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 now recruiting
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NCI Childhood Cancer Data Initiative (CCDI) Led Pediatric, Adolescent, and Young Adult Rare Cancer Registry for Very Rare Solid Tumors
Background: All childhood cancers are rare, but some are called very rare. Very rare cancers are diagnosed in 2 or fewer out of 1 million people each year. Researchers want to gather data so they can learn more about these very rare cancers. They hope to use the data to develop future treatments. O…
- Stage
- Not phased
- Ages
- 0 to 120
- Site
- National Institutes of Health Clinical Center, Bethesda, Maryland
- Run by
- National Cancer Institute (NCI)
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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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Indocyanine Green (ICG) Guided Sentinel Lymph Node Mapping for Pediatric Visceral Solid Tumors
The purpose of the study is to find out the usefulness and safety of a dye called Indocyanine Green (ICG for short). This dye will be used to help the surgeon find lymph nodes draining solid tumors inside the abdomen that need to be removed. This may also help the surgeon to find if the cancer has …
- Stage
- EARLY_Phase 1
- Ages
- Up to 20
- Site
- Lurie Children's Hospital, Chicago, Illinois
- Locations
- 3 in total
- Run by
- St. Jude Children's Research Hospital
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A Study With NKT3964 for Adults With Advanced/Metastatic Solid Tumors
The goal of the Monotherapy Dose Escalation phase (Part 1) 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.…
- Stage
- Phase 1
- Ages
- 19 and older
- Site
- University of Arkansas Medical School, Little Rock, Arkansas
- Locations
- 20 in total
- Run by
- NiKang Therapeutics, Inc.
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Natural History and Biospecimen Acquisition for Children and Adults With Rare Solid Tumors
Background: Approximately 150 cases of cancer per one million per year are considered rare cancers. While all tumors originate from genetic changes, a small percentage of these tumors are familial. Researchers want to study these changes in biological samples from people with rare tumors in order t…
- Stage
- Not phased
- Ages
- 0 and older
- Site
- National Institutes of Health Clinical Center, Bethesda, Maryland
- Locations
- 3 in total
- Run by
- National Cancer Institute (NCI)
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Multi Tumor-Associated Antigen-Specific T Lymphocytes to Treat Patients With High Risk Solid Tumors
This is an open-label phase I dose-escalation study to evaluate the safety of partially human leukocyte antigen (HLA)-matched multi tumor-associated antigen-specific T cell (TAA-T) therapy following lymphodepleting conditioning with or without local tumor ablation for pediatric and adult patients w…
- Stage
- Phase 1
- Ages
- 1 to 70
- Site
- Children's National Hospital, Washington D.C., District of Columbia
- Run by
- Children's National Research Institute
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A Study to Find a Suitable Dose of ASP5834 in Adults With Solid Tumors
Genes contain genetic code which tell the body which proteins to make. Many types of cancer are caused by changes, or mutations, in a gene called KRAS. Researchers are looking for ways to stop the actions of abnormal proteins made from the mutated KRAS gene. ASP5834 is being studied in people with …
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- UCLA Santa Monica Hematology Oncology, Santa Monica, California
- Locations
- 22 in total
- Run by
- Astellas Pharma Inc
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SumMET: Study of [225Ac]Ac-FL-261 in Participants With Solid Tumors Overexpressing c-MET
This is a first-in-human, multicenter, open-label Phase 1/2 study designed to evaluate the safety, efficacy, and tolerability of [225Ac]Ac-FL-261, a targeted radioligand therapy directed at c-MET, in participants with advanced or metastatic solid tumors. Phase 1 will identify the recommended dose t…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Full-Life Technologies Investigational Site, Minneapolis, Minnesota
- Locations
- 2 in total
- Run by
- Full-Life Technologies UK Limited
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A Phase 1/2 Trial of TER-2013 in Patients With Solid Tumors Harboring AKT/PI3K/PTEN Pathway Alterations
This is a Phase 1/2, open-label, multicenter study evaluating the safety, tolerability, pharmacokinetics, pharmacodynamics and anti-tumor activity of TER-2013 in patients with advanced solid tumors harboring AKT/PI3K/PTEN pathway alterations.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- City of Hope, Duarte, California
- Locations
- 25 in total
- Run by
- Terremoto Biosciences Inc.
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A Study of Freeze-Dried Miracle Fruit (MiraBurst) on Participants Receiving Cancer Treatment
This study is for people with a diagnosis of solid tumor cancer who are experiencing changes in taste perception due to cancer treatment. Changes in taste perception, also known as dysgeusia, is a frequent side effect of cancer treatment and can significantly impacts quality of life. These alterati…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Cleveland Clinic Foundation, Cleveland, Ohio
- Run by
- Case Comprehensive Cancer Center
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A Study of DS-3939a in Participants With Solid Tumors
The primary purpose of the study is to evaluate the safety, tolerability, and efficacy of DS-3939a in combination with other anticancer agents or as a monotherapy in participants with solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Highlands Oncology Group (Hog) - Fayetteville, Fayetteville, Arkansas
- Locations
- 76 in total
- Run by
- Daiichi Sankyo
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A Study to Evaluate the Efficacy and Safety of TL118 in Solid Tumors Patients
The main objective of the study will be to evaluate the efficacy of TL118 in participants with solid tumors harboring NTRK gene fusions
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- Adventist Health Glendale, Glendale, California
- Locations
- 20 in total
- Run by
- Teligene US
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Phase I Trial to Determine the Dose and Evaluate the PK and Safety of Lutetium Lu 177 Edotreotide Therapy in Pediatric Participants With SSTR-positive Tumors
The purpose of the study is to determine the appropriate pediatric dosage and evaluate the pharmacokinetics (PK) and safety of Lutetium Lu 177 Edotreotide Targeted Radiopharmaceutical Therapy (RPT) as a monotherapy or following standard of care (SoC) in participants ≥2 to <18 years of age with soma…
- Stage
- Phase 1
- Ages
- 2 to 18
- Site
- Lucile Packard Children's Hospital at Stanford, Palo Alto, California
- Locations
- 9 in total
- Run by
- ITM Solucin GmbH
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Study of Induction PD-1 Blockade in Subjects With Locally Advanced Mismatch Repair Deficient Solid Tumors
The purpose of this study is to find out whether the study drug, TSR-042, followed by standard chemoradiotherapy (the chemotherapy drug capecitabine + radiation therapy) and standard surgery is an effective treatment for advanced dMMR solid tumors. The study will also look at the safety of the stud…
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- Hartford Healthcare (Data Collection), Hartford, Connecticut
- Locations
- 10 in total
- Run by
- Memorial Sloan Kettering Cancer Center
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A Study of Selinexor in People With Wilms Tumors and Other Solid Tumors
The purpose of this study is to find out whether selinexor is an effective treatment for people who have a relapsed/refractory Wilms tumor, rhabdoid tumor, MPNST, BCOR-driven sarcoma, or another solid tumor that makes a higher than normal amount of XPO1 or has genetic changes that increase the acti…
- Stage
- Phase 2
- Ages
- 1 and older
- Site
- Children's Hospital of Los Angeles (Data Collection Only), Los Angeles, California
- Locations
- 16 in total
- Run by
- Memorial Sloan Kettering Cancer Center
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A Study to Evaluate Safety, Pharmacokinetics, and Activity of GDC-7035 as a Single Agent and in Combination in Patients With Advanced Solid Tumors
This is a first-in-human Phase I/II, open-label, multicenter, dose-escalation and expansion study designed to evaluate the safety, pharmacokinetics, and preliminary activity of GDC-7035 as a single agent and in combination with other anti-cancer therapies in participants with advanced or metastatic…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- UC San Diego Moores Cancer Center, La Jolla, California
- Locations
- 49 in total
- Run by
- Genentech, Inc.
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DESCANSO, a Mental Health Intervention for Depression, Insomnia, and Fatigue Symptoms in Latino People With Cancer
The purpose of this study is to improve ways of providing mental health support to Spanish-speaking Latino participants who have cancer and experience depression, insomnia, and fatigue. Investigators will test a special mental health intervention called DESCANSO/REST (Depresión/Depressed Mood, Cans…
- Stage
- Not phased
- Ages
- 21 to 100
- Site
- Memorial Sloan Kettering Cancer Center Basking Ridge (Limited Protocol Activities), Basking Ridge, New Jersey
- Locations
- 8 in total
- Run by
- Ponce Medical School Foundation, Inc.
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Dabrafenib and/or Trametinib Rollover Study
This study is to provide access for patients who are receiving treatment with dabrafenib and/or trametinib in a Novartis-sponsored Oncology Global Development, Global Medical Affairs or a former GSK-sponsored study who have fulfilled the requirements for the primary objective, and who are judged by…
- Stage
- Phase 4
- Ages
- 18 to 100
- Site
- Novartis Investigative Site, Toronto, Ontario
- Locations
- 38 in total
- Run by
- Novartis Pharmaceuticals
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STC-15 as a Part of Combination Therapy With Toripalimab in Selected Advanced Cancers and as Monotherapy in Participants With Selected Sarcomas
This early phase oncology trial will be conducted at various study centers to investigate the safety, tolerability, and antitumor activity of STC-15 (a METTL3 inhibitor) in combination with toripalimab (anti- programmed cell death 1 [PD-1]) in advanced unresectable or metastatic tumors. The Phase 2…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of California, San Francisco, San Francisco, California
- Locations
- 14 in total
- Run by
- STORM Therapeutics LTD
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Safety and Tolerability of TNG456 Alone and in Combination With Abemaciclib in Patients With Solid Tumors With MTAP Loss
This is a first in human study of TNG456 alone and in combination with abemaciclib in patients with advanced or metastatic solid tumors known to have an MTAP loss. The first part of the study is an open-label, dose escalation and the second part is an open label dose expansion in specific solid tum…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Mayo Clinic Scottsdale, Scottsdale, Arizona
- Locations
- 15 in total
- Run by
- Tango Therapeutics, Inc.
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Long-Term Follow-Up of Patients Who Have Participated in Children's Oncology Group Studies
This clinical trial keeps track of and collects follow-up information from patients who are currently enrolled on or have participated in a Children's Oncology Group study. Developing a way to keep track of patients who have participated in Children's Oncology Group studies may allow doctors learn …
- Stage
- Not phased
- Ages
- Any age
- Site
- Children's Hospital of Alabama, Birmingham, Alabama
- Locations
- 164 in total
- Run by
- Children's Oncology Group
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SMP-3124LP in Adults With Advanced Solid Tumors
An Open-label, Phase I Dose Escalation and Phase 2 Dose Expansion Study to Assess Safety, Tolerability, Preliminary Antitumor Activity of SMP 3124LP in Adults with Advanced Solid Tumors
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Cedars Sinai Medical Center, Los Angeles, California
- Locations
- 13 in total
- Run by
- Sumitomo Pharma America, 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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A Study of ASP3082 in Adults With Advanced Solid Tumors
This is an open-label study. This means that people in this study and clinic staff will know that people will receive ASP3082. The study aims to check how safe and well-tolerated ASP3082 is for people with advanced solid tumors that have a specific mutation called KRAS G12D. This study will be in 2…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- City of Hope National Medical Center, Duarte, California
- Locations
- 68 in total
- Run by
- Astellas Pharma Inc
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Phase 1/2 Trial of S241656 in Selected RAS/MAPK Mutation- Positive Malignancies
BDTX-4933-101 is a first-in-human, open-label, Phase 1/2 dose escalation, dose optimization and expansion study designed to evaluate the safety and tolerability of S241656 as monotherapy and in combination with other anti-cancer therapies in participants with selected advanced malignancies. The stu…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Banner Health- MD Anderson Cancer Center, Gilbert, Arizona
- Locations
- 49 in total
- Run by
- Institut de Recherches Internationales Servier
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.