Roy W. Ware, PhD, MBA appointed as Chief Manufacturing and Technology OfficerCaryn Barnett appointed as VP, Clinical OperationsPablo Lee, MD, MBA, appointed as VP, Medical Affairs  CAMBRIDGE, United Kingdom and NEW YORK, February 16, 2026 – Artios Pharma Limited (“Artios”), a clinical-stage biopharmaceutical company pioneering the development of new classes of DNA Damage Response (DDR) medicines to deliver meaningful survival benefits for patients with cancer, today announced the appointment of three senior ...

Financial Data and Key Metrics Changes - The company reported record revenues of $1.13 billion for the third quarter, representing a 7% increase year-over-year [3] - The guidance for revenue was narrowed, reflecting strong performance and disciplined expense management, with an increase in ANI and EPS guidance [4] - A deferred tax asset of $206 million was recognized in the third quarter related to the Chimerix acquisition, which will reduce future tax liabilities [5] - The company ended the quarter with approximately $2 billion in cash and investments, and generated about $1 billion in cash flow for the first nine months of the year [5] Business Line Data and Key Metrics Changes - Epidiolex and Xywav, the two largest brands, showed strong growth, contributing significantly to the overall revenue increase [3] - Xywav has been particularly successful in the idiopathic hypersomnia (IH) market, with 325 new patient ads in IH compared to 125 in narcolepsy during the most recent quarter [18] - Epidiolex is on track to achieve blockbuster status, with an 11% growth year-to-date, needing only 3% growth to reach that milestone [24] Market Data and Key Metrics Changes - The company is experiencing growth in the idiopathic hypersomnia market, which is expected to be about half the size of the narcolepsy market [19] - The competitive landscape in small cell lung cancer is evolving, with new entrants and significant advancements in treatment options [39] - The company anticipates potential headwinds for Xywav in 2026 due to the expected entry of generic versions of Xyrem [20][21] Company Strategy and Development Direction - The company is focused on business development opportunities in oncology and epilepsy, with a strategic fit seen in the Chimerix acquisition [10][15] - There is an emphasis on expanding the presence in brain cancer and glioma, leveraging the capabilities gained from the Chimerix acquisition [11] - The company is open to various transaction types, including licensing deals, to enhance its portfolio [16] Management's Comments on Operating Environment and Future Outlook - Management expressed optimism about the strong momentum heading into 2026, particularly with the performance of Epidiolex and Xywav [3][4] - The company is aware of potential challenges from generic competition but believes it is well-positioned due to the unique attributes of its products [20][21] - Management highlighted the importance of educating physicians about the benefits of using Xywav for IH patients to drive market penetration [23] Other Important Information - The company has made significant investments in patient identification tools and nurse navigator programs to enhance the patient experience with Epidiolex [26][27] - The initial launch of Midaso has exceeded expectations, with strong uptake and positive feedback from physicians [43][45] - The company is actively working on expanding awareness and testing for patients eligible for Midaso treatment [47] Q&A Session Summary Question: What is the rationale behind the Chimerix deal? - The acquisition addresses a significant unmet need in a rare form of glioma and aligns with the company's capabilities and expertise [10] Question: How is the company approaching the SAN2355 licensing agreement? - The licensing agreement aims to build on the company's presence in epilepsy, leveraging the attributes of the Saniona molecule [14] Question: What are the growth drivers for Epidiolex? - Key drivers include patient identification initiatives, nurse navigator programs, and increasing awareness of both seizure and non-seizure benefits [24][26] Question: How is the company positioned in the small cell lung cancer market? - The company is optimistic about Zepzelca's potential in first-line maintenance settings, despite increased competition [39] Question: What is the company's strategy regarding business development? - The company is focused on later-stage assets and is open to various transaction types, including acquisitions and licensing deals [16][62]

Financial Data and Key Metrics Changes - The company reported record revenues of $1.13 billion for the third quarter, representing a 7% increase year-over-year [3] - The guidance for revenue was narrowed, reflecting strong performance and disciplined expense management, with an increase in ANI and EPS guidance [4] - A deferred tax asset of $206 million was recognized in the third quarter related to the Chimerix acquisition, which will reduce future tax liabilities [5] - The company ended the quarter with approximately $2 billion in cash and investments, and generated about $1 billion in cash flow for the first nine months of the year [5] Business Line Data and Key Metrics Changes - Epidiolex and Xywav, the two largest brands, showed strong growth driven by demand, contributing significantly to overall revenue [3] - Xywav has been particularly successful in the idiopathic hypersomnia (IH) market, with 325 new patient ads in IH compared to 125 in narcolepsy [18] - Epidiolex is on track to achieve blockbuster status, with an 11% growth year-to-date and a focus on patient titration and nurse navigator programs to enhance persistence [24][26] Market Data and Key Metrics Changes - The market for idiopathic hypersomnia is estimated to be about half the size of narcolepsy, indicating potential for growth as awareness increases [19] - The company anticipates the entry of generic versions of Xyrem in 2026, which could impact Xywav depending on the number and pricing of generics [20][21] - In the small cell lung cancer market, Zepzelca is positioned to become a standard of care, with significant advancements noted in recent medical meetings [39] Company Strategy and Development Direction - The company is focused on business development opportunities in oncology and epilepsy, with a strategic fit seen in the Chimerix acquisition [10][15] - Jazz Pharmaceuticals aims to build on its presence in brain cancer and glioma, leveraging the expertise gained from the Chimerix team [12] - The company is open to various transaction types, including licensing deals, to enhance its portfolio and address unmet medical needs [16] Management's Comments on Operating Environment and Future Outlook - Management expressed optimism about the strong momentum heading into 2026, particularly with the performance of Epidiolex and Xywav [3][4] - The company is aware of potential headwinds from generic competition and payer actions but feels well-positioned to mitigate these risks [20][21] - There is a strong focus on increasing awareness and understanding of the benefits of products like Xywav and Epidiolex among healthcare providers [23][24] Other Important Information - The company has made significant investments in patient identification tools and commercial initiatives to support the growth of Epidiolex and Xywav [26][27] - Jazz Pharmaceuticals is exploring opportunities in rare and orphan diseases, aiming to leverage its existing capabilities in new therapeutic areas [59] Q&A Session Summary Question: What was the rationale behind the Chimerix acquisition? - The acquisition addressed a significant unmet need in a rare form of glioma and provided strong patent protection, aligning with the company's capabilities and expertise [10][11] Question: How is the company addressing the growth in the epilepsy market? - The company is leveraging its leadership position with Epidiolex and exploring new opportunities to enhance its presence in epilepsy treatments [14][15] Question: What are the growth drivers for Xywav in the sleep franchise? - The majority of new patient ads are coming from the IH indication, with a strong opportunity for continued growth as awareness increases [18][19] Question: How does the company view the competitive landscape in oncology? - The company acknowledges the competitive nature of the oncology market but is optimistic about the potential for Zepzelca and other products to capture market share [39][40] Question: What is the company's approach to managing potential tariff impacts? - The company has built inventory in the U.S. to buffer against tariff impacts and is actively working to mitigate exposure [35][36]

Financial Performance - Total revenues are projected to be between $4175 million and $4275 million[31] - Non-GAAP Adjusted Net Income (ANI) is guided to be between $475 million and $525 million[31] - Adjusted Earnings Per Share (EPS) is expected to be in the range of $765 to $845[31] - Cash reserves at the end of 3Q25 stand at $2 billion[32] - September Year-To-Date (YTD) operating cash flow reached $993 million[32] - Neuroscience revenues accounted for 43% of the total, with Xywav revenues at $431 million, showing an 11% year-over-year growth[88] - Oncology revenues contributed 48%, amounting to $288 million, a 1% increase year-over-year[88] Product Performance - Epidiolex revenues grew by 20% year-over-year, reaching $303 million in 3Q25[17, 46] - Total sleep therapeutic area revenue was $520 million in 3Q25[38] - Rylaze revenues increased by 1% year-over-year, totaling $100 million in 3Q25[51, 52] - Modeyso achieved $11 million in net product sales in 3Q25 following its launch[69]

Core Insights - JAZZ Pharmaceuticals is a unique player in the cannabis sector, focusing on an FDA-approved drug, Epidiolex, rather than traditional cannabis cultivation or sales [1][2] - Epidiolex has become a significant growth driver for JAZZ, contributing over 25% of total product sales and showing a 5% year-over-year increase in sales [3][4] - The global medical cannabis market is projected to exceed $130 billion by 2032, providing JAZZ with a competitive advantage as one of the few established pharmaceutical firms with an FDA-approved cannabis product [5] Company Overview - JAZZ Pharmaceuticals has diversified its portfolio beyond cannabis, maintaining strong positions in neuroscience and oncology [6] - The company's neuroscience segment benefits from the oxybate franchise, particularly Xywav, which is a low-sodium treatment for narcolepsy and idiopathic hypersomnia [7] - JAZZ's oncology portfolio, including drugs like Defitelio and Vyxeos, contributed nearly 28% of product sales in the first half of 2025 [8] Recent Developments - The acquisition of Chimerix for $935 million added Modeyso, an FDA-approved drug for glioma patients, enhancing JAZZ's oncology offerings [9] - Despite setbacks in pipeline development, including the discontinuation of suvecaltamide and underwhelming results for JPZ150, JAZZ continues to explore options for its drug pipeline [10][11] Financial Performance - JAZZ's stock has increased by 5% year-to-date, outperforming the industry average of 4% [12] - EPS estimates for 2025 and 2026 have shown an upward trend, contrasting with declines in estimates for pure-play cannabis companies [13] Market Position - JAZZ Pharmaceuticals is positioned as a balanced biopharma investment, offering exposure to both neuroscience and oncology, with Epidiolex providing a unique entry into the cannabis therapeutics market [16][17]

Core Insights - Altimmune, Inc. has appointed Linda M. Richardson as Chief Commercial Officer, effective September 16, 2025, bringing over 30 years of experience in sales, marketing, and business development across various therapeutic areas [1][2] - The appointment is seen as a strategic move as the company approaches the initiation of Phase 3 development of pemvidutide for Metabolic Dysfunction-Associated Steatohepatitis (MASH) [2] - Richardson believes pemvidutide has significant potential to improve patient outcomes in hepato-metabolic diseases and sees opportunities in Alcohol Use Disorder and Alcohol-associated Liver Disease [2] Company Overview - Altimmune is a late clinical-stage biopharmaceutical company focused on developing peptide-based therapeutics for liver and cardiometabolic diseases [5] - The lead product candidate, pemvidutide, is a GLP-1/glucagon dual receptor agonist targeting MASH, Alcohol Use Disorder, Alcohol-associated Liver Disease, and obesity [5] Inducement Grant Details - As part of her appointment, Richardson will receive options to purchase 278,000 shares and 96,000 restricted stock units (RSUs) [3][4] - The options will vest over four years, with one-fourth vesting on the one-year anniversary of the grant date [3][4]

Summary of Jazz Pharmaceuticals (JAZZ) Update / Briefing on Modesto Company and Industry Overview - **Company**: Jazz Pharmaceuticals - **Product**: Modesto (formerly known as dorbapril) - **Industry**: Oncology, specifically focused on rare brain tumors Key Points and Arguments 1. **FDA Approval**: Modesto received accelerated approval from the FDA on August 6, 2025, for treating adult and pediatric patients with diffuse midline glioma harboring an H3K27M mutation with progressive disease following prior therapy [5][41] 2. **Market Need**: This is the first and only FDA-approved treatment for this ultra-rare and aggressive brain tumor, primarily affecting children and young adults, with an estimated annual incidence of approximately 2,000 patients in the U.S. [10][49] 3. **Launch Readiness**: Following the acquisition of Chimerix, Jazz Pharmaceuticals has prepared for a rapid launch, with Modesto available to patients as of August 15, 2025 [5][6] 4. **Mechanism of Action**: Modesto is a first-in-class small molecule that reverses the loss of H3K27 trimethylation, a hallmark of H3K27M mutant diffuse midline glioma, leading to decreased tumor cell proliferation and death [13][14] 5. **Clinical Data**: In clinical studies, the overall response rate for Modesto was 22%, with a median duration of response of 10.3 months. Approximately 73% of responders maintained their response for at least six months [40][28] 6. **Safety Profile**: Modesto has been well tolerated, with only 2.1% of patients discontinuing due to adverse reactions. Serious adverse reactions occurred in 33% of patients, but no treatment-related deaths were reported [44][36] 7. **Commercial Strategy**: The launch strategy includes targeting academic centers of excellence, with a dedicated neuro-oncology sales team and disease education campaigns to raise awareness about the H3K27M mutation and the importance of testing [50][52] 8. **Pricing**: The wholesale acquisition cost for Modesto is set at $32,000 per bottle, reflecting the value and innovation it brings to patients [54] 9. **Future Trials**: The ongoing Phase III ACTION trial aims to confirm the benefits of Modesto in newly diagnosed patients, with expectations for broader international submissions based on supportive trial results [46][47] Additional Important Information - **Patient Support Services**: Jazz Pharmaceuticals has established robust access and patient support services to help patients navigate reimbursement and ensure access to Modesto [53] - **Long-term Outlook**: The patent for Modesto extends to 2037, with potential for patent term extension, indicating a long-term product lifecycle [58] - **Epidemiology Insights**: The disease was codified in the WHO classification in 2016, and the company is working to increase biopsy rates and improve diagnostic accuracy for H3K27M mutations [100][83] - **Potential for Expansion**: There is ongoing research into the broader applicability of Modesto beyond its current indication, exploring similar biological mechanisms in other tumor types [104][106]

Group 1 - The core point of the article is that Kangpeng Technology has successfully supplied the active pharmaceutical ingredient for Dordaviprone, which has been approved in the U.S. for treating recurrent H3K27M mutant diffuse midline glioma in patients aged 1 and above, marking it as the first drug approved for this patient group globally [1][2] - Dordaviprone was initially developed by Chimerix and later acquired by Jazz Pharmaceuticals for over $900 million in March 2025, indicating significant market interest and investment in this innovative treatment [1] - Kangpeng Technology has established a comprehensive service capability covering "custom synthesis—clinical supply—commercial production," which has been built through deep involvement in early-stage drug development [2] Group 2 - The approval of Dordaviprone is seen as a significant achievement for Kangpeng Technology in the pharmaceutical sector, showcasing its "technical accumulation + strategic layout" [2] - The company aims to leverage the global policy benefits for innovative drugs to capture high-value segments of the industry chain through technological barriers [2] - Kangpeng Technology plans to deepen collaboration with multinational pharmaceutical companies to enhance the quality of active pharmaceutical ingredient supply and expand its social responsibility practices, contributing to the availability of medications for patients [2]

Core Insights - Jazz Pharmaceuticals reported a second-quarter 2025 adjusted loss of $8.25 per share, which was wider than the Zacks Consensus Estimate of a loss of $6.12, primarily due to a one-time charge from the acquisition of Chimerix that impacted earnings by $14.75 per share [1][10] Financial Performance - Total revenues increased by 2% year over year to $1.05 billion, aligning with the Zacks Consensus Estimate [2] - Net product sales rose 2% year over year to $986 million, missing the Zacks Consensus Estimate of $999 million and the model estimate of $1 billion [3] - Royalty revenues from high-sodium oxybate authorized generic remained flat year over year at $54 million, exceeding the Zacks Consensus Estimate of $49 million and the model estimate of $43 million [3] - Other royalties and contract revenues increased by 9% year over year to $6 million [4] Neuroscience Segment - Sales of neuroscience products grew by 3% year over year to $707 million [5] - Combined net product sales for the oxybate business (Xyrem + Xywav) rose about 5% to $451 million, surpassing the Zacks Consensus Estimate of $440 million [5] - Xywav sales reached $415 million, up 13%, attributed to strong uptake in narcolepsy and idiopathic hypersomnia indications [6] - Sales of the epilepsy drug Epidiolex/Epidyolex increased by 2% to nearly $252 million, but fell short of the Zacks Consensus Estimate of $271 million [7] Oncology Segment - Oncology product sales decreased by 1% to $274 million [8] - Rylaze/Enrylaze sales were $101 million, down 7% year over year, missing both the Zacks Consensus Estimate and model estimates [9] - Zepzelca sales were $75 million, down 8% year over year, due to increased competition and treatment protocol updates [11] Operating Costs - Adjusted selling, general and administrative expenses rose by 2% year over year to $310 million [13] - Adjusted research and development expenses decreased by 18% to $167 million [13] Guidance and Market Reaction - The company lowered its 2025 revenue guidance to $4.15-$4.30 billion, reflecting a $100 million cut at the upper end [10][14] - Adjusted earnings per share outlook was raised to $4.80-$5.60, up from the previous range of $4.00-$5.60 [10][18] - Shares of Jazz fell more than 7% in after-market trading following the earnings guidance and wider-than-expected loss [15]

Financial Performance - Total revenues reached $761 million in 2Q25, a 2% year-over-year increase[93] - Neuroscience revenues accounted for 43% of the total, amounting to $335 million in 2Q25[98] - Oncology revenues totaled $274 million in 2Q25[100] - The company updated its full-year 2025 revenue guidance to a range of $415 billion to $430 billion[30, 36] - The company projects non-GAAP adjusted net income to be in the range of $300 million to $350 million, with adjusted EPS between $480 and $560[36] Product Performance - Xywav revenues were $415 million in 2Q25, representing a 13% year-over-year growth[100] - Epidiolex revenues reached $252 million in 2Q25, a 2% year-over-year increase[100] - Rylaze revenues were $101 million in 2Q25, a 7% year-over-year decrease[53] - Zepzelca revenues were $75 million in 2Q25, an 8% year-over-year decrease[59] Pipeline and Corporate Development - The company closed the Chimerix Acquisition for a total consideration of $944 million[32, 33] - The acquisition of Chimerix included an acquired IPR&D expense of $9054 million related to dordaviprone[23, 94, 113] - A PDUFA target action date of October 7, 2025, was set for Zepzelca as maintenance therapy in 1L ES-SCLC[35, 61, 62]