$10 million securities purchase agreement provides efficient and flexible funding in support of strategic multi- million dollar growth initiatives Discussions underway to expand adoption of ChemoFx in the U.S. and accelerate initial launch in Europe PITTSBURGH, July 15, 2025 (GLOBE NEWSWIRE) -- Predictive Oncology Inc. (NASDAQ: POAI), a leader in AI-driven drug discovery, today issued the following shareholder update: To my fellow Shareholders, The past several weeks have been particularly noteworthy and pr ...

SAN DIEGO, July 15, 2025 /PRNewswire/ -- Neurocrine Biosciences, Inc. (Nasdaq: NBIX) today announced results from a new analysis using real-world data from CAHtalog®, a comprehensive registry of patients with classic congenital adrenal hyperplasia in the United States. The analysis demonstrated significant variability in glucocorticoid treatment regimens and frequent changes in health status and outcomes over time in both pediatric and adult patients. These results were presented at the Endocrine Society's ...

Core Insights - MiNK Therapeutics is pioneering allogeneic invariant natural killer T (iNKT) cell therapies, with a focus on treating solid tumors where conventional therapies have struggled [1][2] - The company’s lead product, agenT-797, has shown durable responses in patients with treatment-refractory solid tumors, demonstrating its potential as a next-generation therapy [3][4] Company Overview - MiNK Therapeutics is a clinical-stage biopharmaceutical company focused on developing iNKT cell therapies and precision-targeted immune technologies [7] - The company’s proprietary platform aims to restore immune balance and drive cytotoxic immune responses across various diseases, including cancer and immune-mediated disorders [7][9] Clinical Data - In a recent case, a patient with metastatic testicular cancer achieved complete remission after treatment with agenT-797 combined with anti–PD-1 therapy, remaining disease-free for over two years [3] - Ongoing Phase 2 trials in gastric cancer have shown that agenT-797 can activate the immune system, enhance tumor infiltration, and provide durable disease control in patients who previously failed immunotherapy [4] Unique Mechanism of Action - iNKT cells, when engineered with CARs, maintain their innate tumor-homing and immunomodulatory features while gaining antigen-specific precision, allowing for both direct tumor killing and broad immune reprogramming [5] - MiNK-215, an IL-15–armored, FAP-targeting CAR-iNKT therapy, is designed to penetrate fibrotic tumors and has shown promise in preclinical studies by enhancing T cell infiltration and depleting stromal barriers [6][8] Manufacturing and Scalability - The iNKT platform allows for scalable and cost-effective manufacturing, with the potential for off-the-shelf therapies that do not require complex conditioning or lymphodepletion [8][9]

PolyPid's proprietary and clinically validated, prolonged-release drug delivery technology aims to subcutaneously deliver GLP-1 for approximately 60 days, compared to current standard of care of weekly injections. The GLP-1 delivery platform expands PolyPid's product portfolio beyond the recently successful Phase 3 D- PLEX100 , demonstrating versatility of the Company's proprietary drug delivery platforms in multiple major therapeutic areas. PETACH TIKVA, Israel, July 15, 2025 (GLOBE NEWSWIRE) -- PolyPid Lt ...

Core Insights - SELLAS Life Sciences Group has successfully met all primary endpoints in its Phase 2 trial of SLS009 (tambiciclib) for relapsed/refractory acute myeloid leukemia (r/r AML) [1][3][4] Trial Design and Objectives - The Phase 2 trial was an open-label, single-arm, multi-center study assessing the safety, tolerability, and efficacy of SLS009 in combination with venetoclax and azacitidine at two dose levels: 45 mg and 60 mg [2] - The trial aimed for a target overall response rate (ORR) of at least 20% and a median survival of at least 3 months [2] Efficacy Results - The trial exceeded the target ORR of 20%, achieving an ORR of 44% among AML MR patients at the optimal 30 mg twice a week (BIW) dose and 50% in ASXL1-mutated AML MR patients [6][12] - Median overall survival (mOS) was reported at 8.9 months for AML MR patients and 8.8 months for those refractory to venetoclax-based regimens, significantly surpassing historical benchmarks of 2.4 months [6][12] Safety Profile - SLS009 was well tolerated, with no dose-limiting toxicities observed across all treatment arms, validating its safety profile [9][12] Future Development Plans - Based on the positive Phase 2 results, the company plans to advance SLS009 into a randomized trial targeting newly diagnosed AML populations, with enrollment expected to begin by Q1 2026 [3][10][13] - The upcoming trial will include two cohorts: one for patients unlikely to benefit from standard therapy based on molecular profiling and another for patients showing early resistance to treatment [13][14] Industry Context - The results from the trial highlight a significant advancement in treatment options for patients with r/r AML, addressing a critical unmet medical need in this patient population [11][12]

Oral PL7737 monotherapy produced rapid and significant weight loss after just 4 days of treatment Combination of oral PL7737 and tirzepatide resulted in additive weight loss effects IND-enabling toxicology program ongoing IND submission planned for 4Q2025; Clinical data expected in 1H2026PRINCETON, N.J., July 15, 2025 /PRNewswire/ -- Palatin Technologies, Inc. (OTCQB: PTNT), a biopharmaceutical company developing first-in-class medicines based on molecules that modulate the activity of the melanocortin rec ...

Core Insights - Abeona Therapeutics has activated a Qualified Treatment Center for ZEVASKYN, the first FDA-approved therapy for treating RDEB wounds with a single application [1][2] - ZEVASKYN is a gene-modified cellular therapy developed through a collaboration between Abeona Therapeutics and Stanford Medicine, receiving FDA approval in April 2025 [1][2] - The treatment is now available at Lucile Packard Children's Hospital Stanford and Lurie Children's Hospital of Chicago, marking a significant milestone in its commercial launch [2] Company Overview - Abeona Therapeutics is a commercial-stage biopharmaceutical company focused on developing cell and gene therapies for serious diseases, with ZEVASKYN being its flagship product for RDEB [7] - The company operates a fully integrated cGMP cell and gene therapy manufacturing facility in Cleveland, Ohio, which is responsible for the commercial production of ZEVASKYN [7] Product Details - ZEVASKYN (prademagene zamikeracel) is the first autologous cell sheet-based gene therapy for RDEB, addressing a severe skin disease caused by defects in the COL7A1 gene [3][4] - The therapy incorporates the COL7A1 gene into a patient's skin cells to produce functional type VII collagen, leading to clinically meaningful wound healing and pain reduction [3][4] Patient Support Initiatives - Abeona has established a comprehensive patient support program, Abeona Assist™, to help eligible patients access ZEVASKYN, including assistance with insurance benefits and logistical support [2]

Company Overview - Perspective Therapeutics, Inc. is a radiopharmaceutical company focused on advanced cancer treatments using proprietary technology that employs the alpha-emitting isotope Pb to target cancer cells specifically [2][3] - The company is also developing complementary imaging diagnostics that utilize the same targeting moieties, allowing for personalized treatment and optimized patient outcomes through a "theranostic" approach [2] Clinical Development - The company's melanoma (VMT01), neuroendocrine tumor (VMT-α-NET), and solid tumor (PSV359) programs are currently in Phase 1/2a imaging and therapy trials in the U.S. [3] - Perspective Therapeutics is expanding its regional network of drug product finishing facilities, supported by its proprietary Pb generator, to provide patient-ready products for clinical trials and commercial operations [3] Upcoming Financial Reporting - The company will report its second quarter 2025 financial results and provide a business update on August 13, 2025, before the market opens [1]

Group 1 - Futu Holdings Limited (FUTU) has seen a 7.4% increase in the Zacks Consensus Estimate for its current year earnings over the last 60 days [1] - Pan American Silver Corp. (PAAS) has experienced a 9% increase in the Zacks Consensus Estimate for its current year earnings over the last 60 days [1] - RAPT Therapeutics, Inc. (RAPT) has seen a significant increase of 72.1% in the Zacks Consensus Estimate for its current year earnings over the last 60 days [2] - Hamilton Insurance Group, Ltd. (HG) has experienced an 18.4% increase in the Zacks Consensus Estimate for its current year earnings over the last 60 days [2] - Invesco Ltd. (IVZ) has seen a 7.1% increase in the Zacks Consensus Estimate for its current year earnings over the last 60 days [3]

VANCOUVER, British Columbia, July 15, 2025 (GLOBE NEWSWIRE) -- Rakovina Therapeutics Inc. (“Rakovina” or the “Company”) (TSX-V: RKV) (FSE: 7JO0), a biopharmaceutical company advancing next-generation cancer therapies through artificial intelligence (AI)-powered drug discovery, is pleased to announce that its shares are now eligible for electronic clearing and settlement through The Depository Trust Company (DTC). DTC eligibility streamlines the process for U.S. investors to trade Rakovina shares, enhancing ...