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Staff push for fixes to the 988 hotline; custom gene therapy hints at new path to treat rare diseases

July 12, 2023
Molly Ferguson for STAT

One year into 988 hotline, staff push for fixes to ambitious new system

The national mental health hotline system is still working on securing funding and getting resources and response teams to people who need them.

By Theresa Gaffney


A young girl's custom gene therapy hints at a framework for tailored rare disease treatments

Individualized medicines, are often made to treat debilitating genetic conditions that are too rare to garner interest from pharma companies.

By Bree Iskandar


STAT+ | How are insurers handling the Alzheimer's drug Leqembi and related scans?

As a condition of coverage, Medicare also rolled out a new patient registry to collect more information from physicians prescribing Leqembi.

By Rachel Cohrs



Red blood cells from a person with sickle cell disease.
Jonathan Armstrong/Wellcome

Opinion: Sickle cell cures are coming. African children can't be left behind

Rolling out a new generation of sickle cell cures without a strategy to get them to those with the greatest need is not acceptable.

By Jayasree K. Iyer


STAT+ | Europe issues maximum antitrust fine of $475 million to Illumina over Grail deal

The fine comes after Illumina closed the deal to purchase Grail before getting regulatory clearance.

By Andrew Joseph


STAT+ | How to 'break the logjam'? Economists pitch a plan to curb dire drug shortages

The U.S. continues to see shortages of medicines. Marta Wosińka explains how changes to hospital purchasing and drug facilities could help.

By Ed Silverman


Listen: One Duchenne patient's bittersweet hope for new treatment

"For the older boys, we're running up against the clock a little bit with what we're able to do," says Hawken Miller, who has Duchenne.

By Torie Bosch


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