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Stomach Neoplasms clinical trials

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NCT ID: NCT03026881 Recruiting - Clinical trials for Recurrent and Metastatic Gastric Cancer

A Study of Fluzoparib Given in Combination With Apatinib and Paclitaxel in Gastric Cancer Patients

Start date: January 2017
Phase: Phase 1
Study type: Interventional

Fluzoparib is an oral potent, selective PARP-1 and PARP-2 inhibitor; Apatinib is an oral selective VEGFR inhibitor. This open-label, dose finding phase I trial studies the tolerability and the best dose of Fluzoparib in combination with apatinib and paclitaxel and to see how well this three drugs work together in the treatment of patients with recurrent and metastatic gastric cancer who progress following first-line therapy. The safety and efficacy of fluzoparib in combination with apatinib and paclitaxel will be explored.

NCT ID: NCT03025152 Terminated - Gastric Cancer Clinical Trials

Efficacy and Safety of Hou Gu Mi Xi in Patients With Spleen Qi Deficiency and Radical Gastrectomy for Gastric Cancer

Start date: November 11, 2016
Phase: N/A
Study type: Interventional

This trial aims to determine whether Hou Gu Mi Xi is an effective treatment for improving symptoms and indicators in patients with spleen qi deficiency and radical gastrectomy for gastric cancer.

NCT ID: NCT03023436 Recruiting - Stomach Neoplasm Clinical Trials

Cytoreductive Surgery Combined With HIPEC and Chemotherapy for Gastric Cancer With Peritoneal Metastasis

Start date: January 2016
Phase: Phase 3
Study type: Interventional

This study evaluates the survival benefit and safety of cytoreductive surgery(CRS) combined with HIPEC and chemotherapy in gastric cancer with peritoneal metastasis.

NCT ID: NCT03019588 Terminated - Clinical trials for Gastroesophageal Junction Adenocarcinoma

Efficacy and Safety Study of Pembrolizumab (MK-3475) Versus Paclitaxel in Asian Participants With Advanced Gastric or Gastroesophageal Junction Adenocarcinoma Who Progressed After First-line Therapy With Platinum and Fluoropyrimidine (MK-3475-063/KEYNOTE-063)

Start date: February 16, 2017
Phase: Phase 3
Study type: Interventional

The study will compare the efficacy and safety of treatment with pembrolizumab (MK-3475) versus paclitaxel in Asian, programmed death-ligand 1 (PD-L1) positive participants with advanced gastric or gastroesophageal junction (GEJ) adenocarcinoma who have progressed after failure of any combination chemotherapy containing a platinum and a fluoropyrimidine agent. The primary study hypotheses are that pembrolizumab prolongs Overall Survival (OS) compared to paclitaxel and that pembrolizumab prolongs Progression-free Survival (PFS) per Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1) assessed by blinded central radiologists' review compared to paclitaxel.

NCT ID: NCT03017690 Completed - Clinical trials for Gastroenteropancreatic Neuroendocrine Tumor

Lanreotide and Octreotide Long Acting Release (LAR) for Patients With Advanced Gastroenteropancreatic Neuroendocrine Tumors (GEP-NETs)

Start date: April 12, 2017
Phase:
Study type: Observational

An observational time and motion study in a clinical oncology setting is utilized in order to measure and compare product attributes and overall product efficiency between lanreotide and octreotide LAR.

NCT ID: NCT03016026 Recruiting - Stomach Neoplasms Clinical Trials

Enhanced Recovery After Surgery (ERAS) on Laparoscopy-assisted Distal Gastrectomy

Start date: November 2016
Phase: Phase 2
Study type: Interventional

This study evaluates the safety and effectiveness of enhanced recovery after surgery(ERAS) on laparoscopic distal gastrectomy for gastric cancer.All of participants received an ERAS program.

NCT ID: NCT03015675 Recruiting - Gastric Cancer Clinical Trials

IV Ascorbic Acid in Advanced Gastric Cancer

Start date: March 12, 2017
Phase: Phase 3
Study type: Interventional

Linus Pauling and Dr Ewan Cameron have published two retrospective studies about using high dose vitamin C to treat cancer patients forty years ago. Their studies have shown that high dose vitamin C usage could significantly prolong overall survival of patients with advanced cancer. Recently, preclinical study has shown that human colorectal cancer cells harboring KRAS or BRAF mutations are selectively killed by high levels of ascorbic acid (AA). High dose of AA impairs tumor growth in Apc/KRASG12D mutant mice. Previous phaseⅠclinical trials have found that high dose (1.5g/kg or 90g/m2) iv AA is well tolerated in cancer patients. This protocol is a phase Ⅲ, study of ascorbic acid (AA) infusions combined with treatment with mFOLOX6 versus mFOLOX6 alone as first-line therapy in patients with recurrent or advanced gastric cancer.

NCT ID: NCT03015298 Not yet recruiting - Clinical trials for Gastric Cancer Stage

Comparing the Diagnostic Role of PET/MRI and of PET/CT Among Patients With Gastric Cancer

Start date: January 2017
Phase: N/A
Study type: Observational

The results of PET/MRI and PET/CT in each recruited gastric cancer patients will be compared.

NCT ID: NCT03013712 Recruiting - Prostate Cancer Clinical Trials

A Clinical Research of CAR T Cells Targeting EpCAM Positive Cancer

CARTEPC
Start date: January 2017
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of EpCAM-specific CAR T Cells infusion for EpCAM positive Cancer.

NCT ID: NCT03013010 Recruiting - Adenocarcinoma Clinical Trials

PREACT Study: Locally Advanced Gastric Cancer, Chemoradiotherapy vs. Chemotherapy Followed by D2 Surgery and Adjuvant Chemotherapy

PREACT
Start date: December 2016
Phase: Phase 3
Study type: Interventional

Although the incidence of gastric cancer has been substantially declining for several decades, it is still the sixth most common cancer and the fourth most frequent cause of cancer death worldwide. Surgery is still the only curative option for gastric cancer. However, most patients are unable to undergo surgery because of late stage, unresectable disease. The prognosis for these patients is very poor. Although the Magic trial showed that perioperative chemotherapy can increase the rate of curative surgery and significantly improve overall survival in patients with operable gastric or lower esophageal adenocarcinomas, no pCR events were reported in this trial. The intervention arm in PREACT consists of pre-operative chemotherapy, pre-operative radiochemotherapy, surgery and post-operative chemotherapy. The control arm consists of pre-operative chemotherapy, surgery, and post-operative chemotherapy. The primary purpose of PREACT is to investigate whether the addition of radiochemotherapy to chemotherapy is superior to chemotherapy alone in the pre-operative setting in improving disease free survival in patients with locally advanced gastric or esophagogastric junction adenocarcinoma.