COLUMBIA, Md.--(BUSINESS WIRE)--CELSION CORPORATION (NASDAQ: CLN) announced today that two clinical sites are currently screening patients after receiving IRB approval for the Phase III study titled “A Phase III, Randomized, Double-Blinded, Dummy-Controlled Study of the Efficacy and Safety of ThermoDox® (Thermally Sensitive Liposomal Doxorubicin) in Combination with Radiofrequency Ablation (RFA) Compared to RFA-Alone in the Treatment of Non-Resectable Hepatocellular Carcinoma (HCC).” In the USA, North Shore Hospital-Albert Einstein Medical School, led by Principal Investigator Dr. Thanjavur S. Ravikumar, MD, is currently screening patients and will be the lead clinical center in North America. In Hong Kong, Queen Mary Hospital, University of Hong Kong led by Principal Investigator Dr. Ronnie T. Poon, MD, is also currently pre-screening patients for the Phase III study and will be the lead clinical center in Asia.
