Patents have been shown to be the main determinant to guarantee market exclusivity of originator biologicals , with patent disputes causing uncertainty on a patent’s validity and subsequently potentially influencing launch dates of competitor products, such as biosimilars . In addition, the launch date of a biosimilar might be affected by strategies for prolongation of exclusivity rights on the originator product, such as filing additional patents for a new formulation, new indication or new dosage regime .
Do patent strategies delay market entry of biosimilar monoclonal antibodies in Europe?
Biosimilars/Research | Posted 22/05/2020 0 Post your comment
Moorkens et al. describe a patent landscape analysis of therapeutic monoclonal antibodies (mAbs) in Europe and the legal challenges to patent an originator product and alleged infringement activities, with a focus on consequences for biosimilar developers . The authors give an overview of basic patents, supplementary protection certificates (SPCs), SPC extensions and regulatory market exclusivities for a selection of nine therapeutic mAbs (adalimumab, bevacizumab, cetuximab, eculizumab, etanercept, infliximab, ranibizumab, rituximab and trastuzumab). This overview is supplemented by three specific case studies, providing a detailed analysis of patents, patent applications and case law for bevacizumab, cetuximab and trastuzumab. Patent filing strategies for adalimumab, etanercept, infliximab and rituximab were already covered in other publications [5-7].
The authors report that the key protection for an originator product was provided by the basic patent and SPC (possibly extended). Additional patents that were filed after the basic patent appeared to be hard to obtain in Europe and were often insufficient to block market entry of biosimilars. Nevertheless, these secondary patents appeared in some cases to be a substantial hurdle for biosimilar developers, to overcome via patent litigation or to invent around, creating uncertainty on the launch date of a biosimilar. However, the authors concluded that these hurdles are surmountable, as many of the opposition and litigation cases were won by biosimilar developers. Table 1 summarizes these main findings for each of the three detailed case studies included, and the four mAbs that were discussed in other publications.
|Table 1: Summary of results on whether patent strategies are delaying market entry of biosimilar monoclonal antibodies in Europe |
|Brand name||Active substance||Secondary patents delaying market entry of biosimilars|
|Humira||adalimumab||Eventually no. All litigation cases were settled before expiry of SPC by grant of a non-exclusive licensing agreement|
|Avastin||bevacizumab||Probably no. It remains to be seen whether biosimilars launch in June 2020|
|Erbitux||cetuximab||No. Potential hurdles were not identified (but no biosimilars launched as yet)|
|Enbrel||etanercept||No. Potential hurdles were not identified|
|Remicade||infliximab||No. However, a licensing agreement might exist|
|MabThera||rituximab||Yes. However, these hurdles were overcome via patent litigation|
|Herceptin||trastuzumab||Yes. However, these hurdles were overcome via patent litigation|
|SPC: supplementary protection certificate.|
Conflict of interest
The authors of the research paper  reported conflict of interest, including being involved in consulting, advisory work and speaking engagements for a number of pharmaceutical companies. For full details of the authors’ conflict of interest, see the research paper .
Abstracted by Evelien Moorkens, PhD Researcher Market Access Biosimilars, Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, Belgium
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