Pharmaceutical Insights
Navigate pharmaceutical trends with our insights on targets, institutional pipelines, clinical advances, and new drugs.
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Recent blog posts
Zelenirstat: A Quick Look at Its R&D Progress and Clinical Results from the 2024 ASCO_GI
Zelenirstat: A Quick Look at Its R&D Progress and Clinical Results from the 2024 ASCO_GI
20 February 2024
Zelenirstat, an effective oral NMT inhibitor, showed promising results in treating advanced relapsed/refractory cancer at 2024's ASCO_GI.
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Galderma's Nemolizumab for Prurigo Nodularis and Eczema Approved for Submission in US and EU
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Galderma's Nemolizumab for Prurigo Nodularis and Eczema Approved for Submission in US and EU
20 February 2024
Galderma declares submission approval of Nemolizumab for treating Prurigo Nodularis and Eczema in America and Europe.
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Master Tretinoin Search on Synapse
Drug Insights
2 min read
Master Tretinoin Search on Synapse
20 February 2024
Vesanoid, also known as Tretinoin, is a vitamin A derivative that has been given the green light for treating acne vulgaris and specific forms of promyelocytic leukemia.
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Biogen's SKYCLARYS® Wins EU Approval: A Breakthrough for Friedreich’s Ataxia
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Biogen's SKYCLARYS® Wins EU Approval: A Breakthrough for Friedreich’s Ataxia
20 February 2024
Biogen Secures European Commission for New Drug SKYCLARYS® (omaveloxolone), Pioneering Treatment for Friedreich’s Ataxia.
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An analysis of Tinengotinib's R&D progress and its clinical results presented at the 2024 ASCO_GI Annual Meeting
An analysis of Tinengotinib's R&D progress and its clinical results presented at the 2024 ASCO_GI Annual Meeting
20 February 2024
Tinengotinib, a selective multi-kinase inhibitor, effectively targets FGFR2 fusion/rearrangement and resistance mutations in early trials involving cholangiocarcinoma patients.
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CSL Unveils Phase 3 AEGIS-II Results on CSL112 (Apolipoprotein A-I) Efficacy and Safety
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CSL Unveils Phase 3 AEGIS-II Results on CSL112 (Apolipoprotein A-I) Efficacy and Safety
20 February 2024
CSL Reveals Key Findings of Phase 3 AEGIS-II Study Assessing Effectiveness and Security of CSL112 (Human Apolipoprotein A-I).
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Unveiling Clopidogrel: How to Search for it on Synapse
Drug Insights
2 min read
Unveiling Clopidogrel: How to Search for it on Synapse
20 February 2024
Clopidogrel Bisulfate, a medication trademarked as Plavix®, was approved by Bristol Myers Squibb in the US in 1997.
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Adverum Biotech's Phase 2 LUNA Study Shows Promising Ixo-vec Results for Wet AMD
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Adverum Biotech's Phase 2 LUNA Study Shows Promising Ixo-vec Results for Wet AMD
20 February 2024
Adverum Biotech Reports Encouraging Initial Results for Safety and Effectiveness in Phase 2 LUNA Study of Ixo-vec for Wet Age-Related Macular Degeneration Patients.
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Decoding Tasurgratinib: a comprehensive study of its R&D trends and its clinical results in 2024 ASCO_GI
Decoding Tasurgratinib: a comprehensive study of its R&D trends and its clinical results in 2024 ASCO_GI
20 February 2024
Tasurgratinib (E7090) is an orally available selective inhibitor of FGFR 1–3, the recommended dose is 140 mg per day per the dose-escalation part of a first-in-human phase 1 study.
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Hemab Therapeutics reveals promising early results for Glanzmann's Thrombasthenia drug, HMB-001, at 2024 EAHAD Congress
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Hemab Therapeutics reveals promising early results for Glanzmann's Thrombasthenia drug, HMB-001, at 2024 EAHAD Congress
19 February 2024
At the EAHAD Congress in 2024, Hemab Therapeutics Unveils Encouraging Initial Findings for Their Drug, HMB-001, Targeting Glanzmann's Thrombasthenia.
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Expert Tips for Searching Hydralazine on Synapse
Drug Insights
2 min read
Expert Tips for Searching Hydralazine on Synapse
19 February 2024
Hydralazine Hydrochloride, marketed under the trade name Dralzine®, is an antihypertensive medication that has been approved since 1952 for the treatment of hypertension.
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China Grants First-Ever Approval to Crovalimab for Paroxysmal Nocturnal Hemoglobinuria (PNH) Therapy
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China Grants First-Ever Approval to Crovalimab for Paroxysmal Nocturnal Hemoglobinuria (PNH) Therapy
19 February 2024
Chugai Pharmaceutical announced that China's National Medical Products Administration approved its innovative C5 monoclonal antibody, crovalimab.
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