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Phase 3 FLOW Study: 1mg Ozempic® Reduces Kidney Disease Risk
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Phase 3 FLOW Study: 1mg Ozempic® Reduces Kidney Disease Risk
28 June 2024
The Phase 3 FLOW study presented at the 84th ADA Scientific Sessions showed a 1 mg dose of Ozempic® (semaglutide) injection decreased the risk of kidney disease-related events.
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Innovent Reveals Phase 3 Results of Mazdutide for Weight Control at ADA 84th Sessions
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Innovent Reveals Phase 3 Results of Mazdutide for Weight Control at ADA 84th Sessions
28 June 2024
Innovent Unveils Phase 3 Study Outcomes of Mazdutide for Weight Control at the ADA's 84th Scientific Sessions.
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EU Commission Approves Roche's OCREVUS: First Biannual Injection for Multiple Sclerosis
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EU Commission Approves Roche's OCREVUS: First Biannual Injection for Multiple Sclerosis
28 June 2024
The European Commission has approved Roche's OCREVUS for subcutaneous use, making it the first and only twice-yearly injection for relapsing and primary progressive multiple sclerosis.
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Alnylam Reports Positive Outcomes from HELIOS-B Phase 3 Vutrisiran Trial, Meeting All Primary and Secondary Endpoints
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Alnylam Reports Positive Outcomes from HELIOS-B Phase 3 Vutrisiran Trial, Meeting All Primary and Secondary Endpoints
28 June 2024
Alnylam Announces Successful Topline Results from HELIOS-B Phase 3 Trial of Vutrisiran, Showing Statistical Significance in Primary and All Secondary Endpoints in Both Combined and Monotherapy Groups.
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Adicet Bio Receives FDA Approval for IND Application of ADI-270 in Kidney Cancer
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Adicet Bio Receives FDA Approval for IND Application of ADI-270 in Kidney Cancer
28 June 2024
This IND will enable the assessment of ADI-270, for the therapeutic intervention in relapsed/refractory renal cell carcinoma.
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Scholar Rock Reveals SRK-439 Data: Preserves Lean Mass, Reduces Fat Mass Rebound Post-GLP-1 Agonist
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Scholar Rock Reveals SRK-439 Data: Preserves Lean Mass, Reduces Fat Mass Rebound Post-GLP-1 Agonist
27 June 2024
Scholar Rock Unveils New SRK-439 Preclinical Data Showing Notable Lean Mass Preservation and Reduced Fat Mass Rebound After Stopping GLP-1 Receptor Agonist.
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Altimmune Reveals Pemvidutide's Effects on Cardioinflammatory Lipids at ADA's 84th Session
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Altimmune Reveals Pemvidutide's Effects on Cardioinflammatory Lipids at ADA's 84th Session
27 June 2024
Altimmune Shares Findings on Pemvidutide's Impact on Cardioinflammatory Lipid Levels at ADA’s 84th Annual Scientific Sessions.
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Mim8 Outperforms On-Demand Treatments in Haemophilia A Patients
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Mim8 Outperforms On-Demand Treatments in Haemophilia A Patients
27 June 2024
Novo Nordisk A/S: Mim8 showed better reductions in annual bleeding rates (ABR) than on-demand treatments and previous prophylaxis in haemophilia A patients.
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DA-1726 Outperforms Survodutide in Pre-Clinical Weight Reduction and Health Metrics
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DA-1726 Outperforms Survodutide in Pre-Clinical Weight Reduction and Health Metrics
27 June 2024
In pre-clinical models, DA-1726 from NeuroBo Pharmaceuticals outperformed Survodutide in weight reduction, maintaining lean body mass, and lowering lipid levels.
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Sun Pharma's GL0034 Shows Promising Weight Loss in Obesity at ADA's 84th Session
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Sun Pharma's GL0034 Shows Promising Weight Loss in Obesity at ADA's 84th Session
27 June 2024
Sun Pharma's GL0034 (Utreglutide) Showcases Remarkable Weight Loss and Metabolic Improvements in Obesity at ADA's 84th Session.
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Takeda Unveils Promising Phase 2b Mezagitamab Data for Primary Immune Thrombocytopenia Treatment
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Takeda Unveils Promising Phase 2b Mezagitamab Data for Primary Immune Thrombocytopenia Treatment
27 June 2024
Takeda Reveals New Data from Phase 2b Study of Mezagitamab, Showing Potential to Innovate Primary Immune Thrombocytopenia Treatment.
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EMA Validates Bristol Myers Squibb's Subcutaneous Nivolumab Application
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EMA Validates Bristol Myers Squibb's Subcutaneous Nivolumab Application
27 June 2024
Bristol Myers Squibb's application for subcutaneous nivolumab has been validated by the European Medicines Agency.
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