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10 September 2015
BTG plc announced today that Wellstat Therapeutics’ new drug application (NDA) for uridine triacetate has been accepted for review by the United States Food and Drug Administration (FDA). The NDA seeks FDA approval of uridine triacetate as treatment for patients at risk of serious toxicity following an overdose of the chemotherapy agent 5-fluorouracil (5-FU) and patients exhibiting symptoms of serious toxicity within 96 hours of 5-FU administration. Used in combination with other drugs or radiation, 5-FU is a mainstay of chemotherapy across a variety of solid tumors, including those of the colon, stomach, esophagus, breast, pancreas and head and neck.
The FDA has provided an anticipated Prescription Drug User Fee Act (PDUFA) action date in March 2016. Uridine triacetate is being developed by Wellstat Therapeutics. If approved by the FDA, BTG will market, sell and distribute uridine triacetate for this indication in the US. Wellstat Therapeutics retains certain rights to exercise an option to co-promote uridine triacetate. Terms of the co-promote have not been disclosed.
David M. Wohlstadter, Wellstat’s Chief Strategy Officer and Counsel, commented: “Our partnership with BTG, which will commercialize this important therapy, demonstrates our shared commitment to the oncology community and cancer patients. This important regulatory milestone brings us one step closer to providing the first and only antidote for patients at risk of serious toxicity following an overdose of 5-fluorouracil (5-FU) and patients exhibiting symptoms of serious toxicity within 96 hours of 5-FU administration.”
Carolyn Lewis, BTG’s General Manager of Specialty Pharmaceuticals, commented: “Given how common the use of 5-FU is in patients with solid tumors, the negative health and economic impacts of rapid-onset severe toxicity and unintentional overexposure are significant. This filing by Wellstat Therapeutics underscores our shared commitment to bringing an important potential treatment to patients in critical need of care. If granted, FDA approval of uridine triacetate will provide patients and physicians greater access to this novel, potentially life-saving therapy.”
Published literature as well as historical data suggest that overexposure to 5-FU can result in serious toxicity or death.
In 2009, uridine triacetate received orphan drug designation from the FDA as an antidote in the treatment of 5-fluorouracil poisoning and from the European Medicines Agency (EMA) as a treatment for 5-fluorouracil overdose. Under an expanded access protocol, FDA emergency treatment provisions in the US, and similar emergency use provisions in Europe and the rest of the world, uridine triacetate is currently provided to patients at risk of excess 5-FU toxicity due to overdose and patients exhibiting serious toxicities to 5-FU within 96 hours of 5-FU administration. The NDA for uridine triacetate is based in part on efficacy and safety data from US sites in this protocol.
5-FU is on the World Health Organization’s List of Essential Medicines, a compilation of the most important medications needed in a basic health system. Because 5-FU is administered in different doses and schedules as a frequent component of standard chemotherapy regimens for a variety of cancers, patients can experience dramatically different patterns of toxicity. Overexposure to 5-FU can occur as a result of overdose, genetic variations, impaired clearance or other biochemical factors.
Published literature suggests that each year, approximately 250,000 to 300,000 patients in the US receive multiple treatments with 5-FU, of which 0.5 percent die from 5-FU toxicity. An estimated 10-20 percent of those patients develop serious, sometimes life threatening, 5-FU toxicity or experience an overdose. Non-fatal 5-FU toxicities can result in hospitalization, intensive care utilization and delays in or discontinuation of chemotherapy.
About Uridine Triacetate
Uridine triacetate is an investigational drug currently under review by the FDA for use as a treatment for patients at risk of serious toxicity following an overdose of 5-fluorouracil (5-FU) and patients exhibiting symptoms of serious toxicity within 96 hours of 5-FU administration. Uridine triacetate is converted in the body to uridine, a direct biochemical antagonist of 5-fluorouracil toxicity.
About 5-Fluorouracil (5-FU)
Used in combination with other chemotherapy agents and/or radiation, 5-FU has been for decades a mainstay of various treatment regimens for solid tumors, including those of the colon, stomach, esophagus, breast, pancreas, and head and neck. The drug is most commonly administered by infusion pump at or near what is considered the maximum tolerated dose. Expected side effects of 5-FU include myelosuppression (a reduction in white-blood-cell counts and thus increased risk of infection), diarrhea, nausea, vomiting, and mucositis (a painful inflammation and ulceration of the mucous membranes lining the digestive tract). Overexposure to 5-FU can lead to severe myelosuppression, gastrointestinal hemorrhage, septic shock, multiple organ failure, cardiac and neurological complications and death.
About Wellstat Therapeutics
Wellstat Therapeutics Corporation is a privately-held biopharmaceutical company located in Gaithersburg, Maryland. Wellstat Therapeutics is committed to discovering, developing and commercializing products that will provide new and improved treatments for patients in the fields of oncology and metabolic, neurometabolic and neurodegenerative diseases. For more information, please visit the website at http://www.wellstattherapeutics.com. Wellstat Therapeutics is part of the Wellstat group of companies (http://www.wellstat.com).
BTG is a growing international specialist healthcare company bringing to market innovative products in specialist areas of medicine to better serve doctors and their patients. We have a portfolio of Interventional Medicine products to advance the treatment of liver tumors, advanced emphysema, severe blood clots and varicose veins, and Specialty Pharmaceuticals that help patients overexposed to certain medications or toxins. Inspired by patient and physician needs, BTG is investing to expand its portfolio to address some of today’s most complex healthcare challenges. To learn more about BTG, please visit: www.btgplc.com.
For further information contact:
Andy Burrows, VP Corporate & Investor Relations
+44 (0)20 7575 1741; Mobile: +44 (0)7990 530 605
Stuart Hunt, Investor Relations Manager
+44 (0)20 7575 1582; Mobile: +44 (0)7815 778 536
Chris Sampson, Corporate Communications Director
+44 20 7575 1595; Mobile: +44 7773 251 178
Ben Atwell/Simon Conway
+44 (0)20 3727 1000
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