Gastric and gastroesophageal junction trials often require HER2, PD-L1, or Claudin 18.2 testing. Perioperative versus metastatic protocols are different records. This hub is a snapshot of recruiting ClinicalTrials.gov cards, not a treatment ranking. Sourced from ClinicalTrials.gov. Not a recommendation to join any study.
RecruitingPhase 1 / Phase 2Duarte, California
Phase 1 / Phase 2: testing INBRX-106 - Hexavalent OX40 agonist antibody for Solid TumorThis is a Phase 1/2, open-label, non-randomly assigned, 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) pembrolizumab (Keytruda®). KEYTRUDA is a registered trademark of Merck Sharp \& Dohme LLC, a subsidiary of Merck \& Co., Inc., Rahway, NJ, USA.
NCT04198766 · Official ClinicalTrials.gov record · Inhibrx Biosciences, Inc
RecruitingNot a traditional drug phaseBethesda, Maryland
Surgery in Gastrointestinal Stromal Tumors (GISTs) for Treatment, Tumor Modeling, and Genomic AnalysisObjective: To follow people with GISTs and collect tumor tissue so that it can be studied in the lab. Eligibility: People age 6 and older who have a GIST.
NCT04557969 · Official ClinicalTrials.gov record · National Cancer Institute (NCI)
RecruitingNot a traditional drug phaseAnchorage, Alaska
Not a traditional drug phase: Questionnaire Administration for Acute Lymphoblastic LeukemiaThis study collects blood and tissue samples from patients with cancer and without cancer to evaluate tests for early cancer detection. Collecting and storing samples of blood and tissue from patients with and without cancer to study in the laboratory may help researchers develop tests for the early detection of cancers.
NCT05334069 · Official ClinicalTrials.gov record · Alliance for Clinical Trials in Oncology
RecruitingNot a traditional drug phaseDuarte, California
cfDNA Assay Prospective Observational Validation for Early Cancer Detection and Minimal Residual DiseaseThis is an watch-and-measure (no experimental treatment required) case-control study to train and validate a genome-wide methylome enrichment platform to detect multiple cancer types and to differentiate amongst cancer types. The cancers included in this study are brain, breast, bladder, cervical, colorectal, endometrial, esophageal, gastric, head and neck, hepatobiliary, leukemia, lung, lymphoma, multiple myeloma, ovarian, pancreatic, prostate, renal, sarcoma, and thyroid.
NCT05366881 · Official ClinicalTrials.gov record · Adela, Inc
RecruitingPhase 3Birmingham, Alabama
Phase 3: testing Fluorouracil for Advanced Esophageal AdenocarcinomaThis phase III trial compares the effect of modified fluorouracil, leucovorin calcium, oxaliplatin, and irinotecan (mFOLFIRINOX) with or without nivolumab to the effect of modified fluorouracil, leucovorin calcium, and oxaliplatin (mFOLFOX) with or without nivolumab for the treatment of patients with advanced, unresectable, or metastatic HER2 negative esophageal, gastroesophageal junction, or gastric adenocarcinoma. The usual approach for patients who are not in a study is treatment with FOLFOX with some receiving an immunotherapy drug, either nivolumab or pembrolizumab, in addition to FOLFOX chemotherapy.
NCT05677490 · Official ClinicalTrials.gov record · Alliance for Clinical Trials in Oncology
RecruitingPhase 2Shanghai
Phase 2: testing sintilimab+metronomic POLF for Gastric CancerTo evaluate how well it works and safety of Neoadjuvant of Sintilimab Combined Weekly Metronomic Chemotherapy (POLF) in resectable locally advanced gastric cancer.
NCT06054906 · Official ClinicalTrials.gov record · Huashan Hospital
RecruitingPhase 2 / Phase 3Little Rock, Arkansas
Phase 2 / Phase 3: testing Nivolumab for Advanced Esophageal AdenocarcinomaThis phase II/III trial compares the addition of nivolumab to the usual treatment of paclitaxel and ramucirumab to paclitaxel and ramucirumab alone in treating patients with gastric or esophageal adenocarcinoma that may have spread from where it first started to nearby tissue, lymph nodes, or distant parts of the body (advanced). A monoclonal antibody is a type of protein that can bind to certain targets in the body, such as molecules that cause the body to make an immune response (antigens).
NCT06203600 · Official ClinicalTrials.gov record · National Cancer Institute (NCI)
RecruitingPhase 1Los Angeles, California
Phase 1: testing MGC026 Dose Escalation for Advanced Solid TumorThe 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 escalation portion and a cohort expansion portion in Module A of the study. Combination therapy with pembrolizumab will occur in Module B of the study Participants will receive vobramitamab tavatecan by intravenous (IV) infusion.
NCT06242470 · Official ClinicalTrials.gov record · MacroGenics
RecruitingPhase 1Houston, Texas
Phase 1: testing Azenosertib for Clinical Stage III Gastric Cancer AJCC v8This phase I trial tests the safety, side effects, and best dose of azenosertib in combination with trastuzumab deruxtecan in treating patients with HER2-positive gastric or gastroesophageal junction cancer and other HER2-positive solid tumors that have spread to nearby tissue or lymph nodes (locally advanced), that have spread from where it first started (primary site) to other places in the body (metastatic), or that cannot be removed by surgery (unresectable). Azenosertib is in a class of medications called kinase inhibitors.
NCT06364410 · Official ClinicalTrials.gov record · National Cancer Institute (NCI)
RecruitingPhase 2New York, New York
Phase 2: testing Avutometinib for Gastric CancerThis study wants to determine if the combination study treatment with avutometinib and defactinib will prolong life in participants, is effective in decreasing the size of the tumor(s), and if it is safe in subjects with diffuse-type stomach cancer.
NCT06487221 · Official ClinicalTrials.gov record · Ryan H. Moy, MD, PhD
RecruitingPhase 2Bethesda, Maryland
Phase 2: testing [18F]FAPI-74 for SarcomaBackground: Fibroblast-activation protein (FAP) is an enzyme that appears in high numbers in cancer-associated fibroblasts of certain cancer types. \[18F\]FAPI-74 is a new PET (positron emission tomography) tracer, a substance that is injected into a person s body before an imaging scan.
NCT06503146 · Official ClinicalTrials.gov record · National Cancer Institute (NCI)
RecruitingPhase 1Little Rock, Arkansas
Phase 1: testing NKT3964 for Solid TumorThe goal of the this drug alone Dose Escalation phase (Part 1) of the study is to measure 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 this drug alone Expansion phase of the study (Part 2) is to measure the preliminary anti-tumor activity of NKT3964 at the RDE based on objective response rate (ORR) and determine the preliminary recommended Phase 2 dose (RP2D).
NCT06586957 · Official ClinicalTrials.gov record · NiKang Therapeutics, Inc.
RecruitingPhase 1Duarte, California
Phase 1: testing Nab-paclitaxel for Clinical Stage IVB Gastric Cancer AJCC v8This phase I trial tests the safety, side effects and best dose of nab-paclitaxel pressurized intraperitoneal aerosolized chemotherapy (PIPAC) in combination with second-line chemotherapy, paclitaxel and ramucirumab, and tests how well they work in treating stomach cancer that has spread from where it first started to the tissue that lines the abdominal wall and organs (peritoneal metastases). Paclitaxel is in a class of medications called antimicrotubule agents.
NCT06675136 · Official ClinicalTrials.gov record · City of Hope Medical Center
RecruitingPhase 2Prescott, Arizona
Phase 2: testing Zanidatamab for Breast CancerThis study wants to measure the how well it works 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.
NCT06695845 · Official ClinicalTrials.gov record · Jazz Pharmaceuticals
RecruitingPhase 2Birmingham, Alabama
Phase 2: testing BAY2927088 for Advanced Solid TumorsResearchers are looking for a better way to treat people who have solid tumors with HER2-activating mutations. Before a treatment can be approved for people to take, researchers do clinical trials to better understand its safety and how it works.
NCT06760819 · Official ClinicalTrials.gov record · Bayer
RecruitingPhase 3Anchorage, Alaska
Phase 3: testing Rilvegostomig for HER2-positive Gastric CancerThis is a Phase Ⅲ, randomly assigned, open-label, Sponsor-blinded, 3-arm, global, multicenter study assessing the how well it works and safety of rilvegostomig in combination with fluoropyrimidine and T-DXd (Arm A) compared to trastuzumab, chemotherapy, and pembrolizumab (Arm B) in HER2-positive locally advanced or metastatic gastric or GEJ adenocarcinoma participants whose tumors express PD L1 CPS ≥ 1. Rilvegostomig in combination with trastuzumab and chemotherapy will be evaluated in a separate arm (Arm C) to assess the contribution of each component in the experimental arm.
NCT06764875 · Official ClinicalTrials.gov record · AstraZeneca
RecruitingPhase 2 / Phase 3Edegem
Phase 2 / Phase 3: [18F]AlF-FAPI-74 PET/CT for Oesophageal CancerThe aim of the project is to demonstrate superior detection ratio of \[18F\]AlF-FAPI-74 PET/CT compared to \[18F\]FDG PET/CT or conventional imaging in treatment-naïve, newly diagnosed patients with oesophagogastric adenocarcinoma (clinical T1-4N0-3M0) and pancreatic ductal adenocarcinoma (clinical T1-4N0-2M0-1) and describe the clinical utility of \[18F\]AlF-FAPI-74 PET/CT in oncological patients with a clinically challenging situation.
NCT06782412 · Official ClinicalTrials.gov record · KU Leuven
RecruitingPhase 1Bethesda, Maryland
Phase 1: testing cyclophosphamide for MesotheliomaBackground: Mesothelioma is an aggressive cancer that grows in the linings of the body; this can include the membranes that line the heart, lungs, and internal organs. Mesothelin (MSLN) is a protein that appears in high numbers in many tumors, including mesothelioma.
NCT06885697 · Official ClinicalTrials.gov record · National Cancer Institute (NCI)
RecruitingPhase 3Birmingham, Alabama
Phase 3: testing zolbetuximab for Locally Advanced Unresectable Gastroesophageal Junction (GEJ) Adenocarcinoma or CancerZolbetuximab is being studied in people with cancer in and around the stomach or where the food pipe (esophagus) joins the stomach, called gastroesophageal junction (GEJ) cancer. Zolbetuximab with chemotherapy may be used to treat stomach and GEJ cancer when the cancer cells do not have a protein called HER2 (human epidermal growth factor receptor 2) on their surface (HER2-negative) but do have a protein called Claudin 18.2 (Claudin 18.2-positive).
NCT06901531 · Official ClinicalTrials.gov record · Astellas Pharma Global Development, Inc.
RecruitingNot a traditional drug phaseDublin, California
Not a traditional drug phase: Exercise intervention for Localized Malignant Solid NeoplasmThis clinical trial studies whether an exercise program can be successfully delivered to patients receiving treatment for cancer through virtual sessions and allow patients to exercise in their own home. Treatments for cancer can cause side effects such as fatigue and loss of strength.
NCT07059884 · Official ClinicalTrials.gov record · Alliance for Clinical Trials in Oncology
RecruitingPhase 2Newark, Delaware
Phase 2: testing Sonesitatug Vedotin for Gastroesophageal AdenocarcinomaGEMINI-PeriOp GC study will assess the safety, tolerability, pharmacokinetics (PK) and preliminary anti-tumor activity of novel agents or novel combinations as perioperative treatment in participants with locally advanced resectable gastric, gastroesophageal junction (GEJ), or esophageal adenocarcinoma who have not received previous treatment for the disease.
NCT07069712 · Official ClinicalTrials.gov record · AstraZeneca
RecruitingPhase 2Abbotsford, Victoria
Phase 2: testing Psilocybin therapy for Adjustment DisorderThis study is assessing the how well it works and safety of NPX-5 in psilocybin-assisted psychotherapy for the treatment of adjustment disorder due to cancer diagnosis. This study is for people who are aged between 18 and 80 years old and suffer from anxiety after adjusting to an acutely stressful event of their cancer diagnosis.
NCT07072728 · Official ClinicalTrials.gov record · Psyence Australia Pty Ltd
RecruitingPhase 1Duarte, California
Phase 1: testing LY4257496 for Breast NeoplasmsThe main purpose of this study is to evaluate safety, tolerability, and how well it works of LY4257496 alone and as part of relevant standard of care (SOC) combination therapy in participants with Gastrin-releasing Peptide Receptor (GRPR)-positive advanced cancer, including but not limited to breast, colorectal, prostate, endometrial, esophageal, gastroesophageal (GE) junction, and gastric cancer. The study will also measure the safety, tolerability, and how well it works of LY4257529 to identify cancer with high levels of a protein called GRPR.
NCT07114601 · Official ClinicalTrials.gov record · Eli Lilly and Company
RecruitingPhase 1 / Phase 2Seoul
Phase 1 / Phase 2: testing Lenvatinib for STOMACH NEOPLASMTo investigate how well it works and safety of lenvatinib in combination with nivolumab plus chemotherapy in gastric cancer patients with peritoneal metastasis and grade ≥ 2 ascites.
NCT07149090 · Official ClinicalTrials.gov record · Asan Medical Center
RecruitingPhase 2 / Phase 3Phoenix, Arizona
Phase 2 / Phase 3: testing Pumitamig for Untreated Advanced or Metastatic Gastric, Gastroesophageal Junction, or Esophageal AdenocarcinomaThis study wants to measure the safety and how well it works of Pumitamig in combination with chemotherapy versus Nivolumab in combination with chemotherapy in participants with previously untreated advanced or metastatic gastric, gastroesophageal junction, or esophageal adenocarcinoma
NCT07221149 · Official ClinicalTrials.gov record · Bristol-Myers Squibb
RecruitingNot a traditional drug phaseLos Angeles, California
Not a traditional drug phase: Actigraphy for Clinical Stage I Esophageal Adenocarcinoma American Joint Committee on Cancer (AJCC) v8This clinical trial tests an individually tailored, supervised, remote exercise intervention to improve physical function for stage I-III gastroesophageal cancer survivors. Modern treatments for gastroesophageal cancer are effective at treating the cancer but are often aggressive, can be difficult for patients to tolerate, and can lead to significant debilitation and a loss of independence.
NCT07439484 · Official ClinicalTrials.gov record · Jonsson Comprehensive Cancer Center
RecruitingPhase 2Chicago, Illinois
Phase 2: testing Neoadjuvant chemotherapy for Gastric AdenocarcinomaThis is a single-center, randomly assigned, open-label clinical trial designed to measure the impact of low-dose olanzapine on weight loss, appetite, and nutritional outcomes in patients with gastric cancer receiving neoadjuvant chemotherapy. Eligible patients will be randomly assigned to receive olanzapine 2.5 mg orally once daily (QD) in addition to standard neoadjuvant chemotherapy, beginning prior to initiation of chemotherapy and continuing until surgical resection.
NCT07581405 · Official ClinicalTrials.gov record · University of Illinois Chicago
RecruitingPhase 3Saint Louis Park, Minnesota
Phase 3: testing ASP2138 for Gastric AdenocarcinomaClaudin 18.2 or CLDN18.2 is a protein found on cells in the digestive system. Researchers are looking at ways to attack CLDN18.2 to help control tumors.
NCT07673887 · Official ClinicalTrials.gov record · Astellas Pharma Global Development, Inc.
RecruitingNot a traditional drug phaseAlexandroupoli
A Study in Greece Observing How Patients With Stomach and Esophageal Cancer Are Diagnosed and Treated in Ev…This is a retrospective-prospective watch-and-measure (no experimental treatment required), multicenter, single-country study aiming to describe the epidemiological characteristics and management strategies in patients with stage II-IVB gastric/GEJ adenocarcinoma in routine clinical practice in Greece.
NCT07800754 · Official ClinicalTrials.gov record · AstraZeneca
RecruitingPhase 1Fuzhou, Fujian
Phase 1: testing CG-7321 for Advanced Solid TumorsThis is a Phase I, open-label, multi-center study to measure the safety, tolerability, pharmacokinetics (PK), and preliminary how well it works of CG-7321 capsules as this drug alone or in combination with fulvestrant in subjects with advanced solid tumors. The study consists of: * Part Ia (this drug alone): Dose escalation (accelerated titration followed by 3+3 design) from 2mg to 50mg twice daily (BID), plus dose expansion cohorts in advanced solid tumors including HR+/HER2- breast cancer, ovarian cancer, gastric cancer, and other tumor types.
NCT07923214 · Official ClinicalTrials.gov record · Chengdu Cynogen Bio-pharmaceutical Tech. Co., Ltd.