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Active clinical trials for "Carcinoma, Squamous Cell"

Results 1111-1120 of 1867

Vaccine Therapy in Treating Patients With Persistent or Recurrent Cervical Cancer

Cervical AdenocarcinomaCervical Adenosquamous Carcinoma3 more

This phase II trial studies the side effects and how well vaccine therapy works in treating patients with cervical cancer that does not go to remission despite treatment (persistent) or has come back (recurrent). Vaccines therapy may help the body build an effective immune response to kill tumor cells.

Completed58 enrollment criteria

Brivanib Alaninate in Treating Patients With Persistent or Recurrent Cervical Cancer

Cervical AdenocarcinomaCervical Adenosquamous Carcinoma4 more

This phase II trial studies how well brivanib alaninate works in treating patients with cervical cancer that has come back. Brivanib alaninate may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth or by blocking blood flow to the tumor.

Completed65 enrollment criteria

InductionChemo-Radio-Antibody-Treatment

Squamous Cell Carcinoma of the HeadSquamous Cell Carcinoma of the Neck

This is an open-label, randomized, Phase II-study to evaluate the efficacy of a standard-TPF induction chemotherapy (IC) and an alternative TPF induction chemotherapy followed by radio-antibody-therapy, in patients with unresectable LA-SCC of the HN region (oro-hypopharynx carcinoma, cancer of the oral cavity). The primary objective of the study is to assess the feasibility of an experimental 'fractionated' TPF regimen compared to a current standard TPF regimen. Composite endpoint of compliance and feasibility in terms of response (RECIST1.1) and hematological acute toxicity (CTCAE v.4.02) on time application of RAT following an experimental or standard TPF IC. Secondary endpoints are Treatment intensity achieved Toxicity (according to CTCAE v.4.02) Response rates after completion of induction chemotherapy and after completion of entire protocol treatment (RECIST1.1) Survival (progression-free, metastasis-free, recurrence-free, overall) 1 year after randomisation Quality of life according to EORTC QoL C30 & HN35 The study will be conducted at 5-6 investigational sites in Germany recruiting 90 patients in total. Eligible patients will have a diagnosis of histologically confirmed SSC of the HN. Patients will receive one of 2 different regimens of TPF IC followed by cetuximab together with radiotherapy (RAT) or a standard radiochemotherapy(RCT) regimen.

Completed39 enrollment criteria

Temsirolimus + Weekly Paclitaxel + Carboplatin for Recurrent or Metastatic Head and Neck Squamous...

Squamous Cell CancerHead and Neck Cancer

The purpose of this study is to find out the good and bad effects that occur when temsirolimus is added to standard chemotherapy with carboplatin and paclitaxel.

Completed25 enrollment criteria

Study of Cetuximab in Combination With Chemotherapy in Patients With Recurrent and/or Metastatic...

Squamous Cell Carcinoma of the Head and Neck

The primary objective of this trial is to assess the antitumor activity of cetuximab when given in combination with cisplatin + 5-Fluorouracil (5-FU) for the first-line treatment of recurrent and/or metastatic squamous cell carcinoma of the head and neck (SCCHN) in Japanese subjects.

Completed31 enrollment criteria

Randomized Multicenter Study of 5 vs 6 Weekly Fraction of RT in the Treatment of SCC of the Head...

CarcinomaSquamous Cell

Randomized multicenter study of 5 vs 6 weekly fraction of RT in the treatment of SCC of the head and neck

Completed1 enrollment criteria

Phase II Study of Skin Toxicity Dosing of IRESSA (Gefitinib) in Squamous Cell Carcinoma of the Head...

Head and Neck Neoplasms

The purpose of this study is to demonstrate the activity (response rate and rate of stable disease) of Iressa administered as a single agent escalated to a dose that produces grade 2 skin toxicity in patients with recurrent and/or metastatic squamous cell carcinoma of the head and neck (SCCHN).

Completed16 enrollment criteria

Erlotinib Hydrochloride and Cetuximab in Treating Patients With Advanced Gastrointestinal Cancer,...

Adenocarcinoma of the ColonAdenocarcinoma of the Rectum65 more

This phase I trial is studying the side effects and best dose of erlotinib hydrochloride when given together with cetuximab and to see how well they work in treating patients with advanced gastrointestinal cancer, head and neck cancer, non-small cell lung cancer, or colorectal cancer. Erlotinib hydrochloride may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Monoclonal antibodies, such as cetuximab, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. Erlotinib hydrochloride and cetuximab may also stop the growth of tumor cells by blocking blood flow to the tumor. Giving erlotinib hydrochloride together with cetuximab may kill more tumor cells.

Completed25 enrollment criteria

Erlotinib,Radiation and Cisplatin in Patients With Complete Resected Squamous Cell Carcinoma of...

Squamous Cell Carcinoma of the Head and Neck

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.

Completed37 enrollment criteria

Dasatinib in Treating Patients With Recurrent or Metastatic Head and Neck Cancer

Metastatic Squamous Neck Cancer With Occult Primary Squamous Cell CarcinomaRecurrent Metastatic Squamous Neck Cancer With Occult Primary34 more

This phase II trial studies how well dasatinib works in treating patients with head and neck cancer that has come back or spread to other areas of the body. Dasatinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth.

Completed29 enrollment criteria
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