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ThermoDox is being evaluated in a Phase III clinical trial for primary liver cancer (the HEAT Study), a Phase II clinical trial for colorectal liver metastasis and a Phase II clinical trial for recurrent chest wall breast cancer.
Celsion Corporation (NASDAQ: CLSN), a leading oncology drug development company, announced financial results for the third quarter ended September 30, 2009 and highlighted the progress made in the commercialization of ThermoDox[R], Celsion's heat activated liposomal encapsulation of doxorubicin for the treatment of hepatocellular carcinoma (HCC), the most common form of primary liver cancer, and recurrent chest wall breast cancer.
Clinical Safety and Efficacy results presented for 40mg/m2 completed dose cohort of Phase I/II Recurrent Chest Wall Breast Cancer study Higher dose cohort reaches enrollment completion COLUMBIA, Md.
ThermoDox has already demonstrated remarkable evidence of clinical activity in Phase I studies for primary liver cancer and recurrent chest wall breast cancer.
Celsion is conducting a second registrational trial to evaluate ThermoDox in combination with hyperthermia to treat recurrent chest wall cancer.
ThermoDox is currently being evaluated in the Phase III HEAT trial for the treatment of hepatocellular carcinoma (HCC) and in a Phase I/II trial for patients with recurrent chest wall breast cancer.
Also in the second quarter of 2009, we enrolled our first patients in the Phase I/II recurrent chest wall (RCW) breast cancer clinical trial and we announced that ThermoDox[R] was the subject of three presentations at the Society for Thermal Medicine Annual Meeting, further increasing the drug's exposure within the physician and scientific communities.
Abstract will provide interim results of Phase I/II Recurrent Chest Wall Breast Cancer study COLUMBIA, Md.