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Metastatic Pancreatic Carcinoma clinical trials

View clinical trials related to Metastatic Pancreatic Carcinoma.

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NCT ID: NCT03033225 Completed - Pancreatic Neoplasm Clinical Trials

Ultrasound-Guided Verteporfin Photodynamic Therapy for the Treatment of Unresectable Solid Pancreatic Tumors or Advanced Pancreatic Cancer, VERTPAC-02 Study

Start date: December 6, 2016
Phase: Phase 2
Study type: Interventional

This phase II trial studies how well ultrasound-guided verteporfin photodynamic therapy works for the treatment of patients with solid pancreatic tumors that cannot be removed by surgery (unresectable) or pancreatic cancer that has spread to other places in the body (advanced). Photodynamic therapy is a type of laser device that is guided by ultrasound imaging and used in combination with the drug verteporfin that may be less invasive and as effective as current treatment methods for patients with pancreatic cancer.

NCT ID: NCT00480584 Completed - Clinical trials for Metastatic Pancreatic Carcinoma

A Phase I Trial of Capecitabine in Combination With Gemcitabine and Erlotinib for Advanced Pancreatic Cancer

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

This is a phase I clinical trial examining the safety, feasibility, and toxicity of gemcitabine and erlotinib when given in combination with capecitabine in adult patients with locally advanced unresectable or metastatic pancreatic adenocarcinoma. Treatment will be administered at Moffitt on an outpatient basis and consists gemcitabine once per week for 3 weeks, followed by a week off treatment. Erlotinib (tablet) taken by mouth continuously starting with day one of cycle 1 with capecitabine taken twice per day on days 1-14 of each cycle followed by a 2 week off treatment rest period. An accelerated dose-escalation scheme will be employed with 4 planned dose levels. Whenever patients have been enrolled at a given dose with at most 1 DLT, the protocol will be stopped and the dose will be called the maximum tolerated dose (MTD). Patients will be treated at the recommended phase II dose (RPTD) to confirm tolerability at that dose. In the absence of treatment delays due to adverse events, treatment may continue for 6 cycles or until disease progression and patients may continue on the study regimen unless they experience an adverse event that meets the criteria for a dose limiting toxicity.

NCT ID: NCT00137761 Completed - Clinical trials for Metastatic Pancreatic Carcinoma

Docetaxel in Combination With Iressa in Previously Treated Patients With Pancreatic Cancer

Start date: October 2004
Phase: Phase 2
Study type: Interventional

The purpose of this study is to find out what activity the combination of docetaxel and Iressa have against metastatic pancreatic cancer.