ERT to Acquire PHT Corporation

February 27, 2015
Applied Clinical Trials Editorial Staff

Applied Clinical Trials

PHILADELPHIA and BOSTON – February 27, 2015 –– ERT, a leading global solution provider for high- quality patient safety and efficacy endpoint data collection, and PHT Corporation (PHT), the eClinical innovator leading the adoption of patient-driven mobile apps for improved clinical research, announced today that they have signed a definitive agreement under which ERT will acquire PHT. Financial terms of the transaction were not disclosed.

The transaction combines the flexible eCOA platform and world-class customer service of PHT with the leading clinical trial technology and service offerings of ERT, creating the most innovative and comprehensive solution for patient endpoint collection and data analytics for global clinical trials.

“We are thrilled to announce this strategic merger with PHT,” said Jim Corrigan, President and CEO of ERT. “This combination is about better serving our customers and delivering solutions to support the tremendous growth projected for the eCOA industry. By joining forces we are creating a truly innovative eCOA offering with global reach across therapeutic areas. Additionally, the transaction accelerates our strategy of innovating better health by becoming the software-enabled solution provider of choice; supporting clinical trials from early phase through regulatory submission and post-market research; and adding to our existing eCOA, respiratory, cardiac and data analytics portfolio.”

“This is a compelling combination that brings together two industry pioneers committed to using technology to transform clinical research and help bring new therapies to market,” said Philip Lee, President and CEO of PHT. “Our two companies share the same entrepreneurial drive, culture of innovation and unwavering focus on customer success and together we will be very well positioned to deliver best-in-class solutions to support patient-centric data collection in clinical trials.”

The combined company will have an increased global footprint throughout North America, Europe and in Asia, while serving all phases of clinical research for small and mid-sized biopharma to CROs and large pharmaceutical companies, including the top 30 pharmaceutical companies in the world. The combined scientific and regulatory expertise as well as the deep technical and operational teams in place will continue to bring innovative, patient-centric solutions to the clinical research industry.

The transaction is subject to regulatory review and is expected to close within the next several weeks. 

About ERT

ERT (www.ert.com) is a leading provider of high-quality patient safety and efficacy endpoint data collection solutions for use in clinical drug development. ERT delivers a combination of technology, services, and consulting that increase the accuracy and reliability of patient data and improve the efficiency of the clinical development process throughout the product lifecycle. ERT delivers the most widely deployed solutions in centralized cardiac safety, respiratory services, suicide risk assessment and Clinical Outcome Assessments (COAs) – which includes patient, clinician, and observer reported outcomes as well as data analytics across the trials. By efficiently integrating these solutions through a system built upon a scientific and regulatory foundation, ERT collects, analyzes, and delivers safety and efficacy data critical to the approval, labeling, and reimbursement of pharmaceutical products. ERT is a global organization with headquarters in Philadelphia, PA and offices throughout the U.S., U.K., Japan, and Germany.

About PHT Corporation

PHT Corporation is the eClinical innovator leading the adoption of patient-driven mobile apps for improved clinical research. The PHT electronic clinical outcome assessment (eCOA) system collects and reports secure real-time patient data from the latest mobile devices. PHT scientific, regulatory and technological expertise combined with quality outcomes data enable clients to make research decisions with confidence. Sponsors and CROs have leveraged the PHT Patient Suite in 750+ trials resulting in 22 regulatory approvals. PHT is headquartered in Boston and an office in Geneva. 

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