SOUTH SAN FRANCISCO, Calif., Nov. 13, 2025 (GLOBE NEWSWIRE) -- Senti Biosciences, Inc. (Nasdaq: SNTI) (“Senti Bio”), a clinical-stage biotechnology company developing next-generation cell and gene therapies using its proprietary Gene Circuit platform, today reported financial results for the third quarter of 2025 and provided a summary of recent pipeline and corporate highlights. “Our team is laser focused on driving SENTI-202 clinical development forward. With important milestones achieved in the third qua ...

Core Insights - The earnings season has concluded, highlighting the performance of drug development inputs and services stocks, particularly West Pharmaceutical Services [1] Industry Overview - Companies in drug development inputs and services are essential in the pharmaceutical and biotechnology value chain, providing support for drug discovery, preclinical testing, and manufacturing, leading to stable demand due to outsourcing by pharmaceutical companies [2] - The industry faces challenges such as high capital requirements, customer concentration, and sensitivity to changes in biopharma R&D budgets and regulatory frameworks [2] - Future growth is expected from increased investment in biologics, cell and gene therapies, and advancements in precision medicine, which will drive demand for sophisticated tools and services [2] - A trend towards outsourcing in drug development is noted for enhancing nimbleness and cost efficiency, benefiting the industry [2] - Potential challenges include pricing pressures from healthcare cost containment efforts and an evolving regulatory environment that could hinder innovation or client activity [2] Company Performance - The seven tracked drug development inputs and services stocks reported strong Q3 results, with revenues exceeding analysts' consensus estimates by 3.1% [3] - West Pharmaceutical Services reported revenues of $804.6 million for Q3, reflecting a year-on-year increase of 7.7% and surpassing analysts' expectations by 2.1% [5] - The company experienced broad-based strength across its Proprietary Products and Contract Manufacturing segments, with double-digit growth in its HVP Components business driven by GLP-1 products and an improving demand environment [6]

Core Insights - McKesson is redefining its role in the healthcare ecosystem by shifting focus from pharmaceutical distribution to higher-margin services in oncology, multispecialty care, and biopharma solutions [1] - The company aims for sustainable long-term growth through technology, automation, and specialized care while planning to separate its Medical-Surgical business to sharpen focus [1] Short-Term Growth Drivers - McKesson is experiencing strong momentum in pharmaceutical distribution and specialty therapy demand, with the U.S. pharmaceutical market projected to grow at a 7% CAGR from 2019 to 2029, and oncology spending expected to increase by 60% from 2025 to 2029 [2] - Management has guided for fiscal 2026 adjusted operating profit of $6.2-$6.4 billion, adjusted EPS of $38.05-$38.55, and free cash flow of $4.4-$4.8 billion, reflecting robust operating leverage supported by investments in distribution center automation [3] Long-Term Growth Drivers - McKesson's U.S. Oncology Network includes over 3,300 providers and supports 1.4 million patients annually, which is central to its strategy of integrating clinical care and biopharma services [6] - The company is leveraging technology platforms like Ontada and iKnowMed to enhance its specialty care value chain [7] - Emerging therapeutic modalities, particularly in cell and gene therapies, represent a significant growth opportunity, supported by investments in cold-chain infrastructure and automation [8] Medical-Surgical Separation - McKesson plans to separate its Medical-Surgical business, which generated $11.4 billion in fiscal 2025 revenues and $1.1 billion in adjusted EBITDA, starting with an IPO of a minority stake and a full separation by the second half of calendar 2027 [11][12] Challenges - McKesson faces regulatory and legal risks, particularly related to historical opioid litigation, and operational challenges in integrating recent acquisitions like PRISM Vision [15] - The competitive landscape in specialty distribution and oncology services is intensifying, with risks associated with large-scale technology deployments and the pace of regulatory approvals for cell and gene therapies [16] Peer Comparison - McKesson is diversifying to improve margins and streamline operations, similar to peers Cardinal Health and Cencora, who are also focusing on higher-margin oncology and specialty care [17][21] - Cardinal Health is building a multi-platform healthcare solutions portfolio, while Cencora is extending its business model to include high-growth specialty services [18][22] Conclusion - McKesson is at an inflection point, targeting higher-margin growth avenues while shedding non-core assets, with strong near-term earnings momentum and long-term strategic initiatives [26][27] - The planned separation of Medical-Surgical highlights management's intent to sharpen focus, presenting a balanced opportunity for investors as the company evolves into a specialty-driven healthcare solutions leader [28]

Core Insights - Dr. Park CDMO has selected Thermo Fisher Scientific to equip its new viral vector manufacturing facility, aiming to enhance large-scale production and global access to cell and gene therapies [1][4] Group 1: Company Overview - Dr. Park specializes in Adeno-associated virus-based (AAV-based) viral vector production, currently operating at a capacity of 5,000 L per batch and producing up to 40 clinical-grade batches annually [2] - The new Phase 1 facility was inaugurated on August 5, 2025, with plans to achieve cGMP certification in 2026 and to expand capacity to 10,000 L per batch in the future [2] Group 2: Technological Integration - The facility will utilize several advanced solutions from Thermo Fisher, including the HyPerforma™ 1,000 L Single-Use Bioreactor and DynaSpin™ Single-Use Centrifuge, aimed at streamlining production processes and enhancing efficiency [3] - These technologies are designed to improve process control and automation, thereby supporting rapid scale-up from clinical to commercial production while maintaining high standards of quality and regulatory compliance [3] Group 3: Strategic Collaboration - The collaboration between Dr. Park CDMO and Thermo Fisher is seen as crucial for advancing viral vector manufacturing in South Korea, reflecting the growing importance of robust manufacturing infrastructure for cell and gene therapies [4][5] - Both companies emphasize the need for collaboration to accelerate the development and delivery of therapies to patients, addressing the rising global demand for gene therapy [5]

Company Overview - Senti Biosciences, Inc. is a clinical-stage biotechnology company focused on developing next-generation cell and gene therapies using its proprietary Gene Circuit platform [2] - The company aims to create new medicines that can precisely target and kill cancer cells while sparing healthy cells, enhancing specificity to target tissues, and allowing for control even after administration [2] Upcoming Presentation - Kanya Rajangam, M.D., Ph.D., President, Head of Research & Development and Chief Medical Officer of Senti, will present at the MedInvest Biotech & Pharma Conference on September 24, 2025, at 9:55 AM PT [1] - A live webcast of the presentation will be available on the company's website [2] Investor Engagement - Management will be available for one-on-one meetings with qualified members of the investor community registered for the conference [2] - The company encourages investors and the public to review information posted on its website and social media platforms regularly [3]

Core Insights - Senti Biosciences, Inc. is a clinical-stage biotechnology company focused on developing next-generation cell and gene therapies using its proprietary Gene Circuit platform [2][4] - The company recently announced the recommended Phase 2 dose selection for its first-in-class Logic Gated off-the-shelf CAR-NK cell therapy, SENTI-202, aimed at treating relapsed/refractory hematologic malignancies, including acute myeloid leukemia (AML) [3] Company Overview - Senti Bio is leveraging synthetic biology to engineer Gene Circuits that enhance precision and control in new medicines, specifically targeting cancer cells while sparing healthy cells [4] - The company's pipeline includes cell therapies designed to address challenging liquid and solid tumor indications, with preclinical evidence supporting the efficacy of Gene Circuits in both NK and T cells [4] Recent Developments - The participation in the Virtual Investor segment highlights the company's ongoing efforts to communicate its advancements and strategies to potential investors [2][3] - The focus on SENTI-202 represents a significant step in Senti Bio's clinical development, indicating progress in its research and development initiatives [3]

Core Insights - Senti Biosciences, Inc. is advancing its clinical development of SENTI-202, having completed the dose finding phase and confirmed the recommended Phase 2 dose (RP2D) for treating relapsed/refractory AML [2][7] - The company received Orphan Drug Designation from the U.S. FDA for SENTI-202, enhancing its potential market position [7] - Senti Bio aims to grow its pipeline and expects to release additional efficacy and durability data from its ongoing Phase 1 study by the end of the year [2] Recent Pipeline and Corporate Updates - The company has completed the dose finding phase for SENTI-202 and is currently in the dose expansion phase [2][7] - Senti Bio received a $1.0 million tranche from the California Institute for Regenerative Medicine (CIRM) to support the clinical development of SENTI-202 [7] - New appointments to the leadership team include Bryan Baum to the Board of Directors and Dr. James B. Trager to the Scientific Advisory Board [7] Financial Results for Q2 2025 - As of June 30, 2025, Senti Bio reported cash and cash equivalents of approximately $21.6 million, down from $48.3 million as of December 31, 2024 [7][13] - Research and development expenses increased to $10.0 million for Q2 2025, compared to $9.2 million in Q2 2024, primarily due to higher external services and supplies costs [7][15] - General and administrative expenses rose to $6.8 million in Q2 2025 from $4.2 million in Q2 2024, mainly due to increased personnel-related expenses [7][15] - The net loss for Q2 2025 was $14.7 million, or $0.56 per share, compared to a net loss of $11.2 million in Q2 2024 [7][15][16]

Core Insights - MaxCyte reported an 18% year-over-year decline in total revenue for Q2 2025, with GAAP revenue at $8.5 million, missing analyst expectations by approximately $1.1 million [1][2] - The company revised its full-year 2025 guidance, now forecasting core revenue to be flat to down 10%, a significant change from previous expectations of 8% to 15% growth [9][10] Financial Performance - GAAP net losses widened to $12.4 million, compared to the prior-year period, with EPS (GAAP) at $(0.12), a 33.3% increase in losses year-over-year [2][7] - Core revenue increased by 7.9% year-over-year to $8.2 million, despite the overall revenue decline [2][5] - Gross margin decreased from 86% in Q2 2024 to 82% in Q2 2025, reflecting lower SPL revenue [2][7] Business Operations - The installed base of ExPERT instruments grew by 12.6% to 814 units compared to Q2 2024, indicating continued adoption in the cell and gene therapy market [5] - SPL Program-related revenue fell dramatically from $2.9 million in Q2 2024 to $0.3 million in Q2 2025, with only 42% of core revenue coming from SPL clients, down from 51% [5][6] Strategic Focus - Recent strategic priorities include expanding the installed base of ExPERT instruments, signing new SPL agreements, and enhancing gene-editing safety through the SeQure Dx acquisition [4][8] - The company aims to stabilize recurring revenue and support clients in developing therapies through clinical and regulatory pathways [4] Future Outlook - Management expects SPL Program-related revenue to reach approximately $5 million for 2025, requiring significant acceleration in milestone achievements and royalties in the second half of the year [9][10] - Cash reserves stood at $165.2 million, with expectations of at least $155 million in total cash, cash equivalents, and investments by the end of 2025 [10]

Core Insights - Senti Biosciences, Inc. is participating in a Virtual Fireside Chat hosted by Chardan Capital Markets on June 9, 2025, featuring key executives discussing the company's advancements in biotechnology [1][2]. Company Overview - Senti Biosciences is a clinical-stage biotechnology company focused on developing next-generation cell and gene therapies using its proprietary Gene Circuit platform [1][3]. - The company aims to create therapies that can precisely target and kill cancer cells while sparing healthy cells, enhancing specificity to target tissues, and allowing for controllability post-administration [3]. - Senti's pipeline includes cell therapies engineered with Gene Circuits targeting both liquid and solid tumors, with preclinical evidence supporting their efficacy in NK and T cells [3]. Additional Information - For further details, Senti Biosciences encourages stakeholders to visit their official website and follow their social media channels for updates and disclosures [4].

Core Insights - Cellectis reported financial results for Q1 2025, highlighting progress in clinical studies and partnerships, particularly with AstraZeneca [1][2][9] Financial Results - As of March 31, 2025, Cellectis had a cash position of $246 million, down from $264 million at the end of 2024, providing a runway into H2 2027 [10][11] - Consolidated revenues and other income for Q1 2025 were $12.0 million, an increase from $6.5 million in Q1 2024, primarily due to a $5.9 million increase in revenue recognized under the AstraZeneca joint research collaboration agreement [13][14] - R&D expenses for Q1 2025 were $21.9 million, slightly down from $22.3 million in Q1 2024, while SG&A expenses decreased to $4.7 million from $5.1 million [15][16] - The consolidated net loss attributable to shareholders was $18.1 million for Q1 2025, compared to a net income of $5.6 million in Q1 2024 [19][20] Pipeline Highlights - Cellectis is advancing its clinical programs, including the BALLI-01 study for lasme-cel (UCART22) in relapsed or refractory B-cell acute lymphoblastic leukemia, with results expected in Q3 2025 [3][6][7] - The NATHALI-01 study for eti-cel (UCART20x22) in relapsed or refractory B-cell non-Hodgkin lymphoma is ongoing, with readout expected in late 2025 [4][7] Research and Development - Cellectis presented research data on TALEN®-mediated non-viral transgene insertion and TALE base editing at the ASGCT annual meeting, showcasing advancements in gene editing technologies [5][8] - The company is focusing on the development of its pipeline, including manufacturing and clinical trial expenses for UCART22 and UCART20x22 [12] Partnerships - Ongoing R&D activities under the AstraZeneca partnership include three programs: one allogeneic CAR T for hematological malignancies, one for solid tumors, and one in vivo gene therapy for a genetic disorder [9][6]