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Takeda Pharmaceutical Company Limited: Takeda: FDA gewährt vorrangige Prüfung des NDA-Antrags für Mobocertinib (TAK-788) zur Behandlung von Patienten mit EGFR-Exon-20-insertionspositivem, metastasiertem, nicht-kleinzelligem Lungenkarzinom

Takeda Pharmaceutical Company Limited: Takeda: FDA gewährt vorrangige Prüfung des NDA-Antrags für Mobocertinib (TAK-788) zur Behandlung von Patienten mit EGFR-Exon-20-insertionspositivem, metastasiertem, nicht-kleinzelligem Lungenkarzinom
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App für Jugendliche: ideologische Radikalisierung erkennen

App für Jugendliche: ideologische Radikalisierung erkennen
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