Cellceutix Files IND for New Cancer Drug Clinical Trials

Planned Clinical Trials to be Hosted by Dana-Farber and Beth Israel Deaconess Medical Center

Cellceutix (OTCBB:CTIX) files IND for new cancer drug.
Cellceutix (OTCBB:CTIX) files IND for new cancer drug.
  • Cellceutix (OTCBB:CTIX) files IND for new cancer drug.
    Cellceutix (OTCBB:CTIX) files IND for new cancer drug.
    Cellceutix (OTCBB:CTIX) files IND for new cancer drug.
    Cellceutix (OTCBB:CTIX) files IND for new cancer drug.

Cellceutix Corporation (OTCBB:CTIX) ("the Company"), a biopharmaceutical company focused on discovering and developing small molecule drugs to treat unmet medical conditions, is pleased to report that the Company has filed its Investigational New Drug (IND) application for Kevetrin™, a novel anti-cancer drug, with the U.S. Food and Drug Administration (FDA). The Company must now wait 30 calendar days before initiating the clinical trial. During this time, the FDA reviews the data in the IND and determines the conditions under which human trials can commence.

The Phase I trial is planned to take place at Dana-Farber Cancer Institute and its partner hospitals including Beth Israel Deaconess Medical Center.  The clinical trial will test Kevetrin™ against a variety of different cancer types in patients with advanced-stage cancers.  Primary endpoints for the study will be safety, tolerable dosing levels and establishing the dose for a future Phase II clinical trial.

Cellceutix is focused on developing Kevetrin™ as a new class of chemotherapy for treatment of solid tumors.   Mechanism of action studies showed Kevetrin’s unique ability to affect both wild and mutant types of p53, and that Kevetrin strongly induced apoptosis, characterized by activation of Caspase 3 and cleavage of PARP.  Activation of p53 also induced apoptosis by inducing the expression of p53 target gene PUMA. p53 is an important tumor suppressor that acts to restrict proliferation by inducing cell cycle checkpoints, apoptosis,  or cellular senescence. It is often referred to as the “Guardian Angel of the Human Genome.

“The filing of the IND represents a historic day for Cellceutix and its shareholders.  We cannot possibly express how pleased we are to be making the shift to a clinical stage company,” stated Leo Ehrlich, CEO of Cellceutix.

About Dana-Farber/Harvard Cancer Center

More information on Dana-Farber/Harvard Cancer Center can be found at http://www.dfhcc.harvard.edu/

About Cellceutix

Cellceutix Corporation is a preclinical cancer, anti-inflammatory and autism drug developer. More information is available on the Cellceutix web site at www.cellceutix.com

Safe Harbor Forward-Looking Statements

To the extent that statements in this press release are not strictly historical, including statements as to revenue projections, business strategy, outlook, objectives, future milestones, plans, intentions, goals, future financial conditions, future collaboration agreements, the success of the Company's development, events conditioned on stockholder or other approval, or otherwise as to future events, such statements are forward-looking, and are made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. The forward-looking statements contained in this release are subject to certain risks and uncertainties that could cause actual results to differ materially from the statements made. Factors that may impact Cellceutix's success are more fully disclosed in Cellceutix's most recent public filings with the U.S. Securities and Exchange Commission.

Contact:

Cellceutix Corp.

Leo Ehrlich

(978) 236-8717     

info@cellceutix.com

 

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