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Refractory Cancer clinical trials

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NCT ID: NCT01932047 Enrolling by invitation - Refractory Cancer Clinical Trials

Patients Who Refractory Cancer Conqueror for Bio New Drug Development Translational Research Establishment

Start date: April 2010
Phase: N/A
Study type: Observational [Patient Registry]

■ Unmet medical needs for Refractory cancer Conquest - Many advanced cancers are still detected Despite remarkable technological advances for the early diagnosis of cancer in the field last 20 years. In the type of progressive carcinoma is very high malignancy despite a variety of therapeutic target treatment for refractory cancer. The refractory cancer patients who main focus of this research defined as the adult solid tumor patients who have failed standard therapy according to the criteria NCCN / ASCO (American Society of imsangam) / KCSG (Study Group for chemotherapy). The survival rate of refractory cancer patients are estimated to be 30-40% of the total patients with metastatic solid tumors and these refractory cancers are difficult to deal with or control to conventional treatment so shows almost close to 100% mortality. Therefore the new development of therapies for conquer of refractory cancer are urgently required. ■ Preclinical translational research Unmet Needs of Bio-new drug development for conquer of refractory cancer - The stage of preclinical translational research (Translational Research) connects between the early stages of development and clinical trials in the stage drug development. The establishment of foundation based on the translational research is very necessary and this must have proven ability to treat refractory cancer. The most anti-cancer drugs developed by existing preclinical testing method actually does not show a remarkable effect in many cases in the clinical trials, even if showed a remarkable inhibitory cancer effect in animal testing. The exact molecular diagnosis to treat targets and paradigm for the development of new drugs at the same time requires for target treatment. The tailored cell lines by patients and the proven technology by animal models and unmet need for preclinical translational research is increasing