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    Timothy AndersonBofA Securities

    Timothy Anderson's questions to Eli Lilly and Co (LLY) leadership

    Timothy Anderson's questions to Eli Lilly and Co (LLY) leadership • Q1 2025

    Question

    Timothy Anderson followed up on formulary positioning, noting that exclusive 'one-of-one' deals might occur regardless of Lilly's preference. He asked what percentage of covered lives today are already in such exclusive plans and for Lilly's view on how this will evolve.

    Answer

    Patrik Jonsson, President of Cardiometabolic Health, responded that 'one-on-one' formulary positions are currently rare in the obesity market. He reiterated that while the CVS announcement was not a complete surprise given Zepbound's strong performance, Lilly will continue to execute its growth strategy across all PBMs, Medicaid, and its self-pay channels to maintain momentum.

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    Timothy Anderson's questions to Eli Lilly and Co (LLY) leadership • Q4 2024

    Question

    Timothy Anderson of Wolfe Research asked if the 2025 guidance requires an acceleration in prescription uptake trends or if it can be achieved with the current trajectory.

    Answer

    An executive clarified that the 2025 guidance is built upon the assumption of a continuation of the total prescription growth seen in 2024, not necessarily requiring a significant acceleration in the growth rate.

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    Timothy Anderson's questions to Biogen Inc (BIIB) leadership

    Timothy Anderson's questions to Biogen Inc (BIIB) leadership • Q1 2025

    Question

    Timothy Anderson asked about the market differentiation between LEQEMBI and Lilly's Kisunla, particularly around finite dosing, and whether patients are discontinuing LEQEMBI therapy.

    Answer

    CEO Christopher Viehbacher responded that the choice between products will ultimately be up to physicians and patients. He emphasized the importance of continued therapy, noting that data shows plaque can return after removal. He stressed that the primary focus for both Biogen and Lilly should be on expanding the overall market to treat the vast number of patients in need, rather than competing for share in a still-nascent market.

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    Timothy Anderson's questions to Pfizer Inc (PFE) leadership

    Timothy Anderson's questions to Pfizer Inc (PFE) leadership • Q1 2025

    Question

    Timothy Anderson asked about the likely regulatory path for potential pharmaceutical tariffs, the expected timing for more clarity, and whether tariffs might be limited to non-friendly nations.

    Answer

    CEO Albert Bourla expressed cautious optimism, noting that pharmaceuticals were initially excluded from broad tariffs. He stated the administration's focus is on national security threats via a 232 investigation, which he believes distinguishes between friendly and adversary countries, making it a different situation than broad-based tariffs.

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    Timothy Anderson's questions to Pfizer Inc (PFE) leadership • Q4 2024

    Question

    Timothy Anderson asked about Pfizer's business development strategy for obesity, suggesting a single late-entry asset may struggle and questioning if Pfizer is looking to acquire a portfolio of assets.

    Answer

    Executive Andrew Baum agreed that managing obesity will likely require a portfolio of tools. He confirmed that Pfizer is actively evaluating all opportunities in the space to find assets that can deliver the most value to both patients and shareholders.

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    Timothy Anderson's questions to AbbVie Inc (ABBV) leadership

    Timothy Anderson's questions to AbbVie Inc (ABBV) leadership • Q1 2025

    Question

    Timothy Anderson from Bank of America questioned the potential for the administration to limit direct-to-consumer drug advertising and asked if the long-acting nature of AbbVie's amylin analog implies a strategic need for a long-acting GLP-1 partner.

    Answer

    CCO Jeffrey Stewart acknowledged that while it's difficult to predict DTC reform, AbbVie could pivot its investments to disease awareness campaigns or other channels if needed. CSO Roopal Thakkar addressed the obesity question, stating that while the amylin analog has potential as a monotherapy, the company has not ruled out any particular mechanism for combination, and the asset's neutral pH formulation makes it amenable to various partners.

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    Timothy Anderson's questions to AbbVie Inc (ABBV) leadership • Q4 2024

    Question

    Timothy Anderson asked about the expected impact of GLP-1 obesity drugs on the aesthetics business and what changes AbbVie would prefer to see from PBM reform.

    Answer

    SVP Carrie Strom described the GLP-1 trend as both a short-term headwind (share of wallet) and a long-term tailwind (new patient generation), stating the company is helping providers integrate aesthetics for this new patient group. CEO Robert Michael stated that AbbVie has no strong preference on PBM reform, expressing confidence in their ability to compete on product attributes in either a rebate-based or discount-based system, citing strong international performance as evidence.

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    Timothy Anderson's questions to Gilead Sciences Inc (GILD) leadership

    Timothy Anderson's questions to Gilead Sciences Inc (GILD) leadership • Q1 2025

    Question

    Timothy Anderson asked about the potential for lenacapavir for PrEP to cannibalize Descovy sales and requested an estimate for the number of patients who could be on lenacapavir by the end of the year.

    Answer

    Chief Commercial Officer Johanna Mercier did not provide specific product guidance but indicated the initial opportunity for lenacapavir involves switching patients from daily oral therapies, which constitute 95% of the market and include Descovy. She also highlighted a significant opportunity with naive patients. Mercier anticipates the overall PrEP market will grow exponentially, with lenacapavir's launch acting as an accelerant.

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    Timothy Anderson's questions to Gilead Sciences Inc (GILD) leadership • Q4 2024

    Question

    Timothy Anderson questioned the launch trajectory for lenacapavir in PrEP, noting that consensus estimates could be high initially, and asked for commentary on the expected ramp dynamics and any comparable launch benchmarks.

    Answer

    Chief Commercial Officer Johanna Mercier stated that while the company does not give product-specific guidance, they anticipate a ramp-up period for access, targeting 75% coverage at 6 months and 90% at 12 months. She noted the specialty pharmacy/buy-and-bill model may take time to scale but expressed confidence in a meaningful impact in 2025, growing more significantly in 2026.

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    Timothy Anderson's questions to Merck & Co Inc (MRK) leadership

    Timothy Anderson's questions to Merck & Co Inc (MRK) leadership • Q1 2025

    Question

    Timothy Anderson of Bank of America pressed for an update on providing long-term guidance to alleviate investor concerns about the KEYTRUDA patent cliff in 2028.

    Answer

    CEO Robert Davis reiterated confidence in the long-term outlook, pointing to a pipeline of over 20 new products with a potential of over $50 billion by the mid-2030s. He stated that while there is no current plan to issue specific line-by-line guidance, the company continues to evaluate the possibility.

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    Timothy Anderson's questions to Merck & Co Inc (MRK) leadership • Q4 2024

    Question

    Timothy Anderson pressed on the KEYTRUDA LOE, asking when Merck might provide quantified long-term guidance. He also requested a perspective on two upcoming competitor readouts: AstraZeneca's AVINZA trial and the SUMMIT trial for a PD-1/VEGF bispecific.

    Answer

    CEO Robert Davis addressed guidance, stating there is no current plan for a quantified long-term forecast but emphasized the $50B+ potential from the pipeline will provide proof points over time. Dr. Dean Li, President of Merck Research Labs, commented on competitors, expressing confidence in Merck's TROP2 program and noting that for PD-1/VEGF combinations, demonstrating an Overall Survival (OS) benefit, not just PFS, is critical.

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    Timothy Anderson's questions to Bristol-Myers Squibb Co (BMY) leadership

    Timothy Anderson's questions to Bristol-Myers Squibb Co (BMY) leadership • Q1 2025

    Question

    Timothy Anderson asked if Bristol Myers Squibb would resume providing long-term guidance and if management could provide assurance on a potential floor for trough EPS. He also requested color on which specific brands have transfer pricing arrangements.

    Answer

    CEO Christopher Boerner stated the company will not provide long-term guidance as a standard practice, focusing instead on annual guidance. He did not give a specific trough EPS floor but affirmed the goal is to minimize its depth and duration. CFO David Elkins clarified that transfer pricing is determined by tax law and is not the appropriate framework for analyzing potential tariff impacts.

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    Timothy Anderson's questions to Bristol-Myers Squibb Co (BMY) leadership • Q4 2024

    Question

    Timothy Anderson of Bank of America asked for clarification on the difference between the company's 2025 revenue guidance and consensus estimates, and questioned if the earnings trough is still expected in the late 2020s or if new products could pull it forward.

    Answer

    CFO David Elkins explained that the revenue guidance is broadly in line with consensus after accounting for a ~$500 million foreign exchange headwind, with minor differences related to the legacy portfolio. CEO Christopher Boerner stated that while the general timing of the earnings trough remains the same, the company is actively working to change its depth and duration through brand growth, pipeline acceleration, and strategic acquisitions like Karuna, which has improved the growth velocity exiting the decade.

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    Timothy Anderson's questions to Johnson & Johnson (JNJ) leadership

    Timothy Anderson's questions to Johnson & Johnson (JNJ) leadership • Q1 2025

    Question

    Timothy Anderson from Bank of America asked about the risk of tariffs impacting the company's transfer pricing structures and requested details on which products and geographies use them.

    Answer

    CFO Joseph Wolk declined to comment on transfer pricing for competitive reasons. CEO Joaquin Duato redirected the focus to the company's strategy of onshore manufacturing, stating that their $55 billion investment plan will result in all advanced medicines for the U.S. market being made in the U.S., which he framed as the most effective long-term solution.

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    Timothy Anderson's questions to Johnson & Johnson (JNJ) leadership • Q4 2024

    Question

    Timothy Anderson questioned if the entry of STELARA biosimilars might drive patient volume towards TREMFYA, similar to market shifts seen with HUMIRA biosimilars, and asked about the expected level of price erosion for TREMFYA in 2025.

    Answer

    Executive Jennifer Taubert confirmed that the HUMIRA erosion curve is a good proxy for STELARA and agreed that patients are likely to shift to newer, more effective therapies like TREMFYA. She highlighted TREMFYA's differentiation in IBD and stated that the company has already invested appropriately to secure strong market access and commercial coverage, which is factored into their financial guidance.

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    Timothy Anderson's questions to Moderna Inc (MRNA) leadership

    Timothy Anderson's questions to Moderna Inc (MRNA) leadership • Q4 2024

    Question

    Timothy Anderson questioned why the next-generation COVID vaccine is excluded from 2025 revenue guidance despite a near-term PDUFA date, and asked what the FDA gains by placing the fully-enrolled Norovirus trial on clinical hold.

    Answer

    CFO Jamey Mock explained the exclusion is a new policy to not guide for unapproved products, stating they 'learned their lesson' and it shouldn't be over-interpreted. President Stephen Hoge clarified the Norovirus hold is not for disclosure purposes, as they had already been proactive, but is part of the FDA's prudent review of the situation.

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    Timothy Anderson's questions to Amgen Inc (AMGN) leadership

    Timothy Anderson's questions to Amgen Inc (AMGN) leadership • Q4 2024

    Question

    Timothy Anderson asked why the EYLEA biosimilar, Pavblu, couldn't be a very significant product, given Amgen is the only seller, and requested insight into its contribution to the 2025 guidance.

    Answer

    While declining to give product-specific guidance, executives expressed strong optimism. Murdo Gordon, EVP of Global Commercial Operations, noted very positive and enthusiastic feedback from retina specialists, who appreciate the high-quality biosimilar in an easy-to-use prefilled syringe. Peter Griffith, EVP and CFO, reinforced the company's goal to double its 2025 biosimilar sales by 2030.

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    Timothy Anderson's questions to GSK plc (GSK) leadership

    Timothy Anderson's questions to GSK plc (GSK) leadership • Q2 2024

    Question

    Timothy Anderson of Wolfe Research, LLC asked about the Zantac litigation, specifically inquiring about the earliest realistic timeline for a potential broad settlement to resolve the issue for the company.

    Answer

    Emma Walmsley, CEO, responded by reiterating GSK's position that there is no consistent or reliable scientific evidence linking Zantac to cancer. She stated the company will continue to vigorously defend itself and manage the litigation in the best interest of shareholders, without speculating on hypothetical settlement timelines to protect the company's position in the judicial process.

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    Timothy Anderson's questions to Sanofi SA (SNY) leadership

    Timothy Anderson's questions to Sanofi SA (SNY) leadership • Q2 2024

    Question

    Timothy Anderson requested an update on the timing for tolebrutinib readouts and asked for a base-case expectation, questioning whether the drug is likely to be approvable or if it could be a 'total zero.'

    Answer

    Houman Ashrafian, EVP and Head of R&D, confirmed the timing remains late August or early September and expressed optimism about the drug's path, given the high unmet need in secondary progressive MS and interesting Phase II results. CEO Paul Hudson added that the key will be whether its ability to cross the blood-brain barrier translates into clinical differentiation.

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    Timothy Anderson's questions to AstraZeneca PLC (AZN) leadership

    Timothy Anderson's questions to AstraZeneca PLC (AZN) leadership • Q2 2024

    Question

    Timothy Anderson asked if upcoming TROPION-Breast02 data for Dato-DXd would allow for a direct comparison to Gilead's TRODELVY and prove superiority. He also inquired about operating margins in emerging markets.

    Answer

    CEO Pascal Soriot stated that emerging market margins are viable, profitable, and closer to European levels than the U.S., driving significant growth. EVP, Oncology R&D, Susan Galbraith, expressed optimism that the TROPION-Breast02 data will confirm a best-in-class profile for Dato-DXd, highlighting its differentiation through a stable linker that results in lower toxicity and better combinability.

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    Timothy Anderson's questions to Novartis AG (NVS) leadership

    Timothy Anderson's questions to Novartis AG (NVS) leadership • Q2 2024

    Question

    Timothy Anderson of Wolfe Research asked why pharmaceutical companies are complying with CMS's request to remain quiet about ongoing IRA price negotiations, despite there being no formal gag order.

    Answer

    CEO Vasant Narasimhan stated he had little insight into CMS's motivations but noted that since the price-setting process involves multiple rounds of discussion, there is no benefit to going public while talks are ongoing. He speculated that the impact on the first wave of drugs may seem manageable as they are near their loss of exclusivity, but warned the policy will become 'uglier' as more drugs are included earlier in their lifecycles.

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