| Date | Ticker | Company | Drug | Type | Phase | PoA | Mkt Size | Notes |
|---|---|---|---|---|---|---|---|---|
|
2026-04-28 Today |
INSM | PDUFA | Phase 2 | โ | $6B | For NTM lung disease. sNDA filing. Extracted from SEC filing: 8-K | ||
|
2026-04-30 in 2 days |
AXSM | PDUFA | โ | 92% | $4B | APR 30 2026 2 days ๐ PDUFA Auvelity (supplemental) (dextromethorphan HBr / bupro...) $AXSM | ||
|
2026-04-30 in 2 days |
AXSM | PDUFA | โ | 92% | โ | APR 30 2026 2 days ๐ PDUFA Auvelity (supplemental) (dextromethorphan HBr / bupro...) $AXSM | ||
|
2026-05-09 in 81 days |
LNTH | PDUFA | NDA | โ | โ | For Prostate cancer. NDA filing. Extracted from SEC filing: 8-K | ||
|
2026-05-12 in 84 days |
AGIO | PDUFA | NDA | โ | โ | For pyruvate kinase deficiency. NDA filing. Extracted from SEC filing: 8-K | ||
|
2026-06-05 in 177 days |
ARVN | PDUFA | โ | 85% | $10B | JUN 5 2026 38 days ๐ PDUFA (vepdegestrant (ARV-471)) $ARVN Arvinas / Pfizer ยท NDA ESR1-mut | ||
|
2026-06-05 in 177 days |
ARVN | PDUFA | โ | 85% | โ | JUN 5 2026 38 days ๐ PDUFA (vepdegestrant (ARV-471)) $ARVN Arvinas / Pfizer ยท NDA ESR1-mut | ||
|
2026-06-07 in 179 days |
ARGX | PDUFA | Phase 3 | โ | $500M | For generalized myasthenia gravis. BLA filing. Extracted from SEC filing: 6-K | ||
|
2026-06-08 in 180 days |
ABBV | PDUFA | โ | 90% | $6B | JUN 8 2026 41 days ๐ PDUFA (cendakimab) $ABBV AbbVie / Arena Pharma ยท NDA Eosinophilic eso | ||
|
2026-06-08 in 180 days |
RYTM | PDUFA | NDA | โ | โ | For Obesity caused by genetic deficiencies. NDA filing. Extracted from SEC filing: 8-K | ||
|
2026-06-08 in 180 days |
ABBV | PDUFA | โ | 90% | โ | JUN 8 2026 41 days ๐ PDUFA (cendakimab) $ABBV AbbVie / Arena Pharma ยท NDA Eosinophilic eso | ||
|
2026-06-16 in 188 days |
SNY | PDUFA | Phase 3 | โ | $8B | For hemophilia. BLA filing. Extracted from SEC filing: 6-K | ||
|
2026-06-18 in 190 days |
IMCR | PDUFA | Phase 3 | โ | $8B | For unresectable or metastatic uveal melanoma. BLA filing. Extracted from SEC filing: 8-K | ||
|
2026-06-18 in 190 days |
EVFM | PDUFA | NDA | โ | โ | For Prevention of pregnancy. NDA filing. Extracted from SEC filing: 8-K | ||
|
2026-06-28 in 200 days |
MNKD | PDUFA | Phase 3 | โ | $8B | For Type 1 diabetes. NDA filing. Extracted from SEC filing: 8-K | ||
|
2026-06-30 in 202 days |
AZN | PDUFA | โ | 85% | $12B | JUN 30 2026 63 days ๐ PDUFA (camizestrant (AZD9833)) $AZN AstraZeneca ยท NDA HR+/HER2- adva | ||
|
2026-06-30 in 202 days |
AZN | PDUFA | โ | 92% | $8B | JUN 30 2026 63 days ๐ PDUFA Truqap (supplemental) (capivasertib (Truqap) + abir...) $AZN A | ||
|
2026-06-30 in 202 days |
VRDN | PDUFA | โ | 88% | $2B | JUN 30 2026 63 days ๐ PDUFA (veligrotug) $VRDN Viridian Therapeutics ยท BLA Thyroid eye dis | ||
|
2026-06-30 in 202 days |
KYTX | PDUFA | โ | โ | โ | Kyverna plans to file a U.S. NDA in H1 2026 for its CAR-T therapy in stiff person syndrome | ||
|
2026-06-30 in 202 days |
DYN | PDUFA | โ | โ | โ | For Duchenne muscular dystrophy. Dyne Therapeutics plans to file for FDA approval of z-ros | ||
|
2026-06-30 in 202 days |
AZN | PDUFA | โ | 85% | โ | JUN 30 2026 63 days ๐ PDUFA (camizestrant (AZD9833)) $AZN AstraZeneca ยท NDA HR+/HER2- adva | ||
|
2026-06-30 in 202 days |
VRDN | PDUFA | โ | 88% | โ | JUN 30 2026 63 days ๐ PDUFA (veligrotug) $VRDN Viridian Therapeutics ยท BLA Thyroid eye dis | ||
|
2026-07-07 in 279 days |
VERA | PDUFA | โ | 88% | $8B | JUL 7 2026 70 days ๐ PDUFA (atacicept) $VERA Vera Therapeutics ยท BLA IgA nephropathy (IgAN | ||
|
2026-07-07 in 279 days |
VERA | PDUFA | โ | 88% | โ | JUL 7 2026 70 days ๐ PDUFA (atacicept) $VERA Vera Therapeutics ยท BLA IgA nephropathy (IgAN | ||
|
2026-07-10 in 282 days |
SWTX | PDUFA | โ | 93% | $2B | JUL 10 2026 73 days ๐ PDUFA (mirdametinib) $SWTX SpringWorks Therapeutics ยท NDA NF1-associ | ||
|
2026-07-10 in 282 days |
SWTX | PDUFA | โ | 93% | โ | JUL 10 2026 73 days ๐ PDUFA (mirdametinib) $SWTX SpringWorks Therapeutics ยท NDA NF1-associ | ||
|
2026-07-17 in 289 days |
CELC | PDUFA | โ | 90% | $1B | JUL 17 2026 80 days ๐ PDUFA (gedatolisib) $CELC Celcuity ยท NDA HR+/HER2-/PIK3CA wild-type | ||
|
2026-07-17 in 289 days |
CELC | PDUFA | โ | 90% | โ | JUL 17 2026 80 days ๐ PDUFA (gedatolisib) $CELC Celcuity ยท NDA HR+/HER2-/PIK3CA wild-type | ||
|
2026-07-25 in 297 days |
BIIB | PDUFA | โ | 92% | $15B | JUL 25 2026 88 days ๐ PDUFA Leqembi (lecanemab) $BIIB Eisai / Biogen ยท sNDA Subcutaneous f | ||
|
2026-07-25 in 297 days |
BIIB | PDUFA | โ | 92% | โ | JUL 25 2026 88 days ๐ PDUFA Leqembi (lecanemab) $BIIB Eisai / Biogen ยท sNDA Subcutaneous f | ||
|
2026-07-29 in 301 days |
NVO | PDUFA | โ | 80% | $1B | JUL 29 2026 92 days ๐ PDUFA (denecimig (Mim8)) $NVO Novo Nordisk ยท BLA Hemophilia A (with | ||
|
2026-07-29 in 301 days |
NVO | PDUFA | โ | 80% | โ | JUL 29 2026 92 days ๐ PDUFA (denecimig (Mim8)) $NVO Novo Nordisk ยท BLA Hemophilia A (with | ||
|
2026-08-01 in 373 days |
CBDY | PDUFA | NDA | โ | $400M | For Recurrent Respiratory Papillomatosis (RRP). BLA filing. AI-extracted from news: INOVIO | ||
|
2026-08-01 in 373 days |
MRNA | PDUFA | Phase 3 | โ | $8B | For Influenza vaccine. FDA reversed its Refusal-to-File decision on Moderna's mRNA-1010 fl | ||
|
2026-08-05 in 377 days |
MRNA | PDUFA | Phase 3 | โ | $15B | For influenza. The FDA reversed its earlier Refusal-to-File decision and agreed to review | ||
|
2026-08-17 in 389 days |
PRAX | PDUFA | โ | 90% | $1B | AUG 17 2026 111 days ๐ PDUFA (ulixacaltamide (PRAX-944)) $PRAX Praxis Precision Medicines | ||
|
2026-08-17 in 389 days |
PRAX | PDUFA | โ | 90% | โ | AUG 17 2026 111 days ๐ PDUFA (ulixacaltamide (PRAX-944)) $PRAX Praxis Precision Medicines | ||
|
2026-08-20 in 392 days |
REGN | PDUFA | Phase 3 | โ | $400M | For Fibrodysplasia Ossificans Progressiva (FOP). BLA filing. AI-extracted from news: Garet | ||
|
2026-08-20 in 392 days |
ARGX | PDUFA | Phase 3 | โ | $1B | For generalized myasthenia gravis. BLA filing. Extracted from SEC filing: 6-K | ||
|
2026-08-22 in 394 days |
CAPR | PDUFA | โ | 67% | $1B | AUG 22 2026 116 days ๐ PDUFA (deramiocel) $CAPR Capricor Therapeutics ยท BLA Duchenne muscu | ||
|
2026-08-22 in 394 days |
CAPR | PDUFA | โ | 67% | โ | AUG 22 2026 116 days ๐ PDUFA (deramiocel) $CAPR Capricor Therapeutics ยท BLA Duchenne muscu | ||
|
2026-08-25 in 397 days |
JAZZ | PDUFA | NDA | โ | โ | SBLA filing. Extracted from: Jazz Pharmaceuticals Announces FDA Acceptance and Priority Re | ||
|
2026-08-25 in 397 days |
DRUG | PDUFA | NDA | โ | โ | SBLA filing. Extracted from news: Jazz Pharmaceuticals Announces FDA Acceptance and Priori | ||
|
2026-08-25 in 397 days |
RHHBY | PDUFA | Phase 2 | โ | $15B | NDA filing. AI-extracted from news: FDA Accepts Bristol Myers Squibb (BMY) NDA for Iberdom | ||
|
2026-09-01 in 473 days |
SNY | PDUFA | NDA | โ | โ | For Diabetes. NDA filing. Extracted from SEC filing: 6-K | ||
|
2026-09-02 in 474 days |
CFOO | PDUFA | NDA | โ | $3B | For pediatric solid tumors. NDA filing. AI-extracted from news: InnoCareโs next-generation | ||
|
2026-09-02 in 474 days |
TAK | PDUFA | NDA | โ | $2B | For Polycythemia Vera. NDA filing. AI-extracted from news: Takeda and Protagonist Announce | ||
|
2026-09-15 in 487 days |
ALNY | PDUFA | โ | 90% | $4B | SEP 15 2026 140 days ๐ PDUFA (zilebesiran) $ALNY Alnylam Pharmaceuticals ยท NDA Hypertensio | ||
|
2026-09-15 in 487 days |
ALNY | PDUFA | โ | 90% | โ | SEP 15 2026 140 days ๐ PDUFA (zilebesiran) $ALNY Alnylam Pharmaceuticals ยท NDA Hypertensio | ||
|
2026-09-27 in 499 days |
PRAX | PDUFA | โ | 93% | $1B | SEP 27 2026 152 days ๐ PDUFA (relutrigine) $PRAX Praxis Precision Medicines ยท NDA SCN2A- a | ||
|
2026-09-27 in 499 days |
CBDY | PDUFA | NDA | โ | โ | For patients with cholangiocarcinoma (CCA) with FGFR2 fusions or rearrangements who have r | ||
|
2026-09-27 in 499 days |
PRAX | PDUFA | โ | 93% | โ | SEP 27 2026 152 days ๐ PDUFA (relutrigine) $PRAX Praxis Precision Medicines ยท NDA SCN2A- a | ||
|
2026-09-30 in 502 days |
ROIV | PDUFA | โ | 93% | $2B | SEP 30 2026 155 days ๐ PDUFA (brepocitinib) $ROIV Priovant Therapeutics / Roivant Sciences | ||
|
2026-09-30 in 502 days |
VNDA | PDUFA | NDA | โ | โ | For Non-24-hour sleep-wake disorder in the blind. sNDA filing. Extracted from SEC filing: | ||
|
2026-09-30 in 502 days |
ROIV | PDUFA | โ | 93% | โ | SEP 30 2026 155 days ๐ PDUFA (brepocitinib) $ROIV Priovant Therapeutics / Roivant Sciences | ||
|
2026-10-01 in 573 days |
REGN | PDUFA | โ | 93% | $2B | OCT 1 2026 156 days ๐ PDUFA (pozelimab) $REGN Regeneron ยท BLA VEXAS syndrome (complement C | ||
|
2026-10-01 in 573 days |
GSK | PDUFA | NDA | โ | $2B | For chronic graft-versus-host disease. NDA filing. Extracted from SEC filing: 6-K | ||
|
2026-10-01 in 573 days |
REGN | PDUFA | โ | 93% | โ | OCT 1 2026 156 days ๐ PDUFA (pozelimab) $REGN Regeneron ยท BLA VEXAS syndrome (complement C | ||
|
2026-10-07 in 579 days |
RARE | PDUFA | Phase 3 | โ | $200M | For Sanfilippo Syndrome Type A (MPS IIIA). BLA filing. AI-extracted from news: Ultragenyx | ||
|
2026-10-17 in 589 days |
VTRS | PDUFA | โ | โ | โ | For Presbyopia. Viatris announced FDA acceptance of a supplemental New Drug Application fo | ||
|
2026-10-20 in 592 days |
KALV | PDUFA | โ | 93% | $2B | OCT 20 2026 175 days ๐ PDUFA (donidalorsen) $KALV KalVista Pharmaceuticals ยท NDA Hereditar | ||
|
2026-10-20 in 592 days |
KALV | PDUFA | โ | 93% | โ | OCT 20 2026 175 days ๐ PDUFA (donidalorsen) $KALV KalVista Pharmaceuticals ยท NDA Hereditar | ||
|
2026-10-29 in 601 days |
MRK | PDUFA | Phase 2 | โ | $12B | For Adults with Active Psoriatic Arthritis If the sBLA is approved. sbla filing. AI-extra | ||
|
2026-10-30 in 602 days |
CYTK | PDUFA | โ | 92% | $8B | OCT 30 2026 185 days ๐ PDUFA MYQORZO (supplemental) (aficamten (MAPLE-HCM sNDA)) $CYTK Cyt | ||
|
2026-10-30 in 602 days |
CYTK | PDUFA | โ | 92% | โ | OCT 30 2026 185 days ๐ PDUFA MYQORZO (supplemental) (aficamten (MAPLE-HCM sNDA)) $CYTK Cyt | ||
|
2026-11-01 in 673 days |
SMMT | PDUFA | Phase 3 | โ | $8B | Extracted from: Summit gets November PDUFA date for its PD-1xVEGF bispecific | ||
|
2026-11-10 in 682 days |
ALNY | PDUFA | โ | 90% | $4B | NOV 10 2026 196 days ๐ PDUFA (elebsiran) $ALNY Alnylam / Roche ยท NDA Hepatitis B virus (HB | ||
|
2026-11-10 in 682 days |
ALNY | PDUFA | โ | 90% | โ | NOV 10 2026 196 days ๐ PDUFA (elebsiran) $ALNY Alnylam / Roche ยท NDA Hepatitis B virus (HB | ||
|
2026-12-01 in 773 days |
ACLX | PDUFA | NDA | โ | โ | Extracted from: Gilead Doubles Down on CAR T With $7.8B Arcellx Acquisition | ||
|
2026-12-01 in 773 days |
MRK | PDUFA | Phase 3 | โ | $8B | For Renal cell carcinoma (RCC). Exelixis presented data on Zanzalintinib for renal cell ca | ||
|
2026-12-05 in 777 days |
VRTX | PDUFA | โ | 92% | $2B | DEC 5 2026 221 days ๐ PDUFA Journavx (suzetrigine) $VRTX Vertex Pharmaceuticals ยท sNDA Mod | ||
|
2026-12-05 in 777 days |
VRTX | PDUFA | โ | 92% | โ | DEC 5 2026 221 days ๐ PDUFA Journavx (suzetrigine) $VRTX Vertex Pharmaceuticals ยท sNDA Mod | ||
|
2026-12-18 in 790 days |
RHHBY | PDUFA | NDA | โ | โ | For adult patients with oestrogen receptor (ER)-positive. Extracted from news: FDA accepts | ||
|
2026-12-18 in 790 days |
ADVB | PDUFA | NDA | โ | โ | For adult patients with oestrogen receptor (ER)-positive. Extracted from: FDA accepts New | ||
|
2026-12-27 in 799 days |
IDIA | PDUFA | NDA | โ | $1B | BLA submitted. AI-extracted from: CG Oncology Conference: Credo Posts 75.5% CR in BOND-003 | ||
|
2026-12-27 in 799 days |
CNTA | PDUFA | NDA | โ | $15B | For epilepsy. NDA submitted. AI-extracted from: Praxis tees up another approval filing; Ge | ||
|
2026-12-31 in 803 days |
NVO | PDUFA | โ | โ | โ | For sickle cell disease. Novo Nordisk's etavopivat demonstrated significant efficacy in la | ||
|
2026-12-31 in 803 days |
RHHBY | PDUFA | โ | โ | โ | Roche outlined its rejuvenation strategy for oncology and haematology, expecting to file u | ||
|
2027-01-01 in 9673 days |
EXEL | PDUFA | Phase 3 | โ | $6B | For advanced hepatocellular carcinoma. sNDA filing. Extracted from SEC filing: 8-K | ||
|
2027-01-01 in 9673 days |
TAK | PDUFA | NDA | โ | $2B | For Polycythemia Vera. NDA filing. AI-extracted from news: Takeda, Protagonist Say FDA Acc | ||
|
2027-01-03 in 9675 days |
ARGX | PDUFA | Phase 3 | โ | $500M | For generalized myasthenia gravis. BLA filing. Extracted from SEC filing: 6-K | ||
|
2027-01-28 in 9700 days |
VNDA | PDUFA | Phase 2 | โ | $3B | For Rare Skin Disease. BLA filing. AI-extracted from news: Vanda Pharmaceuticals Says US F | ||
|
2027-02-12 in 9784 days |
DCPH | PDUFA | NDA | โ | $200M | For relapsed or refractory PCNSL. NDA accepted. AI-extracted from: Deciphera Pharmaceutica | ||
|
2027-02-12 in 9784 days |
OCUL | PDUFA | NDA | โ | $12B | For wet-AMD. NDA submitted. AI-extracted from: Ocular: 'Buy' As AXPAXLI Program For Wet-AM | ||
|
2027-02-17 in 9789 days |
MLTX | PDUFA | NDA | โ | $8B | For inflammatory arthritis. BLA submitted. AI-extracted from: MoonLake has 'confidence' ah | ||
|
2027-03-01 in 9873 days |
GSK | PDUFA | Phase 2 | โ | $15B | For multiple myeloma. BLA filing. Extracted from SEC filing: 6-K | ||
|
2027-03-04 in 9876 days |
XENE | PDUFA | Phase 3 | โ | $15B | For epilepsy. NDA submitted. AI-extracted from: Xenon gets Phase 3 win with epilepsy drug, | ||
|
2027-04-04 in 9976 days |
CFOO | PDUFA | NDA | โ | $12B | For Unresectable or Metastatic HER2-Positive Adult Breast Cancer. BLA accepted. AI-extract | ||
|
2027-04-10 in 9982 days |
NHPAP | PDUFA | NDA | โ | $4B | sBLA accepted. AI-extracted from: Mabwell Announces Acceptance of Supplemental Biologics L |