MARKHAM, ON, April 3, 2012 /CNW/ - Cytochroma today announced that the United States Patent and Trademark Office (USPTO) issued a Notice of Allowance for US Patent Application No. 13/244,945. This patent application, entitled "Method for Treating Secondary Hyperparathyroidism in CKD", covers the anticipated method of use of the Company's lead product, CTAP101 Capsules, which is in phase 3 development for treating patients with Stage 3 or 4 chronic kidney disease (CKD), secondary hyperparathyroidism (SHPT) and vitamin D insufficiency.
CTAP101 Capsules has been evaluated in four clinical studies to date, including a Phase 2b study which ended in late 2011. The positive results obtained in the Phase 2b study will be highlighted at a medical conference later this year.
"We are pleased to reach yet another significant milestone for CTAP101 Capsules and be one step closer to introducing this important new medication for chronic kidney disease patients suffering with secondary hyperparathyroidism and vitamin D insufficiency, a sizable population with few treatment options," commented Dr. Charles W. Bishop, President and CEO of Cytochroma. "This newly allowed patent application will help ensure protection for CTAP101 Capsules from generic competition until 2028."
About CTAP101 Capsules
CTAP101 Capsules is being developed as a first-in-class treatment for patients with Stage 3 or 4 CKD with SHPT and vitamin D insufficiency. The product is designed to reliably correct vitamin D insufficiency by raising serum vitamin D pro-hormone concentrations to adequate levels (30 ng/mL or higher), thereby lowering elevated plasma parathyroid hormone (PTH) without the side effects often associated with vitamin D hormone therapies.
About Chronic Kidney Disease
CKD is characterized by a progressive decline in kidney function. The kidney normally removes waste and excess water from the blood and regulates circulating vitamin D hormones. As CKD advances, blood levels of vitamin D prohormones and hormones decrease, causing vitamin D insufficiency and SHPT. CKD is classified in five different stages - mild (stage 1) to severe (stage 5) disease - as measured by glomerular filtration rate. According to the National Kidney Foundation, CKD afflicts over 26 million people in the US, including more than eight million patients with moderate (stages 3 and 4) CKD. In stage 5 CKD, kidney function is minimal to absent and patients require regular dialysis or a kidney transplant for survival.
About Secondary Hyperparathyroidism (SHPT)
SHPT is a condition in which the parathyroid glands secrete excessive amounts of PTH into the blood due to renal and/or vitamin D insufficiency. Prolonged and excessive PTH secretion causes excessive calcium and phosphorus to be released from bone into the blood, leading to elevated serum calcium and phosphorus, various bone diseases and calcification of cardiovascular tissues. SHPT affects 40-60% of patients with moderate CKD and approximately 90% of patients with severe CKD.
Cytochroma is a clinical stage specialty pharmaceutical company focused on developing and commercializing proprietary products to treat and prevent the clinical consequences of vitamin D insufficiency and SHPT associated with CKD. The Company specializes in developing new therapies which are designed to safely and effectively treat patients with stage 3, 4 and 5 CKD. Cytochroma also has a portfolio CYP24 and phosphate-uptake inhibitors in early stage development.
For more information about Cytochroma, please visit www.cytochroma.com.
For further information:
Executive Director, Corporate Development
Tel: +1 (905) 479-5306 ext. 333
Robert Stanislaro (FTI Consulting)
Tel: +1 (212) 850-5657