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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 ,

Antengene Announces Publication of Abstract on XPO1 Inhibitor Selinexor in Relapsed or Refractory Multiple Myeloma at ASCO 2021 and EHA 2021


Antengene Announces Publication of Abstract on XPO1 Inhibitor Selinexor in Relapsed or Refractory Multiple Myeloma at ASCO 2021 and EHA 2021
-Results from the MARCH trial showed an ORR of 33.3% in triple-class-exposed RRMM patients with the Sd regimen, and 44.4% in patients who previously received CAR-T therapies-
-Selinexor is currently the only commercially available XPO1 inhibitor-
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SHANGHAI and HONG KONG, June 3, 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, announced that the results from the Phase II MARCH trial of selinexor plus low dose dexamethasone (the Sd regimen) for the treatment of Chinese patients with relapsed or refractory multiple myeloma (RRMM) are published at the 20 ....

United States , Asia Pacific , Antengene Corporation , American Society Of Clinical Oncology , European Hematology Association , Drug Administration , Prnewswire Antengene Corporation Limited , Antengene Corporation Limited , Virtual Congress , National Comprehensive Cancer Network , Chinese Society Of Clinical Oncology , Corporation Limited , Clinical Oncology , Annual Meeting , Hematology Association , Chinese Society , Asia Pacific Region , Patients Beyond , ஒன்றுபட்டது மாநிலங்களில் , ஆசியா பெஸிஃபிக் , அமெரிக்கன் சமூகம் ஆஃப் மருத்துவ புற்றுநோயியல் , ஐரோப்பிய ஹீமாட்டாலஜி சங்கம் , மெய்நிகர் காங்கிரஸ் , தேசிய விரிவான புற்றுநோய் வலைப்பின்னல் , சீன சமூகம் ஆஃப் மருத்துவ புற்றுநோயியல் , நிறுவனம் வரையறுக்கப்பட்டவை ,