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<oembed><version>1.0</version><provider_name>Future News 24</provider_name><provider_url>https://futurenews24.com</provider_url><author_name>Future News 24</author_name><author_url>https://futurenews24.com/index.php/author/mridulpahuja20/</author_url><title>rAAV manufacturing price evaluation: Indication-specific price per dose and discount methods - Future News 24</title><type>rich</type><width>600</width><height>338</height><html>&lt;blockquote class="wp-embedded-content" data-secret="gL5AdJ02lm"&gt;&lt;a href="https://futurenews24.com/index.php/2026/07/21/s41434-026-00631-3/"&gt;rAAV manufacturing price evaluation: Indication-specific price per dose and discount methods&lt;/a&gt;&lt;/blockquote&gt;&lt;iframe sandbox="allow-scripts" security="restricted" src="https://futurenews24.com/index.php/2026/07/21/s41434-026-00631-3/embed/#?secret=gL5AdJ02lm" width="600" height="338" title="&#x201C;rAAV manufacturing price evaluation: Indication-specific price per dose and discount methods&#x201D; &#x2014; Future News 24" data-secret="gL5AdJ02lm" frameborder="0" marginwidth="0" marginheight="0" scrolling="no" class="wp-embedded-content"&gt;&lt;/iframe&gt;&lt;script&gt;
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</html><thumbnail_url>https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs41434-026-00631-3/MediaObjects/41434_2026_631_Fig1_HTML.png</thumbnail_url><thumbnail_width>1024</thumbnail_width><thumbnail_height>1024</thumbnail_height><description>Recombinant adeno-associated virus (rAAV) vectors underpin many approved and late-stage gene therapies, yet manufacturing costs remain a major driver of therapy price. Here, we present the first comprehensive, platform-resolved cost analysis of rAAV production across three industrially relevant suspension platforms: transient transfection, baculovirus infection, and producer cell line (PCL). Using a bottom-up model, we decompose total cost-of-goods (COGs) into upstream, downstream, drug product, and quality control contributions at bioreactor scales from 50&#x2009;L to 2000 L. We show that, on a per-batch basis, baculovirus infection is the most cost-efficient platform, followed by transient transfection and PCLs however, when costs are normalized to vector titer (cost per 1 &#xD7; 10&#xB9;&#xB2; vg), the ranking shifts, with transient transfection becoming the lowest-cost platform under the modeled assumptions, followed by baculovirus infection and PCL platforms, underscoring the dominant influence of productivity on unit cost. We identify platform-specific cost drivers&#x2014;plasmids, transfection reagent, and media in transient transfection; media and perfusion consumables in PCL platforms; and affinity capture chromatography in baculovirus processes&#x2014;with buffer preparation consistently representing the largest downstream material cost across platforms. We further quantify the impact of process development levers: transfection optimization and perfusion-based intensification reduce cost per dose by up to an order of magnitude, whereas affinity resin reuse and capsid enrichment strategies provide modest, incremental savings. Incorporating indication-specific annual viral genome demand reveals how process optimization and scale-up together reduce batch burden and lower dose cost by up to two orders of magnitude, suggesting the potential for improved supply feasibility, even for high-dose neuromuscular indications, under the modeled assumptions of productivity improvement and process optimization. Together, these results provide a quantitative framework linking platform choice, process scale, and unit operations to rAAV manufacturing COGs.</description></oembed>
