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 now recruiting
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M0324 as Monotherapy and in Combination With Pembrolizumab or Chemotherapy in Participants With Selected Advanced Solid Tumors
The purpose of this first-in-human study is to identify a recommend dose(s) for subsequent larger studies (recommended dose(s) for expansion, RDE), examining increasing doses of M0324, primarily looking at safety, but also preliminary signs of efficacy, pharmacokinetics (PK), and pharmacodynamics (…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Yale Cancer Center, New Haven, Connecticut
- Locations
- 5 in total
- Run by
- EMD Serono Research & Development Institute, Inc.
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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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XTX501 in Patients With Metastatic Non-Small Cell Lung Cancer and Advanced Solid Tumors
This is a first-in-human, multicenter, Phase 1/2, open-label study designed to evaluate the safety and tolerability of XTX501 as monotherapy in participants with metastatic non-small cell lung cancer (NSCLC) and select advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Investigator Site, Canton, Ohio
- Locations
- 3 in total
- Run by
- Xilio Development, Inc.
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SW-682 in Advanced Solid Tumors
This is a first-in-human (FIH), Phase 1a/1b open-label, multicenter, dose escalation and dose expansion study of SW-682 in adult participants with metastatic or unresectable advanced solid tumors with or without Hippo pathway alterations that are refractory to, or have progressed, during or after a…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- HonorHealth Research Institute, Scottsdale, Arizona
- Locations
- 8 in total
- Run by
- SpringWorks Therapeutics, Inc., a healthcare company of Merck KGaA, Darmstadt, Germany
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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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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
- 60 in total
- Run by
- Synthekine
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Study of Lunresertib Alone or in Combination With RP-3500 or Zedoresertib (Debio 0123) in Patients With Advanced Solid Tumors
The primary purpose of this study is to assess the safety and tolerability of lunresertib alone and in combination with RP-3500 or in combination with zedoresertib in patients with eligible advanced solid tumors, determine the maximum tolerated dose (MTD) and assess preliminary anti-tumor activity.
- Stage
- Phase 1
- Ages
- 12 and older
- Site
- #1025, University of California San Francisco, San Francisco, California
- Locations
- 26 in total
- Run by
- Debiopharm International SA
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Study of SGN1 in Patients With Advanced Solid Tumor
Objectives:To assess the safety and tolerability followed by a dose expansion study to characterize safety, and preliminary efficacy of SGN1 in participants with refractory solid tumors. Study Rationale:The mechanism of action for SGN1 is based on the fact that most tumors are methionine dependent.…
- Stage
- Phase 1
- Ages
- 18 to 75
- Site
- Guangdong Clifford Hospital, Guangzhou, Guangdong
- Locations
- 9 in total
- Run by
- Guangzhou Sinogen Pharmaceutical Co., Ltd
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A Study of MGC026 in Participants With Advanced Solid Tumors
The study is designed to understand the safety, tolerability, pharmacokinetics, immunogenicity, and preliminary antitumor activity of vobramitamab tavatecan (MGC026) in participants with relapsed or refractory, unresectable, locally advanced or metastatic solid tumors The study has a dose escalatio…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- The Angeles Clinic and Research Institute, Los Angeles, California
- Locations
- 12 in total
- Run by
- MacroGenics
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Phase 1/2 Study of Intravenous Injection of STX-003 in Advanced Solid Tumors as Monotherapy or in Combination With Pembrolizumab
Protocol Title: Phase 1/2, Open-label, Multi-center, First-in-human Study of the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Anti-tumor Activity of STX-003 Delivered by Intravenous Injection in Patients with Advanced Solid Tumors as a Monotherapy or in Combination with Pembrolizuma…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- HonorHealth Research Institute, Scottsdale, Arizona
- Locations
- 4 in total
- Run by
- Strand Therapeutics Inc.
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A Study of DS-1103a Combination Therapy in Participants With Advanced Solid Tumors
This study will evaluate the safety and efficacy of DS-1103a combination therapy in participants with advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Florida Cancer Specialists, Sarasota, Florida
- Locations
- 15 in total
- Run by
- Daiichi Sankyo
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A Study of HER3-DXd in Subjects With Locally Advanced or Metastatic Solid Tumors
This is a proof-of-concept study designed to investigate HER3-DXd monotherapy in locally advanced unresectable or metastatic solid tumors. The study is enrolling cohorts of participants with melanoma [cutaneous/acral], squamous cell carcinomas of the head and neck (SCCHN), HER2-negative gastric can…
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- City of Hope, Duarte, California
- Locations
- 96 in total
- Run by
- Daiichi Sankyo
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Study of GS-5319 Given Alone or in Combination in Adults With Solid Tumors
The goal of this clinical study is to learn more about the study drug, GS-5319, its dosing, safety and tolerability when given as a single medication and as a combined medication in adults with solid tumors, where the participants show a specific gene alteration in the tumor. The gene helps produce…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Massachusetts General Hospital, Boston, Massachusetts
- Locations
- 12 in total
- Run by
- Gilead Sciences
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A Study of LY4052031 in Participants With Advanced or Metastatic Urothelial Cancer or Other Solid Tumors
The purpose of this study is to find out whether the study drug, LY4052031, is safe, tolerable and effective in participants with advanced, or metastatic solid tumors including urothelial cancer. The study is conducted in two parts - phase Ia (dose-escalation, dose-optimization) and phase Ib (dose-…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- City of Hope National Medical Center, Duarte, California
- Locations
- 39 in total
- Run by
- Eli Lilly and Company
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ARC101 in Advanced Solid Tumors
This first-in-human study will evaluate the safety, tolerability, pharmacokinetics, and antitumor activity of ARC101 in patients with advanced cancer.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Sunshine Coast University Private Hospital, Birtinya, Queensland
- Locations
- 13 in total
- Run by
- Third Arc Bio
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An Investigational Study of BGB-58067 As a Single Agent and in Combination With Anticancer Agents in Participants With Advanced Solid Tumors
This is an open-label, multicenter, first-in-human dose escalation and dose expansion study to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and preliminary antitumor activity of BGB-58067 alone, in combination with BG-89894 (discontinued), in combination with standard of c…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Cancer and Blood Specialty Clinic, Los Alamitos, California
- Locations
- 101 in total
- Run by
- BeOne Medicines
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GI-101/GI-101A as a Single Agent or in Combination With Pembrolizumab or Lenvatinib in Advanced Solid Tumors
The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics, and therapeutic activity of GI-101/GI-101A as a single agent or in combination with pembrolizumab or lenvatinib over a range of advanced and/or metastatic solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Tisch Cancer Institute (TCI), Icahn School of Medicine, New York, New York
- Locations
- 13 in total
- Run by
- GI Innovation, Inc.
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Study of ART6043 in Advanced/Metastatic Solid Tumors Patients (POLKA)
This interventional study will evaluate the safety, tolerability, pharmacokinetics, and preliminary efficacy of ART6043 as monotherapy or in combination with olaparib.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Hospital Universitario Clínico San Cecilio, Granada, Andalusia
- Locations
- 27 in total
- Run by
- Artios Pharma Ltd
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First-in-Human Study of DS-3939a in Participants With Advanced Solid Tumors
This study will evaluate the safety, tolerability, and efficacy of DS-3939a in participants with advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Florida Cancer Specialists, Sarasota, Florida
- Locations
- 61 in total
- Run by
- Daiichi Sankyo
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BGB-43395 Alone or as Part of Combination Therapies in Participants With Breast Cancer and Other Advanced Solid Tumors
This is a dose escalation and dose expansion study to compare how well BGB-43395, a selective cyclin-dependent kinase 4 (CDK4) inhibitor, works as monotherapy or in combination with fulvestrant, letrozole, or elacestrant in participants with hormone receptor positive (HR+) and human epidermal growt…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Sarah Cannon Research Institute (Scri) At Health One, Denver, Colorado
- Locations
- 61 in total
- Run by
- BeOne Medicines
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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 to Evaluate ARV-6723 Alone and With Pembrolizumab in Participants With Advanced Solid Tumors
This is a study to evaluate the safety and potential anti-tumor activity of an investigational drug called ARV-6723, in participants with advanced solid tumors. This is an open-label study which means that participants and study staff will know that all participants will receive ARV-6723. The inves…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Clinical Trial Site, New York, New York
- Locations
- 4 in total
- Run by
- Arvinas Inc.
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Study of APR-1051 in Patients With Advanced Solid Tumors
The purpose of this study is to assess the safety and effectiveness of APR-1051 through the performance of a Phase 1, open-label, safety, PK, and preliminary efficacy study of oral APR-1051 in patients with advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Rutgers Cancer Institute, New Brunswick, New Jersey
- Locations
- 7 in total
- Run by
- Aprea Therapeutics
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A Clinical Study to Test if an Investigational Treatment Called BNT326 is Safe and Potentially Beneficial When Used Alone or in Combination With Other Investigational Treatments Such as BNT327, for People With Advanced Malignant Tumors
This study will evaluate the safety, efficacy, optimal dose, and pharmacokinetics (PK) of BNT326 as monotherapy (Part 1) and as combination treatment with immunotherapeutic agents (Part 2) in participants with histologically or cytologically confirmed solid tumors that are advanced (i.e., either me…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Hartford Healthcare, Hartford, Connecticut
- Locations
- 77 in total
- Run by
- BioNTech SE
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Anti-GD2 ADC M3554 in Advanced Solid Tumors
The purpose of this study is to establish the recommended doses and further evaluate the safety and preliminary antitumor activity of M3554 in participants with soft tissue sarcoma (STS) and glioblastoma, IDH-wildtype. Study details include: Study Duration per participant: Approximately 4 months
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Dana-Farber Cancer Institute, Boston, Massachusetts
- Locations
- 11 in total
- Run by
- EMD Serono Research & Development Institute, 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.