YPrime Awarded Global Phase II Oncology Clinical Trial Which Will Utilize Proprietary eClinical Supply Forecasting Tool Combined With IRT
BOSTON and MALVERN, Pa., April 7, 2015 /PRNewswire/ -- Y-Prime, Inc., announced today that it has been awarded an international Phase II clinical trial to assess a new treatment for patients with Non-Small Cell Lung Carcinoma (NSCLC). This study will be conducted utilizing their proprietary eClinical Supply Forecasting tool (eCSF), along with their state-of-the-art Interactive Response Technology (IRT).
Throughout this trial, YPrime will be supporting world class selected sites to conduct the study with data driven metrics pulled from these tools. YPrime is dedicated to applying its leading edge eClinical technology to help forward unmet medical needs in the Biotech and Pharmaceutical industry.
"Our team is very pleased to continue helping Biotech and Pharmaceutical companies track patient activity and ensure the clinical supply chain runs smoothly with international studies. We have added significant value by playing a critical role in the successful integration of eClinical solutions for this virtual Biopharma organization." said Shawn Blackburn, President and Co-founder of YPrime.
Including Women of Childbearing Age in Clinical Research
March 26th 2024In recognition of International Women's Month, we're featuring this recent talk between Associate Editor Miranda Schmalfuhs and Marie Teil, Global Head of UCB’s Women of Childbearing Age Program. They speak about the specific challenges women with chronic illnesses face when accessing appropriate treatment and participating in clinical trials, UCB's Women of Childbearing Age Program and it’s most successful strategies, and much more.
Improving Engagement While Maintaining Data Integrity & Validity
March 19th 2024In recognition of Women's Health Month, we're featuring this recent talk between Associate Editor Miranda Schmalfuhs and uMotif's Chief Product Officer, Julia Lakeland, discuss new technologies improving patient engagement and reducing the emotional and logistical burdens of participation, ethical considerations that should be addressed when implementing those technologies, while ensuring patient privacy, and much more.
