Advanced Solid Tumor Clinical Trials in Fairfax, Virginia
33 studies are recruiting for advanced solid tumor in Fairfax, Virginia 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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The Evaluation of PC14586 in Patients With Advanced Solid Tumors Harboring a TP53 Y220C Mutation (PYNNACLE)
The Phase 2 monotherapy portion of this study is currently enrolling and will evaluate the efficacy and safety of PC14586 (INN rezatapopt) in participants with locally advanced or metastatic solid tumors harboring a TP53 Y220C mutation. The Phase 1 portion of the study will assess the safety, toler…
- Stage
- Phase 1
- Ages
- 12 and older
- Site
- Virginia Cancer Specialists, Fairfax, Virginia
- Locations
- 77 in total
- Run by
- PMV Pharmaceuticals, Inc
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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), and in combination with standard …
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Next Oncology Virginia, Fairfax, Virginia
- Locations
- 101 in total
- Run by
- BeOne Medicines
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A First-in-Human Study of BG-C0902 Alone and in Combination With Other Therapeutic Agents in Patients With Advanced Solid Tumors
This study is a first-in-human (FIH), Phase 1a/1b study of BG-C0902, a fully humanized anti-epidermal growth factor receptor (EGFR) and anti-mesenchymal-epithelial transition (MET) antibody, conjugated via an enzymatically cleavable linker to a topoisomerase 1 (TOPO1) inhibitor payload. The study a…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Next Oncology Virginia, Fairfax, Virginia
- Locations
- 14 in total
- Run by
- BeOne Medicines
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Study of BG-T187 Alone and in Combination With Other Therapeutic Agents in Participants With Advanced Solid Tumors
This is a first-in-human (FIH), Phase 1a/1b, open-label, multicenter, dose escalation and dose expansion study to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics, and preliminary antitumor activity of BG-T187 alone and in combination with other therapeutic agents in parti…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Next Oncology Virginia, Fairfax, Virginia
- Locations
- 34 in total
- Run by
- BeOne Medicines
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A Study of LY4050784 in Participants With Advanced or Metastatic Solid Tumors
The main purpose of this study is to find out whether the study drug, LY4050784, is safe, tolerable and effective in participants alone or in combination with other anticancer agents. In addition, with locally advanced or metastatic solid tumors with a BRG1 (Brahma-related gene 1, also known as SMA…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- USO-Virginia Cancer Specialists, PC, Fairfax, Virginia
- Locations
- 33 in total
- Run by
- Eli Lilly and Company
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Phase 1 Study of MRTX1719 in Solid Tumors With MTAP Deletion
This is a Phase 1, open-label, multicenter, study of the safety, tolerability, PK, PD, and anti-tumor activity of MRTX1719 patients with advanced, unresectable or metastatic solid tumor malignancy with homozygous deletion of the MTAP gene.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Virginia Cancer Specialists, PC, Fairfax, Virginia
- Locations
- 25 in total
- Run by
- Bristol-Myers Squibb
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A Study of DS5361b in Participants With Advanced Solid Tumors
This study aims to assess the safety, tolerability, and preliminary efficacy and to determine the MTD of DS5361b in monotherapy and combination with pembrolizumab in participants with advanced or metastatic solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Research Site, Fairfax, Virginia
- Locations
- 7 in total
- Run by
- Daiichi Sankyo
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A Study to Assess a New Medicine Called IPN01195 When Administered Alone in Adults With Advanced Solid Tumours
The purpose of this study is to determine the appropriate dosage, safety and effectiveness of a new study drug IPN01195 in adults with advanced solid tumours. The participants in this study will have advanced solid tumours. 'Advanced solid tumours' refers to cancers that can occur in several places…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Virginia Cancer Specialist- Fairfax, Fairfax, Virginia
- Locations
- 13 in total
- Run by
- Ipsen
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A First-in-Human Trial of BLU-924 (SAR449336) in Advanced Solid Tumors Harboring KRAS Mutations
A first in human study to evaluate the safety, tolerability, pharmacokinetics, and antitumor activity of BLU-924 / SAR449336, a pan-KRAS inhibitor, in participants with advanced Pancreatic Cancer, Non-Small Cell Lung Cancer, or Colorectal Cancer harboring KRAS mutations.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Next Oncology Virginia Cancer Specialist, Fairfax, Virginia
- Locations
- 3 in total
- Run by
- Blueprint Medicines Corporation
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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
- NEXT Oncology, Fairfax, Virginia
- Locations
- 11 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
- NEXT Virginia, Fairfax, Virginia
- Locations
- 11 in total
- Run by
- Gilead Sciences
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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
- NEXT Oncology -Virginia, Fairfax, Virginia
- Locations
- 5 in total
- Run by
- Aprea Therapeutics
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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, Fairfax, Virginia
- Locations
- 3 in total
- Run by
- Arvinas Inc.
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Study of Orally Administered MOMA-313 in Participants With Advanced or Metastatic Solid Tumors
This Phase 1, multi-center, open-label, dose escalation and dose optimization study is designed to assess the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PDx), and preliminary clinical activity of MOMA-313 administered orally as a single agent or combination therapy in patients w…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Investigative Site #112, Fairfax, Virginia
- Locations
- 18 in total
- Run by
- MOMA Therapeutics
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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
- NEXT Virginia, Fairfax, Virginia
- 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
- Virginia Cancer Specialists, Fairfax, Virginia
- Locations
- 30 in total
- Run by
- Coherus Oncology, Inc.
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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
- NEXT Oncology Virginia, Fairfax, Virginia
- Locations
- 15 in total
- Run by
- Nuvectis Pharma, Inc.
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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
- NEXT Virginia, Fairfax, Virginia
- Locations
- 29 in total
- Run by
- Pyxis Oncology, 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
- 017, Fairfax, Virginia
- Locations
- 45 in total
- Run by
- MediLink Therapeutics (Suzhou) Co., Ltd.
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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, Fairfax, Virginia
- Locations
- 10 in total
- Run by
- Plexium, Inc.
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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
- NEXT Virginia, Fairfax, Virginia
- Locations
- 8 in total
- Run by
- Peel Therapeutics Inc
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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
- NEXT Virginia, Fairfax, Virginia
- Locations
- 19 in total
- Run by
- NiKang Therapeutics, Inc.
-
A Study of DB-1310 in Advanced/Metastatic Solid Tumors
This is a dose-escalation and dose-expansion Phase 1/2a trial to evaluate the safety and tolerability of DB-1310 in subjects with advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- NEXT Virginia, Fairfax, Virginia
- Locations
- 24 in total
- Run by
- DualityBio Inc.
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First in Human Study of TORL-1-23 in Participants With Advanced Cancer
This first-in-human study will evaluate the safety, tolerability, pharmacokinetics, and antitumor activity of TORL-1-23 in patients with advanced cancer
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Virginia Cancer Specialists, Fairfax, Virginia
- Locations
- 14 in total
- Run by
- TORL Biotherapeutics, LLC
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JZP898 Intravenous Infusion as Monotherapy and Combination With Pembrolizumab in Adults With Advanced/Metastatic Solid Tumors
This Phase 1 first-in-human study will investigate the safety, tolerability, pharmacokinetics (PK), immunogenicity, and preliminary antitumor activity of JZP898 monotherapy as well as JZP898 in combination with pembrolizumab in adult participants with advanced or metastatic solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Virginia Cancer Specialists, Fairfax, Virginia
- Locations
- 10 in total
- Run by
- Jazz Pharmaceuticals
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.