Core Viewpoint - NovoCure Ltd. reported higher revenues for the fourth quarter and fiscal year 2025, indicating strong financial performance and growth potential for 2026 [1][2]. Financial Performance - Total preliminary net revenues for Q4 were $174.4 million, an increase of 8% from the same period last year [2]. - For fiscal 2025, total preliminary net revenues reached $655.4 million, also reflecting an 8% increase compared to the prior year [3]. - Revenue breakdown for Q4 included $101.6 million from the U.S., $21.6 million from Germany, $20.5 million from France, and $10.2 million from Japan, with an additional $15.8 million from other markets [2][3]. Future Outlook - The CEO stated that NovoCure is positioned for exciting growth opportunities in 2026, with plans for multiple product launches and a clear path to profitability [2]. - The company will cease reporting new prescriptions for indications that have been commercially available for over one year but will continue to report active patients segmented by product and market [3].

Summary of China Pharma and Biotech Conference Call Industry Overview - **Sector Outlook**: The China Pharma and Biotech sector is experiencing a positive outlook with valuations returning to a more rational range compared to mid-2025. Most stocks have seen a decline of 20-30%, and major healthcare indices are below 2023 post-COVID reopening levels, providing a solid base for growth in 2026 [1][10][11]. - **Growth Drivers**: Accelerated growth and quality improvement in the sector are anticipated, driven by the unique advantages of Chinese drugmakers that support globalization and sector re-rating trends [1][10]. Key Insights on China Biopharma - **R&D Efficiency**: China's early R&D model has matured, with clinical trials costing 60-70% less than in the U.S. Preclinical research averages 1.5 years, and Phase 1 trials take less than 2 years, significantly faster than global standards [2]. - **Global Pipeline Contribution**: China's share of the global biopharma pipeline has increased to 43% in 2025, up from 38% in 2024. However, the percentage of First-in-Class (FIC) drugs remains lower than in developed markets (17% vs. 37%) [2]. - **Out-licensing Trends**: The trend of outbound deals is expected to continue, with innovative models like platform deals and co-development agreements emerging. These deals are seen as avenues for revenue maximization, although they may not impact stock prices as significantly as in 2025 [2][13]. Stock-Specific Catalysts for 2026 - **Oncology Developments**: A significant number of trials (20+) in Non-Small Cell Lung Cancer (NSCLC) are expected to report data, with key players including Kelun, Innovent, and Akeso. New modalities such as multispecific antibodies and ADCs are also anticipated to provide proof of concept data [3]. - **GLP-1 Drugs**: HRS-9531 (Hengrui) and TG103 (CSPC) have submitted New Drug Applications (NDA) in the second half of 2025, with expected approvals in late 2026 or 2027 [3]. Top Stock Picks - **Innovent**: Anticipated strong sales growth for mazdutide and updates on IBI363 trials across various indications [4]. - **Kelun**: Expected to report results from its first global Phase 3 trial and domestic sales growth of approximately 40% [4]. - **Hansoh & Hengrui**: Projected recurring license income to contribute 10-15% of revenue, with net income growth of 20-30% CAGR from 2024 to 2027 [4]. Investment Ratings - **Outperform Ratings**: Hansoh, Kelun-Biotech, Innovent, and Jiangsu Hengrui are rated as outperform [6]. - **Market-Perform Ratings**: Akeso, BeOne Medicines (BeiGene), Sino Biopharm, Zai Lab, and CSPC are rated as market-perform [6]. Financial Projections - **Stock Performance**: The report includes a detailed table of stock ratings, target prices, and financial projections for various companies, indicating significant upside potential for selected stocks [5][9]. Additional Insights - **Market Dynamics**: The sector has transitioned from exuberance to equilibrium, with a notable correction in stock prices since October 2025, following a period of rapid growth [10][11]. - **Approval Trends**: The number of innovative drug approvals by the National Medical Products Administration (NMPA) has accelerated, with 69 approvals in 2025, while the FDA remains receptive to Chinese drug candidates [33]. This summary encapsulates the key points from the conference call, highlighting the positive outlook for the China Pharma and Biotech sector, the efficiency of R&D processes, stock-specific catalysts, and investment recommendations.

Summary of Whitehawk Therapeutics FY Conference Call Company Overview - **Company**: Whitehawk Therapeutics (NasdaqCM:AADI) - **Focus**: Development of antibody-drug conjugates (ADCs) for solid tumors - **Recent Developments**: Formed through the in-licensing of a three-asset ADC portfolio from Ushi Biologics, initiated in December of the previous year and completed earlier this year [4][4] Key Programs and Platforms ADC Platform - **Evolution**: Transition from tubulin inhibitor-based payloads to topoisomerase class ADCs, focusing on stability and payload release [6][6] - **Unique Features**: High-stability ADCs that limit free payload release, aiming for better potency with fewer side effects [7][7] Lead Assets 1. **HAWK-007 (PTK7-targeted ADC)** - **Target Validation**: Previously targeted by Pfizer and AbbVie, showing early efficacy but suffering from side effects [13][13] - **Clinical Development**: IND submission planned for this year, with preclinical data expected in the first half of 2026 [14][14] - **Tumor Relevance**: Broadly expressed in 70% of tumors, initially targeting lung, ovarian, and endometrial cancers [16][16] - **Efficacy Benchmarks**: Aiming for 35%-40% overall response rate (ORR) in non-small cell lung cancer and 50% in gynecological cancers [19][19] 2. **HAWK-016 (MUC16-targeted ADC)** - **Target Characteristics**: Highly expressed in gynecological cancers, with a unique approach to bypass circulating CA125 [23][23] - **Clinical Timeline**: IND submission in Q4, with trials starting in Q1 2026 [25][25] - **Potential Expansion**: Possible relevance in pancreatic cancer and non-small cell lung cancer [26][26] 3. **HAWK-206 (SEZ6-targeted ADC)** - **Target Validation**: Overexpressed in small cell lung cancer and neuroendocrine neoplasia, with a focus on improving safety and efficacy [34][34] - **Clinical Development**: IND submission planned for mid-2026, with trials starting in the second half of the year [38][38] - **Efficacy Benchmarks**: Aiming for 50%-60% ORR in small cell lung cancer and above 30% in neuroendocrine neoplasia [39][39] Competitive Landscape - **Emerging Competitors**: Increased interest in PTK7, with companies like Day One and Lilly entering the space [20][20] - **MUC16 Competition**: Previous attempts by Genentech faced challenges due to targeting issues; Regeneron is also pursuing a similar approach [27][27][29][29] - **SEZ6 Market Dynamics**: Limited competition in neuroendocrine cancers, with potential advantages over DLL3 and B7-H3 programs [40][40][41][41] Financial Position and Future Outlook - **Cash Runway**: Sufficient funds through early 2028, starting with $163 million from recent financing [45][45] - **Data Expectations**: Initial clinical data for all three programs expected around Q1 2027, with preclinical data anticipated in the first half of 2026 [31][31][50][50] - **Strategic Focus**: Emphasis on executing current programs and potential for future partnerships, particularly for high-potential assets like PTK7 [46][46] Conclusion - **Transition Year**: 2026 is positioned as a pivotal year for Whitehawk, moving from preclinical to clinical stages with a focus on demonstrating differentiation and efficacy across its ADC portfolio [48][48][49][49]

Summary of Key Points from the Greater China Healthcare Corporate Day Industry Overview - **Industry**: Healthcare in Greater China, including biopharma, CROs, medtech, services, pharmacies, and vaccines - **Sentiment**: Positive sentiment observed in biopharma and CRO sectors, with a focus on undervalued assets following recent market pullbacks [1][1] - **Key Companies**: Wuxi Apptec, Duality, Hansoh, 3SBio, and Tigermed highlighted as companies of interest due to their overseas businesses and partnered assets [1][1] Biopharma Insights - **R&D and Commercialization**: Most biopharma companies are on track with R&D and commercialization efforts. Innovative drug sales and milestone payments are expected to drive near-term revenues [2][2] - **Revenue Projections**: - Huadong Medicine: Rmb2 billion in 2025F and Rmb3 billion in 2026F [2][2] - Sino Biopharm: Projected organic profit growth of over 20% in 2025F and double-digit growth in 2026F [2][2] - **Pricing Pressure**: Volume-based procurement (VBP) continues to impact the generics segment, although biosimilar VBP may remain limited to provincial levels [2][2] CRO and CDMO Performance - **CDMO Orders**: Strong orders and backlog reported for CDMO companies, outperforming CROs due to robust overseas demand [3][3] - **CRO Recovery**: Mild recovery signals noted for domestic CRO demand, despite lagging booking income [3][3] Medtech Sector - **Investor Sentiment**: Generally muted, with some positive indicators in segments like in-vitro diagnosis (IVD) [4][4] - **Company Guidance**: - New Industries: Expected 10% revenue growth in 2026F [4][4] - Yuyue Medical: Anticipates 10% revenue growth for 2025F and higher growth in 2026F [4][4] - **Pharmacies and TCM**: Positive feedback received, with expectations for M&A to drive growth in 2026E [4][4] Company-Specific Updates - **Kelun Biotech**: Maintained sales target of Rmb800 million to Rmb1 billion for sac-TMT (TROP2 ADC) in 2025, with potential for significant milestone payments from 2027F [7][7] - **Abbisko**: R&D progressing well, with potential NDA submission in the US for Pimicotinib expected in Q425 [8][8] - **Hutchmed**: Maintained 2025 oncology revenue guidance of US$270-350 million, with expectations for better performance in 2026 [11][11] - **Zai Lab**: Revised down 2025 revenue guidance to over US$460 million, but noted good growth trends for Zejula [14][14] - **3SBio**: Pfizer planning multiple clinical trials for SSGJ-707, with significant near-term milestone payments expected [24][24] Vaccines and Pharmacies - **CanSino**: Highlighted a diverse product portfolio, including COVID-19 vaccines and other candidates, with healthy inventory levels [39][39] - **Gushengtang**: Targeting 10-15% organic revenue growth in 2026, with notable progress in overseas business [44][44] Risks and Challenges - **Market Risks**: Potential risks include worse-than-expected price cuts from GPO programs, intensified competition, and regulatory challenges [50][50] This summary encapsulates the key insights and projections from the Greater China Healthcare Corporate Day, highlighting the positive sentiment in the biopharma and CRO sectors, along with specific company updates and potential risks in the healthcare industry.

Core Insights - Zai Lab is a global biopharmaceutical company with a focus on oncology, immunology, neuroscience, and infectious diseases, currently having seven products approved in China [1][2] - The company expects significant revenue growth, projecting total revenue to reach US$2.0 billion by 2028, driven by the sales ramp-up of existing products and the approval of new products [1][2] Group 1: Product Portfolio and Revenue Growth - Zai Lab's first commercial product, ZEJULA, was approved in China in 2019, and the company currently has seven commercialized products [1] - In 2024, the company's total revenue is projected to be US$399 million, representing a 50% year-over-year increase, primarily due to the sales ramp-up of new products like VYVGART and NUZYRA [1] - Efgartigimod, an FcRn antagonist, is expected to become a blockbuster product, with domestic sales reaching US$94 million in 2024, an increase of 835% year-over-year [2] Group 2: Pipeline Development and Future Prospects - The company is actively expanding its product pipeline, focusing on areas such as antibody-drug conjugates (ADCs) and bispecific antibodies (biAbs), with several products granted Fast Track Designation by the FDA [2] - ZL-1310 has shown promising results in clinical trials, with plans to initiate a global pivotal trial in the second half of 2025 [2] - The company anticipates filing at least one new IND application annually, indicating a robust pipeline development strategy [2] Group 3: Financial Projections - The company is projected to achieve non-GAAP operating profit in the fourth quarter of 2025, with revenue estimates of US$553 million in 2025, US$802 million in 2026, and US$1.203 billion in 2027 [3] - A net loss of US$134 million is expected in 2025, transitioning to a net profit of US$15 million in 2026 and US$173 million in 2027 [3] - The target price derived from DCF valuation is HK$35.2, indicating a 39% upside potential [3]

Summary of China Pharma and Biotech Sector Conference Call Industry Overview - The Chinese pharmaceutical and biotech sector is experiencing a significant rally, with the Hang Seng Biotech and MSCI China Healthcare indices showing year-to-date (YTD) returns of 57% and 38%, respectively, outperforming broader market indices which are at 16-20% [1][10][26] - Public financing has increased fourfold in the first half of 2025 compared to the same period in 2024, driving IPO activity on the Hong Kong Stock Exchange, particularly in biotech [1][40] - Despite the rally, valuations have sharply re-rated, with China's biotech price-to-sales multiples now aligning with global peers, suggesting limited further upside compared to the peaks of 2020-2021 [1][11] Key Growth Drivers - Oncology and metabolic diseases are identified as primary growth drivers, with significant market potential in PD-1-based bispecific antibodies and GLP-1 drug classes [3][4] - The global market for PD-1-based bispecific antibodies could reach US$70-80 billion, while the domestic GLP-1 market is projected to hit CNY87 billion by 2035 [3] - Chinese companies are competitive in clinical results, particularly in lung cancer treatments, and domestic GLP-1 drugs are matching international efficacy [3][4] Company Highlights - **Akeso**: Leading in PD-1/VEGF bispecific antibodies with multiple phase 3 trials; however, overall survival results remain uncertain [4] - **Innovent**: Offers a diversified portfolio across various disease areas and leads in advanced antibody modalities [4] - **Hansoh**: Transitioning to innovation-driven growth with strong sales in its 3rd-generation EGFR inhibitor and significant GLP-1 business development deals [4] R&D and Innovation - The sector is shifting from me-too drugs to best-in-class and first-in-class assets, focusing on novel targets and drug combinations [2][38] - Clinical trial activity is robust, with Chinese assets comprising over 50% of new global trials in 2025 [2][42] - The number of new clinical trials has shown stable growth, with a notable increase in innovative drug approvals [42][65] Policy Environment - Government policies have fluctuated but are currently favorable, balancing innovation stimulation with price control [2][43] - Recent supportive policies include initiatives to cover innovative drugs under commercial insurance, indicating a long-term positive outlook for the sector [43] Out-Licensing Trends - Out-licensing activity has surged in 2025, with total deal value reaching US$59 billion, surpassing the previous year's total [72] - The focus has shifted from PD-1 drugs to PD-1/VEGF and GLP-1 assets, with significant deal values and upfront payments [75][72] - Despite the increase in total deal value, upfront payments in China still lag behind developed markets, indicating a need for caution regarding the sustainability of this growth [73][81] Investment Implications - Companies such as Akeso, Hansoh, Innovent, and Hengrui are rated as Outperform, while BeiGene, CSPC, Sino Biopharm, and Zai Lab are rated as Market-Perform [7] - The current rally may require new catalysts beyond existing out-licensing deals to sustain momentum, as valuation headroom appears limited [5][22] Conclusion - The Chinese pharma and biotech sector is evolving into a mature, innovation-driven industry with growing global competitiveness, tempered by valuation caution and sector uncertainties [5][11]

Summary of China Pharma and Biotech Conference Call Industry Overview - The China healthcare sector is experiencing its strongest rally since mid-2023, with the Hang Seng Biotech and MSCI China Healthcare indices showing year-to-date (YTD) returns of 57% and 38%, respectively, outperforming broader indices like Hang Seng and MSCI China at 20% and 16% [1][10] - The current market is at 30% of the peak seen during the last healthcare boom in 2020-2021, with a notable shift towards mature companies and top players rather than early-stage firms [1][2] - Public financing has surged, increasing 4 times in 1H25 compared to 1H24, with about two-thirds of IPO and follow-on offerings yielding positive returns [1][12] Market Valuation and Opportunities - Valuations in the China healthcare sector are now at or above global counterparts, with MSCI China healthcare P/S ratios crossing over with S&P 500 healthcare [2] - Individual stock performance varies significantly, with funds showing interest in companies with lower valuation multiples and potential for out-licensing deals [2][52] - Specific companies like CSPC are considered overheated with a PEG ratio of 14.5x, while Hengrui (2.3x) and Sino Biopharm (2.0x) are viewed as cheaper alternatives [3][44] Biotech Sector Insights - Biotech companies are valued based on market cap to projected 2032 revenue, ranging from 2-5x. Companies like BeiGene (2.7x) and Zai Lab (1.2x) are seen as undervalued, while Akeso (4.7x) and Kelun Biotech (5.6x) are considered relatively pricey [4][48] - The biotech sector has seen a significant increase in market capitalization, rising from US$102 billion to US$160 billion YTD 2025 [11] Clinical Trials and R&D - The number of clinical trial starts in China has shown consistent growth, with local assets making up over 50% of the global pipelines for the first time in 2025 [1][33] - Innovative drug modalities, particularly in oncology, have seen a resurgence in clinical trials, indicating sustained R&D efforts despite previous market downturns [32][36] Out-licensing Trends - There has been a boom in outbound licensing deals, with companies like RemeGen and Innovent leading the way. This trend is expected to continue, although there are concerns about saturation in certain drug classes [34][52] - The out-licensing model has remained resilient against geopolitical challenges, with no significant shifts in FDA attitudes towards China-originated drugs [34] Investment Implications - The report rates Akeso, Hansoh, Innovent, and Hengrui as Outperform, while BeiGene, CSPC, Sino Biopharm, and Zai Lab are rated as Market-Perform [7] - A methodological shift in valuation is noted, with increased emphasis on multiple-based valuation for mature companies, while biotechs will continue to use P/S and DCF models [8] Conclusion - The China pharma and biotech sector is on an upward trajectory, driven by strong market sentiment, increased public financing, and a robust pipeline of clinical trials. However, caution is advised regarding valuation levels and the sustainability of the current rally, particularly in the context of out-licensing deals and market saturation [52][53]

Summary of China Pharma and Biotech Conference Call Industry Overview - The focus is on the **China Pharma and Biotech** sector, particularly the out-licensing activities and their sustainability in 2025 [1][7]. Key Insights - **Out-licensing Growth**: As of June 17, 2025, the total value of China's out-licensing deals reached **$54 billion**, surpassing the **$47 billion** total for the entire year of 2024. This indicates a significant increase in deal-making activity [1][9]. - **US-bound Deals**: Historically, about half of China's licensing deals have been with US partners. In 2025, **57%** of the deal value is attributed to US-bound deals, suggesting that geopolitical tensions have not significantly impacted these transactions [1][9][11]. - **Global Licensing Trends**: The total value of global license transfers has been steadily increasing, with a notable contribution from China. In 2025, China's outbound deal value exceeded that of developed markets for the first time [2][13][15]. Emerging Drug Classes - **New Favorites**: The PD-1/VEGF bispecific and GLP-1 drug classes have emerged as the new favorites in out-licensing, with the former attracting deals worth over **$20 billion** and upfront payments exceeding **$3 billion** [4][38]. - **Historical Context**: Previous booms in 2020-2021 were primarily driven by PD-1 and TIGIT drugs, which ultimately faced saturation and deal terminations. The current growth drivers may also face similar risks of overheating and saturation [3][5][39]. Market Dynamics - **R&D Efficiency**: China's R&D efficiency has improved significantly, with clinical trial costs being approximately **1/5** of those in the US. This has led to a substantial increase in the size and quality of local players' pipelines [7]. - **Investment in R&D**: Despite market challenges, top pharma and biotech players in China continue to invest heavily in R&D, leading to a growing number of first-in-class assets [7]. Deal Activity - **Mega-deals**: There have been **23 license transfers** to global players with total deal values exceeding **$500 million**, with over **two-thirds** of these deals valued at **$1 billion or more** [8][9]. - **Upfront Payments**: The average upfront payment for China's outbound deals is lower than that of developed markets, with a typical range of **3-5%** of total deal value compared to around **10%** in developed markets [2][14]. Future Outlook - **Cautious Optimism**: While long-term growth in out-licensing is expected, there are short-term concerns regarding the sustainability of the current boom, particularly with the potential saturation of key drug classes [5][39]. - **Market Share Potential**: Despite the significant role of top 20 multinational corporations (MNCs) in China's out-licensing deals, China's share of these MNCs' licensing deals remains low, indicating potential for market share gains [44][50]. Conclusion - The China Pharma and Biotech sector is experiencing unprecedented growth in out-licensing activities, driven by improved R&D efficiency and strategic partnerships, particularly with US firms. However, the sustainability of this growth remains a concern as the market evolves and potential saturation looms for key drug classes.

Investment Rating - The report indicates a positive outlook for the China healthcare sector, with a recovery underway and improving investor sentiment, particularly in the biotech segment, which has seen a year-to-date performance increase of 37% [1]. Core Insights - The report highlights a significant recovery in the China healthcare sector, driven by improving investor sentiment and bottoming valuations, with offshore healthcare stocks up 21% year-to-date [1]. - Biotech companies are expected to benefit from licensing-out themes and resilience to geopolitical uncertainties, with key events like ASCO in June serving as potential catalysts for individual stock performance [1]. - There is a growing interest in domestic demand, particularly in capital expenditures and hospital traffic, with robust equipment tendering observed [1]. - The report anticipates a consumption recovery in areas such as refractive surgeries and orthodontics, although the sustainability of this recovery is contingent on the broader macroeconomic outlook [6]. - The report emphasizes the importance of global collaboration and licensing opportunities for pharmaceutical companies, with a focus on upcoming data releases at ASCO to enhance business development visibility [16]. Summary by Relevant Sections Biotech - The biotech sector is focusing on global licensing deals and achieving break-even points, with significant catalysts expected from the upcoming ASCO conference [13][14]. - Companies like Zai Lab and Innovent are highlighted for their innovative drug pipelines and potential for global collaboration [14][15]. Pharma - The pharmaceutical industry experienced soft growth in Q1 2025, but companies with strong product cycles, such as Hengrui, are showing better earnings trends [16]. - Collaboration opportunities are expected to increase, particularly with data releases at ASCO [16]. CDMO - CDMO companies reported better-than-expected results in Q1 2025, with strong order growth and maintained guidance for FY25 [17]. - Companies like WuXi Apptec and Asymchem are noted for their resilience in earnings delivery [17]. Medical Consumables - The report indicates challenges in inpatient surgeries due to reimbursement controls, but opportunities exist in the obesity and GLP-1 segments [19]. - Surgical volumes are expected to remain challenging, with ongoing pricing pressures [19]. Capital Equipment - Strong tendering activity was noted, but pricing pressures from value-based purchasing (VBP) are leading to longer revenue realization timelines [21]. - Companies like United Imaging and Mindray are expected to see positive growth in the coming quarters [21]. Retail Pharmacy - The retail pharmacy sector is undergoing a market clearing process, with a net decrease in drugstores for the first time, indicating a consolidation trend [26]. - Yifeng is highlighted as a resilient player in this space, benefiting from operational efficiency [26].

Summary of Key Points from the Conference Call Industry Overview - **Industry**: China Pharma and Biotech - **Focus**: Updates from ASCO 2025 regarding various cancer treatments, particularly in extensive stage small cell lung cancer (ES-SCLC) and non-small cell lung cancer (NSCLC) Core Insights and Arguments 1. **Zai Lab's ZL-1310 (DLL3 ADC)**: - Reported a 68% overall response rate (ORR) in the dose escalation group (n=28) for ES-SCLC - Notable results in 2L patients: 67% ORR across doses (n=33) and 79% ORR in the 1.6 mg/kg group (n=14) [1][8] - Safety profile shows 23% Grade ≥3 treatment-related adverse events (TRAE) [1] - Potential for best-in-class (BIC) status, pending survival data [1] 2. **Innovent's IBI363 (PD-1/IL-2 bispecific)**: - High ORR of 37% and median progression-free survival (mPFS) of 9.3 months in squamous NSCLC patients who failed PD-(L)1 treatment [2][10] - Efficacy significantly surpasses Dato-Dxd (Daiichi Sankyo/AstraZeneca) in cross-trial comparisons [2] 3. **Hengrui's SHR-1826 (c-met ADC)**: - Demonstrated a 29% confirmed ORR and 40% unconfirmed ORR in NSCLC patients with c-met alterations [2][10] - C-met alterations are prevalent in 10-60% of NSCLC globally, indicating a substantial market opportunity [2] 4. **Market Potential**: - NSCLC has a total addressable market (TAM) of approximately US$30 billion, with 1L treatment representing over 60% of this market [4] - Breast cancer market estimated at US$35 billion, with emerging products but no significant efficacy improvements over leading global products [4] 5. **Investment Ratings**: - Outperform ratings maintained for Akeso, Hansoh, Innovent, and Hengrui [6] - Market-Perform ratings for BeiGene, CSPC, Sino Biopharm, and Zai Lab [6] Additional Important Content - All updates are derived from Phase 1 trials, typically lacking control groups [3] - The competitive landscape includes various other companies and products, with specific mentions of Akeso, 3S Bio, and Kelun Biotech in relation to their respective therapies [4][7] - The report emphasizes the importance of survival data for ZL-1310 to validate its potential in the market [1][8] This summary encapsulates the critical developments and insights from the conference call, highlighting the advancements in cancer therapies and their implications for the market and investment opportunities.