Gastric Cancer Clinical Trials in Dallas, Texas
14 studies are recruiting for gastric cancer in Dallas, Texas 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.
Search these by distance from you
Studies now recruiting
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Safety and Efficacy of NEO212 in Patients With Astrocytoma IDH-mutant, Glioblastoma IDH-wildtype or Brain Metastasis
This multi-site, Phase 1/2 clinical trial is an open-label study to identify the safety, pharmacokinetics, and efficacy of a repeated dose regimen of NEO212 alone for the treatment of patients with radiographically-confirmed progression of Astrocytoma IDH- mutant, Glioblastoma IDH-wildtype, and the…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Baylor, Scott and White Research Institute, Dallas, Texas
- Locations
- 8 in total
- Run by
- Neonc Technologies, Inc.
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Sonesitatug Vedotin in Combination With Capecitabine With or Without Rilvegostomig in Participants With Advanced or Metastatic Gastric, Gastroesophageal Junction, or Esophageal Adenocarcinoma Expressing Claudin18.2
The purpose of this study is to evaluate the efficacy and safety of sonesitatug vedotin in combination with capecitabine with or without rilvegostomig in first-line (1L) Claudin18.2 (CLDN18.2)-positive, human epidermal growth factor receptor 2 (HER2)-negative, gastric, gastroesophageal junction (GE…
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- Research Site, Dallas, Texas
- Locations
- 311 in total
- Run by
- AstraZeneca
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Study of TDXd, Chemotherapy, Pembrolizumab, and Trastuzumab in First-Line Metastatic HER2-Positive Gastric or Gastroesophageal Junction Cancer
This clinical trial is designed to assess the efficacy and safety of the triplet combination of trastuzumab deruxtecan (ENHERTU, T-DXd, DS-8201a) plus a fluoropyrimidine plus pembrolizumab versus standard of care (SoC) chemotherapy plus trastuzumab plus pembrolizumab as first-line therapy in partic…
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- UT Southwestern Medical Center, Dallas, Texas
- Locations
- 250 in total
- Run by
- Daiichi Sankyo
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A Study of Bispecific Antibody MCLA-158 in Patients With Advanced Solid Tumors
This is a Phase 1/2 open-label, multi-center, multi-national study with an initial dose escalation part to determine the recommended Phase II dose (RP2D) of MCLA-158 single agent in patients with mCRC. The dose escalation part has been completed and the RP2D will be further evaluated in an expansio…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Texas Oncology, Dallas, Texas
- Locations
- 54 in total
- Run by
- Merus B.V.
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Study of INBRX-106 and INBRX-106 in Combination With Pembrolizumab (Keytruda®) in Subjects With Locally Advanced or Metastatic Solid Tumors (Hexavalent OX40 Agonist)
This is a Phase 1/2, open-label, non-randomized, 4-part trial to determine the safety profile and identify the maximum tolerated dose (MTD) and/or recommended Phase 2 dose (RP2D) of INBRX 106 administered as a single agent or in combination with the anti-PD-1 checkpoint inhibitor (CPI) pembrolizuma…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Sarah Cannon Research Institute at Mary Crowley, Dallas, Texas
- Locations
- 42 in total
- Run by
- Inhibrx Biosciences, Inc
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Study of Orally Administered MOMA-341 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-341 administered orally as a single agent or combination therapy in patients w…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Investigative Site #127, Dallas, Texas
- Locations
- 15 in total
- Run by
- MOMA Therapeutics
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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
- University of Texas Southwestern Medical Center - Simmons Cancer Center, Dallas, Texas
- Locations
- 62 in total
- Run by
- Seagen, a wholly owned subsidiary of Pfizer
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A Phase 2 Study of Zanidatamab in Patients With HER2-expressing Tumors
The purpose of this study is to evaluate the efficacy and safety of zanidatamab for the treatment of participants with previously treated solid tumors that have Human Epidermal Growth Factor Receptor 2 (HER2) Immunohistochemistry (IHC) 3+ overexpression.
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- Texas Oncology - DFW, Dallas, Texas
- Locations
- 28 in total
- Run by
- Jazz Pharmaceuticals
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A Study of TRK-950 When Used in Combination With Ramucirumab and Paclitaxel in Patients With Gastric Cancer
This study will assess the efficacy, safety, optimal dose and ADA and NAbs development of TRK-950 at two separate dose levels in combination with ramucirumab and paclitaxel (RAM+PTX) as compared with RAM + PTX treatment alone in participants with gastric or gastro-esophageal junction (GEJ) adenocar…
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- Texas Oncology Dallas Methodist, Dallas, Texas
- Locations
- 27 in total
- Run by
- Toray Industries, Inc
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[18F]FPyQCP PET Imaging of Fibroblast Activation Protein in Selected Oncology Indications
This is a multi-center, open-label, single-arm, Phase 1/2 study designed to evaluate the safety, radiation dosimetry, and preliminary diagnostic performance of [18F]FPyQCP in detecting colorectal cancer (CRC), gastric cancer (GC), pancreatic ductal adenocarcinoma (PDAC), invasive lobular breast can…
- Stage
- Phase 1
- Ages
- 18 to 80
- Site
- University of Texas Southwestern Medical Center, Dallas, Texas
- Run by
- Blue Earth Diagnostics
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BAL0891 in Patients With Advanced Solid Tumors or Relapsed or Refractory Acute Myeloid Leukemia
This study is a multiple cohort, multicenter, open-label Phase 1 study with dose-escalation substudies investigating intravenous (IV) BAL0891 as monotherapy, and in combination with tislelizumab or paclitaxel, to determine the safety and tolerability of increasing doses of BAL0891 in patients with …
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Baylor University Medical Center, Dallas, Texas
- Locations
- 17 in total
- Run by
- SillaJen, 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
- UT Southwestern, Dallas, Texas
- Locations
- 19 in total
- Run by
- NiKang Therapeutics, Inc.
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Study of TJ033721 (Givastomig) in Subjects With Advanced or Metastatic Solid Tumors
This is an open label, multi-center, multiple dose Phase 1 study to evaluate the safety, tolerability, MTD PK, and PD of TJ033721 (givastomig) in subjects with advanced or metastatic solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Mary Crowley Cancer Research, Dallas, Texas
- Locations
- 21 in total
- Run by
- I-Mab Biopharma US Limited
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A Study of DR-0202 in Patients With Locally Advanced or Metastatic, Relapsed or Refractory Carcinomas
A phase 1a/1b, multicenter, open-label, dose escalation/expansion, multiple-dose study to evaluate the safety and activity of DR-0202 in patients with locally advanced or metastatic, relapsed or refractory carcinomas
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Dren Investigational Site, Dallas, Texas
- Locations
- 10 in total
- Run by
- Dren Bio
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.
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