Can a plasma-based treatment boost Gilead’s remdesivir? NIH starts phase 3 trial to find out

When the first placebo-controlled data for Gilead’s remdesivir came out, analysts agreed it was no “silver bullet” for COVID-19. But it didn’t have to be, said Gilead CEO Daniel O’Day, who saw it as a steppingstone to other treatments and one that could even be combined to work better. Now, the National Institutes of Health (NIH) will test that theory as it kicks off a global study pairing the antiviral drug with plasma-based treatments.

How will Alkermes’ schizophrenia prospect affect those on opioids? FDA raises concerns ahead of AdComm

An FDA decision is looming for Alkermes’ ALKS 3831, a treatment for schizophrenia and bipolar I disorder that adds an opioid antagonist to a well-known antipsychotic to negate the weight gain and metabolic issues that come with the latter. An FDA panel will meet Friday to help the agency decide the treatment’s fate—and their major focus will be how the opioid antagonist will affect patients also taking opioids like morphine or oxycodone.

Scribe Therapeutics emerges with $20M, Biogen pact to clear CRISPR hurdles

CRISPR evolved in bacteria as a form of “genetic vandalism,” as George Church, Ph.D., puts it, to fend off pathogens. That means it works very well in bacteria but runs into various obstacles when researchers try to put it to work in humans. Jennifer Doudna’s latest CRISPR company plans to surmount those hurdles with an entirely new CRISPR platform that does not rely on molecules found in nature.

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