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Recent blog posts
Pharma Frontiers: Daily Digest of Global Pharmaceutical News – Jul 26
Pharma Frontiers
11 min read
Pharma Frontiers: Daily Digest of Global Pharmaceutical News – Jul 26
26 July 2024
Jul 26th 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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Is Adagrasib approved by the FDA?
Drug Insights
4 min read
Is Adagrasib approved by the FDA?
26 July 2024
Adagrasib, marketed under the brand name Krazati, is an oral medication used to treat adults with non-small cell lung cancer (NSCLC).
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Promising Phase 2 Results for OSE Immunotherapeutics' Lusvertikimab in Treating Ulcerative Colitis
Latest Hotspot
3 min read
Promising Phase 2 Results for OSE Immunotherapeutics' Lusvertikimab in Treating Ulcerative Colitis
26 July 2024
OSE Immunotherapeutics Reports Promising Phase 2 Trial Outcomes for Lusvertikimab in Ulcerative Colitis Treatment.
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Check out our latest report
siRNA Drug Amvuttra Patent Research and Practical Operation Guide

siRNA Drug Amvuttra Patent Research and Practical Operation Guide

Small interfering RNA (siRNA) are short double-stranded RNA molecules, typically 21-25 nucleotides long. On June 14, 2022, Alnylam's siRNA drug Amvuttra® (Vutrisiran) was approved by the FDA for treating polyneuropathy in adults with hereditary transthyretin-mediated (hATTR) amyloidosis. As Alnylam's flagship product, Amvuttra generated $560 million in sales in 2023. Compared to Alnylam's Onpattro, Amvuttra has lower manufacturing costs, requires less frequent dosing, and offers convenient subcutaneous injection, potentially leading more patients to switch to Amvuttra. Over 20 companies globally are developing siRNA drugs, but Alnylam dominates the market with a robust patent strategy covering Amvuttra's core components, delivery agents, sequences, and modifications. Alnylam utilizes divisional and continuation applications to maintain extensive patent protection, serving as a model for siRNA drug patenting. This report focuses on siRNA drug patent searches, using Alnylam's Amvuttra as a case study to illustrate the research process. It also provides an overview of the latest patent landscapes in the U.S. and China.

Global Drug R&D Express (May 2024)

Global Drug R&D Express (May 2024)

This report compiles and summarizes the basic information of all the first-to-market and special review drugs globally for the month of May totaling 95 drugs. Among them, 1 first-to-market drugs and 2 drugs under special review were selected for detailed analysis. The report provides an in-depth interpretation of these drugs, covering various aspects such as basic information, development status, technological barriers, mechanism of action, clinical trials, and competitive landscape.

Patent Research and Operational Guide for Daiichi Sankyo's ADC Drug DS-8201

Patent Research and Operational Guide for Daiichi Sankyo's ADC Drug DS-8201

Antibody-Drug Conjugates (ADCs) have a tripartite structure: Antibody-Linker-Payload. Currently, 272 ADCs are in clinical trials worldwide. Despite the withdrawal of Belantamab mafodotin, 14 ADCs remain on the market. ADC development is highly competitive, with strategic patent deployment being critical. For example, DS-8201's patents on each component offer primary protection, while novel combinations and pharmacological properties drive patent iteration and extend market exclusivity. Comprehensive extraction and aggregation of these source, core, and iterative patents are essential for high-quality patent research reports to guide infringement analysis, biosimilar development, and investment strategies. This report focuses on ADC patent searches, using DS-8201 as a case study to outline the research process and map the latest patent landscapes in China and the United States.

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