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Carcinoma clinical trials

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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: NCT02683200 Completed - Clinical trials for Metastatic Malignant Neoplasm in the Liver

MRI-Guided Stereotactic Body Radiation Therapy in Treating Patients With Liver Metastases or Liver Cancer

Start date: June 3, 2015
Phase: Early Phase 1
Study type: Interventional

This pilot clinical trial studies magnetic resonance imaging (MRI)-guided stereotactic body radiation therapy (SBRT) in treating patients with liver metastases or liver cancer. SBRT is a specialized radiation therapy that delivers a single, high dose of radiation directly to the tumor and may kill more tumor cells and cause less damage to normal tissue. Combining MRI with SBRT may help doctors to highlight the tissues surrounding the tumor better.

NCT ID: NCT02677337 Completed - Clinical trials for Renal Cell Carcinoma

NCCN Renal Cell Registry

Start date: March 2016
Phase: N/A
Study type: Interventional

This study will consist of three parts: 1) a retrospective chart review of patients treated for mRCC from July 2013 until the start of the educational intervention; 2) an educational program for DCN community oncology providers and DCN community patients with mRCC, lasting 8 - 10 months, and 3) a second retrospective chart review of patients treated for mRCC starting at the time of the educational intervention until the intervention is completed.

NCT ID: NCT02674009 Completed - Clinical trials for Carcinoma, Basal Cell

Observational Study to Determine the Effectiveness and Safety of Vismodegib (Erivedge®) in Participants With Locally Advanced Basal Cell Carcinoma (laBCC)

NIELS
Start date: September 17, 2015
Phase:
Study type: Observational

The primary purpose for this multi-center, non-interventional study is to evaluate the duration of response defined as duration from first documented response of complete response (CR) or partial response (PR) until disease progression (as determined by the treating physician) for participants with laBCC.

NCT ID: NCT02672475 Completed - Clinical trials for Stage IV Breast Cancer

Galunisertib and Paclitaxel in Treating Patients With Metastatic Androgen Receptor Negative (AR-) Triple Negative Breast Cancer

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

This phase I trial studies the side effects and best dose of Galunisertib when given together with paclitaxel in treating patients with androgen receptor negative or triple negative breast cancer that has spread to other places in the body. Some tumors need growth factors, which are made by the body's white blood cells, to keep growing. Galunisertib may interfere with growth factors and help cause tumor cells to die. Drugs used in chemotherapy, such as paclitaxel, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving Galunisertib together with paclitaxel may kill more tumor cells.

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: NCT02670122 Completed - Clinical trials for Hepatocellular Carcinoma

Prospective Study to Evaluate Safety of Deb-TACE With 100µ Beads in Patients With Non Resectable HCC

Start date: March 2015
Phase:
Study type: Observational

This is an observational, multicenter, single arm, prospective study to evaluate safety and tolerability of selective and ultraselective drug eluting beads transcatheter intraarterial chemoembolization (DEB-TACE) with up to 3 ml of well calibrated 100 µ microspheres and up to 150 mg of doxorubicin, for the treatment of non resectable hepatocellular carcinoma (HCC). The hypothesis is that 100 µ beads penetrate deeper into the tumor than those eluting beads with larger volumes without increasing the risk and complications of DEB-TACE.

NCT ID: NCT02667886 Completed - Clinical trials for Clear Cell Renal Cell Carcinoma

Trial of X4P-001 in Patients With Advanced Renal Cell Carcinoma

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

The purpose of the study is to test different doses of X4P-001 given alone and in combination with axitinib in patients diagnosed with advanced renal cell carcinoma. The goals of the study are to determine the safety and tolerability of X4P-001, as well as the potential effect it may have on the body and the cancer tumor.

NCT ID: NCT02667574 Completed - Clinical trials for Basal Cell Carcinoma

Study Evaluating the Interest of Vismodegib as Neo-adjuvant Treatment of Basal Cell Carcinoma (BCC)

VISMONEO
Start date: November 18, 2014
Phase: Phase 2
Study type: Interventional

Open-label, non-comparative, multicenter, phase II study of Vismodegib in patients with locally advanced BCC.

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.