Core Viewpoint - Inspira Technologies is planning a strategic expansion into liquid biopsy diagnostics, aiming to preserve shareholder value while enabling future dividend distributions from its core respiratory and life-support technologies [1][2]. Company Strategy - The proposed acquisition of a liquid biopsy platform is seen as a significant value inflection point, enhancing Inspira's diagnostics capabilities with long-term potential [2]. - The transaction is structured to optimize value allocation between the new platform and Inspira's existing respiratory business through a Contingent Value Rights (CVR) framework [2][12]. - The acquisition is positioned as a natural extension of Inspira's competencies in blood-based diagnostics and real-time monitoring, leveraging its proprietary HYLA™ blood sensor platform [2][7]. Liquid Biopsy Technology - The targeted liquid biopsy platform analyzes intact circulating tumor cells (CTCs) from blood samples, offering a more direct view of tumor characteristics over time [3]. - Initial focus is on breast cancer, where changes in biomarkers can significantly impact treatment options, enabling minimally invasive testing to monitor tumor evolution [4][5]. - The technology is designed for routine clinical use and has shown high concordance with traditional tissue biopsy in preliminary validations, with plans for adaptability across various solid tumor indications [5][6]. Current Operations - Inspira's existing operations in respiratory care and life-support are advancing, with the FDA-cleared INSPIRA™ ART100 system deployed in leading U.S. hospitals [7]. - The company is expected to generate revenue from previously announced purchase orders during 2026 [7]. Financial Aspects - The proposed equity investment of up to $15 million is intended to support ongoing operations and further development of existing platforms, with $12 million specifically allocated for this purpose [8][12]. - The acquisition structure allows Inspira to acquire the liquid biopsy business in exchange for up to 40% of its issued share capital, ensuring economic benefits for current shareholders through the CVR framework [12]. Transaction Timeline - The acquisition and equity investment are expected to close concurrently, pending customary conditions, including shareholder and regulatory approvals, with a target for execution of definitive agreements within approximately four weeks from January 5, 2026 [12].

Core Viewpoint - Tempus AI, Inc. reported strong third-quarter FY25 earnings, leading to a reiterated Buy rating from BTIG analyst Mark Massaro with a price target of $96, despite current selling pressure on the stock [1]. Earnings Details - Tempus AI reported revenue of $334.21 million, exceeding analyst estimates of $328.73 million, representing an 84.7% year-over-year increase [2]. - The adjusted loss per share was 11 cents, better than the estimated loss of 17 cents [2]. - For FY25, the company raised its revenue guidance to $1.265 billion from a previous estimate of $1.260 billion [2]. Analyst View - The analyst anticipates that Tempus will secure additional pharmaceutical contracts for its data and services business [3]. - There is an expectation for average selling prices (ASPs) to increase due to a shift towards higher-priced tests, such as the xT CDx priced at $4,500 per test (up from $2,900 for xT LDT) and the xF liquid biopsy assay at $3,288 per test (up from $2,919) [3]. - Expansion of commercial payor coverage for xF and xT CDx is expected, along with continued development of Tempus's algorithm business [3]. Market Positioning - Tempus is positioned at the intersection of key trends including precision medicine, oncology (including liquid biopsies), AI and machine learning, and the shift towards personalized drug development and companion diagnostics for pharmaceutical companies [4]. - As of the publication date, Tempus shares were down 2.74% at $82.18 [4].

Core Insights - Roche expects mid single-digit growth in Group sales and high single-digit growth in core earnings per share for 2025, along with an increase in dividends [1][4]. Financial Performance - Group sales for the first half of 2025 reached CHF 30.9 billion, a 7% increase at constant exchange rates (CER) and a 4% increase in CHF compared to 2024 [2][5]. - The Pharmaceuticals Division reported sales of CHF 24.0 billion, reflecting a 10% increase at CER and a 6% increase in CHF [6][16]. - The Diagnostics Division's sales remained stable at CHF 7.0 billion, showing a 3% decline in CHF [12][31]. - Core operating profit increased by 11% (6% in CHF) to CHF 12.0 billion, driven by higher sales and effective cost management [5][6]. - Core earnings per share rose by 12% (8% in CHF), while IFRS net income increased by 23% (17% in CHF) to CHF 7.8 billion [6][31]. Key Growth Drivers - The top five growth drivers in the Pharmaceuticals Division included Phesgo, Xolair, Hemlibra, Vabysmo, and Ocrevus, which collectively generated CHF 10.6 billion in sales, an increase of CHF 1.7 billion at CER compared to the first half of 2024 [7][9]. - Sales in the United States grew by 10%, driven by the continued growth of Xolair and the uptake of Hemlibra, Ocrevus, Vabysmo, and Phesgo [9][10]. - The International region saw a 14% increase in sales, led by Phesgo, Hemlibra, and Vabysmo, with China reporting a 9% increase [12][13]. Regulatory Approvals and Pipeline Developments - Roche received several important regulatory approvals, including US approval for Susvimo for diabetic retinopathy and EU approval for Itovebi for advanced breast cancer [3][15]. - Four potentially practice-changing therapies advanced into the final phase of clinical development, including NXT007 for haemophilia A and prasinezumab for early-stage Parkinson's disease [3][4]. - The introduction of the Elecsys PRO-C3 test aims to improve precision in evaluating liver fibrosis severity [22][19]. Strategic Collaborations - Roche announced a collaboration with Broad Clinical Labs to accelerate the adoption of SBX sequencing technology, focusing on genetic disorders in critically ill newborns [20][18].

As filed with the Securities and Exchange Commission on June 30, 2023. UNITED STATES SECURITIES AND EXCHANGE COMMISSION Washington, D.C. 20549 AMENDMENT NO. 1 TO FORM S-1 REGISTRATION STATEMENT UNDER THE SECURITIES ACT OF 1933 Allarity Therapeutics, Inc. (Exact name of registrant as specified in its charter) (State or other jurisdiction of incorporation or organization) (Primary Standard Industrial Delaware 2834 87-2147982 (I.R.S. Employer Identification No.) Classification Code Number) 24 School Street, 2n ...