Pharmaceutical Insights
Navigate pharmaceutical trends with our insights on targets, institutional pipelines, clinical advances, and new drugs.
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Recent blog posts
Pharma Frontiers: Daily Digest of Global Pharmaceutical News – Aug 20
Pharma Frontiers
10 min read
Pharma Frontiers: Daily Digest of Global Pharmaceutical News – Aug 20
20 August 2024
Aug 20th 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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Immutep Reports Initial Dosage in Phase I Trial of IMP761, an Innovative LAG-3 Agonist Antibody
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3 min read
Immutep Reports Initial Dosage in Phase I Trial of IMP761, an Innovative LAG-3 Agonist Antibody
20 August 2024
Immutep Limited has announced the successful dosing of the initial participant in the first-in-human Phase I trial of IMP761.
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Sionna Therapeutics Starts Two Phase 1 Clinical Trials with SION-719 and SION-451 for Cystic Fibrosis
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3 min read
Sionna Therapeutics Starts Two Phase 1 Clinical Trials with SION-719 and SION-451 for Cystic Fibrosis
20 August 2024
Sionna Therapeutics announced that the first participants have been dosed in two Phase 1 trials of SION-719 and SION-451 in healthy volunteers.
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First Patient Treated in Aegle Therapeutics' Phase 1/2a AGLE-102™ Trial for Dystrophic Epidermolysis Bullosa
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3 min read
First Patient Treated in Aegle Therapeutics' Phase 1/2a AGLE-102™ Trial for Dystrophic Epidermolysis Bullosa
20 August 2024
Aegle Therapeutics Corp. reveals the initial patient treated in the Phase 1/2a study of AGLE-102™ for Dystrophic Epidermolysis Bullosa.
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U.S. FDA Fast-tracks Approval for Gilead's Livdelzi in Treating Biliary Cholangitis
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4 min read
U.S. FDA Fast-tracks Approval for Gilead's Livdelzi in Treating Biliary Cholangitis
19 August 2024
The U.S. FDA has granted accelerated approval to Gilead's Livdelzi (Seladelpar) for treating primary biliary cholangitis.
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Arrowhead Pharmaceuticals to Start Clinical Trials for Two New RNAi Obesity Drugs, ARO-INHBE and ARO-ALK7
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4 min read
Arrowhead Pharmaceuticals to Start Clinical Trials for Two New RNAi Obesity Drugs, ARO-INHBE and ARO-ALK7
19 August 2024
Arrowhead Pharmaceuticals, Inc. (NASDAQ: ARWR) disclosed preclinical data and outlined its strategy to move two advanced RNAi-based candidates, ARO-INHBE and ARO-ALK7.
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Incyte and Syndax Declare FDA Clearance for Niktimvo™ (axatilimab-csfr) to Treat Chronic GVHD
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4 min read
Incyte and Syndax Declare FDA Clearance for Niktimvo™ (axatilimab-csfr) to Treat Chronic GVHD
19 August 2024
Incyte and Syndax Pharmaceuticals announced that Niktimvo™ (axatilimab-csfr), an anti-CSF-1R antibody, has been approved by the U.S. Food and Drug Administration (FDA).
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TransCode Therapeutics Initiates First Phase Clinical Study
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3 min read
TransCode Therapeutics Initiates First Phase Clinical Study
19 August 2024
TransCode Therapeutics has reported the start of its multicenter, open-label, Phase 1 clinical trial for its primary therapeutic candidate, TTX-MC138.
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EMA Accepts Marketing Submission for AVT06, an Aflibercept Biosimilar to Eylea®
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3 min read
EMA Accepts Marketing Submission for AVT06, an Aflibercept Biosimilar to Eylea®
19 August 2024
Alvotech declared that the European Medicines Agency (EMA) has accepted a Marketing Authorization Application for AVT06, Alvotech’s planned biosimilar to Eylea® (aflibercept).
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CV6 Therapeutics Begins Dosing Patients in Phase 1a Trial for Novel dUTPase Inhibitor CV6-168
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3 min read
CV6 Therapeutics Begins Dosing Patients in Phase 1a Trial for Novel dUTPase Inhibitor CV6-168
19 August 2024
CV6 Therapeutics has reported the successful administration of the second patient in its Phase 1a clinical trial assessing CV6-168 in combination with infusional 5-fluorouracil (5-FU) for cancer treatment.
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Pharma Frontiers: Daily Digest of Global Pharmaceutical News – Aug 15
Pharma Frontiers
12 min read
Pharma Frontiers: Daily Digest of Global Pharmaceutical News – Aug 15
15 August 2024
Aug 15th 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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UroGen Submits UGN-102 NDA, Targets FDA Approval for Intermediate-Risk Bladder Cancer Treatment
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3 min read
UroGen Submits UGN-102 NDA, Targets FDA Approval for Intermediate-Risk Bladder Cancer Treatment
15 August 2024
UroGen Submits NDA for UGN-102, Aiming for FDA Approval as the First Treatment for Intermediate-Risk, Low-Grade Non-Muscle Invasive Bladder Cancer.
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