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Carcinoma clinical trials

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NCT ID: NCT02129322 Withdrawn - Clinical trials for Hepatocellular Carcinoma

Effect of Adjuvant Therapy by Sorafenib, Oxaliplatin and S-1

Start date: July 2015
Phase: Phase 2
Study type: Interventional

The study is designed to investigate the effect of adjuvant therapy by Sorafenib, Oxaliplatin and S-1 to prevent the tumor recurrence for hepatocellular carcinoma after liver transplantation

NCT ID: NCT02119728 Withdrawn - Clinical trials for Recurrent Squamous Cell Carcinoma of the Lip and Oral Cavity

Photodynamic Therapy With HPPH in Treating Patients With Squamous Cell Carcinoma of the Oral Cavity

Start date: n/a
Phase: Phase 2
Study type: Interventional

This randomized phase II trial studies how well photodynamic therapy with HPPH works in treating patients with squamous cell carcinoma of the oral cavity. Photodynamic therapy uses HPPH that becomes active when it is exposed to a certain kind of light. When the drug is active, cancer cells are killed. This may be effective against squamous cell carcinoma of the oral cavity.

NCT ID: NCT02105350 Withdrawn - Clinical trials for Biliary Tract Carcinoma

A Study of MEK162 With Gemcitabine and Oxaliplatin in Biliary Cancer

Start date: June 2015
Phase: Phase 1
Study type: Interventional

This is a phase I study (an early study to check the safety of a new drug or drug combination) to find the safest and most tolerated dose of the combination of oxaliplatin with gemcitabine and MEK 162 in patients with biliary cancer (including gallbladder cancers and cancers associated with the bile ducts leading from the gallbladder and to and from the liver) that is not curable by surgery and/or has spread beyond the biliary tree (place where cancer started). Everyone will receive the same standard doses of oxaliplatin and gemcitabine but may receive different doses of MEK 162. MEK 162 is a new drug which plays an important role in the regulation of cell growth and has been shown to shrink tumours in patients with biliary cancer and other types of human cancers. This type of drug has also been shown to shrink tumours when given in combination with cisplatin and gemcitabine in research studies done in animals and in some patients with biliary cancer.

NCT ID: NCT02083536 Withdrawn - Ovarian Cancer Clinical Trials

LDFWART With Docetaxel in Patients With Platinum-Resistant Recurrent Ovarian Carcinoma

Start date: May 2014
Phase: Phase 1
Study type: Interventional

The ultimate clinical aim of this proposed phase I trial is to evaluate the toxicity and determine the recommended phase II dose of combining the effect of LDFWART following administration of docetaxel for 6 cycles in patients with recurrent platinum-resistant ovarian cancer.

NCT ID: NCT02041819 Withdrawn - Clinical trials for Squamous Cell Carcinoma of Esophagus

Neoadjuvant Chemotherapy of Nimotuzumab Plus Nab-Paclitaxel in Squamous Cell Carcinoma of Esophagus

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

Nimotuzumab, a humanized monoclonal antibody against epidermal growth factor receptor (EGFR),has been shown to be effective and safe in some studies with head-neck cancers.Nab-paclitaxel regimen in advanced NSCLC has a better tumor response rate and safety than solvent-based paclitaxel.However,the safety and efficacy of Nimotuzumab plus nab-paclitaxel regimen is uncertain in neoadjuvant therapy in esophageal cancer.The investigators then initiated a phase II clinical trial with Nimotuzumab plus Nab-paclitaxel/cisplatin as the neoadjuvant chemotherapy in patients with locally advanced esophageal squamous cell carcinoma to observe the efficacy and safety of the combination.

NCT ID: NCT02034968 Withdrawn - Clinical trials for Stage IV Esophageal Squamous Cell Carcinoma

Nimotuzumab Plus Nab-paclitaxel and Cisplatin in Treating Patients With Advanced Esophageal Carcinoma

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

There have been reports suggesting that anti-epidermal growth factor antibody nimotuzumab is advantageous for advanced esophageal cancer patients in combination with chemotherapy or radiotherapy.And,albumin-bound paclitaxel was characterized with high tolerated doses with greater efficacy,and with greater concentration in tumor tissue compared with normal tissues.So,The objective of this single-arm phase II trial was to evaluate the benefit of nimotuzumab plus nab-paclitaxel and cisplatin in patients with advanced esophageal carcinoma.

NCT ID: NCT02033538 Withdrawn - Clinical trials for Squamous Cell Carcinoma of Esophagus

Neoadjuvant Chemotherapy of Nanoparticle Albumin-bound Paclitaxel in Squamous Cell Carcinoma of Esophagus

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

Albumin-bound paclitaxel regimen in advanced NSCLC has a better tumor response rate and safety than solvent-based paclitaxel. However, the safety and efficacy is uncertain in neoadjuvant therapy in esophageal cancer. The objective of this single-arm phase II trial was to evaluate the benefit of neoadjuvant chemotherapy with nanoparticle albumin-bound paclitaxel plus 5-fluorouracil in patients with locally advanced esophageal squamous cell carcinoma.

NCT ID: NCT02014831 Withdrawn - Clinical trials for Squamous Cell Carcinoma of the Penis

Efficacy and Safety of Cetuximab in Metastatic Penile Carcinoma (PENILANE)

PENILANE
Start date: February 2016
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of Cetuximab in metastatic penile carcinoma

NCT ID: NCT02011594 Withdrawn - Clinical trials for Stage IV Esophageal Squamous Cell Carcinoma

Phase II Study of Maintenance Treatment of Nimotuzumab for Advanced Esophageal Carcinoma

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

There have been reports suggesting that anti-epidermal growth factor antibody nimotuzumab is advantageous for advanced esophageal cancer patients in combination with chemotherapy or radiotherapy. However, whether maintenance therapy of nimotuzumab provides benefit to advanced esophageal cancer patients is not known.

NCT ID: NCT02004210 Withdrawn - Clinical trials for Hepatocellular Carcinoma

A Phase 3 Trial Comparing TACE and TARE in Unilobar Advanced Hepatocellular Carcinoma

Start date: April 2013
Phase: Phase 3
Study type: Interventional

The aim of this study is to compare the efficacy of conventional transarterial chemoembolization(TACE) and transarterial radioembolization in patients with unilobar advanced hepatocellular carcinoma.