ClinPhone will be exhibiting its complete range of clinical trial technology services at the 42nd DIA Annual Meeting.
Technologies being showcased at booth # 1009 include ClinPhone's TrialWorks®, ePRO (Electronic Patient Reported Outcomes), ClinPhone's integration suite for Electronic Data Capture Systems (EDC) and Clinical Trial Management Software (CTMS), Randomization and Trial Supply Management services. ClinPhone will also be launching an exciting new service which is to be announced during the show.
Showcasing at booth # 1009 will be ClinPhone's TrialWorks®, our enterprise-level, globally scalable Web-based CTMS. This user-friendly system is used by more pharmaceutical, biotech and CRO organizations than any other CTMS, and supports our clients in the day-to-day tracking, reporting and management of regulatory and clinical information. Two ancillary components will also be available: the Universal Transfer Tool (UTT), used to import relevant data from other clinical trial technologies, and our new TrialWorks® Monitoring Module (TMM), which allows monitors/CRAs to work offline and to automatically create monitoring reports. TrialWorks®, the UTT, and the TMM collectively enable ClinPhone to offer its customers the "total" clinical trial management solution.
ClinPhone is also promoting its ePRO solution at DIA which delivers real-time, cost-effective electronic patient reported outcomes data. The 21 CFR part 11 compliant technology eliminates concerns over limitations on data quality and integrity of paper diaries and questionnaires by using the company's powerful Interactive Voice Response (IVR) system. ClinPhone ePRO is simple and intuitive to use, offering unparalleled diary compliance, study site access to patient data and simultaneous application in an unlimited number of languages and countries.
Also being demonstrated at booth # 1009 is ClinPhone's integration technology for EDC and CTMS systems. This offers customers a flexible interface between their EDC and/or CTMS software and ClinPhone's real-time trial management systems. This application creates an environment where critical randomization and dispensing data are seamlessly shared between systems in real-time. Unlike other integration solutions, ClinPhone's enables data to originate in either system and also offers protocol-specific integration touch-points.
Driving Diversity with the Integrated Research Model
October 16th 2024Ashley Moultrie, CCRP, senior director, DEI & community engagement, Javara discusses current trends and challenges with achieving greater diversity in clinical trials, how integrated research organizations are bringing care directly to patients, and more.
Obe-Cel Achieves High Response Rates, Durable Outcomes in r/r B-Cell Acute Lymphoblastic Leukemia
December 3rd 2024CAR T-cell therapy obecabtagene autoleucel produced high response rates, durable outcomes, and low toxicity in adult patients with relapsed or refractory B-cell acute lymphoblastic leukemia, especially benefiting those with low-to-intermediate bone marrow burden.
AI in Clinical Trials: A Long, But Promising Road Ahead
May 29th 2024Stephen Pyke, chief clinical data and digital officer, Parexel, discusses how AI can be used in clinical trials to streamline operational processes, the importance of collaboration and data sharing in advancing the use of technology, and more.
Opdivo plus Yervoy Significantly Outperforms Chemotherapy in MSI-H/dMMR Metastatic Colorectal Cancer
December 2nd 2024Phase III CheckMate 8HW trial results demonstrated that the combination of Opdivo (nivolumab) and Yervoy (ipilimumab) significantly improves progression-free survival and has a better safety profile compared to chemotherapy in the first-line treatment of MSI-H or dMMR metastatic colorectal cancer.