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Carcinoma, Squamous Cell clinical trials

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NCT ID: NCT02764593 Completed - Clinical trials for Head and Neck Squamous Cell Carcinoma (HNSCC)

Safety Testing of Adding Nivolumab to Chemotherapy in Patients With Intermediate and High-Risk Local-Regionally Advanced Head and Neck Cancer

Start date: June 2016
Phase: Phase 1
Study type: Interventional

This study will evaluate the safety of adding nivolumab to several chemotherapy platforms with weekly cisplatin, high-dose cisplatin, cetuximab or radiation therapy alone.

NCT ID: NCT02760498 Completed - Clinical trials for Advanced Cutaneous Squamous Cell Carcinoma

Study of REGN2810 in Patients With Advanced Cutaneous Squamous Cell Carcinoma

Start date: April 7, 2016
Phase: Phase 2
Study type: Interventional

Groups 1 to 4 To estimate the clinical benefit of cemiplimab monotherapy for patients with: metastatic (nodal or distant) cutaneous squamous cell carcinoma (CSCC), or unresectable locally advanced CSCC Group 6 To provide additional efficacy and safety data for cemiplimab monotherapy in patients with advanced CSCC (metastatic [nodal or distant] or locally advanced treated with cemiplimab

NCT ID: NCT02759575 Completed - Clinical trials for Head and Neck Cancer

A Study of Chemoradiation Plus Pembrolizumab for Locally Advanced Laryngeal Squamous Cell Carcinoma

Start date: April 2016
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this research study is to test the safety and the benefit of adding pembrolizumab (a therapy that activates the immune system to fight cancer) to standard of care treatment for larynx cancer. The standard of care treatment will include chemotherapy and radiation for 7 weeks.

NCT ID: NCT02752932 Completed - Clinical trials for Head and Neck Squamous Cell Carcinoma

TumorGraft- Guided Therapy for Improved Outcomes in Head and Neck Squamous Cell Cancer- A Feasibility Study

Xenograft
Start date: November 2015
Phase: N/A
Study type: Interventional

Primary objectives: 1. Evaluate the feasibility of rapidly accruing 30 participants with recurrent metastatic head and neck squamous cell carcinoma for the development of patient derived xenographs (PDX) from fresh, real time biopsies in which sensitivity to < 4 Ontario funded chemotherapeutic regimen will be tested. Written feedback to the primary oncologist will be provided. 2. There is also a curative intent cohort of 30 participants undergoing surgical resection with curative intent. These PDX models will undergo exome sequencing with written feedback. 3. Feasibility in both surgical and recurrent cohorts will be a measure of i) engraftment rate, ii) patient status at the time of drug testing completion and iii) rate of accrual.

NCT ID: NCT02741570 Completed - Clinical trials for Head and Neck Cancer

Study of Nivolumab in Combination With Ipilimumab Compared to the Standard of Care (Extreme Regimen) as First Line Treatment in Patients With Recurrent or Metastatic Squamous Cell Carcinoma of the Head and Neck

CheckMate 651
Start date: October 5, 2016
Phase: Phase 3
Study type: Interventional

The main purpose of this study is to compare nivolumab and ipilimumab with the extreme regimen as first line treatment in patients with recurrent or metastatic squamous cell of the head and neck cancer

NCT ID: NCT02715596 Completed - Clinical trials for Squamous Cell Carcinoma of Head and Neck

Changes in Body Composition After EPA Supplementation in Head and Neck Patients

hepaneck
Start date: December 23, 2015
Phase: Phase 3
Study type: Interventional

Evaluates the effect of EPA supplementation in terms of muscle mass in patients with squamous cell carcinoma of the head and neck locally advanced

NCT ID: NCT02707588 Completed - Clinical trials for Squamous Cell Carcinoma of the Head and Neck

Tolerance and Efficacy of Pembrolizumab or Cetuximab Combined With RT in Patients With Locally Advanced HNSCC

PembroRad
Start date: May 18, 2016
Phase: Phase 2
Study type: Interventional

The general aim of the study is to evaluate the anti-tumour activity and the tolerance profile of Pembrolizumab + RT in comparison to cetuximab + RT in patients with locally advanced HNSCC and to explore potential correlations between treatment outcome and the immune landscape.

NCT ID: NCT02684253 Completed - Clinical trials for Head and Neck Squamous Cell Carcinoma (HNSCC)

Screening Trial of Nivolumab With Image Guided, Stereotactic Body Radiotherapy (SBRT) Versus Nivolumab Alone in Patients With Metastatic Head and Neck Squamous Cell Carcinoma (HNSCC)

Start date: February 11, 2016
Phase: Phase 2
Study type: Interventional

Nivolumab is an antibody (a type of human protein) that is designed to boost your body's immune system. It does this by allowing immune cells to grow and fight the cancer. Nivolumab has been approved by the FDA for the treatment of melanoma (a form of skin cancer) and lung cancer. It is currently under study for the treatment of head and neck squamous cell cancer.

NCT ID: NCT02672254 Completed - Clinical trials for Cutaneous Squamous Cell Carcinoma

New Strategies Against Cutaneous Squamous Cell Carcinoma

Start date: January 2016
Phase: N/A
Study type: Observational

The gold treatment for local invasive cutaneous squamous cell carcinoma is surgical excision. Nevertheless, surgery is not always an option as a consequence of the age and/or the health status of the patient. One of the objectives of this study is to assess the effects of cisplatin concomitantly with a subsequent low-energy X-rays irradiation in vitro. In order to enhance the effectiveness of this combined treatment, the temporal fractionation of the platinated compound is expected to be performed.

NCT ID: NCT02666534 Completed - Clinical trials for Microinvasive Squamous Cell Carcinoma

Efficacy of AFL-assisted PDT in Microinvasive Squamous Cell Carcinoma

Start date: January 2012
Phase: Phase 1
Study type: Interventional

Surgical excision is the standard treatment for cutaneous SCC. However, many patients diagnosed with SCC are elderly and ineligible for surgery. Ablative fractional laser- assisted photodynamic therapy (AFL-PDT) offered a higher efficacy than conventional Methylaminolevulinate (MAL)-PDT.