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Antengene Announces Acceptance of IND Application in China for the Phase II Clinical Trial of Single-Agent Selinexor for the Treatment of Myelofibrosis (MF)


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SHANGHAI and HONG KONG, July 5, 2021 /PRNewswire/ Antengene Corporation Limited ( Antengene , SEHK: 6996.HK), a leading innovative biopharmaceutical company dedicated to discovering, developing and commercializing global first-in-class and/or best-in-class therapeutics in hematology and oncology, recently announced that China s National Medical Products Administration (NMPA) has accepted the Investigational New Drug (IND) application for single agent selinexor, a first-in-class orally available Exportin 1 (XPO1) inhibitor, for the treatment of patients with myelofibrosis (MF) in China.
MF is a clonal hematologic neoplasm which can emerge either as primary MF, polycythemia vera (PV) or essential thrombocythemia (ET)
[1]. Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is currently the only curative treatment for MF. However, such treatment is difficult to carry out and has a low rate of success. According to the ....

New Zealand , South Korea , Jay Mei , Asia Pacific , S El Jamal , Karyopharm Therapeutics Inc , Antengene Corporation , European Commission , Drug Administration , China National Medical Products Administration , Prnewswire Antengene Corporation Limited , Antengene Corporation Limited , Connective Tissue Oncology Society , Israeli Ministry Of Health , Ministry Of Food , National Comprehensive Cancer Network , Corporation Limited , National Medical Products Administration , Investigational New Drug , Karyopharm Therapeutics , Greater China , Israeli Ministry , Safety Monitoring Board , New Drug Applications , Priority Review , Orphan Drug Designation ,

FDA Won't Meet PDUFA Dates For AbbVie' RINVOQ In Psoriatic Arthritis & Ankylosing Spondylitis

FDA Won't Meet PDUFA Dates For AbbVie' RINVOQ In Psoriatic Arthritis & Ankylosing Spondylitis
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