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News

FDA, DAWNZERA and hereditary angioedema

Digest more
 · 1d
DAWNZERA™ (donidalorsen) approved in the U.S. as first and only RNA-targeted prophylactic treatment for hereditary angioedema
Ionis Pharmaceuticals, Inc. (Nasdaq: IONS) announced today that the U.S. Food and Drug Administration (FDA) has approved DAWNZERA™ (donidalorsen) for prophylaxis to prevent attacks of hereditary angioedema (HAE) in adult and pediatric patients 12 years of age and older.

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PharmExec · 12h
FDA Approves Ionis Pharmaceuticals’ Dawnzera for Hereditary Angioedema
Pharmaceutical Technology on MSN · 19h
FDA approves Ionis’ donidalorsen for HAE attack prevention
BioSpace
17h

Ionis Wins Approval For First RNA-Targeted Prophylactic for Rare Swelling Disease

Dawnzera is the first and so far only RNA-targeting therapy approved as a prophylactic treatment for hereditary angioedema ...
Asianet Newsable on MSN1d

Retail Traders Pile Into Ionis As Wall Street Hikes Price Targets On FDA Approval Of Swelling Disorder Therapy

BofA Securities raised its target to $64 with a ‘Buy’ rating, while Stifel lifted its target to $43 with a ‘Hold,’ both ...
pharmaphorum
22h

Ionis brings long-acting treatment option to HAE patients

Ionis has won an FDA green light for an RNA-based hereditary angioedema (HAE) treatment, Dawnzera, that can be ...

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