Deep clinical phenotyping, imaging ... All participants are made aware of the potential for industry collaboration in the participant information sheet and are specifically asked to provide consent to ...

Can you think of other elements that should be included in the MIST template to provide a good handover? Do you think any of the elements should be excluded? Can you see any value in receiving ...

CTX310 is in an ongoing Phase 1 first-in-human dose escalation clinical trial targeting ANGPTL3 in four patient ... and DL4 [0.8 mg/kg]) with at least 30 days of follow-up for each participant as of a ...

We aimed to explore the adverse effects of colonoscopy A&F using a feedback intervention theory (FIT) dark logic model before the National Endoscopy Database Automated Performance Reports to Improve ...

Introduction Early phase cancer clinical trials have become ... CONSENT will be a randomised controlled trial examining the effect of both a short (2 page), jargon-free, plain language participant ...

The trial protocol and all amendments were approved by the UK Health Research Authority (West Midlands Research Ethics Committee 13/WM/0419). Potential participants were provided with a participant ...

Over the last couple of quarters, we've taken several critical steps related to PAVmed's corporate structure and balance sheet ... one of the clinical sites was -- that wasn't a participant ...

A steering committee involving the research team, clinical staff and people with T1D will meet regularly to ensure the trial is conducted ... the study design and participant-facing documents (ie, ...

Most notably, the bipartisan bill ensures that the first $2,000 in payments a clinical trial sponsor provides to a participant is not subject to taxation and doesn’t count against income ...