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Novartis’ recent $5.2 billion licensing deal with Argo Biopharma marks a pivotal moment in the RNAi cardiovascular therapeutics sector, underscoring the company’s commitment to dominating a market poised for exponential growth. According to a report by Reuters, the agreement includes upfront payments of $160 million, potential milestone payments totaling $5.2 billion, and tiered royalties, reflecting Novartis’ confidence in Argo’s RADS™ platform for long-acting siRNA therapies [1]. This collaboration, the third between the two firms, builds on a January 2024 deal valued at $185 million upfront and $4 billion in total potential value, signaling a strategic bet on RNAi’s ability to address unmet needs in cardiovascular disease [2].
The RNAi therapeutics market is projected to grow from $5.2 billion in 2024 to $28.6 billion by 2034, at a compound annual growth rate (CAGR) of 18.6%, driven by advancements in delivery systems like lipid nanoparticles and GalNAc conjugates [5]. Cardiovascular applications, in particular, are gaining traction due to their potential to target genetic drivers of diseases such as hypertriglyceridemia and hypertension. Novartis’ Leqvio (inclisiran), an RNAi therapy for LDL-C reduction, has already demonstrated clinical success, with 85% of patients achieving LDL-C targets within 90 days in the V-DIFFERENCE Phase IV study [5]. This positions
to capitalize on a $600 billion cardiovascular disease market, where adherence challenges and high treatment costs remain significant barriers [3].Competitively, Novartis’ move outpaces peers like
and . , a pioneer in RNAi, reported $310 million in Q1 2025 revenue from itsATTR-CM drug AMVUTTRA (vutrisiran) and is advancing zilebesiran, a hypertension candidate, into a global Phase 3 trial [4]. However, Novartis’ partnerships with Argo and BOW Pharmaceuticals—another $5.2 billion deal for siRNA therapies targeting ANGPTL3—provide a broader pipeline and diversified risk profile [3]. , while strong in antisense oligonucleotides, faces higher manufacturing costs and regulatory hurdles compared to Novartis’ lipid nanoparticle-based delivery systems [1].From a long-term R&D ROI perspective, Novartis’ investments align with the projected $15% CAGR of the RNAi technology market, which is expected to reach $8.27 billion by 2032 [2]. The company’s focus on partnerships reduces upfront R&D costs, as seen in its collaboration with Alnylam for Leqvio, which generated $500 million in revenue within 18 months of launch [2]. By leveraging Argo’s platform for less frequent dosing, Novartis addresses adherence issues—a critical factor in chronic disease management—and enhances the commercial viability of its therapies.
Challenges remain, including high development costs and manufacturing scalability. However, Novartis’ established commercial infrastructure and Alnylam’s expertise in RNAi formulation mitigate these risks. As stated by a Bloomberg analysis, the RNAi cardiovascular therapeutics segment is “poised to redefine standard-of-care treatments,” with Novartis’ aggressive licensing strategy positioning it as a market leader [5].
**Source:[1] Novartis signs up to $5.2 billion licensing deal with China's biotech Argo heart drugs [https://www.reuters.com/business/healthcare-pharmaceuticals/novartis-signs-up-52-billion-licensing-deal-with-chinas-biotech-argo-heart-drugs-2025-09-03/][2] Novartis returns to Argo for $5B cardiovascular collab [https://www.fiercebiotech.com/biotech/novartis-returns-argo-multi-faceted-5b-cardiovascular-collab][3] Argo Biopharma's Strategic Alliance with Novartis [https://www.ainvest.com/news/argo-biopharma-strategic-alliance-novartis-paradigm-shift-cardiovascular-innovation-biotech-valuation-2509/][4] Alnylam Anticipates Strong Growth in 2025 Driven by RNAi ... [https://trial.medpath.com/news/acbaa1781f5ba852/alnylam-pharmaceuticals-reports-strong-financial-growth-and-advances-in-rnai-therapeutics][5] Antisense and RNAi Therapeutics Market Growth [https://market.us/report/global-antisense-and-rnai-therapeutics-market/]
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