Using Flow Cytometry in Biomanufacturing
Method Serves as a Powerful Tool for Analyzing Cells and Secreted Proteins in Suspension
Cell by Cell Mapping of the Cancer Transcriptome
Capturing Tumor Heterogeneity for Better Therapeutics and Diagnostics
Scaledown Keeps Processes on the Up and Up
Minireactors, Sampling Techniques, and Statistical Analyses Can Keep Optimization Conversations Going
Streamlining Stem Cell Manufacturing
The Factory System Will Help the Stem Cell Industry Standardize, Integrate, and Automate Unit Operations
Raising the Bar for Human Clinical Trials
Standards for authorizing first-time trials of drugs in humans are lax, and should be strengthened in several ways, McGill University researchers argue in a paper published in Nature. While regulators in North America and Europe evaluate safety before human trials can proceed, they do not currently demand meaningful evidence for potential efficacy, say the investigators.
Trials of ineffective therapies place burdens on society even if research participants aren't harmed directly, the researchers argue. Drug development soaks up financial and research resources; patients and healthy volunteers involved in testing a dud treatment miss out on more promising ones; and expenses wasted on ineffective therapies are often passed on to healthcare systems in the form of higher drug prices. The argument for better scrutiny of animal studies may be especially timely, since the incoming U.S. president has indicated he intends to weaken requirements for clinical evidence of efficacy before drugs are approved.