Pharmaceutical Insights
Navigate pharmaceutical trends with our insights on targets, institutional pipelines, clinical advances, and new drugs.
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Recent blog posts
Allyx Therapeutics Reports Initial Parkinson’s Patient Treated with ALX-001
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Allyx Therapeutics Reports Initial Parkinson’s Patient Treated with ALX-001
6 September 2024
Allyx Therapeutics has begun a new clinical trial for its key drug, ALX-001, administering it to the first patient to assess safety, pharmacokinetics, and potential therapeutic effects in Parkinson’s disease.
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Zealand and Boehringer Ingelheim Collaborate on Latest Development of GLP-1R/GCGR Dual Agonist Survodutide
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Zealand and Boehringer Ingelheim Collaborate on Latest Development of GLP-1R/GCGR Dual Agonist Survodutide
6 September 2024
Zealand Pharma and Boehringer Ingelheim (BI) announced breakthrough clinical trial results for Survodutide, a novel drug targeting metabolic dysfunction-associated steatohepatitis (MASH).
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Merck and EyeBio Initiate Phase 2b/3 Trial for Restoret™ in Diabetic Macular Edema Treatment
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Merck and EyeBio Initiate Phase 2b/3 Trial for Restoret™ in Diabetic Macular Edema Treatment
6 September 2024
Merck and EyeBio Announce Start of Phase 2b/3 Clinical Study for Restoret™ to Treat Diabetic Macular Edema.
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Kelun-Biotech: First Dual-Antibody ADC in Collaboration with Merck Submits China IND
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Kelun-Biotech: First Dual-Antibody ADC in Collaboration with Merck Submits China IND
6 September 2024
September 5, the NMPA Center for Drug Evaluation (CDE) announced that the clinical trial application (IND) for SKB571, an injectable drug from Kelun-Biotech, has been accepted.
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FDA Approves BlueRock Therapeutics' IND for iPSC-Derived Cell Therapy OpCT-001 Targeting Photoreceptor Diseases
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FDA Approves BlueRock Therapeutics' IND for iPSC-Derived Cell Therapy OpCT-001 Targeting Photoreceptor Diseases
6 September 2024
BlueRock Therapeutics has obtained FDA approval for their IND application for OpCT-001, a cell therapy derived from iPSCs, targeting primary photoreceptor diseases.
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Pharma Frontiers: Daily Digest of Global Pharmaceutical News – Sep 6
Pharma Frontiers: Daily Digest of Global Pharmaceutical News – Sep 6
6 September 2024
Sep 6th 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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Vasa Therapeutics Initiates Phase 1 Trial of VS-041 for Heart Failure Treatment
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Vasa Therapeutics Initiates Phase 1 Trial of VS-041 for Heart Failure Treatment
6 September 2024
Vasa Therapeutics Begins Phase 1 Human Trial of VS-041 for Treating Heart Failure with Preserved Ejection Fraction.
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GC Biopharma and Hanmi Pharmaceutical get U.S. FDA IND approval for Phase 1/2 trial
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GC Biopharma and Hanmi Pharmaceutical get U.S. FDA IND approval for Phase 1/2 trial
6 September 2024
GC Biopharma revealed that its joint effort with Hanmi Pharmaceutical on the Fabry treatment 'LA-GLA' (GC1134A/HM15421) has been granted IND approval by the U.S. FDA to initiate a Phase 1/2 clinical study.
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REGENXBIO Reports Positive Results for RGX-121, Showing Lasting Systemic Impact
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REGENXBIO Reports Positive Results for RGX-121, Showing Lasting Systemic Impact
6 September 2024
REGENXBIO Inc. revealed encouraging findings from the Phase I/II/III CAMPSIITE® study of RGX-121, aimed at treating Mucopolysaccharidosis Type II (MPS II).
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Evommune Begins Phase 2 Study of Oral MRGPRX2 Antagonist EVO756 in Chronic Inducible Urticaria
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Evommune Begins Phase 2 Study of Oral MRGPRX2 Antagonist EVO756 in Chronic Inducible Urticaria
5 September 2024
Evommune has announced the initiation of a Phase 2 trial for EVO756, with the first patient now enrolled.
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LENZ Therapeutics Submits NDA to FDA for Novel Eye Drop Treatment for Presbyopia
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LENZ Therapeutics Submits NDA to FDA for Novel Eye Drop Treatment for Presbyopia
5 September 2024
LENZ Therapeutics, a biopharmaceutical company dedicated to developing the first and only eye drop based on aceclidine (LNZ100) to improve near vision in presbyopia patients.
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EU Approves Merck's KEYTRUDA and Padcev Combo for Advanced Urothelial Cancer
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EU Approves Merck's KEYTRUDA and Padcev Combo for Advanced Urothelial Cancer
5 September 2024
The EC has authorized the use of Merck's KEYTRUDA® (pembrolizumab) in combination with Padcev® (enfortumab vedotin-ejfv) as an initial therapy for adults with inoperable or metastatic urothelial cancer.
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