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Jazz Pharmaceuticals to Present Compelling Clinical and Pre-Clinical Data Advancing Oncology Research at AACR 2026
Prnewswire· 2026-03-18 11:44
Core Insights - Jazz Pharmaceuticals is set to present significant clinical and pre-clinical data at the 2026 American Association for Cancer Research (AACR) Annual Meeting, showcasing advancements in its oncology portfolio, particularly with zanidatamab, dordaviprone, and JZP898 [1][2][3] Group 1: Zanidatamab Developments - Zanidatamab is a HER2-targeted bispecific antibody that has shown meaningful benefits for adult patients with previously treated, unresectable or metastatic HER2+ biliary tract cancer [3][7] - The NeoZanHER trial data indicate that zanidatamab treatment resulted in a statistically significant decrease in tumor size and volume, with 30% of patients achieving pathologic complete response [4][5] - Presentations will explore zanidatamab's utility across HER2-expressing solid tumors and innovative biomarker-driven clinical trial designs [4] Group 2: Dordaviprone Insights - Dordaviprone, a protease activator and dopamine D2 receptor inhibitor, is being evaluated for its efficacy in renal cell carcinoma and small-cell lung cancer models [2][6] - Presentations will include data on the synergistic effects of dordaviprone in reducing renal cell carcinoma cell viability [6] Group 3: JZP898 Overview - JZP898 is an investigational, conditionally activated interferon alpha-2b cytokine pro-drug designed for activation within the tumor microenvironment, currently in Phase 1 development [2][34] - Preclinical data supporting JZP898's activity and immune engagement will be presented, highlighting its potential in solid tumors [4][6] Group 4: Regulatory Designations and Approvals - Zanidatamab has received multiple FDA designations, including Breakthrough Therapy and Fast Track designations for various indications, emphasizing its potential in treating HER2+ cancers [8] - The FDA granted accelerated approval for zanidatamab in treating unresectable or metastatic HER2-positive biliary tract cancer based on overall response rate and duration of response [7][8]
Astellas To Present Pioneering Advances Across Its Portfolio and Pipeline at ESMO 2025
Prnewswire· 2025-10-01 06:00
Core Insights - Astellas Pharma is set to present significant clinical data at the ESMO congress, showcasing advancements in its oncology programs, particularly in muscle-invasive bladder cancer and hormone-sensitive prostate cancer [1][2][3] Astellas' Oncology Programs - The company will present ten abstracts, including new data for PADCEV (enfortumab vedotin) combined with pembrolizumab in muscle-invasive bladder cancer, which will be featured in an ESMO Presidential Symposium [1][2] - Final overall survival data for XTANDI (enzalutamide) in high-risk, biochemically recurrent non-metastatic hormone-sensitive prostate cancer will also be shared [1][2] Clinical Trials and Data - The EV-303 trial (KEYNOTE-905) will evaluate enfortumab vedotin plus pembrolizumab as neoadjuvant and adjuvant treatment in patients with muscle-invasive bladder cancer who are not eligible for cisplatin-based chemotherapy [3][4] - Long-term follow-up data from the EV-302 trial will explore the utility of enfortumab vedotin in patients with challenging baseline characteristics, including older patients and those with comorbidities [3][4] - The EMBARK trial will present final data assessing overall survival with enzalutamide in combination with leuprolide and as monotherapy in patients with non-metastatic hormone-sensitive prostate cancer [3][4] Innovative Treatments - Astellas is advancing its investigational bispecific T cell engager ASP2138, targeting CLDN18.2 in solid tumors, with initial clinical data being presented [2][3][5] - The company continues to explore treatment options for gastric and gastroesophageal junction cancers with new clinical data for ASP2138 [2][5]
Veeva and Sarah Cannon Research Institute Form Strategic Collaboration to Advance Oncology Clinical Trials
Prnewswire· 2025-06-04 11:03
Core Insights - Veeva Systems and Sarah Cannon Research Institute (SCRI) have formed a strategic collaboration to enhance the efficiency of oncology clinical trials across SCRI's 200+ research sites [1][2] - The adoption of Veeva Clinical Platform aims to unify SCRI's contract research organization (CRO) and site management organization (SMO) for improved data flow and trial processes [1][2] Company Overview - Sarah Cannon Research Institute is a leading oncology research organization with a focus on community-based clinical trials, having conducted over 850 first-in-human clinical trials and contributed to the majority of new cancer therapies approved by the FDA in the last decade [4] - Veeva Systems is recognized as the global leader in cloud software for the life sciences industry, serving over 1,000 customers, including major biopharmaceutical companies and emerging biotechs [5] Technology and Innovation - The Veeva Clinical Platform is a comprehensive solution that integrates various clinical operations and data applications, streamlining the clinical trial process from start to finish [3] - The collaboration is expected to standardize operations on a single platform, enabling SCRI to deliver faster and more cost-effective clinical trials [3]