FDA PDUFA Calendar
The FDA PDUFA Calendar is a chronological calendar of PDUFA target dates. These are dates by which the FDA aims to deliver their decision regarding an NDA or BLA filing. These decisions can however come before the PDUFA target date.
The FDA will typically issue one of the following decisions:
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CRL - complete response letter - rejection letter noting reasons
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Marketing approval - approved to market under the given label
Sometimes the FDA requires an advisory committee meeting prior to the approval decision. This meeting is a public discussion with committee members of various relevant backgrounds, which usually concludes in a vote regarding the efficacy and safety of the drug in question. The FDA is may use this discussion and vote as a guideline for their decision but by no means are bound to this discussion or vote.
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Ticker | Drug | Indication | PDUFA Date |
|---|---|---|---|
RARE | UX111 (ABO-102) | Sanfilippo syndrome type A (MPS IIIA) | Aug 18, 2025 |
PTCT | Vatiquinone (PTC743) | FA (Friedreich Ataxia) | August 19, 2025 |
IONS | Donidalorsen (IONIS-PKK-LRx) | HA (Hereditary Angioedema) | August 21, 2025 |
PGEN | PRGN-2012 AdenoVerse™ (zopapogene imadenovec) | Recurrent respiratory papillomatosis (RRP) | Aug 27, 2025 |
TVTX | FILSPARI (Sparsentan) | IgAN (IgA nephropathy) | August 28, 2025 |
BIIB | Leqembi (Lecanemab) SC formulation | Early Alzheimer’s Disease | August 31, 2025 |
CAPR | Deramiocel (CAP-1002) | DMD (Duchenne Muscular Dystrophy) | August 31, 2025 |
AGIO | PYRUKYND (Mitapivat) (pyruvate kinase R (PKR) activator) | Adult patients with non-transfusion-dependent and transfusion-dependent alpha- or beta-thalassemia | September 7, 2025 |
CRNX | Paltusotine (SST2 agonist) | Acromegaly (Adults) | September 25, 2025 |
CYTK | Aficamten | oHCM (Obstructive Hypertrophic Cardiomyopathy | September 26, 2025 |
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