MedPath

Clinical Trial News

GSK's GSK5764227 Receives FDA Breakthrough Therapy Designation for Osteosarcoma

  • GSK5764227, a B7-H3-targeted antibody-drug conjugate, has been granted Breakthrough Therapy Designation by the FDA for osteosarcoma treatment.
  • The designation aims to accelerate the development and review of GSK5764227 for relapsed or refractory osteosarcoma in adults.
  • This is the third regulatory designation for GSK5764227, highlighting its potential in treating serious conditions with limited therapeutic options.
  • The FDA's decision is based on preliminary clinical evidence suggesting substantial improvement over existing therapies for bone cancer.

Teva and IBM Watson Partner to Accelerate AI-Driven Drug Repurposing Initiative

  • Teva Pharmaceuticals and IBM Watson Health have launched a collaborative project using artificial intelligence to identify new therapeutic applications for existing drug compounds.
  • The partnership leverages Watson's cognitive computing capabilities to analyze Teva's compound portfolio, with initial focus on developing abuse-deterrent opioids and extended-release schizophrenia treatments.
  • The collaboration extends to developing predictive models for chronic conditions like asthma, incorporating weather data to help prevent disease exacerbations through patient-centric digital solutions.

Kymab and EpimAb Form Strategic Alliance to Develop Novel Bispecific Antibodies for Cancer Treatment

• UK-based Kymab partners with China's EpimAb Biotherapeutics, combining Kymouse antibody platform with FIT-Ig technology to develop innovative bispecific antibodies for immuno-oncology applications.
• The collaboration grants Kymab development rights outside China while EpimAb retains rights within China, with both companies eligible for milestone payments and royalties.
• The partnership aims to leverage Kymab's nine existing immuno-oncology projects and four therapeutic approaches, including NK- and T-cell activation and macrophage-mediated cancer cell destruction.

Nivolumab Shows Promise in Advanced Head and Neck Cancer Treatment

  • Nivolumab significantly extends survival in advanced head and neck cancer patients compared to chemotherapy, offering a new treatment option.
  • A clinical trial demonstrated that 36% of patients treated with nivolumab were alive after one year, versus 17% with chemotherapy.
  • Combination therapy of nivolumab and ipilimumab shows potential in reducing tumor size in advanced kidney cancer patients.
  • Immunotherapy, like nivolumab, harnesses the immune system to target and destroy cancer cells, with fewer side effects.

Ribociclib Shows Promise in Advanced Breast Cancer Treatment

• Ribociclib, a CDK 4/6 inhibitor by Novartis, significantly improved progression-free survival when combined with letrozole in patients with hormone receptor-positive advanced breast cancer. • The MONALEESA-2 trial demonstrated a 63.0% progression-free survival rate at 18 months for ribociclib plus letrozole, compared to 42.2% with letrozole alone. • Common side effects of ribociclib include neutropenia, infection, hair loss, diarrhea, and nausea, with a small percentage of patients experiencing a prolonged QT interval. • Ribociclib's efficacy and potential high cost raise questions about its accessibility and how it compares to similar drugs like palbociclib.

Strategic Framework for Early Asset Development: Integrating Clinical, Patient, and Commercial Value

• Early-stage pharmaceutical development faces significant challenges due to data gaps and evolving treatment landscapes, requiring teams to predict market conditions 5-10 years ahead.
• Successful asset development demands integration of three key value streams: clinical feasibility, patient benefits, and commercial viability, with emphasis on evidence-based decision making.
• Modern healthcare development increasingly prioritizes patient voice and real-world outcomes, while navigating an increasingly competitive reimbursement landscape with multiple approved therapies.

Verily Partners with Dutch Institutions to Launch Large-Scale Parkinson's Disease Study

  • Google's life sciences division Verily collaborates with Radboud University Medical Center and ParkinsonNet to study disease progression in 650 Parkinson's patients using advanced imaging and wearable technology.
  • The study aims to understand individual variations in Parkinson's disease progression and treatment response, potentially enabling more personalized treatment approaches for the 10 million affected globally.
  • Researchers will utilize real-time data collection through advanced brain imaging, molecular analysis, and wearable devices, with findings to be made freely available to Dutch hospitals and international researchers.

Inspiring Hope Ideathon Launches Global Initiative to Boost Clinical Trial Participation

  • INC Research and CISCRP partner to launch the Inspiring Hope Ideathon in Boston, aiming to generate innovative solutions for increasing clinical trial awareness and participation rates.
  • With clinical trial participation at just 5% of eligible patients and a current demand for 58 million trial participants, the initiative seeks to address a critical gap in medical research advancement.
  • The global competition has attracted over 70 entries worldwide, bringing together diverse stakeholders from technology companies, patient advocacy groups, and healthcare professionals to tackle trial recruitment challenges.

New Immunotherapy for Leukemia Shows Promise in Small Clinical Trial

A novel immunotherapy approach for acute myeloid leukemia (AML) has demonstrated promising results in a small clinical trial, showing a 50% response rate among patients with poor prognoses. The treatment involves 'training' natural killer (NK) cells in the lab to enhance their ability to attack leukemia cells, offering hope for patients with limited treatment options.

FDA Approves Sandoz's Erelzi as First Enbrel Biosimilar in US

  • Sandoz's Erelzi (etanercept-szzs) has received FDA approval as the first biosimilar to Amgen's Enbrel, covering all indications of the reference product for inflammatory diseases.
  • The approval marks a significant milestone in the US biosimilars landscape, potentially impacting the $5 billion annual US market for Enbrel.
  • The biosimilar approval aligns with healthcare cost reduction goals, with IMS Health projecting potential savings of up to $110 billion by 2020 across the US and five largest EU countries.

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.