TY - JOUR
T1 - Could patents interfere with the development of a cardiovascular polypill?
AU - Beall, Reed F.
AU - Schwalm, Jon David R.
AU - Huffman, Mark D.
AU - McCready, Tara
AU - Yusuf, Salim
AU - Attaran, Amir
N1 - Funding Information:
JDS, TM, and SY have declared that PHRI receives funding for investigating the polypill from Cadila, but the authors have not received any personal compensation, stocks or share or employment with Cadila or any other company. SY received an honorarium and travel expenses once to attend a meeting in the last 5 years. SY is listed as an inventor on patents relating to the treatment of cardiovascular disease. MDH receives support from the World Heart Federation to serve as its senior program advisor for its Emerging Leaders program, which is funded by unrestricted educational grants from AstraZeneca, Boehringer Ingelheim, and Bupa. All other authors (RFB and AA) have nothing to declare.
Funding Information:
Authors declare that each of their roles in the development of this manuscript satisfies the ICMJE criteria for authorship. No direct funding was received spe‑ cific to this manuscript; however, this article is relevant to RFB’s doctoral stud‑ ies, which have been funded through a Vanier Doctoral Scholarship by the Canadian Institutes of Health Research (CIHR) of the Government of Canada.
Publisher Copyright:
© 2016 The Author(s).
PY - 2016/8/18
Y1 - 2016/8/18
N2 - Background: The Wellcome Trust, the World Health Organization, and cardiologists have advocated for the idea of a "polypill" containing multiple cardiovascular drugs to be co-formulated into a single pill for over a decade. Some cardiologists have asserted that the drugs commonly considered for inclusion into such a polypill are older and therefore free of patent protection. We tested this assertion. This project was requested by the World Heart Federation (WHF). Methods, data and materials: Two cardiologists from the WHF provided a list of 48 cardiovascular drugs for evaluation. We designated the United States and Canada as the base jurisdictions for this patent study. We linked patent data from these countries' national medicine patent registers to patent information in over 96 other countries using Derwent and INPADOC via Thomson Innovation. We expanded our study beyond the aforementioned data linkage through a systematic search of the World Intellectual Property Organization's PatentScope, which was based primarily upon the drugs' active ingredient names. Results: In the United States and Canada, eight of the drugs were only available in the patent-protected, brand name formulation in one or both countries. Another 21 drugs had relevant patents, but generic equivalents were nevertheless available. Only 19 drugs (40 %) appeared entirely post-patent. Broadening the co-formulation searches globally, the overwhelming majority of drugs (40/48) were mentioned in patent applications for cardiovascular drug combinations. Conclusion: The assertion that most of these cardiovascular drugs are post-patent is accurate, but only in the sense that many of the original patents on these active ingredients have expired and that generic alternatives are usually available. The landscape of patents covering novel (co-) formulations is far more complex, however. Most research and development for cardiovascular combination medicines are likely to be undertaken by companies whose original patents on the active ingredient will soon expire or have recently expired. Cardiologists looking to accelerate polypill development may consider approaching such companies to partner.
AB - Background: The Wellcome Trust, the World Health Organization, and cardiologists have advocated for the idea of a "polypill" containing multiple cardiovascular drugs to be co-formulated into a single pill for over a decade. Some cardiologists have asserted that the drugs commonly considered for inclusion into such a polypill are older and therefore free of patent protection. We tested this assertion. This project was requested by the World Heart Federation (WHF). Methods, data and materials: Two cardiologists from the WHF provided a list of 48 cardiovascular drugs for evaluation. We designated the United States and Canada as the base jurisdictions for this patent study. We linked patent data from these countries' national medicine patent registers to patent information in over 96 other countries using Derwent and INPADOC via Thomson Innovation. We expanded our study beyond the aforementioned data linkage through a systematic search of the World Intellectual Property Organization's PatentScope, which was based primarily upon the drugs' active ingredient names. Results: In the United States and Canada, eight of the drugs were only available in the patent-protected, brand name formulation in one or both countries. Another 21 drugs had relevant patents, but generic equivalents were nevertheless available. Only 19 drugs (40 %) appeared entirely post-patent. Broadening the co-formulation searches globally, the overwhelming majority of drugs (40/48) were mentioned in patent applications for cardiovascular drug combinations. Conclusion: The assertion that most of these cardiovascular drugs are post-patent is accurate, but only in the sense that many of the original patents on these active ingredients have expired and that generic alternatives are usually available. The landscape of patents covering novel (co-) formulations is far more complex, however. Most research and development for cardiovascular combination medicines are likely to be undertaken by companies whose original patents on the active ingredient will soon expire or have recently expired. Cardiologists looking to accelerate polypill development may consider approaching such companies to partner.
UR - http://www.scopus.com/inward/record.url?scp=84982295492&partnerID=8YFLogxK
U2 - 10.1186/s12967-016-0997-3
DO - 10.1186/s12967-016-0997-3
M3 - Article
C2 - 27538505
AN - SCOPUS:84982295492
SN - 1479-5876
VL - 14
JO - Journal of Translational Medicine
JF - Journal of Translational Medicine
IS - 1
M1 - 242
ER -