On December 23, 2020, the PTAB sua sponte extended the pendency of Galderma v. Medy-Tox, PGR2019-00062, after determining good cause existed due to travel restrictions caused by the COVID-19 pandemic. The PGR involves U.S. Patent No. 10,143,728, titled “Long lasting effect of new botulinum toxin formulations.” PGR2019-00062 is one of only a handful of PGRs where pendency has been extended beyond one year for good cause.
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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