Leah focuses her practice on patent litigation in the life sciences industry. She has experience with matters involving oncology treatments, drug compounds and methods of treatment, and dietary supplements. Leah co-authored the chapter on patent issues relating to diagnostics in the 2026 edition of PLI’s Pharmaceutical and Biotech Patent Law. She has a B.S. in Biology, summa cum laude, with a co-major in Pre-Medical Studies.
Information contained in the Venable BiologicsHQ database relates to FDA-approved drug products listed in the CDER Purple Book or on the FDA website (www.fda.gov). Information relating to FDA licensed products, FDA-approved indications, and aBLA and 505(b)(2) applications is obtained from public sources including the U.S. FDA website (www.fda.gov). Information relating to litigations is given only for cases active from January 31, 2010 onward. Information relating to foreign biosimilar / biologics follow-on products approved in Australia, Canada, the E.U., Japan and South Korea is from public sources. Statistics graphics are compiled from information contained in the Venable BiologicsHQ database.
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