Pharmaceutical Insights
Navigate pharmaceutical trends with our insights on targets, institutional pipelines, clinical advances, and new drugs.
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Recent blog posts
Is Delandistrogene moxeparvovec approved by the FDA?
Drug Insights
3 min read
Is Delandistrogene moxeparvovec approved by the FDA?
5 August 2024
Delandistrogene moxeparvovec, known by the brand name Elevidys, received FDA approval for the treatment of Duchenne muscular dystrophy in children on June 22, 2023.
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FDA Clears IND for Umoja's UB-VV111: A CD19 CAR T-Cell Therapy for Blood Cancers
Latest Hotspot
3 min read
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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Is Vyvgart Hytrulo approved by the FDA?
Drug Insights
3 min read
Is Vyvgart Hytrulo approved by the FDA?
5 August 2024
Vyvgart Hytrulo received FDA approval on June 20, 2023. It is approved for the treatment of adults with generalized myasthenia gravis (gMG) who are anti-acetylcholine receptor (AChR) antibody positive.
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EMA Approves Bio-Thera's BAT1706: A Bevacizumab Biosimilar to Avastin®
Latest Hotspot
2 min read
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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Is Suflave approved by the FDA?
Drug Insights
3 min read
Is Suflave approved by the FDA?
5 August 2024
Suflave was approved by the FDA on June 15, 2023. It is a prescription laxative used to cleanse the bowel in preparation for colonoscopy in adults.
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Connext Successfully Gives Initial CNT201 Dose for Dupuytren’s Contracture
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3 min read
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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Pharma Frontiers: Daily Digest of Global Pharmaceutical News – Aug 2
Pharma Frontiers
10 min read
Pharma Frontiers: Daily Digest of Global Pharmaceutical News – Aug 2
2 August 2024
Aug 2nd 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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FDA Approves Vertex's Suzetrigine for Moderate-to-Severe Acute Pain
Latest Hotspot
3 min read
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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Is Posluma approved by the FDA?
Drug Insights
4 min read
Is Posluma approved by the FDA?
2 August 2024
The US Food and Drug Administration (FDA) approved Posluma injection on May 25, 2023.
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PepGen Announces Promising Low-Dose Results in Phase 2 CONNECT1-EDO51 Trial for Duchenne Muscular Dystrophy Treatment
Latest Hotspot
3 min read
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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Is Durlobactam/Sulbactam approved by the FDA?
Drug Insights
3 min read
Is Durlobactam/Sulbactam approved by the FDA?
2 August 2024
durlobactam/sulbactam, marketed under the brand name Xacduro, is FDA approved. The approval was granted on May 23, 2023.
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Formycon initiates Phase III clinical trial for Keytruda® biosimilar candidate FYB206
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3 min read
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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