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The responses, guidance, and advisories provided by the Pharmaceutical Advertising Advisory Board (PAAB), including but not limited to those available through the PAAB Forum, the PAAB website, and any PAAB correspondences, are specifically intended to assist individuals navigating the PAAB preclearance system. Repurposing or reproducing this content without written consent from the PAAB Commissioner is strictly prohibited. This prohibition includes, but is not limited to, use in machine learning or AI models.

Draft Guidance on Burden of Disease Presentations

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  • Jennifer CarrollJ Offline
    Jennifer CarrollJ Offline
    Jennifer Carroll
    wrote on last edited by
    #1

    Happy Friday @Manufacturer and @Agency

    Based on input from various stakeholders, PAAB has drafted a guidance on disease burden to expand the range of information that may be acceptable for presentations of disease information in advertising. This draft is now in circulation for consultation until April 24th. If you would like more information, please reach out to Pauline Dong.

    palanskiP 1 Reply Last reply
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    • Jennifer CarrollJ Jennifer Carroll

      Happy Friday @Manufacturer and @Agency

      Based on input from various stakeholders, PAAB has drafted a guidance on disease burden to expand the range of information that may be acceptable for presentations of disease information in advertising. This draft is now in circulation for consultation until April 24th. If you would like more information, please reach out to Pauline Dong.

      palanskiP Offline
      palanskiP Offline
      palanski
      wrote on last edited by
      #2

      @jennifer-carroll This is an exciting change! I'm sure we're all wondering why the PAAB is evolving its stance on this subject, which has in the past generally been a no-go zone. Could you provide any context?

      Jennifer CarrollJ 1 Reply Last reply
      1
      • palanskiP palanski

        @jennifer-carroll This is an exciting change! I'm sure we're all wondering why the PAAB is evolving its stance on this subject, which has in the past generally been a no-go zone. Could you provide any context?

        Jennifer CarrollJ Offline
        Jennifer CarrollJ Offline
        Jennifer Carroll
        wrote on last edited by
        #3

        Hey @palanski

        Great question. PAAB’s strategic plan for 2023-2025 includes a focus on increasing the extent to which HCPs value health product advertising and industry-generated patient information. This is the primary motivation for the shift outlined in the disease burden document. This shift is one element of a multi-pronged approach towards that aim. The standards outlined in the document were generated in consideration of our global benchmarking and stakeholder consultation activities.

        While health product manufacturers’ have expressed a long-standing desire to provide more detailed presentations of disease states, it took some time to establish a set of standards that effectively aligned that desire with the interests of patients and HCPs. The objective of PAAB is to ensure that disease information (including burden of disease) does not suggest use and efficacy for outcomes which the brand has not been demonstrated to address. This objective remains however PAAB has looked to explore ways that we can meet this objective while allowing more latitude on disease presentations.

        In short, the document seeks to outline principles that will mitigate the risk that the disease burdens be interpreted as outcomes that the drug can improve. The document also reiterates the requirement that the disease information and descriptions of disease burden must pertain to the promoted product’s indication.

        Our hope is that manufactures will view the guidance document as a collaborative means to providing greater flexibility in relation to disease information presentations in HCP advertising, disease information presentations in patient information, and disease burdens conveyed in creative imagery.

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