Healthcare Industry News: abiraterone
News Release - July 20, 2017
Churchill Pharmaceuticals Announces NDA Filing Acceptance for YONSA(TM) by the U.S. FDAThe NDA contains data to support approval for YONSA, (abiraterone acetate) ultramicrosize tablets, for the treatment of Metastatic Castration-Resistant Prostate Cancer (mCRPC)
Churchill Pharmaceuticals also announces positive results from the pivotal STAAR Study evaluating serum testosterone levels in patients with mCRPC in a head-to-head comparison trial of YONSA to Zytiga®
KING OF PRUSSIA, Pa., July 20, 2017 -- (Healthcare Sales & Marketing Network) -- Churchill Pharmaceuticals, LLC (Churchill), a privately held company devoted to expanding treatment options with oral oncology agents, announces that the New Drug Application (NDA) for YONSA™ (abiraterone acetate) ultramicrosize tablets has been accepted for filing by the U.S. Food and Drug Administration (FDA). Under the Prescription Drug User Fee Act (PDUFA), the FDA has set a target date of March 19, 2018 to complete its review.
"We are pleased that the NDA for YONSA has been accepted. The notification from the FDA indicated that the application is sufficiently complete to permit a substantive review and that no potential review issues have been identified. Our team looks forward to working closely with the FDA throughout the review process," stated Scott Megaffin, President, Churchill.
"YONSA represents a new potential treatment option for the nearly 30,000 men diagnosed annually in the U.S. with mCRPC," stated Ben Steinmetz, Senior Vice President, Commercial, Churchill. "YONSA sets the stage in our initial commercial approach with an exciting and innovative opportunity to deliver on the Churchill commitment to responsibly enhance product access to critical therapies."
About YONSA™ (abiraterone acetate) ultramicrosize tablets
YONSA is an investigational oral agent, formulated as abiraterone acetate ultramicrosize tablets. YONSA is a CYP17 inhibitor being developed for the treatment of metastatic castration-resistant prostate cancer in combination with methylprednisolone. The active ingredient is converted in vivo to abiraterone, an androgen biosynthesis inhibitor, that inhibits 17 a-hydroxylase/C17,20-lyase (CYP17). This enzyme is expressed in testicular, adrenal and prostatic tumor tissues and is required for androgen biosynthesis. YONSA ultramicrosize tablets have double the bioavailability of the comparator formulation of abiraterone acetate. YONSA has been formulated using the SoluMatrix Fine Particle Technology™.
The *STAAR Study
The STAAR Study (CHL-AA-201, A Randomized, Open-Label, Active-Controlled, Multi-Center Study to Evaluate Serum Testosterone Levels in Patients with Metastatic Castration-Resistant Prostate Cancer) was an 84-day study in the U.S. comparing YONSA in combination with methylprednisolone against Zytiga® in combination with prednisone. The primary endpoint was comparative lowering of serum testosterone at pharmacodynamic steady-state. Additional secondary endpoints included safety assessments, PSA and pharmacokinetic measurements. The full results of the STAAR Study will be presented at a future scientific meeting.
About Churchill Pharmaceuticals, LLC
Churchill is focused on providing value to cancer care by developing quality orally delivered oncology products with optimized clinical profiles. Our commitment to responsibly deliver these products to the patients, payers and healthcare communities we serve is at the core of our business. Churchill has a license from iCeutica to the SoluMatrix Fine Particle Technology™.
For more information, please visit www.churchillpharma.com and www.iceutica.com
Source: Churchill Pharmaceuticals
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