Faruqi & Faruqi, LLP Securities Litigation Partner James (Josh) Wilson Encourages Investors Who Suffered Losses In Novo To Contact Him Directly To Discuss Their Options If you purchased or acquired securities in Novo between May 7, 2025, to July 28, 2025 and would like to discuss your legal rights, call Faruqi & Faruqi partner Josh Wilson directly at 877-247-4292 or 212-983-9330 (Ext. 1310). [You may also click here for additional information] NEW YORK, Sept. 25, 2025 (GLOBE NEWSWIRE) -- Faruqi & Faruqi, L ...

Core Viewpoint - A class action lawsuit has been filed against Novo Nordisk A/S by Berger Montague PC on behalf of investors who acquired Novo's publicly traded securities during the specified class period from May 7, 2025, to July 28, 2025 [1][2] Company Summary - Novo Nordisk A/S is a global pharmaceutical company headquartered in Denmark [3] - The lawsuit alleges that Novo understated the impact of the personalization exception to the compounded GLP-1 exclusion, which has allowed continued use of compounded alternatives to its products [3] - The company is accused of overstating the likelihood that patients using less expensive compounded drugs would switch to its branded products, leading to an overestimation of its long-term growth potential [3] Financial Impact - On July 29, 2025, Novo announced a reduction in its sales and profit outlook for fiscal 2025, citing slower-than-expected growth for its products Wegovy® and Ozempic® due to competition from compounded GLP-1 products [4] - Following this announcement, Novo's stock price fell from $69.00 per share on July 28, 2025, to $53.94 per share on July 29, representing a decline of approximately 21.83% in a single day [4]

Summary of Zealand Pharma Conference Call Company Overview - **Company**: Zealand Pharma (OTCPK:ZLDP.Y) - **Date**: September 25, 2025 - **Key Speaker**: David M. Kendall, Chief Medical Officer Core Industry Insights Partnership and Product Development - Zealand Pharma has established a partnership with Roche, focusing on the petrelintide asset, which is progressing towards phase 3 trials [3][5] - Ongoing phase 2 studies are expected to yield results in the first half of next year [3] - The company aims to position itself as a key player in the obesity and metabolism space, beyond its existing Zegalogue franchise [4] Market Dynamics - The obesity market is evolving rapidly, with projections indicating that 40% to 50% of the global population will be overweight or obese in the coming decade [8] - There is a shift towards patient-driven demand for weight management therapies, contrasting with traditional provider-driven approaches [9][10] - Zealand Pharma believes that amylin-based therapies, particularly petrelintide, could become foundational in managing obesity [4][5] Product-Specific Insights Petrelintide Development - Petrelintide is expected to achieve weight loss comparable to GLP-1 therapies, with estimates of mid-teens to 20% weight loss [12][13] - The phase 2b trial aims to leverage tolerability and lower starting doses with monthly dose escalations [19] - The trial design will focus on a representative population, including a balanced gender ratio and higher BMI [20] Competitive Landscape - Petrelintide is positioned as a better-in-class option compared to other amylin agonists, with a 100% response rate in early studies [26] - The adverse event profile of petrelintide is expected to be favorable compared to competitors like kagrelintide and LRL-NTIDE [28][30] - Zealand Pharma is confident in the safety and efficacy of petrelintide, with no significant neuropsychiatric side effects reported [36][37] Regulatory and Market Considerations - The regulatory landscape is evolving, with expectations for higher efficacy and tolerability standards for new therapies [44][45] - Zealand Pharma is monitoring the potential for oral formulations but believes that injectables will remain the dominant delivery method in the obesity market [48][50] Future Outlook - Zealand Pharma is optimistic about the potential of petrelintide and its partnership with Roche to capture a significant share of the obesity market [11][35] - The company is preparing for phase 3 trials and is focused on optimizing trial designs to meet regulatory requirements and market needs [12][14] Conclusion - Zealand Pharma is strategically positioned in the growing obesity market with innovative therapies like petrelintide, backed by a strong partnership with Roche and a focus on patient-driven demand for weight management solutions [5][11]

Group 1 - The article highlights the ongoing construction in Kalundborg, Denmark, to accommodate the increasing demand for Novo Nordisk's Wegovy weight-loss drug [1] - The town of Kalundborg is referred to as "Novo Town," indicating its strong association with Novo Nordisk and its operations [1] - Therapist Heidi Thron Rune has adapted to the noise from the construction, reflecting the significant impact of Novo Nordisk's business on the local community [1]

Summary of Key Points from the Asia CDMO Day Conference Industry Overview - **Industry Focus**: The conference centered on the Contract Development and Manufacturing Organization (CDMO) sector within the healthcare industry, particularly in Asia, including companies from mainland China, India, Taiwan, Korea, and Singapore [7][8]. Core Insights - **Current Demand and Future Outlook**: - Resilient demand is noted currently, driven by CMO projects and emerging modalities such as GLP-1/peptide capacity and Antibody-Drug Conjugates (ADCs) [7]. - The demand for obesity drugs is significantly influencing manufacturing orders, with ADCs and bispecific antibodies (BsAbs) identified as growth areas [7]. - A mixed recovery is expected for early-stage R&D in 2025 due to weak funding in 2024 and the first half of 2025, but a positive outlook is anticipated for 2026, especially among Chinese players [7][8]. - **Geopolitical Impact**: - Investors are less concerned about geopolitical uncertainties, focusing instead on tangible deliverables like earnings and order momentum [2]. - CDMOs are implementing strategic measures to mitigate risks, such as offshore facilities and M&A plans in the US, with business operations largely unaffected by geopolitical issues [2][9]. - **Performance of Chinese CDMOs**: - Chinese CDMOs have outperformed global peers with a 47% re-rating over the past six months, attributed to positive investor sentiment and strong earnings [3][6]. Capital Expenditure Trends - **Capex Execution**: - Capital expenditure (capex) is on track for FY25, with a focus on expanding peptide and ADC capabilities, as well as strategic offshore sites despite higher costs [7][44]. - Chinese CDMOs typically allocate a higher percentage of revenue to capex (average 20% of sales) compared to Indian counterparts (13%) [12]. - **Diverging Strategies**: - There is a notable divergence in capex strategies between Chinese and Indian CDMOs, with Indian firms adopting a more conservative approach tied to visible demand [12][44]. Demand Dynamics - **Recovery Variability**: - The industry is experiencing uneven recovery across the value chain, particularly in early-stage services, with a noted decline in small molecule projects due to funding challenges [14][15]. - High-quality and emerging modalities, especially peptides for obesity and ADCs, continue to see strong demand [14][15]. - **Emerging Opportunities**: - The GLP-1 market is expected to grow significantly, with projections indicating a potential increase in the total addressable market (TAM) in India from Rs13 billion in FY26 to Rs126 billion by FY31 [18]. ADC Market Insights - **Expansion in ADC Capabilities**: - CDMO players are expanding their ADC capabilities to capture growth opportunities, with WuXi XDC reporting a backlog of US$1,329 million in 1H25, reflecting a 48% year-on-year increase [23][25]. - The global ADC market is projected to grow at a CAGR of 31% from 2024 to 2030 [26]. Conclusion - The Asia CDMO sector is poised for growth, driven by resilient demand for innovative therapies and strategic investments in capacity expansion. The geopolitical landscape is less of a concern for investors, who are focusing on operational performance and future growth potential. The divergence in capex strategies between Chinese and Indian CDMOs highlights differing approaches to market opportunities and risk management.

Core Viewpoint - A class action lawsuit has been filed against Novo Nordisk A/S for allegedly providing misleading statements regarding its growth potential and market performance during the class period from May 7, 2025, to July 28, 2025 [8]. Allegation Details - The lawsuit claims that Novo made overly positive statements while concealing material adverse facts about its growth potential, particularly regarding the compounded GLP-1 market and the likelihood of patients switching to Novo's branded alternatives [8]. - The complaint highlights that Novo's assertions about its market potential were significantly overstated, leading to investor losses when the company later lowered its sales and profit outlook [8]. Market Impact - Following Novo's announcement on July 29, 2025, regarding lowered growth expectations for its products Wegovy and Ozempic, the company's stock price fell from $69.00 to $53.94 per share, representing a decline of approximately 21.83% in one day [8]. Next Steps - Investors who purchased Novo shares during the class period and suffered losses are encouraged to contact the law firm Bragar Eagel & Squire for more information and to discuss their legal rights [4]. - The deadline for investors to apply to be appointed as lead plaintiff in the lawsuit is September 30, 2025 [8]. About the Law Firm - Bragar Eagel & Squire, P.C. is a nationally recognized law firm that represents individual and institutional investors in complex litigation across the United States [5].

Core Viewpoint - Kuehn Law, PLLC is investigating potential breaches of fiduciary duties by certain officers and directors of Hims & Hers Health, Inc. related to misleading statements and actions that may have jeopardized shareholder interests [1]. Group 1: Allegations Against Hims & Hers Health, Inc. - Insiders at Hims & Hers Health allegedly misrepresented or failed to disclose involvement in the deceptive promotion and sale of illegitimate versions of Wegovy, which posed risks to patient safety [1]. - There is a substantial risk that the company's collaboration with Novo Nordisk could be terminated due to these actions [1]. - Positive statements regarding the company's business, operations, and prospects were claimed to be materially misleading and lacked a reasonable basis [1].

Core Viewpoint - Faruqi & Faruqi, LLP is investigating potential claims against Novo Nordisk A/S due to allegations of misleading statements regarding the company's growth potential and market capabilities, particularly related to its GLP-1 products [3][4]. Group 1: Legal Investigation - The law firm is encouraging investors who suffered losses exceeding $100,000 in Novo between May 7, 2025, and July 28, 2025, to contact them for discussing legal options [1]. - A federal securities class action has been filed against Novo, with a deadline of September 30, 2025, for investors to seek the role of lead plaintiff [1][5]. Group 2: Allegations Against Novo - The complaint alleges that Novo and its executives violated federal securities laws by making false or misleading statements and failing to disclose the true state of the company's growth potential [3]. - Specific claims include that Novo's potential to capitalize on the compounded market was greatly understated, and the likelihood of patients switching to Novo's branded alternatives was overstated [3]. Group 3: Stock Performance Impact - Following Novo's announcement of lowered sales and profit outlook on July 29, 2025, the company's stock price fell from $69.00 per share on July 28, 2025, to $53.94 per share on July 29, 2025, marking a decline of approximately 21.83% in one day [4].

Core Insights - Eli Lilly and Company is recognized as one of the best pharmaceutical stocks, particularly excelling in obesity treatments and expanding its global presence [1] Group 1: Product Development and Market Expansion - The obesity drug franchise, led by Mounjaro (tirzepatide), has rapidly expanded beyond the U.S. to regions including Europe, Asia, the Middle East, Mexico, Brazil, India, and China [2] - New clinical trial data indicates that Orforglipron, an oral GLP-1 agonist, has outperformed Novo Nordisk's Rybelsus in blood sugar control and weight loss for type 2 diabetes patients [3] Group 2: Manufacturing and Investment - Eli Lilly announced a $5 billion facility near Richmond, Virginia, focused on bioconjugates and monoclonal antibodies, as part of a broader $27 billion investment plan for four U.S. plants [4] - This investment is aimed at enhancing capabilities in next-generation oncology and autoimmune therapies [4] Group 3: Regulatory Approvals and Acquisitions - The Alzheimer's drug donanemab (Kisunla) has received an FDA-approved dosing schedule and positive feedback from European regulators [5] - The acquisition of Verve Therapeutics for $1.3 billion is expected to strengthen Eli Lilly's innovation capabilities [5] Group 4: Pricing Strategy and Policy Impact - Eli Lilly introduced a flat-rate $499 monthly pricing model for Zepbound, aimed at improving affordability [6] - Upcoming U.S. policy changes, including Medicaid coverage for GLP-1 weight-loss drugs in 2026 and Medicare in 2027, could further enhance demand [6]

Core Viewpoint - Rosen Law Firm is reminding investors who purchased Novo Nordisk A/S securities between May 7, 2025, and July 28, 2025, of the September 30, 2025, deadline to become lead plaintiffs in a class action lawsuit [1] Group 1: Class Action Details - Investors who bought Novo Nordisk securities during the specified period may be entitled to compensation without any out-of-pocket fees through a contingency fee arrangement [1] - A class action lawsuit has already been filed, and interested parties must move the Court by September 30, 2025, to serve as lead plaintiff [2] - The lawsuit alleges that defendants made misleading statements about Novo Nordisk's growth potential while concealing material adverse facts [4] Group 2: Law Firm Credentials - Rosen Law Firm has a strong track record in securities class actions, having achieved the largest settlement against a Chinese company at the time and being ranked No. 1 for securities class action settlements in 2017 [3] - The firm has recovered hundreds of millions of dollars for investors, securing over $438 million in 2019 alone [3] - Founding partner Laurence Rosen was recognized as a Titan of Plaintiffs' Bar by Law360 in 2020, highlighting the firm's expertise [3]