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[12], Lutathera is a major technological advancement for the detection of tumors. by @adacap_news. Advanced Accelerator Applications (AAA) is a pharmaceutical group specialized in the field of nuclear medicine.
INDICATIONLutathera® is a radiolabeled somatostatin analog indicated for the treatment of somatostatin receptor-positive gastroenteropancreatic neuroendocrine tumors (GEP-NETs), including foregut, midgut and hindgut neuroendocrine tumors in adults.
AAA fully recognizes that some associates are eager to return to the office while others may prefer to continue to work from home. endobj 147.360000 0] L U T A T H E R A � \( l u t e t i u m L u 1 7 7 d o t a t a t e \) i n j e c t i o n , f o r i n t r a v e n o u s u s e I n i t i a l U . 50.3999999 0] To help associates, the local leadership team will provide local guidance and support. /Filter /FlateDecode ", NETs are rare tumors originating in the neuroendocrine cells of numerous organs, including the gastrointestinal tract, pancreas and lung. 3. [0 /XYZ 69.5999999 >> This is applicable to all countries and markets. It selectively targets over-expressed somatostatin receptors while also giving off gamma emissions to allow physicians to visualize where in the body both the drug and the tumor are.
/GSa 3 0 R [0 /XYZ 69.5999999 [1] Patient survival with advanced GEP-NETs depends on stage and histology. LUTATHERA ® (lutetium Lu 177 dotatate) is a prescription medicine used to treat adults with a type of cancer known as gastroenteropancreatic neuroendocrine tumors (GEP-NETs) that are positive for the hormone receptor somatostatin, including GEP-NETs in the foregut, midgut, and hindgut. /XObject << Starting May 11, 2020, Accelerators Applications (AAA), a Novartis Company, will introduce company-wide a flexible working model that invites associates, country-by-country, to return to the office and restart on-site field activities, when possible and appropriate, based on the respective local situation and risk assessment. Advanced Accelerator Applications develops, produces and commercializes drugs for targeted radioligand therapy and precision radioligand imaging. >> [0 /XYZ 69.5999999
"The approval of Lutathera marks an important achievement and an innovation greatly needed for the NET cancer community," said Susanne Schaffert, Ph.D., Chairperson and President, Advanced Accelerator Applications. CTT1057 is an 18F-labeled investigational diagnostic candidate in development for PET imaging of prostate cancer. 1 0 obj [19] The expert concluded that the proposed operations at AAA are safe and pose no hazard to the citizens of Millburn. Global cancer care 5 0 obj endobj Our work is guided by our commitment to bring new innovations to patients. Please see full Prescribing Information at: http://www.adacap.com/wp-content/uploads/2018/01/Lutathera_lutetium_Lu_-177_dotatate_PI_2018_01.pdf. "For 30 years, Novartis has supported the NET community with the development of therapeutics in NET and carcinoid syndrome. /MediaBox [0 0 612 792] [3] A pre-planned interim overall survival analysis determined that Lutathera treatment lead to a 48% reduction in the estimated risk of death (hazard ratio 0.52, 95% CI: 0.32-0.84) compared to treatment with 60 mg octreotide LAR. 541.919999 0]
Strosberg J, El-Haddad G, Wolin E, et al. Our theragnostic radioligand platform involves radiolabeling a targeting molecule with fluorine 18 (F-18), gallium 68 (Ga-68), or other radionuclides used for precision radioligand imaging, or with lutetium 177 (Lu-177), actinium 225 (Ac-225) or other radionuclides used for treatment to create a targeted radioligand therapy. 3. [10] The dotatate binds to the GEP-NET positive somatostatin receptor cells commonly present on neuroendocrine tumors. Advanced Accelerator Applications (AAA) (NASDAQ: AAAP) est un groupe pharmaceutique spécialisé en médecine nucléaire moléculaire. LUTATHERA- lutetium lu 177 dotatate injection Advanced Accelerator Applications USA, Inc HIGHLIGHTS OF PRESCRIBING INFORMATION These highlights do not include all the information needed to use LUTATHERA safely and effectively. )*�u4�P� Each kit has received orphan drug designation from both the EMA and the FDA.[15][16]. Advanced Accelerator Applications is a newly established subsidiary of Novartis Lutathera expands Novartis' neuroendocrine tumor portfolio, building on long heritage and leadership ; Basel, January 26, 2018 - Novartis AG (NYSE: NVS) today announced that Advanced Accelerator Applications, a subsidiary of Novartis Groupe S.A., has received US Food and Drug Administration (FDA) approval of … [10] Its approval for Advanced Accelerator Applications was announced on January 26, 2018 by the US Food and Drug Administration. Advanced Accelerator Applications (AAA) is a pharmaceutical group specialized in the field of nuclear medicine.
/Creator (��) We continue to assess the situation and adapt accordingly. [3] Lutathera® (lutetium Lu 177 dotatate) Important Safety information[3].
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