Recent blog posts
FDA Approves Vertex's Suzetrigine for Moderate-to-Severe Acute Pain
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FDA Approves Vertex's Suzetrigine for Moderate-to-Severe Acute Pain
2 August 2024
Vertex reveals FDA approval of New Drug Application for Suzetrigine for treating moderate-to-severe acute pain.
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PepGen Announces Promising Low-Dose Results in Phase 2 CONNECT1-EDO51 Trial for Duchenne Muscular Dystrophy Treatment
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PepGen Announces Promising Low-Dose Results in Phase 2 CONNECT1-EDO51 Trial for Duchenne Muscular Dystrophy Treatment
2 August 2024
PepGen reports encouraging results from low-dose group in ongoing CONNECT1-EDO51 Phase 2 trial for treating Duchenne Muscular Dystrophy with PGN-EDO51.
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Formycon initiates Phase III clinical trial for Keytruda® biosimilar candidate FYB206
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Formycon initiates Phase III clinical trial for Keytruda® biosimilar candidate FYB206
2 August 2024
Formycon AG announced the first enrollment in the Phase III "Lotus" study comparing FYB206/pembrolizumab with leading cancer drug Keytruda for safety and efficacy.
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Celldex Reports Successful Phase 2 Results for Barzolvolimab in Chronic Inducible Urticaria
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Celldex Reports Successful Phase 2 Results for Barzolvolimab in Chronic Inducible Urticaria
2 August 2024
Celldex Therapeutics announces successful findings from Phase 2 trial of Barzolvolimab for chronic inducible urticaria.
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undefined European Commission gives green light to Roche's Vabysmo for treating retinal vein occlusion (RVO)
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undefined European Commission gives green light to Roche's Vabysmo for treating retinal vein occlusion (RVO)
2 August 2024
Roche disclosed today that the European Commission has given the green light to Vabysmo® (faricimab) .
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Galderma's Relfydess™ has been approved for use in Europe
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Galderma's Relfydess™ has been approved for use in Europe
2 August 2024
Galderma has successfully completed the European decentralized procedure, leading to a favorable decision for RelfydessTM.
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Compugen Announces FDA Clearance of IND for COM503 for the Treatment of Solid Tumors
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Compugen Announces FDA Clearance of IND for COM503 for the Treatment of Solid Tumors
2 August 2024
Compugen has announced that the U.S. Food and Drug Administration has approved the investigational new drug application to begin a Phase 1 trial for COM503.
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Alpha Cognition’s Oral Therapy ZUNVEYL® Receives FDA Approval to Treat Alzheimer’s Disease
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Alpha Cognition’s Oral Therapy ZUNVEYL® Receives FDA Approval to Treat Alzheimer’s Disease
2 August 2024
Alpha Cognition has reported that the U.S. Food and Drug Administration has given the green light to ZUNVEYL® (benzgalantamine).
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NewAmsterdam Pharma Reports Positive Results from BROOKLYN Phase 3 Trial on Obicetrapib in Heterozygous Familial Hypercholesterolemia
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NewAmsterdam Pharma Reports Positive Results from BROOKLYN Phase 3 Trial on Obicetrapib in Heterozygous Familial Hypercholesterolemia
2 August 2024
NewAmsterdam Pharma Announces Positive Topline Data from Pivotal Phase 3 BROOKLYN Clinical Trial Evaluating Obicetrapib in Patients with Heterozygous Familial Hypercholesterolemia.
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European Commission Approves CStone's Sugemalimab (Cejemly®) for First-Line Non-Small Cell Lung Cancer Treatment
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European Commission Approves CStone's Sugemalimab (Cejemly®) for First-Line Non-Small Cell Lung Cancer Treatment
2 August 2024
CStone Announces European Commission Approval of Sugemalimab (Cejemly®) as First-Line Treatment for Non-Small Cell Lung Cancer.
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Nectin Therapeutics Licenses Novel Antibodies to Immunome
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Nectin Therapeutics Licenses Novel Antibodies to Immunome
2 August 2024
According to the agreement, Immunome has obtained exclusive rights to a collection of antibodies directed at an undisclosed target.
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CHMP has adopted a negative opinion on lecanemab for the EU
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CHMP has adopted a negative opinion on lecanemab for the EU
2 August 2024
European Medicines Agency Rejects Eisai's Lecanemab for Alzheimer’s Treatment.
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