RUBY-FILL® is an approved cutting edge technology for PET myocardial perfusion imaging (MPI) under rest and pharmacological stress conditions to evaluate regional myocardial perfusion in adult patients with suspected or existing coronary artery disease. MONTREAL, Quebec – October 3, 2016 Jubilant DraxImage Inc., (“DraxImage”) a wholly Owned Subsidiary of Jubilant Pharma Ltd, announced today that the U.S. Food and Drug Administration has approved RUBY-FILL®, an innovative technology for Positron Emission Tomography (PET) myocardial perfusion imaging (MPI). Comprised of a Rubidium-82 (Rb-82) Generator and precedent setting Elution System, RUBY-FILL® is used to produce a personalized patient dose of Rubidium Rb 82 chloride used to evaluate regional myocardial perfusion in adult patients with suspected or existing coronary artery disease (CAD) which is an important component of diagnosing CAD. “We are proud to bring to the US market a groundbreaking, state-of-the-art technology for myocardial perfusion imaging. RUBY-FILL® expands DraxImage’s nuclear medicine portfolio and is a part of our commitment to provide healthcare providers and their patients with innovative health care solutions for those with suspected or existing coronary artery disease,” comments GP Singh, CEO of Jubilant Pharma Ltd. “Our knowledge of the role and value of PET nuclear cardiology, specifically Rb- 82 Chloride PET in known or suspected coronary artery disease, advanced significantly as we progressed through the comprehensive and rigorous FDA review process,” said Norman LaFrance, MD, Chief Medical Officer and Senior VP, Medical & Regulatory Affairs, for Jubilant Pharma and Jubilant DraxImage. “With its advanced weight based dose accuracy and multiple infusion options, among other product capabilities, RUBY-FILL® will enhance the way patients with known or suspected coronary artery disease are both diagnosed and managed.” Commercial launch plans for RUBY-FILL® is expected to be in the October-December 2016 quarter. RUBY-FILL® Rubidium 82 Generator and RUBY Rubidium Elution System The RUBY-FILL® Generator contains an accelerator produced Strontium-82, which decays to Rubidium-82. When the generator is eluted with saline it produces a sterile, non-pyrogenic solution of Rb-82 Chloride. Due to the short half-life (75 s) of Rb-82, the use of an elution system is required for delivery of the Rb-82 Chloride into a patient for the purposes of performing Myocardial Perfusion Imaging with PET. PET imaging with Rb-82 Chloride may be performed under rest and/or stress conditions. The Rubidium Elution System has been exclusively designed to be used with the RUBY-FILL® generator and to deliver accurate doses of Rb-82 Chloride to patients. For more information, please contact: Medical & Regulatory Affairs email@example.com or visit http://www.draximage.com/en/pipeline/cardiovascular-pet.html Important Safety Information WARNING: UNINTENDED STRONTIUM 82 (Sr 82) AND STRONTIUM 85 (Sr 85) RADIATION EXPOSURE Please see full prescribing information for complete boxed warning Unintended radiation exposure occurs when the levels of Sr 82 or Sr 85 in the rubidium Rb 82 chloride injection exceed specific limits. Perform generator eluate tests: 1) Determine Rb 82, Sr 82, Sr 85 levels in the eluate: Once daily, prior to any drug administration, and With additional daily tests after detection of an Alert Limit. 2) Stop use of the generator at its Expiration Limit. Click here to view full prescribing information About Jubilant DraxImage Jubilant DraxImage Inc., a wholly Owned Subsidiary of Jubilant Pharma Ltd, which is held by Jubilant Life Sciences Ltd, develops, manufactures and commercializes radiopharmaceuticals used for the diagnosis and treatment of diseases. The company is dedicated to nuclear medicine and serves customers and through them patients, globally, with high quality and reliable products and services. The company is the market leader in North America for I-131 products (diagnosis and treatment of thyroid disorder and cancer, MAA (lung perfusion imaging), DTPA (renal and brain imaging) and MDP (bone imaging), and also markets other products such as Sestamibi, Xenon and Gluceptate. The company has a strong development pipeline of new products and commitment in bringing new products to market. For more info: www.draximage.com About Jubilant Life Science Jubilant Life Sciences Limited is an integrated global Pharmaceutical and Life Sciences Company engaged in Pharmaceuticals, Life Science Ingredients and Drug Discovery Solutions. The Pharmaceuticals segment, through its wholly owned subsidiary Jubilant Pharma Ltd, is engaged in manufacture and supply of APIs, Solid Dosage Formulations, Radiopharmaceuticals, Allergy Therapy Products and Contract Manufacturing of Sterile and Non Sterile products through 6 USFDA approved facilities in India, US and Canada. The Life Science Ingredients segment is engaged in Specialty Intermediates, Nutritional Products and Life Science Chemicals through 5 manufacturing facilities in India. The Drug Discovery Solutions segment provides proprietary in-house innovation and collaborative research and partnership for out-licensing through 3 world class research centres in India and US. Jubilant Life Sciences Ltd has a team of around 6,500 multicultural people across the globe and is committed to deliver value to its customers spread across over 100 countries. The Company is well recognized as a ‘Partner of Choice’ by leading pharmaceuticals and life sciences companies globally. For more info: www.jubl.com. 2 Responses to “JDI RECEIVES FDA APPROVAL for products” Kimiichi Uno,M.D. March 20, 2017 Please supply RUBY-FILL® Generator in Tokyo. Reply Suzanne Bissonnette May 8, 2017 Dear Dr. Kimiichi Uno, Thank you for your inquiry. Please contact Jim Kaufman Director PET products at firstname.lastname@example.org Reply Leave a Reply Click here to cancel reply. Name (required) Email (will not be published) (required) Website Comment Share this news!