Ipsen delivers strong results in 2025, driven by solid execution across all therapeutic areas, and provides 2026 guidance

On February 12, 2026 Ipsen, a global specialty-care biopharmaceutical company, reported its financial results for the full year (FY) 2025 and for the fourth quarter of 2025.

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(Press release, Ipsen, FEB 12, 2026, View Source [SID1234663550])

FY 2025 results

On February 12, 2026 Ipsen reported full year 2025 results.

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(Presentation, Ipsen, FEB 12, 2026, View Source [SID1234663546])

Orion Full-Year 2025 Result Presentation

On February 12, 2026 Orion reported Full-Year 2025 Results.

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(Presentation, Orion, FEB 12, 2026, View Source [SID1234663023])

NeoGenomics Introduces PanTracer Pro to Support Timely, Informed Solid Tumor Therapy Selection

On February 12, 2026 NeoGenomics, Inc. (NASDAQ: NEO), a leading provider of oncology diagnostic solutions that enable precision medicine, reported the availability of PanTracer Pro, a new addition to the PanTracer Family, designed to help clinicians navigate increasingly complex molecular testing workflows to make informed decisions for patients with advanced-stage solid tumors.

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As precision oncology continues to evolve, clinicians face growing diagnostic complexity, increasing biomarker requirements, and mounting pressure to initiate treatment quickly, often before a complete molecular profile is available. Fragmented testing workflows, sequential ordering, and tissue limitations can delay care and introduce uncertainty at critical decision points. PanTracer Pro was developed to address these challenges more comprehensively and earlier in the diagnostic pathway.

"Every delay or unanswered question in the diagnostic process can affect how quickly patients begin treatment," said Tony Zook, chief executive officer at NeoGenomics. "PanTracer Pro is designed to help clinicians get the information they need earlier and more reliably, so care teams can plan next steps with greater clarity and confidence across the care journey."

PanTracer Pro integrates broad, comprehensive genomic profiling (CGP) with diagnosis-directed immunohistochemistry (IHC) and ancillary testing selected based on tumor type. By delivering comprehensive, guideline-aligned insights through a single coordinated order, PanTracer Pro enables physicians to ensure relevant biomarkers are assessed upfront rather than through multiple, sequential tests. Turnaround time for the test is 8–10 days, supporting timely real-world treatment decisions.

Beyond streamlining test selection, PanTracer Pro may help identify clinically relevant biomarkers that can be missed with incomplete testing. The ability of PanTracer Pro to combine broad DNA and RNA sequencing across more than 500 cancer-related genes with tumor-specific ancillary testing supports therapy selection, helps identify potential clinical trial options, and facilitates personalized treatment planning based on a patient’s unique tumor biology. When tissue samples are insufficient or unavailable, cases can automatically reflex to PanTracer LBx, NeoGenomics’ pan-solid tumor liquid biopsy assay, allowing clinicians to continue diagnostic workup without restarting the process.

(Press release, NeoGenomics Laboratories, FEB 12, 2026, View Source [SID1234662657])

SURGE Therapeutics Completes Phase 1 Dosing of First-in-Category Intraoperative Immunotherapy and Prepares for Registrational Trial

On February 12, 2026 SURGE Therapeutics (SURGE), a clinical-stage oncology company pioneering intraoperative immunotherapy, reported the final patient has been dosed in its Phase 1 clinical trial of SRG-514, an investigational therapy for breast cancer patients undergoing surgery. The treatment was generally well tolerated in the Phase 1 dose-escalation study, and there were no treatment-related dose-limiting toxicities or treatment-related serious adverse events to date. Based on the data generated to date and discussions with the FDA, the company is preparing to advance SRG-514 directly into a registrational trial.

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SRG-514 is designed to deliver immunotherapy intraoperatively, directly into the resection cavity during the time of tumor removal. The therapy aims to reprogram the local inflammatory response from immunosuppressive to immunostimulatory, with the goal of generating a durable, systemic anti-tumor immune response when tumor burden is at its lowest.

"Intraoperative immunotherapy represents a fundamentally different approach to treating cancer," said Michael Goldberg, Ph.D., CEO & Founder, SURGE Therapeutics. "With SRG-514, we are targeting primary drivers of cancer mortality – post-surgical recurrence and metastasis – by improving how, when, and where immunotherapy is delivered. We are encouraged by the data generated to date and by the broader potential of our programs to serve as pipelines-in-a-product."

"One of the most persistent challenges in oncology is that microscopic disease can remain even after successful tumor removal and later drive cancer recurrence, both locally and distally," said Robert Langer, Sc.D., Institute Professor at MIT and Chair of SURGE’s Scientific Advisory Board. "Applying established principles of drug delivery in the intraoperative setting creates a powerful opportunity to influence immune responses where and when intervention may have the greatest impact."

SRG-514 is a novel thermosensitive formulation of ketorolac, a non-steroidal anti-inflammatory drug commonly used perioperatively. By intervening during surgery, the therapy is designed to provide extended, localized release directly at the tumor resection site and may counteract surgery-induced immune suppression, a biological process that can promote recurrence and metastasis.

Post-surgical recurrence remains one of the most significant unmet needs in oncology, as 90% of cancer-related deaths are driven by local recurrence and metastasis. Each year, approximately 9 million cancer patients worldwide undergo surgical tumor resection, yet an estimated 40% of patients experience disease recurrence within five years. While surgery triggers acute inflammation, standard post-operative therapies are typically not administered until several weeks after surgery, allowing residual cancer cells time to develop strategies to evade immune surveillance.

SURGE’s proprietary SURGERx platform uses an injectable, biodegradable hydrogel optimized for intraoperative administration to deliver a drug in a highly concentrated manner.

The company expects to initiate a registrational trial of SRG-514 in triple-negative breast cancer this year, with potential expansion into additional breast cancer and solid tumor indications. In parallel, the company is advancing two additional intraoperative immunotherapy programs – STM-416 and STM-416p, utilizing the TLR7/8 agonist resiquimod, in bladder cancer and prostate cancer, respectively. Both programs are expected to enter Phase 2 clinical trials this year.

These programs highlight SURGE’s mission to transform surgery from a purely physical intervention into a therapeutic modality to deliver localized immunotherapy to potentially improve patient outcomes.

(Press release, SURGE Therapeutics, FEB 12, 2026, View Source [SID1234662656])