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BioSpace News Archive
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Job Trends
Small and Medium Biotech Companies Still Growing in Uncertain Times
BioSpace spoke with three CEOs: Alto Neuroscience’s Dr. Amit Etkin, Omega Therapeutics’ Mahesh Karande and Rain Therapeutics’ Avanish Vellanki about their companies’ employment growth.
June 26, 2022
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8 min read
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Geoff Herman
Drug Development
Ascletis’ Subcutaneous PD-L1 Antibody ASC22 Demonstrated Potential of Functional Cure of Chronic Hepatitis B as 42.9% of Patients with Baseline HBsAg≤100 IU/mL Obtained Sustained HBsAg Loss
Ascletis Pharma Inc. announces the latest Phase IIb clinical trial results of subcutaneous PD-L1 antibody ASC22 in patients with chronic hepatitis B at an oral parallel session of the International Liver Congress™ 2022 held by the European Association for the Study of the Liver.
June 26, 2022
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5 min read
Policy
Innovent and Lilly Jointly Announce the Approval of TYVYT® (sintilimab injection) by China NMPA in Combination with Chemotherapy as First-line Treatment of Advanced or Metastatic Gastric or Gastroesophageal Junction Adenocarcinoma
Innovent Biologics, Inc. and Eli Lilly and Company, announced that the National Medical Products Administration of China has approved the supplemental New Drug Application for TYVYT® in combination with fluorouracil and platinum-based chemotherapy for the first-line treatment of unresectable, locally advanced, recurrent or metastatic gastric or gastroesophageal junction adenocarcinoma.
June 26, 2022
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16 min read
Antengene Announces Clinical Trial Collaboration with BeiGene to Evaluate Selinexor in Combination with Tislelizumab in T and NK-Cell Lymphoma
Antengene Corporation Limited announced that it has entered into a clinical trial collaboration with BeiGene to evaluate the safety, pharmacokinetics, pharmacodynamics and preliminary efficacy of selinexor in combination with BeiGene’s anti-PD-1 checkpoint inhibitor, tislelizumab.
June 26, 2022
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9 min read
Policy
Astellas Announces FDA Update on the FORTIS Clinical Trial of AT845 in Adults with Late-Onset Pompe Disease
Astellas Pharma Inc. announced that the US Food and Drug Administration has placed a clinical hold on the FORTIS Phase 1/2 trial following the occurrence of a serious adverse event of peripheral sensory neuropathy in one of the trial participants.
June 26, 2022
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6 min read