Core Insights - Compugen Ltd. is a clinical-stage cancer immunotherapy company that utilizes AI/ML for drug target discovery [1] - The company will participate in two upcoming investor conferences, including the Oppenheimer 36th Annual Healthcare Life Sciences Conference and the Leerink Partners 2026 Global Healthcare Conference [1] Company Overview - Compugen is focused on developing cancer immunotherapies through its AI/ML powered computational discovery platform, Unigen™ [1] - The company has two main programs targeting TIGIT: COM902, a fully owned anti-TIGIT antibody in Phase 1, and rilvegostomig, an Fc-reduced PD-1/TIGIT bispecific antibody in Phase 3 development by AstraZeneca [1] - Additional programs include COM701, a potential first-in-class anti-PVRIG antibody, and GS-0321, a high affinity anti-IL-18 binding protein antibody licensed to Gilead [1] Upcoming Events - The Oppenheimer conference will take place on February 26, 2026, featuring a fireside chat at 2 PM ET [1] - The Leerink Partners conference is scheduled for March 9, 2026, with a fireside chat at 8:40 AM ET [1] - Live webcasts of the fireside chats will be available on Compugen's Investor Relations website [1]

Core Insights - TuHURA Biosciences has filed an Investigational New Drug Application (IND) for TBS-2025, a novel VISTA inhibiting antibody, aimed at treating mutNPM1 relapsed/refractory Acute Myeloid Leukemia (AML) in combination with a menin inhibitor [1] - The company plans to initiate a Phase 2 study in early Q2 2026, targeting menin inhibitor naïve patients, with preliminary results expected in Q3 2026 [1] - TBS-2025 is expected to address the unmet medical need in AML treatment, as current therapies have low complete response rates of less than 25% [1] Company Overview - TuHURA Biosciences, Inc. is a Phase 3 immuno-oncology company focused on developing novel therapeutics to overcome resistance to cancer immunotherapy [1] - The company’s lead product, IFx-2.0, is designed to overcome primary resistance to checkpoint inhibitors and is currently in a Phase 3 trial for advanced Merkel Cell Carcinoma [1] - TBS-2025 was acquired through the merger with Kineta Inc. and is moving into Phase 2 development for mutNPM1 r/r AML [1] Scientific Rationale - Scientific evidence indicates that mutations like mutNPM1 drive VISTA expression on leukemic cells, contributing to poor therapy responses and high relapse rates in AML [1] - The removal of the VSIR gene, which encodes for VISTA, in murine models has shown enhanced immune response and improved survival rates [1] - TBS-2025 demonstrated a favorable safety profile in a Phase 1 trial, with an optimal Phase 2 dose anticipated to be 750mg every three weeks [1]

Group 1 - Iovance Biotherapeutics Inc. expects to achieve full-year 2025 revenue guidance of $250 to $300 million in the first full calendar year of Amtagvi sales [1][2] - Amtagvi, the treatment regimen for advanced melanoma, is projected to have peak sales potential of up to $1 billion [1] - The company has $307 million in cash and cash equivalents, which will fund operations through the second quarter of 2027 [2] Group 2 - Lifileucel, an in-development treatment for lung cancer, has a commercial opportunity that could be up to 7 times larger than the current melanoma treatment market [2] - Enrollment and data updates for Lifileucel are expected to be completed this year, with a launch anticipated in the second half of 2027 [2] - Iovance Biotherapeutics specializes in developing and commercializing cell therapies as novel cancer immunotherapy products [2]

Core Viewpoint - OS Therapies Inc. has initiated a Biologics License Application (BLA) submission to the FDA for OST-HER2, targeting the prevention or delay of recurrent pulmonary metastatic osteosarcoma, with expectations for approval by September 30, 2026 [1][5]. Company Developments - The company has submitted the Non-Clinical and Chemistry, Manufacturing, and Controls (CMC) modules of the BLA to the FDA and requested a Rolling Review [1][5]. - A Type D Meeting is anticipated in March 2026 to discuss new Comparative Oncology biomarker data from the Phase 2b clinical trial in humans and a similar trial in canines [1][5]. - The final clinical BLA module is expected to be submitted by the end of March 2026 [5]. Designations and Approvals - OST-HER2 has received Orphan Disease Designation (ODD), Fast Track Designation from the FDA and EMA, and Rare Pediatric Disease Designation (RPDD) from the FDA [3][4]. - If Accelerated Approval is granted before September 30, 2026, the company will be eligible for a Priority Review Voucher (PRV), which it intends to sell [3][4]. Clinical Trial Results - Positive data from the Phase 2b clinical trial of OST-HER2 demonstrated statistically significant benefits in the 12-month event-free survival (EFS) primary endpoint [4]. Future Developments - OS Therapies is advancing its next-generation Antibody Drug Conjugate (ADC) and Drug Conjugates (DC), known as tunable ADC (tADC), utilizing proprietary technology for enhanced delivery of therapeutic payloads [6].

Core Insights - BriaCell Therapeutics Corp. has released new imaging data demonstrating the resolution of metastatic breast cancer lesions in patients with various organ involvements, highlighting the effectiveness of their immunotherapy treatment [1][6]. Patient Outcomes - Patient 11-018, a 66-year-old woman with ER+/PR+/HER2+ metastatic breast cancer, achieved 27 months of survival post-enrollment after 35 cycles of Bria-IMT treatment, showing complete resolution of temporal lobe metastasis and significant improvement in orbital lesions [2][4]. - Patient 15-005, a 44-year-old woman with ER+/PR+/HER2- metastatic breast cancer, remains in stable condition 27 months after treatment, having completed 6 cycles of therapy [9]. - Patient 15-006, a 64-year-old woman with ER+/PR-/HER2- metastatic breast cancer, has survived 25 months post-enrollment after receiving 4 cycles of Bria-IMT treatment [13]. Mechanism of Action - The CD8 ImmunoPET imaging confirms that BriaCell's treatment activates CD8+ cytotoxic T cells, which infiltrate tumors, potentially enhancing long-term patient survival even after treatment cessation [3]. Study Details - The Phase 2 study involved 54 heavily pre-treated metastatic breast cancer patients, with a median of six prior therapies, who received the Bria-IMT regimen alongside a checkpoint inhibitor. Notably, no treatment-related discontinuations have been reported [17].

Core Insights - Adagene Inc. announced an update on its ongoing Phase 1b/2 study of muzastotug in combination with pembrolizumab for patients with microsatellite stable metastatic colorectal cancer (MSS CRC), with data expected in Q1 2026 [1][6] - The company reported unaudited cash and cash equivalents of $74.5 million as of December 31, 2025, which is anticipated to provide sufficient runway until late 2027 [1][3] 2025 Key Accomplishments - The company demonstrated a favorable safety profile for muzastotug at doses 10-20 times higher than first-generation CTLA-4 inhibitors, with encouraging overall response rates and durable responses [5] - Muzastotug received FDA Fast Track designation for use in combination with KEYTRUDA for adult patients with MSS CRC without current or active liver metastases [5] - Adagene secured a strategic investment of up to $25 million from Sanofi to support the randomized Phase 2 study of muzastotug [5] - Collaborations were established with Third Arc Bio for developing next-generation T cell therapies and with Exelixis for advancing a third masked ADC against a solid tumor target [5] 2026 Objectives - The company aims to provide a data update from the ongoing Phase 1b/2 study, including results from 41 patients in the 10 mg/kg cohort and 26 patients in the 20 mg/kg cohort [6] - Complete enrollment of the randomized Phase 2 dose-optimization study with muzastotug, aligned with FDA Project Optimus [6] - Share results from a clinical trial collaboration with Roche evaluating muzastotug in combination with atezolizumab and bevacizumab for liver cancer [6] Company Overview - Adagene Inc. is a clinical-stage biotechnology company focused on developing novel antibody-based cancer immunotherapies using computational biology and artificial intelligence [8] - The company's lead clinical program, muzastotug, is a masked anti-CTLA-4 SAFEbody targeting regulatory T cells in the tumor microenvironment, currently in Phase 1b/2 and Phase 2 studies [10]

Company Overview - OS Therapies Inc. is a leader in listeria-based cancer immunotherapies, focusing on treatments for osteosarcoma and other solid tumors [8] - The company is preparing for an Initial Public Offering (IPO) for its subsidiary OS Animal Health Corp (OSAH) in the first half of 2026 [1][5] - OSAH aims to commercialize OST-HER2, an immunotherapy for canine osteosarcoma and HER2-positive cancers in animals [5][7] Research and Development - A 2023 study highlighted similarities between human and canine osteosarcoma, indicating that a robust immune response improves clinical outcomes [2] - Data from canine studies of OST-HER2 showed upregulation of immune activation biomarkers that correlate with better outcomes [2][3] - OST-HER2 has demonstrated potential in improving patient outcomes in canine osteosarcoma, including preventing metastatic disease and amputation [4] Market Opportunity - The veterinary oncology market is projected to grow from $1.58 billion in 2024 to $4.77 billion by 2034, primarily driven by North America [3] - The canine cancer segment is expected to grow at a rate of 12.56% from 2025 to 2030, attributed to rising cancer prevalence and increased awareness of treatment options [3] Regulatory and Approval Status - OS Therapies is pursuing a Biologics Licensing Application (BLA) for OST-HER2 under the Accelerated Approval Program for human osteosarcoma [3][8] - OST-HER2 has received conditional approval from the USDA for treating canine osteosarcoma and is part of the National Cancer Institute's Comparative Oncology Program [6][8]

Daiichi Sankyo Company FY Conference Summary Company Overview - **Company**: Daiichi Sankyo Company - **Headquarters**: Tokyo, Japan - **Fiscal Year Ending**: March 31, 2026 - **Revenue Forecast**: Approximately 2.1 trillion JPY, an increase of 11% from the previous fiscal year [3] - **Core Operating Profit Forecast**: 350 billion JPY, reflecting a growth of 12% from the previous fiscal year [3] - **Revenue Distribution**: Approximately 70% generated outside Japan, particularly in the United States [3] Key Products and Technologies - **Main Growth Drivers**: HER2-directed ADC Enhertu and Trop2-directed ADC Dataway [3] - **DXd ADC Technology**: Proprietary technology platform with two launched products, Enhertu and Dataway, approved in multiple indications [4] - **Clinical Development**: Seven different ADC assets in clinical development, with promising outcomes in various cancers [4] - **Breakthrough Therapy Designation**: Five DXd ADCs received BTD from FDA, with Enhertu's DESTINY-Breast05 study being the 14th to receive this designation [4] Market Performance - **Global Net Sales (Q2 FY 2025)**: 160 billion JPY, growing 24% year-over-year [6] - **Enhertu Impact**: Over 200,000 patients treated across 85 countries, with significant market share leadership in various cancer indications [6][5] - **Dataway Sales**: Exceeded 10 billion JPY in Q2, with U.S. revenue growing 113% and Japan's revenue growing 59% compared to the previous quarter [8] Clinical Insights - **Enhertu in HER2-positive Metastatic Breast Cancer**: Reduced risk of disease progression or death by 44% compared to standard treatments, with over 40 months of progression-free survival [7] - **Dataway in HR-positive, HER2-negative Metastatic Breast Cancer**: Early experiences reported positively by oncologists, with expectations for triple-negative breast cancer indication [9][10] Future Growth and Strategy - **New Indications**: Anticipated growth from Enhertu and Dataway in 2026, with multiple pivotal trials expected to read out over the next few years [10][11] - **Investment in R&D**: Continued investment in clinical trials and establishing in-house capabilities for clinical development [19][24] - **Shareholder Returns**: Targeting a dividend on equity of 8% or more, with plans for consecutive annual dividend increases [15] Manufacturing and Development - **Global Manufacturing Sites**: 13 sites globally, with ongoing investments in manufacturing capabilities in Germany, China, and the U.S. [14][29] - **Platform Strategy**: Focus on developing multiple ADC technologies, including modified PBD ADC and STING agonist ADC technologies [12][27] Conclusion - **Commitment to Oncology**: Transition from a cardiovascular company to a global oncology leader, with a strong pipeline and innovative ADC technologies [17][19] - **Sustainable Growth**: Aiming for sustainable growth beyond 2030 through continuous innovation and enhanced shareholder returns [20]

Core Viewpoint - OS Therapies Inc. has launched a warrant exercise inducement and exchange offer to nine accredited investors, raising a total of $7.53 million in gross proceeds to support its ongoing projects and regulatory filings [1][3]. Group 1: Financial Details - The gross proceeds of $7.53 million will provide the company with a financial runway into 2027 [3]. - All nine investors who were offered the inducement have agreed to participate in the exercise of their existing warrants [7]. Group 2: Regulatory and Development Plans - The company plans to use the net proceeds to support regulatory filings and commercial preparation activities for its lead asset, OST-HER2, aimed at treating pulmonary metastatic osteosarcoma [3]. - OS Therapies intends to file a Biologics Licensing Application (BLA) with the U.S. FDA by the end of January 2026 and expects to submit Marketing Authorisation Applications (MAA) to the UK and EU regulatory bodies by February and March 2026, respectively [4][5]. - The company is hopeful for regulatory approval for OST-HER2 in the UK by Q2 2026, in the U.S. by Q3 2026, and in Europe by Q4 2026 [4]. Group 3: Product Designations and Market Potential - OST-HER2 has received Orphan Disease Designation and Fast Track Designation from the FDA, as well as Rare Pediatric Disease Designation, which may allow the company to receive a Priority Review Voucher (PRV) if it gains Accelerated Approval before September 30, 2026 [5]. - The most recent PRV sale was valued at $160 million, indicating significant market potential for the company if it successfully monetizes a future PRV [5]. Group 4: Company Overview - OS Therapies is a clinical-stage oncology company focused on developing treatments for osteosarcoma and other solid tumors, leveraging listeria-based cancer immunotherapies [9]. - The company reported positive data from its Phase 2b clinical trial of OST-HER2, demonstrating significant benefits in the primary endpoint of 12-month event-free survival [9].

Core Insights - TG4050 demonstrates strong potential as an individualized cancer immunotherapy, showing 100% two-year disease-free survival in patients with operable head and neck cancers [3][5][8] Clinical Trial Results - The Phase I/II trial of TG4050 involved patients with HPV-negative head and neck squamous cell carcinoma (HNSCC), where one-third of patients typically experience recurrence within two years post-surgery [3] - Half of the participants received TG4050 immediately after primary adjuvant treatment, while the other half received it at the time of disease recurrence [4][16] - The trial results indicate that TG4050 can prevent cancer relapses when used as monotherapy in high-risk, resected, locally advanced HPV-negative HNSCC patients [5] Immunogenicity and T-cell Responses - TG4050 induced neoantigen-specific T-cell responses in 73% of evaluable patients, with these responses being durable for up to one year post-treatment [6][7] - The vaccine was well-tolerated, showing no unexpected safety signals, reinforcing its potential for further development [5][8] Publication and Transparency - The results of the Phase I trial have been published on medRxiv, emphasizing the company's commitment to transparency and scientific rigor [2][8] - The findings are currently under evaluation for publication in a peer-reviewed journal [2] Future Developments - TG4050 is undergoing further evaluation in a randomized Phase I/II clinical trial (NCT04183166), with first immunogenicity data from the Phase II part expected in the second half of 2026 [7][16]