Recent blog posts
Palleon Pharma Presents GLIMMER-01 Findings on E-602 and Cemiplimab for Solid Tumors at SITC Meeting
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Palleon Pharma Presents GLIMMER-01 Findings on E-602 and Cemiplimab for Solid Tumors at SITC Meeting
11 November 2024
Palleon Pharmaceuticals shares findings from the Phase 1/2 GLIMMER-01 study on E-602 combined with Cemiplimab for solid tumor patients at the SITC Annual Meeting.
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NextCure Showcases Preclinical Results for LNCB74 and Clinical Biomarker Data for NC410 at SITC Meeting
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NextCure Showcases Preclinical Results for LNCB74 and Clinical Biomarker Data for NC410 at SITC Meeting
8 November 2024
NextCure presents preclinical findings for LNCB74 and new clinical biomarker results for the NC410 combination at the Society for Immunotherapy of Cancer Annual Meeting.
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EU Approves Dupixent as Exclusive Treatment for Young Children with Eosinophilic Esophagitis
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EU Approves Dupixent as Exclusive Treatment for Young Children with Eosinophilic Esophagitis
8 November 2024
Dupixent has been authorized in the EU as the first and sole treatment for young children suffering from eosinophilic esophagitis.
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Hanmi Launches ‘HM17321’: New Treatment for Obesity and Muscle Loss Linked to GLP-1
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Hanmi Launches ‘HM17321’: New Treatment for Obesity and Muscle Loss Linked to GLP-1
8 November 2024
Hanmi Introduces New Obesity Treatment ‘HM17321’: A Breakthrough in Addressing Muscle Loss Linked to GLP-1.
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Minghui Pharmaceutical Announces Promising Phase I Results for New Bispecific Antibody MHB039A Targeting PD-1 and VEGF
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Minghui Pharmaceutical Announces Promising Phase I Results for New Bispecific Antibody MHB039A Targeting PD-1 and VEGF
8 November 2024
Minghui Pharmaceutical Reports Positive Early Findings from Phase I Trial of MHB039A, a New Bispecific Antibody Targeting PD-1 and VEGF.
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Domvanalimab and Zimberelimab Improve Survival in ARC-10 Lung Cancer Trial
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Domvanalimab and Zimberelimab Improve Survival in ARC-10 Lung Cancer Trial
8 November 2024
Arcus Biosciences reports that the combination of Domvanalimab and Zimberelimab enhanced overall survival in the ARC-10 trial involving patients with high PD-L1 NSCLC.
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OSE Immunotherapeutics Announces Significant Phase 2 Results for Lusvertikimab in Ulcerative Colitis Treatment
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OSE Immunotherapeutics Announces Significant Phase 2 Results for Lusvertikimab in Ulcerative Colitis Treatment
8 November 2024
OSE Immunotherapeutics reports noteworthy and statistically significant findings from the Phase 2 trial of Lusvertikimab, an anti-IL7R monoclonal antibody.
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European Medicines Agency Approves Marketing Authorization Application for AVT05
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European Medicines Agency Approves Marketing Authorization Application for AVT05
8 November 2024
European Medicines Agency Approves Marketing Authorization Application for AVT05, a Biosimilar to Simponi® (golimumab).
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Korro Initiates First Human Study of KRRO-110, Forms Clinical Advisory Board
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Korro Initiates First Human Study of KRRO-110, Forms Clinical Advisory Board
8 November 2024
Korro Bio has announced that it has submitted an application to the Bellberry HREC for a Phase 1/2 clinical trial of KRRO-110 targeting AATD.
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FDA Approves HuidaGene's HG202, First CRISPR/Cas13 Treatment for Macular Degeneration
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FDA Approves HuidaGene's HG202, First CRISPR/Cas13 Treatment for Macular Degeneration
6 November 2024
HuidaGene Therapeutics Secures FDA Approval for HG202, the First CRISPR/Cas13 RNA-Editing Treatment for Macular Degeneration.
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Cytoki Pharma Begins Phase 2 Trial of CK-0045 for Obesity and Type 2 Diabetes
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Cytoki Pharma Begins Phase 2 Trial of CK-0045 for Obesity and Type 2 Diabetes
6 November 2024
Cytoki Pharma has dosed the first patient in its Phase 2 trial for CK-0045, targeting obesity and Type 2 diabetes.
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Viking Therapeutics Shares Fresh Findings on VK2735 Obesity Program at ObesityWeek® 2024
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Viking Therapeutics Shares Fresh Findings on VK2735 Obesity Program at ObesityWeek® 2024
6 November 2024
Viking Therapeutics has announced that new clinical findings from its VK2735 obesity initiative were featured in two poster sessions at ObesityWeek® 2024.
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