📊 Shifts in global clinical trial distribution: Europe's share declines across most segments, while China sees growth, except in biosimilars. More on these regional trends from our Rethinking Clinical Trial Country Prioritization report: https://t.co/QT1YqhDiH3. #ClinicalTrials
What else is needed in the near-term to change the trajectory of the past five years and increase Europe’s share of global oncology trial sites ? #ESMO24
The latest performance data from the UK’s MHRA reveal that clinical trial applications continue to be handled within the target statutory timescales - average of 27 days compared with the statutory timescales of 30 days)
https://t.co/QKUpD7JjHk
The patient perspective on dose optimization for anticancer treatments: A new era of cancer drug dosing— Challenging the “more is better” dogma https://t.co/CtB6DYlaRC
Noteworthy advances in oncology R&D shared during #ASCO24 enhancing the art of cancer care and potentially transforming treatment approaches for patients... https://t.co/LnTGUX7hRx
Although careful consideration is necessary to determine which #clinicaltrials in #oncology are well suited for inclusion of pragmatic design features, there is growing momentum to simplify, broaden access and increase generalizability of study data.... https://t.co/69dfzuccw1
❓As increasing molecular subtyping continues to turn even some common tumour types a set of rare diseases, is there a way to make just-in-time site activation live up to its promise through reducing the administrative and regulatory burden for sites ?
Some key takeaways:
1️⃣: Multiple targeted agents are available across many different tumours, with many more in development, but most patients just aren’t getting tested and so aren’t getting optimal care…
🔬Happening Now: IQVIA Institute Pre-ASCO Symposium in Chicago & virtually. We are discussing the future of precision oncology, including clinical trial site selection, recruitment challenges, real-world data needs, testing practices, and ensuring patient access. #Oncology
❓How do we turn the real world data often buried in medical notes into real world evidence that is generalizable to bring precision medicine clinical trials to patients ?