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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 gel widely available to treat the signs and symptoms of this rare cancer. learn more

 

 
 

 

 


February 27, 2013
Ceptaris Resubmits New Drug Application (NDA) to FDA for Proprietary Gel Formulation of Mechlorethamine Hydrochloride

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