Disc Medicine Rare Disease Drug Picked for Faster Regulatory Review Is Rejected by the FDA
The FDA requires Phase 3 APOLLO trial results to confirm bitopertin’s clinical benefit for erythropoietic protoporphyria, delaying approval despite a 40% biomarker reduction in Phase 2 data.
5 Articles
5 Articles
Disc Medicine Rare Disease Drug Picked for Faster Regulatory Review Is Rejected by the FDA
The FDA asked for more data to determine whether Disc Medicine’s bitopertin is benefiting patients with erythropoietic protoporphyria, a rare blood disorder. Analysts say it’s a surprising delay considering bitopertin is one of the first drugs in a new FDA pilot program that speeds up regulatory review of medicines deemed critical for national security or public health. The post Disc Medicine Rare Disease Drug Picked for Faster Regulatory Review…
FDA rejects Disc Medicine's rare disease drug despite granting it a commissioner voucher
The rejection of Disc Medicine’s rare disease treatment marks the first negative outcome of the FDA's controversial voucher program and suggests drugs that are selected won't be guaranteed an approval. Disc's bitopertin was an early ...
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