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Adenocarcinoma of the Stomach clinical trials

View clinical trials related to Adenocarcinoma of the Stomach.

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NCT ID: NCT03722108 Terminated - Clinical trials for Adenocarcinoma of the Gastroesophageal Junction

Regorafenib Combined With Irinotecan as Second-line in Patients With Metastatic Gastro-oesophageal Adenocarcinomas

REGIRI
Start date: February 7, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

Trial evaluating the efficacy of regorafenib combined with irinotecan compared to irinotecan alone in second-line treatment of patients with metastatic gastro-oesophageal adenocarcinomas.

NCT ID: NCT03647969 Active, not recruiting - Clinical trials for GastroEsophageal Cancer

Modified FOLFOX Plus/Minus Nivolumab and Ipilimumab vs. FLOT Plus Nivolumab in Patients With Previously Untreated Advanced or Metastatic Gastric Cancer

Start date: November 7, 2018
Phase: Phase 2
Study type: Interventional

Patients with Her2 negative, previously untreated metastatic esophagogastric adenocarcinoma will be treated with modified FOLFOX, with modified FOLFOX plus Nivolumab and Ipilimumab or FLOT plus Nivolumab. The groups will be compared for time until progression of the disease (primary endpoint) as well as for response to the treatment, overall survival, safety/tolerability of the treatment and quality of life.

NCT ID: NCT02678182 Recruiting - Clinical trials for Adenocarcinoma of the Stomach

Planning Treatment for Oesophago-gastric Cancer: a Maintenance Therapy Trial

PLATFORM
Start date: February 2015
Phase: Phase 2
Study type: Interventional

To evaluate the efficacy of maintenance therapies following completion of standard first-line chemotherapy in patients with locally advanced or metastatic HER-2 positive or HER-2 negative oesophago-gastric adenocarcinomas.

NCT ID: NCT02202759 Active, not recruiting - Clinical trials for Adenocarcinoma of the Stomach

A Study of MLN0264 in Patients With Cancer of the Stomach or Gastroesophageal Junction

Start date: July 2014
Phase: Phase 2
Study type: Interventional

The purpose of this study is to assess the efficacy, safety and tolerability of MLN0264 in patients with recurrent or metastatic guanylyl cyclase C (GCC)-positive adenocarcinoma of the stomach or gastroesophageal junction.

NCT ID: NCT01962519 Recruiting - Clinical trials for Adenocarcinoma of the Stomach

Early Oral Feeding After Total Gastrectomy for Cancer

Start date: January 2012
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the possibility of shortening postoperative hospital stay after gastrectomy by early oral feeding as a component of an enhanced recovery protocol (ERAS).

NCT ID: NCT01640782 Completed - Clinical trials for Adenocarcinoma of the Gastroesophageal Junction

Intergroup Trial of Adjuvant Chemotherapy in Adenocarcinoma of the Stomach

ITACA-S
Start date: February 2005
Phase: Phase 3
Study type: Interventional

Open label, randomised, multicenter, superiority study for efficacy. Patients with histologically proven adenocarcinoma of the stomach or gastroesophageal junction without gross or microscopic evidence of residual disease after surgery with curative intent and fulfilling all the inclusion/exclusion criteria are eligible for this study.

NCT ID: NCT01561014 Completed - Clinical trials for Adenocarcinoma of the Gastroesophageal Junction

Oxaliplatin, Fluorouracil, Erlotinib Hydrochloride, and Radiation Therapy Before Surgery and Erlotinib Hydrochloride After Surgery in Treating Patients With Locally Advanced Cancer of the Esophagus or Gastroesophageal Junction

Start date: April 2007
Phase: Phase 1
Study type: Interventional

This phase I trial is studying the side effects and best dose of erlotinib hydrochloride when given together with oxaliplatin, fluorouracil, and radiation before surgery and alone after surgery in treating patients with locally advanced cancer of the esophagus and gastroesophageal junction. Drugs used in chemotherapy, such as oxaliplatin and fluorouracil, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Erlotinib hydrochloride may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Radiation therapy uses high-energy x-rays to kill tumor cells. Giving combination chemotherapy together with erlotinib hydrochloride and radiation therapy before surgery may make the tumor smaller and reduce the amount of normal tissue that needs to be removed. Giving erlotinib hydrochloride after surgery may kill any tumor cells that remain after surgery

NCT ID: NCT01472029 Completed - Clinical trials for Adenocarcinoma of the Gastroesophageal Junction

Explorative Phase II Study of Perioperative Treatment in Patients With Adenocarcinoma of the Gastroesophageal Junction or Stomach

HerFLOT
Start date: December 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the rate of complete pathological responses (percentage of patients with pCR referring to the total number of enrolled and eligible patients), as evaluated centrally by a reference pathologist.

NCT ID: NCT01233505 Terminated - Clinical trials for Unspecified Adult Solid Tumor, Protocol Specific

Veliparib, Oxaliplatin, and Capecitabine in Treating Patients With Advanced Solid Tumors

Start date: October 2010
Phase: Phase 1
Study type: Interventional

This phase I trial is studying the side effects and the best dose of veliparib when given together with capecitabine and oxaliplatin in treating patients with advanced solid tumors. Veliparib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as capecitabine and oxaliplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving veliparib together with capecitabine and oxaliplatin may kill more tumor cells.

NCT ID: NCT01095120 Active, not recruiting - Clinical trials for Adenocarcinoma of the Stomach

Tesetaxel as Second-line Therapy for Patients With Advanced Gastric Cancer

Start date: March 2010
Phase: Phase 2
Study type: Interventional

Tesetaxel is an orally administered chemotherapy agent of the taxane class. This study is being undertaken to evaluate the efficacy and safety of tesetaxel administered as second-line therapy to patients with advanced gastric cancer.