Esophageal Squamous Cell Carcinoma Clinical Trials in Fairfax, Virginia
9 studies are recruiting for esophageal squamous cell carcinoma 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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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
- NEXT Oncology, Fairfax, Virginia
- Locations
- 20 in total
- Run by
- Terremoto Biosciences Inc.
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A Study Evaluating the Safety, Efficacy, and Pharmacokinetics (PK) of EVOLVE104 in Participants With Advanced Urothelial and Squamous Cell Carcinomas
The goal of this study is to evaluate the safety and effectiveness of EVOLVE104 in participants with advanced urothelial and squamous cell carcinomas who have previously taken standard treatment options, have declined or have been ineligible for treatment with these medications. Participants with a…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Virginia Cancer Specialists, Fairfax, Virginia
- Locations
- 16 in total
- Run by
- EvolveImmune United, Inc
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Study to Assess Adverse Events and Change in Disease Activity in Adult Participants With Select Advanced Solid Tumor Indications Receiving Intravenous (IV) ABBV-400
Cancer is a condition where cells in a specific part of body grow and reproduce uncontrollably. The purpose of this study is to assess adverse events and change in disease activity when ABBV-400 is given to adult participants to treat advanced solid tumors. ABBV-400 is an investigational drug being…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Inova Schar Cancer Institute - Fairfax - Innovation Park Drive /ID# 262771, Fairfax, Virginia
- Locations
- 54 in total
- Run by
- AbbVie
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A Study of Ifinatamab Deruxtecan in Subjects With Pretreated Advanced or Metastatic Esophageal Squamous Cell Carcinoma (ESCC) (IDeate-Esophageal01)
This study is designed to assess the efficacy and safety of ifinatamab deruxtecan (I-DXd) in patients with unresectable advanced or metastatic esophageal squamous cell carcinoma (ESCC) who have experienced disease progression following treatment with a platinum-based systemic therapy and an immune …
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- Virginia Cancer Specialists, Fairfax, Virginia
- Locations
- 132 in total
- Run by
- Daiichi Sankyo
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A Study of PF-08046054/SGN-PDL1V in Advanced Solid Tumors
This study will test the safety of a drug called PF-08046054/SGN-PDL1V alone and with pembrolizumab in participants with solid tumors. It will also study the side effects of this drug. A side effect is anything a drug does to your body besides treating your disease. Participants will have solid tum…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- NEXT Virginia, Fairfax, Virginia
- Locations
- 62 in total
- Run by
- Seagen, a wholly owned subsidiary of Pfizer
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A Study of Sigvotatug Vedotin in Advanced Solid Tumors
This trial will look at a drug called sigvotatug vedotin (SGN-B6A) alone and with pembrolizumab, with or without chemotherapy, to find out whether it is safe for people who have solid tumors. It will study sigvotatug vedotin to find out what its side effects are. A side effect is anything the drug …
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Virginia Cancer Specialists, Fairfax, Virginia
- Locations
- 158 in total
- Run by
- Seagen, a wholly owned subsidiary of Pfizer
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A Study to Investigate ALE.P02 as Monotherapy in Adult Patients With Selected CLDN1+ Solid Tumors
The purpose of this study is to evaluate the safety, tolerability, pharmacokinetic, pharmacodynamic, preliminary anti-tumor activity, and to determine the recommended Phase II dose (RP2D) of the ALE.P02 monotherapy in adult patients with selected squamous solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- NEXT Oncology Virginia, Fairfax, Virginia
- Locations
- 41 in total
- Run by
- Alentis Therapeutics AG
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A Study of IDE034 in Adult Participants With Locally Advanced/Metastatic Solid Tumors Types
This is a Phase 1a/1b, open-label, multicenter dose escalation and dose expansion clinical study to evaluate the safety, PK, immunogenicity and preliminary efficacy of IDE034 in participants with locally advanced/metastatic solid tumor types that express B7-H3 and PTK7.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- NEXT Texas LLC - Virginia, Fairfax, Virginia
- Locations
- 15 in total
- Run by
- IDEAYA Biosciences
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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.
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.