[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"locally-advanced-esophageal-adenocarcinoma\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:locally-advanced-esophageal-adenocarcinoma":33},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,54],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":43,"lastUpdatePostDateStruct":44,"startDateStruct":47,"completionDateStruct":49,"leadSponsor":51,"locationsCount":5},"100638988","phase-1-futibatinib-with-paclitaxel-and-ramucirumab-for-the-treatment-of-locally-advanced-or-unresectable-gastric-gastroesophageal-junction-or-esophageal-adenocarcinoma-100638988",false,"NCT07594548","Futibatinib With Paclitaxel and Ramucirumab for the Treatment of Locally Advanced or Unresectable Gastric, Gastroesophageal Junction, or Esophageal Adenocarcinoma","A Phase I\u002FIb Dose Escalation Trial of Futibatinib in Combination With Paclitaxel\u002FRamucirumab in Second Line Confirmed Locally Advanced\u002FUnresectable Gastric, Gastroesophageal Junction, or Esophageal Adenocarcinoma","Inclusion Criteria:\n\n* Patients must have histologically or cytologically confirmed locally advanced\u002Funresectable gastric, gastroesophageal junction, or esophageal adenocarcinoma that is microsatellite stable and HER2 negative. (American Joint Committee on Cancer \\[AJCC\\] staging criteria; https:\u002F\u002Fpmc.ncbi.nlm.nih.gov\u002Farticles\u002FPMC5387145\u002F)\n\n  * Note: Histological or cytological test reports from external laboratories outside of Northwestern University (NU) will also be accepted\n* Patients must have measurable disease per Response Evaluation Criteria in Solid Tumors (RECIST) 1.1\n\n  * Note: Patients must have documented unresectable and\u002For metastatic disease on CT or MRI imaging completed prior to registration. Imaging must have been completed within 90 days prior to registration for participants with measurable disease\n* Patients must not have received more than 1 prior line of therapy in the metastatic setting.\n\n  * Note: Patients who have received neoadjuvant or adjuvant therapy must have completed therapy a year prior to registration in this study. Exception: patients with neoadjuvant or adjuvant therapy who have progressed within 6 months\n* Patients must be age ≥ 18 years\n* Patients must exhibit an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1\n* Leukocytes (white blood cells \\[WBC\\]) ≥ 2,000\u002FmcL\n* Absolute neutrophil count (ANC) ≥ 1500\u002FmcL\n* Hemoglobin (Hgb) ≥ 9 g\u002FdL (transfusions within 1 week of registration are not allowed to meet cutoff)\n* Platelets (PLT) ≥ 100,000\u002FmcL (transfusions within 1 week of registration are not allowed to meet cutoff)\n* Total bilirubin ≤ 1.5 x institutional upper limit of normal (ULN)\n* Aspartate aminotransferase (AST) (serum glutamic oxaloacetic transaminase \\[SGOT\\]) ≤ 3 x institutional ULN (unless liver metastases are present, in which case they must be ≤ 5 x ULN)\n* Alanine aminotransferase (ALT) (serum glutamic pyruvic transaminase \\[SGPT\\]) ≤ 3 x institutional ULN (unless liver metastases are present, in which case they must be ≤ 5 x ULN)\n* Creatinine ≤ 1.5 x Institutional ULN or meeting creatinine clearance (CrCl) criteria below\n* Creatinine clearance per the Cockcroft-Gault formula or 24-hour urine collection) ≥ 45 mL\u002Fmin\n* Phosphate \\\u003C ULN\n* International normalized ratio (INR) \\\u003C 1.5\n* Patient's urinary protein is ≤ 1+ on dipstick or routine urinalysis (UA) within 28 days of registration.\n\n  * Note: Random analysis of urine protein with a normal value is sufficient. If urine dipstick or routine analysis indicated proteinuria ≥ 2+, then a 24-hour urine is to be collected and demonstrate \\\u003C 1000 mg of protein in 24 hours to allow participation in the study\n* For patients with a known history of human immunodeficiency virus (HIV), infected patients on effective anti-retroviral therapy must have a viral load undetectable for 6 months prior to registration.\n\n  * Please note: this lab is not a requirement for eligibility, however, if it has been completed previously as part of the patient's health care, it should be documented for eligibility\n* Patients with known history of chronic hepatitis B virus (HBV) infection must be on suppressive therapy with an undetectable viral load.\n\n  * Please note: this lab is not a requirement for eligibility, however if it has been completed previously as part of the patient's health care, it should be documented for eligibility\n* Patients with a known history of hepatitis C virus (HCV) infection must have been treated and cured. For patients with a known HCV infection who are currently on treatment are eligible if they have an undetectable HCV viral load.\n\n  * Please note: this lab is not a requirement for eligibility, however if it has been completed previously as part of the patient's health care, it should be documented for eligibility\n* Patients with treated brain metastases must not have any evidence of progression on the follow-up brain imaging after central nervous system (CNS)-directed therapy.\n\n  * Note: All treatment for brain metastases must have been completed at least 28 days prior to registration\n* Futibatinib and other therapeutic agents used in this trial are known to be teratogenic. For this reason, patients of child-bearing potential (POCBP) and their partners with sperm-producing reproductive capacity must agree to use adequate contraception from time of informed consent, for the duration of study participation, and for 3 months following completion of study drug therapy. Should a POCBP become pregnant or suspect they are pregnant while they or their partner are participating in this study, they should inform their treating physician immediately. Patients with sperm-producing reproductive capacity (PWSPRC) treated or enrolled on this protocol must also agree to use adequate contraception with partners of childbearing potential from time of informed consent, for the duration of study participation, and 3 months after completion of study drug administration\n\n  * Note: A POCBP is any patient (regardless of gender, sexual orientation, having undergone a tubal ligation, or remaining celibate by choice) with an egg-producing reproductive tract who meets the following criteria:\n  * Has not undergone a hysterectomy or bilateral oophorectomy\n  * Has had menses at any time in the preceding 12 consecutive months (and therefore has not been naturally postmenopausal for \\> 12 months)\n* POCBP must have a negative pregnancy test prior to registration on study\n* Patients must have the ability to understand and the willingness to sign a written informed consent document and comply with the study requirements\n* Patients must have the ability to swallow, retain and absorb oral medications\n\nExclusion Criteria:\n\n* Patients with adenosquamous or mixed histology disease\n* Patients who have received\u002Fare receiving other investigational agents, or anticancer\u002Fantineoplastic therapy including chemotherapy, immunotherapy, biological response modifiers, anti-neoplastic endocrine therapy or devices concurrently or within 21 days or 5 times the half-life, whichever is shorter, prior to first dose of cycle 1\n* Patients who have previously received a FGFR inhibitor.\n\n  * Note: Agents that are multi-kinase inhibitors are allowed\n* Patients who have not recovered from adverse events due to prior anti-cancer therapy (i.e., have residual toxicities \\> grade 1) with the exception of alopecia, neuropathy and other non-significant adverse events per NCI CTCAE v 6.0\n* Patients who have a history of allergic reactions attributed to compounds of similar chemical or biologic composition to paclitaxel, ramucirumab, or futibatinib\n* Patients who have major surgical procedure planned during the study or any surgery within 28 days of registration or any subcutaneous venous access device placement within 7 days prior registration\n* Patients with known history or current symptoms of cardiac disease, or history of treatment with cardiotoxic agents, or who have experienced arterial thromboembolic events, including but not limited to myocardial infarction, transient ischemic attack, cerebrovascular accident, or unstable angina, within 6 months prior to registration ,should have a clinical risk assessment of cardiac function using the New York Heart Association Functional Classification.\n\n  * Note: To be eligible for this trial, patients should be class 2B or better\n* History of gastrointestinal perforation and\u002For fistulae within 6 months prior to registration\n* History of active bleeding or significant gastrointestinal (GI) bleeding requiring intervention within 60 days prior to registration\n* History and\u002For current evidence of endocrine alteration of calcium-phosphorus homeostasis. History and\u002For current evidence of ectopic mineralization\u002Fcalcification including but not limited to soft tissue, kidneys, intestine, or myocardia and lung with the exception of calcified lymph nodes and asymptomatic arterial calcification\n* Current evidence of retinal disorder\u002Fkeratopathy including but not limited to bullous\u002Fband keratopathy, corneal abrasion, inflammation\u002Fulceration, keratoconjunctivitis, etc., confirmed by ophthalmologic examination\n* Patients who have an uncontrolled intercurrent illness including, but not limited to any of the following:\n\n  * Hypertension that is not controlled on medication(per treating physician's discretion)\n  * Ongoing or active infection requiring systemic treatment\n  * Symptomatic congestive heart failure\n  * Unstable angina pectoris\n  * Cardiac arrhythmia\n  * Psychiatric illness\u002Fsocial situations that would limit compliance with study requirements\n  * Any other illness or condition that the treating investigator feels would interfere with study compliance or would compromise the patient's safety or study endpoints\n* Patients with a prior or concurrent malignancy whose natural history or treatment has the potential to interfere with the safety or activity assessment of the investigational regimen (per treating physician's discretion)\n* Patients who are pregnant or nursing","ALL","18 Years",{"count":19,"type":20},18,"ESTIMATED","INTERVENTIONAL",[23],"PHASE1","This phase I trial tests the safety, side effects and best dose of futibatinib with paclitaxel and ramucirumab for the treatment of patients with gastric, gastroesophageal junction or esophageal adenocarcinoma that has spread to nearby tissue or lymph nodes (locally advanced) or that cannot be removed by surgery (unresectable). Futibatinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Paclitaxel is in a class of medications called antimicrotubule agents. It stops cancer cells from growing and dividing and may kill them. Ramucirumab is a monoclonal antibody that may prevent the growth of new blood vessels that tumors need to grow. Giving futibatinib with paclitaxel and ramucirumab may be safe and tolerable in treating patients with locally advanced or unresectable gastric, gastroesophageal junction or esophageal adenocarcinoma.",[26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41],"Clinical Stage II Esophageal Adenocarcinoma AJCC v8","Clinical Stage III Esophageal Adenocarcinoma AJCC v8","Clinical Stage III Gastric Cancer AJCC v8","Clinical Stage III Gastroesophageal Junction Adenocarcinoma AJCC v8","Clinical Stage IV Esophageal Adenocarcinoma AJCC v8","Clinical Stage IV Gastric Cancer AJCC v8","Clinical Stage IV Gastroesophageal Junction Adenocarcinoma AJCC v8","Locally Advanced Esophageal Adenocarcinoma","Locally Advanced Gastric Adenocarcinoma","Locally Advanced Gastroesophageal Junction Adenocarcinoma","Metastatic Esophageal Adenocarcinoma","Metastatic Gastric Adenocarcinoma","Metastatic Gastroesophageal Junction Adenocarcinoma","Unresectable Esophageal Adenocarcinoma","Unresectable Gastric Adenocarcinoma","Unresectable Gastroesophageal Junction Carcinoma","NOT_YET_RECRUITING","2026-05-13",{"date":45,"type":46},"2026-05-18","ACTUAL",{"date":48,"type":20},"2027-09-09",{"date":50,"type":20},"2031-09-09",{"name":52,"class":53},"Northwestern University","OTHER",{"id":55,"slug":56,"hasResults":11,"nctId":57,"briefTitle":58,"officialTitle":59,"acronym":4,"eligibilityCriteria":60,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":61,"targetDuration":4,"studyType":21,"phases":63,"briefSummary":65,"conditions":66,"keywords":4,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":72,"completionDateStruct":74,"leadSponsor":76,"locationsCount":78},"100489321","phase-2-propranolol-in-combination-with-pembrolizumab-and-standard-chemotherapy-for-the-treatment-of-unresectable-locally-advanced-or-metastatic-esophageal-or-gastroesophageal-junction-adenocarcinoma-100489321","NCT05651594","Propranolol in Combination With Pembrolizumab and Standard Chemotherapy for the Treatment of Unresectable Locally Advanced or Metastatic Esophageal or Gastroesophageal Junction Adenocarcinoma","A Phase 2 Trial of Chemotherapy, Pembrolizumab, and Propranolol in Advanced Esophageal\u002FGastroesophageal Junction Adenocarcinoma Patients","Inclusion Criteria:\n\n* Age \\>= 18 years of age.\n* Participants must be newly diagnosed, treatment-naive with unresectable locally advanced or metastatic esophageal\u002Fgastroesophageal junction (GEJ) adenocarcinoma. Any prior systemic treatment for resectable disease must be six months or before. Prior PD-1\u002FPD-L1 treatment is allowed as long as the treatment was completed more than 1 year ago.\n* Have an Eastern Cooperative Oncology Group (ECOG) Performance Status of 0-1\n* Available archival Formalin-Fixed Paraffin-Embedded (FFPE) from a prior biopsy collected within 1 year or, participant must be willing to have a tissue biopsy taken prior to start of study treatment.\n* Have measurable disease per Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 criteria present.\n* Platelet \\>= 75,000\u002FuL\n* Hemoglobin \\>= 8 g\u002FdL (without transfusion in the past 14 days)\n* Absolute Neutrophil Count (ANC) \\>= 1500\u002FuL\n* Creatinine clearance (Cockcroft Gault) \\>= 30 mL\u002Fmin\n* Total bilirubin: =\\\u003C 2 × upper limit of normal (ULN) OR direct bilirubin =\\\u003C ULN for participants with total bilirubin levels \\> 2 × ULN\n* Aspartate aminotransferase (AST) (serum glutamic-oxaloacetic transaminase) (SGOT) and alanine transaminase (ALT) (serum glutamic-pyruvic transaminase) (SGPT) =\\\u003C 3 X institutional ULN (=\\\u003C 5 × ULN for participants with liver metastases)\n* Participants of child-bearing potential must have a negative pregnancy test at study entry and then agree to use adequate contraceptive methods (e.g., hormonal or barrier method of birth control; abstinence) prior to study entry. Should a woman become pregnant or suspect she is pregnant while she or her partner is participating in this study, she should inform her treating physician immediately.\n* Ability to swallow and retain oral medication. If a patient is not able to swallow or is experiencing dysphagia that limits ability to swallow oral medication, they are still eligible for study provided they can swallow liquid formula propranolol or have an enteric feeding tube placed which will permit administration of crushed tablets or liquid formula propranolol. Liquid and tablet formulations may be used interchangeably for patients in the event of a shortage of either formulation\n* Participant must understand the investigational nature of this study and sign an Independent Ethics Committee\u002FInstitutional Review Board approved written informed consent form prior to receiving any study related procedure.\n\nExclusion Criteria:\n\n* Patients with HER 2-positive cancer.\n* Patients with active, untreated central nervous system metastases or leptomeningeal disease.\n* Patients with active autoimmune disease, requiring ongoing immunosuppressive therapy or history of transplantation.\n\n  * Patients currently treated with systemic immunosuppressive agents: If a patient is currently on steroids, they must be on a steroid dose less than or equal to an equivalent prednisone dose of 10 mg daily.\n* Has a history of (non-infectious) pneumonitis\u002Finterstitial lung disease that required treatment.\n* Has a concurrent Human Immunodeficiency Virus (HIV) infection.\n* Concurrent active Hepatitis B (defined as Hepatitis B virus surface antigen \\[HBsAg\\] positive and\u002For detectable Hepatitis B virus \\[HBV\\] deoxyribonucleic acid DNA) and Hepatitis C virus (defined as anti-HCV antibody \\[Ab\\] positive and detectable HCV ribonucleic acid \\[RNA\\]) infection. Note: Hepatitis B and C screening tests are not required unless known history of HBV and HCV infection.\n* Participants that are already on beta-adrenergic (B-AR) blockers for various indications.\n* Has received prior radiotherapy within 2 weeks of start of study intervention. Participants must have recovered from all radiation-related toxicities, not require corticosteroids, and not have had radiation pneumonitis. A 1-week washout is permitted for palliative radiation (=\\\u003C2 weeks of radiotherapy) to non-central nervous system (CNS) disease.\n* Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness\u002Fsocial situations that would limit compliance with study requirements.\n* Pregnant or nursing female participants, where pregnancy is defined as the state of a female after conception and until the termination of gestation, confirmed by a positive human chorionic gonadotropin (hCG) laboratory test.\n* Other active cancers that require systemic treatment.\n* Contraindications to the use of beta-blockers, e.g.: uncontrolled depression, unstable angina pectoris, uncontrolled heart failure ( Grade III or IV), hypotension (systolic blood pressure \\\u003C100 mmHg), severe asthma or chronic obstructive pulmonary disease (COPD), uncontrolled type I or type II diabetes mellitus (HbA1C \\> 8.5 or fasting plasma glucose \\> 160 mg\u002Fdl at screening), symptomatic peripheral arterial disease or Raynaud's syndrome, untreated pheochromocytoma etc.\n* Has received a live vaccine or live-attenuated vaccine within 30 days prior to the first dose of trial treatment and while participating in the trial. Examples of live vaccines include, but are not limited to, the following: measles, mumps, rubella, varicella\u002Fzoster etc.\n* Unwilling or unable to follow protocol requirements.\n* Any condition which in the Investigator's opinion deems the participant an unsuitable candidate to receive study drug.",{"count":62,"type":20},40,[64],"PHASE2","This phase II trial tests what effects the addition of propranolol to pembrolizumab and standard chemotherapy (mFOLFOX) may have on response to treatment in patients with esophageal or gastroesophageal junction cancer that cannot be removed by surgery and has spread to nearby tissue or lymph nodes (unresectable locally advanced) or has spread from where it first started (primary site) to other places in the body (metastatic). Propranolol is a drug that is classified as a beta-blocker. Beta-blockers affect the heart and circulation (blood flow through arteries and veins). Cancer patients may be under a tremendous amount of stress with elevated levels of norepinephrine (a hormone produced by the adrenal glands in response to stress). Increased adrenergic stress may dampen the immune system, which beta-blockers, like propranolol, may be able to counteract. Immunotherapy with monoclonal antibodies, such as pembrolizumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Drugs used in the standard chemotherapy regimen, mFOLFOX (leucovorin, fluorouracil and oxaliplatin) work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Adding propranolol to pembrolizumab and standard mFOLFOX chemotherapy may increase the effectiveness of the pembrolizumab + mFOLFOX regimen.",[26,27,29,30,32,33,35,36,38,39,67],"Unresectable Gastroesophageal Junction Adenocarcinoma","RECRUITING","2025-12-10",{"date":71,"type":46},"2025-12-16",{"date":73,"type":46},"2023-03-07",{"date":75,"type":20},"2029-03-30",{"name":77,"class":53},"Roswell Park Cancer Institute",1]