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ซานดิเอโก, May 21, 2019 (GLOBE NEWSWIRE) -- Invivoscribe, Inc., บริษัทระดับโลกที่บูรณาการเฉพาะที่มุ่งเน้นไปที่การปรับปรุงชีวิตด้วย Precision Diagnostics®...
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SAN DIEGO, May 21, 2019 (GLOBE NEWSWIRE) -- A Invivoscribe, Inc.,, uma empresa global verticalmente integrada com foco na melhoria de vidas com Precision Diagnostics®, anuncia hoje a expansão das...
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圣迭戈, May 21, 2019 (GLOBE NEWSWIRE) -- Invivoscribe, Inc.是一家专注于利用Precision...
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SAN DIEGO, May 21, 2019 (GLOBE NEWSWIRE) -- Invivoscribe, Inc., a vertically integrated global company focused on Improving Lives with Precision Diagnostics®, today announces expansion of space and...
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SAN DIEGO, Nov. 30, 2018 (GLOBE NEWSWIRE) -- Invivoscribe se complace en anunciar la aprobación por parte de la FDA tanto del ensayo de mutación LeukoStrat CDx FLT3 como del medicamento de Astellas,...
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SAN DIEGO, Nov. 30, 2018 (GLOBE NEWSWIRE) -- Invivoscribe berbangga untuk mengumumkan bahawa FDA telah meluluskan Asai Mutasi LeukoStrat CDx FLT3 dan ubat Astellas, XOSPATA (gilteritinib fumarate)...
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미국 샌디에이고, Nov. 30, 2018 (GLOBE NEWSWIRE) -- Invivoscribe는 미국 내 FLT3 재발/난치성 급성골수성백혈병(AML) 환자 치료용 LeukoStrat CDx FLT3 Mutation Assay와 아스텔라스(Astellas)의 신약 XOSPATA (길터리티닙 푸마르산염)가 미국 FDA(식품의약청)로부터 허가를...
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SAN DIEGO, Nov. 30, 2018 (GLOBE NEWSWIRE) -- Invivoscribe dengan senang hati mengumumkan persetujuan FDA baik Asai Mutasi LeukoStrat CDx FLT3 dan obat Astellas, XOSPATA (fumarat gilteritinib), untuk...
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美国圣地亚哥, Nov. 30, 2018 (GLOBE NEWSWIRE) -- Invivoscribe十分高兴地宣布,FDA现已批准LeukoStrat CDx FLT3基因突变试验和Astellas的药物XOSPATA(富马酸吉列替尼)被用于治疗美国FLT3阳性的难治性或复发性急性骨髓性白血病(AML)患者。此外,日本MHLW已确认LeukoStrat CDx...
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SAN DIEGO, Nov. 30, 2018 (GLOBE NEWSWIRE) -- Invivoscribe freut sich bekannt geben zu können, dass der LeukoStrat CDx FLT3 Mutation Assay und das Medikament XOSPATA (Gilteritinib-Fumarat) von...