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Active clinical trials for "Adenocarcinoma"

Results 1301-1310 of 2249

Gemcitabine in Treating Patients With Recurrent or Persistent Endometrial Cancer

Endometrial AdenocarcinomaEndometrial Adenosquamous Carcinoma2 more

This phase II trial is studying the side effects of gemcitabine and to see how well it works in treating patients with recurrent or persistent endometrial cancer. Drugs used in chemotherapy, such as gemcitabine, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing.

Completed47 enrollment criteria

Open-Label Phase 2 Efficacy Trial of Cancer Macrobeads in Patients With Treatment-Resistant Pancreatic/Colorectal...

Pancreatic Adenocarcinoma Non-resectablePancreatic Adenocarcinoma Metastatic1 more

This is a clinical research study of an investigational (FDA BB-IND 10091) treatment for patients with pancreatic cancer (all stages) and advanced colorectal cancer that no longer responds to standard therapies. The treatment is being evaluated for its effect on tumor growth. It consists of the placement (implantation) of small beads that contain mouse renal adenocarcinoma cells (RENCA macrobeads). The cells in the macrobeads produce substances that have been shown to slow or stop the growth of tumors in experimental animals and veterinary patients. It has been tested in 31 human subjects with different types of cancers in a Phase I safety trial. Phase II studies in patients with colorectal, pancreatic or prostate cancers are in progress.

Completed46 enrollment criteria

Gemcitabine and Pemetrexed in Primary Unknown Adenocarcinoma

Adenocarcinoma

There is no standard treatment for the patient population being asked to participate in this study. Although one current regimen, used by some investigators, has a high rate of response compared to other therapies, it is associated with moderate to severe toxicity. As gemcitabine and pemetrexed have a broad range of activity against cancer it is reasonable to determine how active and safe they are against patients with this type of cancer.The objective of this study is to determine the anti-tumor activity of pemetrexed and gemcitabine in patients with this condition.

Completed10 enrollment criteria

Vinorelbine in Unresectable or Metastatic Esophageal and Gastric Adenocarcinoma

Esophageal CancerGastric Cancer1 more

The purpose of this study is to collect anti-tumor activity of vinorelbine when given to patients with esophageal or gastric tumors. We will also collect information on the toxicities of vinorelbine in these patients.

Completed14 enrollment criteria

Sorafenib, Docetaxel, and Cisplatin in Treating Patients With Metastatic or Advanced Gastric or...

Adenocarcinoma of the Gastroesophageal JunctionMetastatic Gastric Cancer1 more

This phase II trial is studying how well giving sorafenib together with docetaxel and cisplatin works in treating patients with metastatic or locally advanced gastric or gastroesophageal junction cancer that cannot be removed by surgery. Sorafenib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor. Drugs used in chemotherapy, such as docetaxel and cisplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving sorafenib together with docetaxel and cisplatin may kill more tumor cells.

Completed31 enrollment criteria

Phase I/II Trial of Radiation, Avastin and Tarceva for Pancreatic Adenocarcinoma

Pancreatic Cancer

The primary purpose of this trial is to define the maximum tolerated and/or recommended phase II dose of the combination of Avastin and Tarceva in patients undergoing radiation therapy for carcinoma of the pancreas. An additional primary objective is to describe the frequency and nature of grade III/IV and grade I/II toxicities associated with this regimen. Secondary objectives include describing 1-year disease-free survival and overall survival rates as well as to estimate clinical and pathologic complete response rates associated with this regimen.

Completed27 enrollment criteria

SU5416 and Irinotecan in Treating Patients With Advanced Colorectal Cancer

Adenocarcinoma of the ColonAdenocarcinoma of the Rectum6 more

Phase I/II trial to study the effectiveness of combining SU5416 and irinotecan in treating patients who have advanced colorectal cancer. SU5416 may stop the growth of colorectal cancer by stopping blood flow to the tumor. Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die

Completed33 enrollment criteria

Docetaxel With or Without Thalidomide in Treating Patients With Metastatic Prostate Cancer

Stage IV Prostate CancerAdenocarcinoma of the Prostate1 more

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Thalidomide may stop the growth of prostate cancer by stopping blood flow to the tumor. PURPOSE: Randomized phase II trial to compare the effectiveness of docetaxel with or without thalidomide in treating patients who have metastatic prostate cancer.

Completed2 enrollment criteria

Vaccine Therapy With or Without Sargramostim in Treating Patients With Advanced or Metastatic Cancer...

Adenocarcinoma of the ColonAdenocarcinoma of the Gallbladder40 more

Phase I trial to study the effectiveness of vaccine therapy with or without sargramostim in treating patients who have advanced or metastatic cancer. Vaccines may make the body build an immune response to kill tumor cells. Colony-stimulating factors such as sargramostim may increase the number of immune cells found in bone marrow or peripheral blood. Combining vaccine therapy with sargramostim may make tumor cells more sensitive to the vaccine and may kill more tumor cells

Completed71 enrollment criteria

Assessment of Compliance With Monitoring Conducted by a Physician in Person or by a Nurse in Remote...

Stage I Testicular SeminomaStage I Testicular Nonseminomatous Germ Cell Tumor15 more

This is a multicenter, interventional, randomized study among adult patients recently diagnosed with a rare tumor (<12 months). The study will aim to compare compliance with the personalized post-treatment surveillance plan, established for each patient according to national guidelines, when the surveillance is conducted in person by a hospital-based physician (control arm) or remotely by a trained nurse (experimental arm).

Not yet recruiting14 enrollment criteria
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