1 study that involves patients with a type of cancer called HER2 (Human Epidermal Growth Factor Receptor 2) positive cancer. This study asks patients to volunteer to take part in a research study investigating the safety and efficacy of using special immune cell…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Baylor St. Luke's Medical Center, Houston, Texas
- Run by
- Baylor College of Medicine
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FIH Study to Evaluate Safety, Tolerability, PK, PD & Preliminary Efficacy of AT03-65 With Advanced Solid Tumors
A Phase I, First-in-Human Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Preliminary Efficacy of AT03-65 in Adults with Advanced Solid Tumors
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Oregon Health & Science University (OHSU), Portland, Oregon
- Run by
- Axcynsis Therapeutics Pte Ltd
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A Study of CUSP06 in Patients With Platinum-Refractory/Resistant Ovarian Cancer and Other Advanced Solid Tumors
This phase 1 study will evaluate the safety, tolerability, pharmacokinetics, and efficacy of CUSP06 in patients with platinum-refractory/resistant ovarian cancer and other advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Sarah Cannon Research Institute at HealthONE, Denver, Colorado
- Locations
- 15 in total
- Run by
- OnCusp Therapeutics, Inc.
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Study of PAT in Patients With Solid Tumor Cancers
This is a single center Phase I study with extension of peptide alarm therapy (PAT) administered by intratumoral (IT) injection during the 1st course of a standard of care intravenous PD-1/PD-L1 inhibitor for the treatment of locally advanced or metastatic solid tumor cancers that has failed to be …
- 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 Pilot Prospective Clinical Trial Using Remote Monitoring for Cancer Patients Undergoing Outpatient Chemotherapy
A pilot study using remote monitoring technology developed by Locus Health in cancer patients undergoing chemotherapy treatment.
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Inova Schar Cancer Institute, Fairfax, Virginia
- Run by
- Inova Health Care Services
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Liquid Biopsy-informed Precision Oncology Study to Evaluate Utility of Plasma Genomic Profiling for Therapy Selection
Overall, this project has three main goals: first, to ascertain the feasibility of the approach and identify whether liquid biopsies can detect actionable mutations that can be utilized to generate precision oncology treatment recommendations. Second, the investigators will investigate whether enac…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Johns Hopkins University, Baltimore, Maryland
- Run by
- Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
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A Phase 2 Study of Avutometinib (VS-6766) Plus Defactinib
The purpose of this research is to test the effectiveness and safety of the study drugs (VS-6766 and defactinib), and see what effects (good and bad) these drugs have on the patients with endometrioid cancer, mucinous ovarian cancer, high-grade serous ovarian cancer, or solid gynecological cancer.
- Stage
- Phase 2
- Ages
- 18 to 99
- Site
- AdventHealth, Orlando, Florida
- Locations
- 4 in total
- Run by
- University of Oklahoma
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Umbilical Cord Blood Transplantation From Unrelated Donors
This study is being done to determine how long it takes for the engraftment (recovery of blood cell counts) of umbilical cord stem cells and also how often engraftment of umbilical cord stem cells transplanted from an unrelated donor fails. Another purpose will be to document the rate of disease-fr…
- Stage
- Not phased
- Ages
- 0 to 75
- Site
- Wilmot Cancer Institute, Rochester, New York
- Run by
- University of Rochester
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A Clinical Study of Intratumoral MVR-T3011 (T3011) Given as a Single Agent and in Combination With Intravenous Pembrolizumab in Participants With Advanced or Metastatic Solid Tumors
This is a Phase 1/2a, open-label, study to evaluate the safety and preliminary efficacy of intratumoral T3011 given alone and in combination with intravenous pembrolizumab in partients with advanced or metastatic solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Massachusetts General Hospital, Boston, Massachusetts
- Locations
- 9 in total
- Run by
- ImmVira Pharma Co. Ltd
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Safety and Preliminary Efficacy of OBT076 in Recurrent/Metastatic CD205+ Solid Tumors
The purpose of this study is to evaluate OBT076, which is a drug that combines an antibody with an anti-cancer drug. This class of drugs are called Antibody-Drug Conjugates (ADC). Antibodies are normally produced in the human body by the immune system to fight infections but can be designed to targ…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Institut Jules Bordet, Brussels,
- Locations
- 27 in total
- Run by
- Oxford BioTherapeutics Ltd
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A Beta-only IL-2 ImmunoTherapY Study
This is a Phase 1/2, multi-center, open-label, dose-escalation and expansion study to evaluate safety and tolerability, PK, pharmacodynamic, and early signal of anti-tumor activity of MDNA11 alone or in combination with a checkpoint inhibitor in patients with advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Sharp Memorial Hospital, San Diego, California
- Locations
- 27 in total
- Run by
- Medicenna Therapeutics, Inc.
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FIH Trial of VERT-002 in Patients With Locally Advanced or Metastatic Solid Tumors With MET Alterations
The goal of this clinical trial is to investigate the safety, the activity of VERT-002 (PFL-002), and the optimal safe dose to be used, in participants with solid tumors including non-small cell lung cancer.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Georgetown Lombardi Comprehensive Cancer Center, Washington D.C., District of Columbia
- Locations
- 19 in total
- Run by
- Pierre Fabre Medicament
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First-in-human Study of CRB-601-01 to Treat Patients With Advanced Solid Tumor.
The purpose of this study is to determine the safety, blood concentrations and treatment effect of CRB-601 in combination with immunotherapy in patients who have advanced solid tumors (cancer) and have exhausted other therapeutic options.CRB-601 targets a protein called avb8 integrin which is expre…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- SCRI- Lake Nona DDU, Orlando, Florida
- Locations
- 26 in total
- Run by
- Corbus Pharmaceuticals Inc.
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RAPA-201 Therapy of Solid Tumors
The therapy of solid tumors has been revolutionized by immune therapy, in particular, approaches that activate immune T cells in a polyclonal manner through blockade of checkpoint pathways such as PD-1 by administration of monoclonal antibodies. In this study, the investigators will evaluate the ad…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Hackensack University Medical Center, Hackensack, New Jersey
- Run by
- Rapa Therapeutics LLC
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Study to Evaluate IMP9064 as a Monotherapy or in Combination in Patients With Advanced Solid Tumors
This is a Phase 1/2, multicenter, open-label study to evaluate the safety and efficacy of IMP9064 as monotherapy or in combination with PARP inhibitor Senaparib in patients with advanced solid tumors
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Beijing Cancer Hospital, Beijing, Beijing Municipality
- Locations
- 8 in total
- Run by
- Impact Therapeutics, Inc.
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Study of TU2218 in Combination With KEYTRUDA®(Pembrolizumab) in Patients With Advanced Solid Tumors
This study consists of phase 1b and 2a to evaluate safety, Pharmacokinetics, and efficacy of TU2218 in combination with Pembrolizumab in patients with advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- CHA University Bundang Medical Center, Seongnam,
- Locations
- 11 in total
- Run by
- TiumBio Co., Ltd.
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BP1001-A in Patients With Advanced or Recurrent Solid Tumors
This is a phase I, open-label, study of BP1001-A in participants with advanced or recurrent solid tumors. The dose escalation phase will determine the safety and the maximum tolerated dose (MTD) or maximum administered dose (MAD) of BP1001-A as a single agent. After the MTD or MAD of BP1001-A is es…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Holy Cross Hospital, Silver Spring, Maryland
- Locations
- 4 in total
- Run by
- Bio-Path Holdings, Inc.
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Trial of DFP-14927 in Advanced Solid Tumors
This is a Phase I, open-label, single-arm, dose escalation study of DFP-14927 intravenous infusion administered to patients with refractory or relapsed solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- UCLA Department of Medicine- Hematology/Oncology, Los Angeles, California
- Locations
- 2 in total
- Run by
- Delta-Fly Pharma, Inc.
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Phase 1a and Phase 2 Study for Safety, Preliminary Efficacy, PK and PD of ST-067
This is a multiphase, multicenter study, which includes a Phase 1a open-label, dose escalation monotherapy study of ST-067 given as an SC injection with or without obinutuzumab [Gazyva®] pre-treatment, by IV infusion, and in combination with pembrolizumab. A Phase 2 monotherapy arm is also planned;…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- HonorHealth Research Institute, Scottsdale, Arizona
- Locations
- 6 in total
- Run by
- Simcha IL-18, Inc.
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A First-in-human (FIH), Phase I Study of PTX-912 in Patients with Locally Advanced/Metastatic Solid Tumors
The goal of this clinical trial is to evaluate the safety and tolerability of escalating doses of PTX-912 in patients with locally advanced or metastatic solid tumors. To evaluate the PK and immunogenicity profile of PTX-912. To evaluate the preliminary anti-tumor activity of PTX-912. Participants …
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- City of Hope National Medical Center, Duarte, California
- Locations
- 3 in total
- Run by
- Proviva 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.