PHT Selects HP ElitePad 1000 for its SitePad® System
PHT announced it has selected the Hewlett Packard (HP) ElitePad 1000 G2 with Windows 8.1 for its SitePad® System.
PHT announced it has selected the Hewlett Packard (HP) ElitePad 1000 G2 with Windows 8.1 for its SitePad® System. The SitePad System is used to collect clinician-driven endpoints such as disease progression, impression and assessments as well as patient reported outcomes and quality of life data directly from patients. The SitePad is configured to the requirements of clinical protocols and the study specific data collected is sent securely to StudyWorks™, the PHT online portal for real-time information about study compliance, operations and patient safety monitoring.
Using Patient Reported Outcomes in Dermatology Trials
April 25th 2024In part 3 of this video interview with ACT editor Andy Studna, Melissa Mooney, director, eCOA sales engineering, IQVIA sheds light on the unique challenges of dermatology trials and how clinical outcome assessments can be implemented in them.
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.
FDA Grants Ziftomenib with Breakthrough Therapy Designation for NPM1-Mutant Acute Myeloid Leukemia
April 23rd 2024Data from the Phase Ib portion of the KOMET-001 trial showed that the once-daily oral treatment may provide a substantial improvement over available therapies for relapsed/refractory NPM1-mutant acute myeloid leukemia.
