Feb. 24, 2016, Rochester, NY - iCardiac Technologies, Inc., a market leader in the conduct of respiratory and cardiac safety studies, today announced it was awarded and is now enrolling patients in the largest late phase respiratory and cardiac safety study in the company’s history.
The three-year clinical trial will be conducted at sites across 28 countries and will include approximately 340,000 pulmonary function tests and 90,000 ECG reviews. iCardiac acquired the clinical trials division of nSpire Health in July 2015 and now offers both respiratory and cardiac safety assessment services to drug developers.
“iCardiac has the capacity and the expertise to support sponsors whether they are doing a small Phase II study with 10 sites or a large study with 750 sites,” said Brian Smith, Vice President of Project Operations, at iCardiac. “And whether a study is large or small, iCardiac continues to set itself apart based on our dedication to flexibility and study support, as well as the innovation embedded in our technology.”
About iCardiac Technologies:
iCardiac Technologies, Inc. is an industry-leading centralized core laboratory for cardiac safety and respiratory services. Its high precision cardiac safety assessment methodology has set a new standard for precision and accuracy in all phases of clinical trials. The company serves 8 of the top 10 global pharmaceutical companies, as well as numerous small and mid-sized pharma and biotechnology firms. For more information, please visit: www.icardiac.com.
Unifying Industry to Better Understand GCP Guidance
May 7th 2025In this episode of the Applied Clinical Trials Podcast, David Nickerson, head of clinical quality management at EMD Serono; and Arlene Lee, director of product management, data quality & risk management solutions at Medidata, discuss the newest ICH E6(R3) GCP guidelines as well as how TransCelerate and ACRO have partnered to help stakeholders better acclimate to these guidelines.
Merck Launches Phase III Trials of Once-Monthly Oral HIV PrEP Candidate MK-8527
July 14th 2025In the new EXPrESSIVE clinical trial program, Merck will evaluate MK-8527, a once-monthly, oral PrEP therapy, in populations at high risk of HIV-1 infection, including adolescent girls and women in sub-Saharan Africa.
Baxdrostat Shows Significant Blood Pressure Reduction in Phase III BaxHTN Trial
July 14th 2025In the BaxHTN Phase III study, AstraZeneca’s baxdrostat demonstrated statistically significant and clinically meaningful reductions in systolic blood pressure in patients with uncontrolled or treatment-resistant hypertension.