“We were looking for elite partners that could provide world class service and with PharPoint and Medical Research Consulting Services we have come to terms with two of the best in the industry,” said George Evans, CEO of Cellceutix. “These agreements are the next step in our mission to start the Phase 1 study of Kevetrin ASAP.”

“We are pleased to have the opportunity to work with Cellceutix and to bring our skills to bear on the Kevetrin Phase 1 study,” said Art Holmes, President of PharPoint. Mr. Holmes continued, “From a corporate standpoint, it is exciting to be involved in the start of a promising clinical program, particularly in the field of oncology where there is an urgent need for new therapies.” More information about PharPoint is available at www.pharpoint.com (http://www.pharpoint.com/) .

Kevetrin is being developed to treat drug resistant cancers. The Company has reported that Kevetrin showed greater tumor growth delay than standard therapies in animal models of resistant lung cancer, resistant breast cancer and resistant colon cancer. In data recently presented at the American Association for Cancer Research (AACR), the efficacy of Kevetrin in a mouse model of drug resistant lung cancer was shown to increase with increasing dose. The data presented at the AACR also show that the administration of a second cycle of therapy with Kevetrin in the same animal model continues to delay tumor growth without the development of resistance. For more information about these results, please visit the Cellceutix web site at www.cellceutix.com (http://www.cellceutix.com/) .

“I am looking forward to working with Cellceutix on the Phase I clinical trial of their novel development product, Kevetrin, for the treatment of solid carcinomas,” said Denise T. Resnik, the Owner of Medical Research Consulting Services. “I have had a long-standing consulting relationship with George Evans’s prior employer, and I am sure this relationship will be fruitful as well.”