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Clinical Trial News

Expanding Innovations Receives FDA Clearance for N-GAGE Lumbar Plate System

  • Expanding Innovations received U.S. FDA 510(k) clearance for its N-GAGE Lumbar Plate System, marking the company's first spinal fixation platform.
  • The modular system offers spine surgeons a flexible fixation solution for lateral and anterolateral lumbar fusions using NON-SCREW-based technology.
  • The N-GAGE Plate uniquely pairs with the X-PAC LLIF Expandable Interbody Cage System via a NON-SCREW-based Polyaxial Coupler.
  • This regulatory milestone represents the company's transition from a product-based technology company to a complete procedural solutions provider.

Applied DNA Sciences Announces Leadership Transition as CEO Dr. James Hayward Retires After 20-Year Tenure

  • Applied DNA Sciences announced the retirement of Chairperson and CEO Dr. James A. Hayward effective June 18, 2025, following a distinguished 20-year term leading the biotechnology company.
  • President and COO Judy Murrah has been appointed as the new Chairperson of the Board of Directors and CEO, bringing over a decade of operational leadership at Applied DNA.
  • The leadership transition comes as Applied DNA focuses on its biotherapeutic manufacturing capabilities and seeks to address manufacturing challenges in the nucleic acid therapeutics industry.
  • Ms. Murrah previously held strategic roles at Symbol Technologies and Motorola, contributing to Symbol's growth to approximately $2 billion in revenue and 5,000 employees.

SaverOne Receives US Patent for Advanced Sensor Fusion Technology to Combat Driver Distraction

  • SaverOne 2014 Ltd. has been granted US Patent 12,326,512 for a sensor fusion system that detects and classifies mobile device usage within vehicle cabins to enhance driver safety.
  • The patented technology combines Radio Frequency-based location detection with non-RF sensor data to distinguish between driver and passenger mobile device usage in real-time.
  • This marks SaverOne's 14th granted patent out of a portfolio of 23 patents and applications, strengthening the company's position in transportation safety technology.
  • The innovation addresses a critical safety issue, as mobile phone-related accidents account for approximately 25% of road incidents and cost the US $870 billion annually according to federal data.

Blue Biofuels Secures Seventh U.S. Patent for Cellulose-to-Sugar Technology

  • Blue Biofuels has been granted its seventh U.S. patent, strengthening its intellectual property portfolio for biofuel technologies with 25 additional patent applications pending.
  • The new patent reinforces protection for the company's proprietary Cellulose-to-Sugar (CTS) technology, which converts plant materials into biofuels including ethanol and sustainable aviation fuel.
  • CEO Ben Slager emphasized that the patent demonstrates the strength of their CTS technology and secures competitive advantage as they scale toward commercial deployment.
  • The CTS process can utilize diverse biomass sources including agricultural waste, grasses, and forestry products, offering a sustainable alternative to food crop-based ethanol production.

Medibank Partners with Emyria to Fund Innovative PTSD Treatment Program in Australian Healthcare First

  • Medibank, Australia's largest private health insurer, has entered a multi-year partnership with Emyria to fund the Empax PTSD care program, marking the first time a major private health insurer has funded an ethics-approved, psychiatrist-led trauma therapy program.
  • Eligible Medibank members can now access the comprehensive trauma care program with no out-of-pocket costs at Perth Clinic, with treatment typically valued between AUD $20,000 and AUD $30,000.
  • The Empax model integrates psychiatrist-supervised therapy, specialist care coordination, and continuous real-world data collection, addressing the urgent need for innovative mental health treatments as PTSD affects approximately one in 11 Australians.
  • Independent evaluation by Professor Paul Fitzgerald from Australian National University will assess clinical effectiveness and health economics to build the case for broader reimbursement and systemic adoption.

OCCAM Immune and Cancer Research Institute Form Strategic Partnership to Advance Personalized Immunotherapy

  • OCCAM Immune, a Mount Sinai initiative, has partnered with the Cancer Research Institute to establish long-term immune monitoring across clinical trials, aiming to identify which patients benefit most from specific immunotherapies.
  • The collaboration will begin with a clinical trial in platinum-resistant high-grade serous ovarian cancer, analyzing 160 blood samples and tumor biopsies using RNA/DNA sequencing and immune cell mapping technologies.
  • This partnership combines CRI's decades of immunotherapy experience and global clinical trial access with OCCAM Immune's advanced immune profiling tools to accelerate personalized cancer treatment development.
  • The initiative addresses the critical challenge that immunotherapy doesn't work for all patients, seeking to understand immune system responses to therapy for more precise treatment matching.

Sartorius Stedim Biotech Completes Major Manufacturing Expansion in France to Meet Growing Bioprocessing Demand

  • Sartorius Stedim Biotech has completed a multi-year capacity expansion project at its Aubagne headquarters, nearly doubling cleanroom space to 9,000 square meters with automated production lines for single-use bioprocessing bags.
  • The expansion includes a new 12,000-square-meter automated warehouse facility and 1,900-square-meter cross-functional lab space for product development and customer training, with total site area quadrupling to 90,000 square meters since 2020.
  • The company has invested significantly in sustainable manufacturing practices, achieving ISCC Plus certification for renewable raw materials and ISO 14001 environmental management standards while doubling its French workforce to 1,400 employees over the past decade.

Castle Biosciences and SciBase Partner to Develop AI-Powered Atopic Dermatitis Flare Prediction Test

  • Castle Biosciences and SciBase have signed a collaboration agreement to develop a diagnostic test that predicts flares in atopic dermatitis patients using SciBase's AI-powered Electrical Impedance Spectroscopy technology.
  • The partnership targets up to 24 million atopic dermatitis patients in the United States who experience flares despite maintenance treatment, aiming to enable pre-symptomatic intervention.
  • Castle Biosciences will invest approximately $19 million in SciBase shares and receive North American territory rights, while SciBase retains EU and other international markets.
  • The collaboration leverages Castle's existing dermatology portfolio and commercial infrastructure to expand diagnostic solutions for skin barrier dysfunction affecting over 500 million people globally.

Medtech Products Recalls Little Remedies Honey Cough Syrup Nationwide Due to Bacterial Contamination

  • Medtech Products Inc. voluntarily recalled five lots of Little Remedies Honey Cough Syrup due to contamination with Bacillus cereus bacteria and loss of shelf-stability.
  • The recalled 4 FL OZ bottles were distributed nationwide from December 2022 through June 2025, with no serious adverse events reported to date.
  • Bacillus cereus can cause foodborne illness symptoms including nausea, vomiting, stomach cramps, and diarrhea, with potential for death at high exposure levels.
  • Consumers should stop using recalled products immediately and contact healthcare providers if they experience related symptoms.

City of Hope Receives $23.7 Million ARPA-H Grant to Map Immunotherapy Resistance in Lung Cancer

  • City of Hope has been awarded up to $23.7 million by ARPA-H to create a biomap of tumor changes causing immunotherapy resistance in advanced non-small cell lung cancer.
  • The six-year clinical trial will enroll 535 patients and use real-time monitoring techniques including liquid biopsies and single-cell sequencing to track tumor evolution.
  • Researchers aim to improve progression-free survival by 50% in at least one patient group by adapting treatments as resistance develops.
  • The project addresses the limited reliability of current biomarkers, with existing immunotherapy response rates below 40% in NSCLC patients.

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