Pharmaceutical Insights
Navigate pharmaceutical trends with our insights on targets, institutional pipelines, clinical advances, and new drugs.
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Recent blog posts
FDA Approves Needle-Free Neffy (Epinephrine Nasal Spray) for Type I Allergic Reactions and Anaphylaxis
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5 min read
FDA Approves Needle-Free Neffy (Epinephrine Nasal Spray) for Type I Allergic Reactions and Anaphylaxis
13 August 2024
ARS Pharmaceuticals has recently achieved a milestone with the U.S. Food and Drug Administration (FDA) approval of neffy® (epinephrine nasal spray) 2 mg.
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Merck's Phase 3 Trial Update on Vibostolimab & Pembrolizumab for Small Cell Lung Cancer
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3 min read
Merck's Phase 3 Trial Update on Vibostolimab & Pembrolizumab for Small Cell Lung Cancer
12 August 2024
Merck Shares Update on Phase 3 Trial KeyVibe-008 Testing Vibostolimab and Pembrolizumab Combo in Extensive-Stage Small Cell Lung Cancer.
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FDA Grants Fast-Track Approval to Novartis' Fabhalta for Lowering Proteinuria in IgAN
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3 min read
FDA Grants Fast-Track Approval to Novartis' Fabhalta for Lowering Proteinuria in IgAN
12 August 2024
Novartis gets FDA fast-track approval for Fabhalta® (iptacopan), marking it as the inaugural complement inhibitor to lower proteinuria in primary IgA nephropathy (IgAN).
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Invenra Highlights Exelixis' Phase 1 Trial for XB010 in Advanced Tumor Patients
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2 min read
Invenra Highlights Exelixis' Phase 1 Trial for XB010 in Advanced Tumor Patients
12 August 2024
Invenra Showcases Exelixis’ News: Phase 1 Clinical Trial Begins for XB010 in Advanced Solid Tumor Patients.
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Mediar Therapeutics Starts New Clinical Trial for Innovative Anti-Fibrosis Antibodies
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3 min read
Mediar Therapeutics Starts New Clinical Trial for Innovative Anti-Fibrosis Antibodies
12 August 2024
This study is assessing the safety and tolerability of MTX-474, a human IgG1 antibody created to inhibit EphrinB2 signaling.
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Takeda's ADZYNMA Clears EU Commission for cTTP Treatment
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3 min read
Takeda's ADZYNMA Clears EU Commission for cTTP Treatment
12 August 2024
Takeda Gains European Commission Clearance for ADZYNMA (Recombinant ADAMTS13), the First Recombinant ADAMTS13 Therapy for cTTP.
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FDA Approves Servier's VORANIGO®, First Targeted Treatment for Grade 2 IDH-mutant Glioma
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3 min read
FDA Approves Servier's VORANIGO®, First Targeted Treatment for Grade 2 IDH-mutant Glioma
12 August 2024
The FDA has approved Servier's VORANIGO® (vorasidenib) tablets as the first targeted treatment for Grade 2 IDH-mutant glioma.
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NeuroBo, Dong-A ST, & ImmunoForge Collaborate on Monthly Obesity Treatment DA-1726
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3 min read
NeuroBo, Dong-A ST, & ImmunoForge Collaborate on Monthly Obesity Treatment DA-1726
9 August 2024
NeuroBo Pharmaceuticals, Dong-A ST, and ImmunoForge Sign Agreement to Collaborate on Developing a Monthly DA-1726 Formulation to Treat Obesity.
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Pharma Frontiers: Daily Digest of Global Pharmaceutical News – Aug 9
Pharma Frontiers
12 min read
Pharma Frontiers: Daily Digest of Global Pharmaceutical News – Aug 9
9 August 2024
Aug 9th latest updates in the global new drug development field, including progress in new drug research and development, transaction information, and partnership developments.
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First U.S. Participant Joins Global Clinical Trial for Telitacicept in Myasthenia Gravis: A Milestone
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3 min read
First U.S. Participant Joins Global Clinical Trial for Telitacicept in Myasthenia Gravis: A Milestone
9 August 2024
The initial participant in the U.S. joins the phase III global multi-center clinical trial for telitacicept targeting myasthenia gravis, marking a significant milestone.
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Elevation Oncology's Phase 1 Trial: Promising Early Results for EO-3021 in Advanced Non-Resectable/Metastatic Solid Tumors
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3 min read
Elevation Oncology's Phase 1 Trial: Promising Early Results for EO-3021 in Advanced Non-Resectable/Metastatic Solid Tumors
9 August 2024
Elevation Oncology Releases Encouraging Early Results from Phase 1 Trial of EO-3021 in Patients with Advanced Non-Resectable or Metastatic Solid Tumors.
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Daiichi Sankyo and Merck Sign Global Pact for MK-6070 Development and Sales
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3 min read
Daiichi Sankyo and Merck Sign Global Pact for MK-6070 Development and Sales
9 August 2024
This expansion now encompasses Merck’s investigational product MK-6070, a T-cell engager targeting delta-like ligand 3 (DLL3).
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