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Recent blog posts
GlycoNex Completes Phase 1 Trial of Denosumab Biosimilar, SPD8 Successfully
Latest Hotspot
3 min read
GlycoNex Completes Phase 1 Trial of Denosumab Biosimilar, SPD8 Successfully
22 August 2024
GlycoNex has declared the successful conclusion of a Phase 1 clinical trial for its denosumab biosimilar, SPD8.
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Rising Tides in ADCs: Clinical Progress and Regulatory Outlook for Targeted Cancer Therapies
Hot Spotlight
6 min read
Rising Tides in ADCs: Clinical Progress and Regulatory Outlook for Targeted Cancer Therapies
21 August 2024
Antibody-Drug Conjugates (ADCs), as a part of precision medicine, target tumor cells by combining the specificity of antibodies with the potent effects of cytotoxins.
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European Medicines Agency Reviews Bristol Myers Squibb's CAR T Therapy Breyanzi for Follicular Lymphoma
Latest Hotspot
4 min read
European Medicines Agency Reviews Bristol Myers Squibb's CAR T Therapy Breyanzi for Follicular Lymphoma
21 August 2024
The European Medicines Agency has accepted Bristol Myers Squibb's application for CAR T cell therapy Breyanzi for treating relapsed or refractory follicular lymphoma.
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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.

Global Drug R&D Express (June 2024)

Global Drug R&D Express (June 2024)

This report compiles and summarizes the basic information of all the first-to-market and special review drugs globally for the month of June totaling 89 drugs. Among them, 1 first-to-market drugs and 1 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.

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