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Dispute over Duchenne gene therapy highlights thorny access issues 

September 27, 2024
Pharmalot Columnist, Senior Writer
Sarah Jenssen
Courtesy Deb Jenssen

Dispute over Duchenne gene therapy highlights thorny access issues

Elevidys, a gene therapy developed by Sarepta Therapeutics, has received FDA approval. But insurers are not always quick to provide coverage

By Andrew Joseph


STAT+ | Regeneron, Sanofi blockbuster Dupixent wins FDA approval for COPD

Market analysts have estimated that the new COPD indication could bring in more than $1 billion in additional annual revenue for Dupixent

By Jonathan Wosen


STAT+ | FDA approves schizophrenia drug that could alter how disorder is treated

Cobenfy works by stimulating a pair of muscarinic receptors in the brain, that, in turn, control the release of acetylcholine. 

By Adam Feuerstein



Adobe

STAT+ | Cassava Sciences and former execs, facing SEC charges for misleading claims, agree to fines

Cassava was charged Thursday by the SEC with making misleading claims in 2020 about trials for its Alzheimer's drug, and agreed to pay fines.

By Jonathan Wosen


Sickle cell community scrambles to find safe plan after a drug is pulled from the market

Everyone was caught between two possibilities: Taking the drug might put patients at risk, but abruptly stopping the drug could put patients at risk, too.

By Eric Boodman


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