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Updated: Nov 16, 2025

Generation of Murine Monoclonal Antibodies by Hybridoma Technology
Published on: January 2, 2017
Technological Advancements in Monoclonal Antibodies
José F Santos-Neto1, Fabricia O Oliveira2, Katharine V S Hodel2
1University Center SENAI/CIMATEC, National Service of Industrial Learning-SENAI, Salvador, Bahia, Brazil.
Advancements in biopharmaceutical technologies, including biosimilar drugs and monoclonal antibodies (mAbs), are increasing treatment accessibility. Patent and scientific literature analysis reveals a growing innovation landscape, promising more therapies for chronic diseases and malignancies.
Area of Science:
- Biopharmaceutical technology
- Intellectual property analysis
- Drug development
Background:
- Biopharmaceuticals offer innovative treatments for chronic diseases and cancers.
- Biosimilar products provide more accessible therapeutic options.
- Technological advancements are crucial for biopharmaceutical innovation.
Purpose of the Study:
- To analyze the technological and scientific advancements in biopharmaceuticals using patent and article data.
- To identify key players, trends, and innovation trajectories in the field.
- To understand the impact of biosimilar approvals on treatment accessibility.
Main Methods:
- Patent analysis using Derwent Innovation Index (DWPI) and PatentInspiration databases.
- Scientific literature search using Web of Science for the last 5 years.
- Keyword and IPC code-based search strategy across titles, summaries, and claims.
Main Results:
- Extensive patent data retrieved: 2295 individual patents and 467 families (DWPI); 769 patents and 205 families (PatentInspiration).
- Significant scientific output: 2602 articles from Web of Science.
- Monoclonal antibodies (mAbs) show prominence in scientific research and innovation.
- Analysis includes contributing organizations, geographical distribution, development, and key inventors/authors.
Conclusions:
- The biopharmaceutical landscape, particularly in mAbs and immunotherapies, is rapidly evolving.
- Anticipated regulatory approvals will drive a continuous flow of new biopharmaceutical products.
- Increased scientific and technological publications support wider availability of these essential therapies.
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