Pharmaceutical Insights
Navigate pharmaceutical trends with our insights on targets, institutional pipelines, clinical advances, and new drugs.
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Recent blog posts
Novartis' Leqvio® Significantly Reduces LDL-C in Low to Moderate ASCVD Risk Patients as Standalone Treatment
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Novartis' Leqvio® Significantly Reduces LDL-C in Low to Moderate ASCVD Risk Patients as Standalone Treatment
30 August 2024
Novartis' biannual Leqvio® showed significant and meaningful LDL-C reduction as a solo treatment for patients with low to moderate ASCVD risk.
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Merck Initiates Phase 3 Trial for Bomedemstat in Select Essential Thrombocythemia Cases
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Merck Initiates Phase 3 Trial for Bomedemstat in Select Essential Thrombocythemia Cases
30 August 2024
Merck Begins Phase 3 Study of Bomedemstat, an Experimental Drug for Specific Essential Thrombocythemia Patients.
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Cantargia announces schedules for nadunolimab trials in leukemia and triple negative breast cancer
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Cantargia announces schedules for nadunolimab trials in leukemia and triple negative breast cancer
30 August 2024
Cantargia (Cantargia AB, Nasdaq Stockholm: CANTA) has updated the anticipated schedules for nadunolimab clinical studies.
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Centessa Pharmaceuticals Presents Key Data on ORX142, a Novel OX2R Agonist, from Non-Human Primate Study
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Centessa Pharmaceuticals Presents Key Data on ORX142, a Novel OX2R Agonist, from Non-Human Primate Study
30 August 2024
Centessa Pharmaceuticals Unveils Late-Breaking Poster on Non-Human Primate Data for ORX142, a New Orexin Receptor 2 (OX2R) Agonist.
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Find Therapeutics Receives FDA Approval for Phase 1 Trial of FTX-101 in Chronic Optic Neuropathy
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Find Therapeutics Receives FDA Approval for Phase 1 Trial of FTX-101 in Chronic Optic Neuropathy
30 August 2024
Find Therapeutics Announces FDA Approval for FTX-101 Phase 1 Clinical Trial in Chronic Optic Neuropathy Treatment.
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European Commission Approves PADCEV and KEYTRUDA as First-Line Treatment for Advanced Urothelial Carcinoma
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European Commission Approves PADCEV and KEYTRUDA as First-Line Treatment for Advanced Urothelial Carcinoma
30 August 2024
The European Commission has authorized the use of Astellas’ PADCEV™ (enfortumab vedotin) with KEYTRUDA® (pembrolizumab) as an initial treatment for advanced urothelial carcinoma.
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Yunovia Receives MFDS IND Clearance for Phase 1 MAD Study of GLP-1 Small Molecule Agonist
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Yunovia Receives MFDS IND Clearance for Phase 1 MAD Study of GLP-1 Small Molecule Agonist
30 August 2024
Yunovia revealed on the 26th that the Korean MFDS has approved the IND application for a Phase 1 MAD study of ID110521156.
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Patent Research and Operational Guide for Daiichi Sankyo's ADC Drug DS-8201(3)
Patent Research and Operational Guide for Daiichi Sankyo's ADC Drug DS-8201(3)
30 August 2024
Based on the characteristics of ADC drugs, we have summarized the process for conducting patent research on ADC drugs.
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Axalbion Therapeutics Initiates Phase 2 Trial of New TRPM8 Agonist AX-8 in Chronic Cough Patients
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Axalbion Therapeutics Initiates Phase 2 Trial of New TRPM8 Agonist AX-8 in Chronic Cough Patients
30 August 2024
Axalbion Therapeutics Begins Phase 2 Trial for Chronic Cough by Administering AX-8, a New TRPM8 Agonist, to the First Patient.
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Patent Research and Operational Guide for Daiichi Sankyo's ADC Drug DS-8201(2)
Patent Research and Operational Guide for Daiichi Sankyo's ADC Drug DS-8201(2)
30 August 2024
Based on the characteristics of ADC drugs, we have summarized the process for conducting patent research on ADC drugs.
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Zai Lab Presents ZL-1218 Phase 1 Results at ESMO 2024: Advancing Anti-CCR8 Therapy in Tumors
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Zai Lab Presents ZL-1218 Phase 1 Results at ESMO 2024: Advancing Anti-CCR8 Therapy in Tumors
30 August 2024
Zai Lab to Share Early Findings from Phase 1 Study of ZL-1218, a Potential Anti-CCR8 Antibody for Advanced Tumor Therapy, at ESMO Congress 2024.
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Patent Research and Operational Guide for Daiichi Sankyo's ADC Drug DS-8201(1)
Patent Research and Operational Guide for Daiichi Sankyo's ADC Drug DS-8201(1)
30 August 2024
Currently, 272 ADC drugs have been initiated for clinical trials globally. Excluding the market withdrawal of Belantamab mafodotin (Blenrep®), 14 approved ADC products remain available.
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