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Carcinoma, Squamous Cell clinical trials

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NCT ID: NCT00454779 Completed - Clinical trials for Metastatic or Recurrent Squamous Cell Carcinoma of Head and Neck

PARTNER: Panitumumab Added to Regimen for Treatment of Head aNd Neck Cancer Evaluation of Response

Start date: January 1, 2007
Phase: Phase 2
Study type: Interventional

This is a randomized, open-label, 2-arm, controlled, phase 2, multi-center, estimation clinical trial of docetaxel and cisplatin combination chemotherapy with and without panitumumab in the first-line treatment of subjects with metastatic or recurrent head and neck cancer, as well as a cross-over second-line panitumumab monotherapy of subjects who fail the chemotherapy only arm. This study will be conducted in the United States. Approximately 150 subjects with histologically or cytologically confirmed metastatic and/or recurrent SCCHN.

NCT ID: NCT00454142 Completed - Clinical trials for Stage IV Squamous Cell Carcinoma of the Nasopharynx

Pazopanib Hydrochloride in Treating Patients With Stage IV or Recurrent Nasopharyngeal Cancer

Start date: August 2007
Phase: Phase 2
Study type: Interventional

This phase II trial studies the side effects and how well pazopanib hydrochloride works in treating patients with stage IV or recurrent nasopharyngeal cancer. Pazopanib hydrochloride 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.

NCT ID: NCT00450138 Completed - Clinical trials for Head and Neck Cancer

Open Label, Phase I ZD6474 Head and Neck Cancer Study

Start date: December 2006
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the maximum tolerated dose of ZD6474 given in combination with radiation or in combination with chemotherapy and radiation in patients with squamous cell carcinoma of the head and neck.

NCT ID: NCT00448240 Terminated - Clinical trials for Head and Neck Cancer

Erlotinib (Tarceva) During First Line Standard Platinum Containing Chemo for Advanced Squamous Cell Head and Neck Cancer

Start date: February 2007
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determine if combination Erlotinib, Cisplatin/Carboplatin, and Paclitaxel are effective first line treatment for metastatic, recurrent and persistent squamous cell carcinoma of the head and neck.

NCT ID: NCT00446446 Completed - Cancer Clinical Trials

PRISM (Panitumumab Regimen In Second-line Monotherapy of Head and Neck Cancer)

Start date: October 30, 2007
Phase: Phase 2
Study type: Interventional

To estimate the effect of second-line panitumumab monotherapy on objective response in patients with metastatic or recurrent squamous cell carcinoma of head and neck (SCCHN).

NCT ID: NCT00443261 Terminated - Clinical trials for Squamous Cell Carcinoma

Azacitidine and Cisplatin for Patients With Recurrent or Metastatic Squamous Cell Carcinoma of the Head and Neck

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

To evaluate the safety and toxicity of azacitidine (5-azacitidine, Vidaza®) and cisplatin combination in patients with squamous cell carcinoma of head and neck (SCCHN).

NCT ID: NCT00442455 Completed - Clinical trials for Squamous Cell Carcinoma of the Head and Neck

Erlotinib,Radiation and Cisplatin in Patients With Complete Resected Squamous Cell Carcinoma of the Head and Neck

Start date: January 2006
Phase: Phase 3
Study type: Interventional

The purpose of the study is to determinate the free-progression interval in patients with surgically resected locally advanced squamous cell carcinoma of head and neck treated with the maximum tolerated dose of the combination of erlotinib, radiation therapy and cisplatin, previously established in a safety trial.

NCT ID: NCT00432315 Completed - Clinical trials for Carcinoma, Squamous Cell

Docetaxel in Non Small Cell Lung Cancer (NSCLC)

Start date: May 2001
Phase: Phase 2
Study type: Interventional

Primary objective: • To assess the response rate to induction therapy with docetaxel/CDDP. Secondary objectives: To assess - Resectability after induction therapy - Time to progression - Overall survival - Safety profile - Quality of Life

NCT ID: NCT00427102 Terminated - Clinical trials for Head and Neck Cancer

MRX, Radiation, and Chemotherapy for Patients With Resected Squamous Cell Carcinoma of the Head and Neck

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

Rationale for Study Oral mucositis is a major complication arising from contemporary chemoradiation treatment of patients with head and neck cancer. No effective therapy exists to prevent this complication in this population. MRX-1024 is an investigational agent that has demonstrated in in vitro and in vivo experiments to have the potential to exert a protective effect in normal mucosa cells, without interfering with the intended antitumor effect of radiation. A pilot Phase 1 study of MRX-1024 was conducted in India in patients with head and neck cancer receiving radiation alone or radiation in combination with cisplatin or carboplatin. MRX 1024 doses of 100 mgkg given orally twice a day, five days a week during radiation treatment cycles, were well tolerated and appeared to exert a protective effect against the development of severe mucositis. Twice daily doses of MRX 1024 impose a certain level of inconvenience to the patient, to their clinic companion, and to the general work flow within radiation oncology clinics. This study is designed to study the safety and pharmacokinetics of both single daily dose and twice daily dose regimens of oral MRX 1024 given in conjunction with daily radiation fractions and intermittent high-dose cisplatin to patients with high-risk for recurrence head and neck cancer following surgical resection. The study will also document the incidence and severity of oral mucositis that occurs following such therapy. The results will be instrumental in determining the regimen of MRX 1024 to use in subsequent definitive clinical trials.

NCT ID: NCT00426062 Recruiting - Clinical trials for Squamous Cell Carcinoma

Free Radical Level in SCC of Tongue Patients Tumor, Serum and Saliva

Start date: n/a
Phase: Phase 1
Study type: Observational

Study comparing level of free radicals in tumor tissue, blood serum and saliva in patients with Squamous Cell Carcinoma of tongue and mouth floor. Patients with benign fibroma of oral cavity and normal gingiva around extracted lower wisdom tooth are used for control