News

ONO will be conducting a series of clinical trials in Japan to assess the safety and efficacy of using OPDIVO for a wide range of additional indications, including head and neck cancer.

GuideStar will collaborate with ACRES on its Site Accreditation Standards Initiative as a Strategic Ally.

Radiant Sage has partnered with Oslo, Norway-based imaging CRO Clearpoint Image Review Center to provide expanded imaging operations.

This case study describes how innovative structural design at a study site is leveraging innovative telehealth technologies and nursing home infrastructures to recruit and retain Alzheimer’s patients.

Because identifying and communicating with patients who are willing to participate in trials can be a significant challenge, Synexus says it is keen to adopt a streamlined process that offers consistency across multiple channels.

Slightly more than a thousand healthcare research projects were funded by the European Union between 2007 and 2013, at a cost of $6 billion, revealed Carlos Moedas, European Commissioner for Research, Science and Innovation, at the end of January.

New approach focuses on assessing the effectiveness of four key areas related to risk-minimization and pharmacovigilance activities in Europe.

Survey spotlights the concern levels associated with the adoption of clinical trials using wearable technology.

Study shows sharp reduction in market exclusivity periods for first-in-class treatment entrants.

Search-engine data offers window to public consciousness around clinical trial research, participation.

This three-step process can help managers accurately assess how patient-centric their trials really are.

Despite wealth of data collected, many inefficiencies exist in the site-sponsor transfer of insights from clinical trials.

Analysis of the largest antihypertensive trial ever offers useful blueprint for sites in boosting subject enrollment.

Survey takes deep dive into enrollment hurdles, aims to inform future recommendations for improvement.

Measuring clinically relevant response requires routine and regular collection of outcomes data.

Click the title above to open the Applied Clinical Trials February/March 2016 issue in an interactive PDF format.

French safety authority confirms what had been speculated--Phase I volunteers received the fifth of the highest dose escalation of the investigational drug at the same time, which goes against EMA recommendations.

Oracle will participate as a Global Impact Partner (GIP) and will participate on the SCRS Global Impact Board at an executive level, and work closely with SCRS’ Leadership Council to determine strategic initiatives for SCRS.

Bioclinica has built a post-approval study-specific technology platform along with a Program Coordinating Center (PCC) with dedicated and experienced post-approval research staff.

The alliance’s primary goal is to be flexible and adaptive based on client needs, while mitigating client risk, driving efficiency and improving timelines, and removing barriers that prevent getting treatments to market in a timely fashion.

A "can’t live with them, can’t live without them" attitude is revealed in survey of standard operating procedures in the management and conduct of clinical trials.

In addition to the patient education database, guidelines for the interaction of patient organizations with ethics, health technology assessment, regulatory bodies and industry are being developed with the goal of being released later in the year.