Nick George has more than 30 years of experience developing and evaluating biologics-based patent portfolios.
Nick has devised worldwide patent prosecution strategies for dozens of pre-clinical, clinical, and approved products involving such diverse technologies as therapeutic antibodies, antibody drug conjugates (ADCs), chimeric antigen receptors (CARs), cellular therapeutics (including natural killer [NK], macrophage, monocyte, regulatory T [Treg] cell, and induced pluripotent stem cell [iPSC] therapeutics), gene therapies, gene editing, oncolytic viruses, RNA (ribonucleic acid) therapeutics, peptide therapeutics, diagnostics, and enzyme replacements.
Nick also routinely conducts freedom-to-operate, noninfringement, invalidity, and patentability assessments and performs IP diligence in connection with investments, partnerships, licensing, and private and public financings.
He advises clients ranging from emerging company start-ups to mid- and large-cap biotech and pharmaceutical companies, as well as life sciences venture capital and incubator firms.
Nick holds a Ph.D. in genetics from the University of California, Berkeley and prior to entering patent law did postdoc research at Columbia University (The Chalfie Lab).
執業經驗
- October 19, 2022
East-West Biopharma Summit Road Trip, New York City, October 19, 2022
- Fordham University (J.D. 1997); Columbia University (Postdoctoral Fellow, 1990-1992); University of California, Berkeley (Ph.D. in Genetics 1990); University of Dallas (B.S. in Biology cum laude 1984)
- New York and registered to practice before the United States Patent and Trademark Office