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Ceptaris Therapeutics Inc. is developing a proprietary gel formulation of mechlorethamine hydrochloride (mechlorethamine) for the treatment of early stage (stages I-IIA) mycosis fungoides, a type of CTCL. Based upon results of a pivotal trial, Ceptaris submitted a new drug application (NDA) with the Food and Drug Administration (FDA) in 2011. If approved, Ceptaris’ investigational drug would be the first topical mechlorethamine product available to treat the signs and symptoms of this rare cancer. learn more

 

 
 


February 21, 2012
Ceptaris Secures $15M in Venture Debt Financing

February 14, 2012
Pennsylvania BIO Awards Ceptaris’ Steve Tullman the Frank Baldino CEO of the Year Award

January 18, 2012
Ceptaris Therapeutics Receives EMA Orphan Drug Designation for Proprietary Mechlorethamine Gel

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