Recent blog posts
Tectonic Therapeutic Secures US IND Approval for TX45 Lead Program
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Tectonic Therapeutic Secures US IND Approval for TX45 Lead Program
5 August 2024
Tectonic Therapeutic has announced that the U.S. Food and Drug Administration has approved its Investigational New Drug application for TX45.
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Pamrevlumab Trial Results in Advanced Pancreatic Cancer: FibroGen's Update
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Pamrevlumab Trial Results in Advanced Pancreatic Cancer: FibroGen's Update
5 August 2024
FibroGen Releases Main Outcomes from Two Advanced Pamrevlumab Pancreatic Cancer Trials and Shares Corporate News.
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FDA Clears IND for Umoja's UB-VV111: A CD19 CAR T-Cell Therapy for Blood Cancers
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FDA Clears IND for Umoja's UB-VV111: A CD19 CAR T-Cell Therapy for Blood Cancers
5 August 2024
Umoja Biopharma Receives FDA Approval for IND Application of UB-VV111, a CD19 Targeted CAR T for Blood Cancers.
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EMA Approves Bio-Thera's BAT1706: A Bevacizumab Biosimilar to Avastin®
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EMA Approves Bio-Thera's BAT1706: A Bevacizumab Biosimilar to Avastin®
5 August 2024
The European Medicines Agency (EMA) has given its approval to Bio-Thera Solutions for BAT1706 (Avzivi®, bevacizumab), a biosimilar of Avastin®.
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Connext Successfully Gives Initial CNT201 Dose for Dupuytren’s Contracture
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Connext Successfully Gives Initial CNT201 Dose for Dupuytren’s Contracture
5 August 2024
Connext has revealed the initial successful administration of CNT201, its therapeutic solution for Dupuytren’s contracture, in patients.
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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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