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 3
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Study of STP938 (Dencatistat) in Advanced Solid Tumours
The Phase 1a part of the study is a dose escalation of STP938 as a monotherapy. The Phase 1b part of the study is a safety expansion cohort of STP938 as a monotherapy.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Comprehensive Hematology Oncology, LLC, St. Petersburg, Florida
- Locations
- 7 in total
- Run by
- Step Pharma, SAS
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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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MEM-288 Oncolytic Virus Alone and in Combination With Standard of Care Therapy in Advanced Solid Tumors
This is a multipart, open-label, multi-center dose escalation, dose expansion phase I clinical trial designed to evaluate the safety, tolerability, maximum tolerated dose (MTD), recommended phase 2 dose (RP2D), and preliminary efficacy of MEM-288 in patients with advanced solid tumors. Eligible sub…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Moffitt Cancer Center, Tampa, Florida
- Locations
- 2 in total
- Run by
- Memgen, Inc.
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An Extension Study for Patients Previously Enrolled in Studies With Pelabresib
The purpose of this study is to evaluate the long-term safety and the clinical benefit of pelabresib in patients with hematological and/or solid tumor indications or advanced malignancies. Additionally, participants previously enrolled in studies with pelabresib who received placebo or participants…
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- University of California LA, Los Angeles, California
- Locations
- 15 in total
- Run by
- Novartis Pharmaceuticals
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Dose Determining Study of EXS74539 (REC-4539) in Participants With Select Solid Tumors
The primary purpose of this study is to determine the safety, tolerability, and maximum tolerated dose (MTD) of EXS74539 (REC-4539) in participants with select solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Start Lacn, Los Angeles, California
- Locations
- 3 in total
- Run by
- Exscientia AI Ltd., a wholly owned subsidiary of Recursion Pharmaceuticals, Inc.
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Ex Vivo Expansion (ACT-X)
The purpose of this study is to understand how the body's immune cells respond to a new type of vaccine (neoantigen vaccine) designed to help the immune system recognize and fight cancer. To do this, the study team will collect a research specimen from participants to study their immune cells' reac…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Mayo Clinic in Florida, Jacksonville, Florida
- Run by
- Mayo Clinic
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PET [89Zr]DFO-starPEG in Solid Tumors
This is a first-in-human, pilot study of the novel PET-imaging radiotracer [89Zr]DFO-starPEG. The study is designed to obtain preliminary data to support future development of this agent as an imaging surrogate to visualize enhanced permeability and retention (EPR)-mediated tracer uptake before adm…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of California, San Francisco, San Francisco, California
- Run by
- Robert Flavell, MD, PhD
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A Study to Evaluate the Safety, Tolerability, and Efficacy of MORAb-202 (Herein Referred to as Farletuzumab Ecteribulin), a Folate Receptor Alpha (FRα)-Targeting Antibody-drug Conjugate (ADC) in Participants With Selected Tumor Types
The primary objectives of the study are: (1) in the dose-escalation part: to evaluate safety and tolerability and to determine the recommended Phase 2 dose (RP2D) of farletuzumab ecteribulin (MORAb-202) in participants with selected tumor types (ovarian cancer [OC], endometrial cancer [EC], non-sma…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Stanford Women's Cancer Center, Palo Alto, California
- Locations
- 58 in total
- Run by
- Eisai Inc.
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Let's Get REAL: Family Health Communication Tool in Pediatric Stem Cell Transplant and Cellular Therapy
The investigators will conduct a pilot feasibility and efficacy trial of a newly developed family health communication tool (called Let's Get REAL) in increasing youth involvement in real-time stem cell transplant and cellular therapy decisions (SCTCT). The investigators will pilot the intervention…
- Stage
- Not phased
- Ages
- 8 and older
- Site
- Washington University School of Medicine, St Louis, Missouri
- Run by
- Washington University School of Medicine
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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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VITAS: Atezolizumab in Combination With Chemotherapy for Pediatric Relapsed/Refractory Solid Tumors
This trial is a multi-center, non-randomized, open-label Phase I/II study evaluating the feasibility and efficacy of vincristine, irinotecan, temozolomide, and atezolizumab in children with relapsed/refractory solid tumors.
- Stage
- Phase 1
- Ages
- 0 to 30
- Site
- Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois
- Locations
- 7 in total
- Run by
- University of Texas Southwestern Medical Center
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5-Azacitidine Plus PD-1/PD-L1 Inhibitor With PD-1/PD-L1 Refractory Tumors
This is a Phase I study to determine the optimal biological dose (OBD) of 5-Azacitidine in combination with PD-1/PD-L1 inhibitors in patients with tumors refractory to PD-1/PD-L1 inhibitors, for which such treatments have been approved.
- Stage
- Phase 1
- Ages
- 18 to 99
- Site
- University of Iowa Health Care, Iowa City, Iowa
- Run by
- Mohammed Milhem
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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
- 20 in total
- Run by
- Astellas Pharma Inc
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Givastomig Combined With Nivolumab and Chemotherapy in Adults With CLDN18.2 Positive Metastatic Gastric Cancer (GIVA-2)
The goal of this clinical trial is to learn if givastomig in combination with standard therapy works to treat adults with cancer in the stomach and/or esophagus (GEA adenocarcinoma). It will also help the researchers to learn more about the safety of givastomig. The main questions it aims to answer…
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- I-Mab Site 1016, Goodyear, Arizona
- Locations
- 6 in total
- Run by
- I-Mab Biopharma US Limited
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Brodalumab in the Treatment of Immune-Related Adverse Events
The purpose of this study is to test the safety and effectiveness of using brodalumab in patients who develop side effects from cancer immune therapy. Immune-related side effects are due to activation of the immune system in patients who previously received immunotherapy and the goal of this study …
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Columbia University Irving Medical Center, New York, New York
- Run by
- Brian Henick, MD
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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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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 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
- 19 in total
- Run by
- Teligene US
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Trial to Evaluate the Safety & Tolerability of JBZ-001 in Pts With Advanced Solid and Hematological Malignancies
This will be a phase 1, open-label, dose-escalation and expansion, FIH trial to evaluate the safety, tolerability, PK, PD, and preliminary efficacy of JBZ-001, a DHODH inhibitor, in patients with refractory solid and hematological malignancies. The study design includes two independent parts: dose …
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- The Ohio State University, Columbus, Ohio
- Locations
- 2 in total
- Run by
- Jabez Bioscience, Inc
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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.
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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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A Study of Azenosertib (ZN-c3) in Patients With Ovarian Cancer
This is a Phase 1b open-label, multicenter study, evaluating the safety, tolerability, preliminary clinical activity, pharmacokinetics (PK), and pharmacodynamics of azenosertib (ZN-c3) in combination with other drugs.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Site 0264, Aurora, Colorado
- Locations
- 24 in total
- Run by
- K-Group, Beta, Inc., a wholly owned subsidiary of Zentalis Pharmaceuticals, Inc
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Open-Label Study to Evaluate the Safety, Tolerability, PK, and Efficacy of INX-315 in Patients With Advanced Cancer
Incyclix Bio (Incyclix) is developing INX-315 as an oral, small molecule inhibitor of cyclin dependent kinase 2 (CDK2) for the treatment of human cancers. This first-in-human study is designed to evaluate the safety, tolerability, pharmacokinetics (PK) and preliminary antitumor activity of INX-315 …
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Florida Cancer Specialists, Orlando, Florida
- Locations
- 18 in total
- Run by
- Incyclix Bio
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A Phase 1/2 Study of BHV-1510 (Previously PBI-410) in Advanced Solid Tumors
This is a Phase 1/2, first in human (FIH), open-label, multicenter study of BHV-1510 monotherapy and in Combination with Cemiplimab in participants with previously treated, advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Site-113, Duarte, California
- Locations
- 17 in total
- Run by
- Biohaven Therapeutics Ltd.
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.