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  1. Marchés de Prédiction
  2. Health & Medicine
  3. FDA approves Unicycive's Oxylanthanum carbonate?
FDA approves Unicycive's Oxylanthanum carbonate?

FDA approves Unicycive's Oxylanthanum carbonate?

2.0% (24h)Health & MedicineOne-Off17j
PolymarketPolymarketVérifier la disponibilitéSans KYC2% de frais
Probabilité implicite actuelle
Oui
Oui 79%+0.0%
Qualite du marche

49 / 100

Faible qualité
Volume 24h

7,9 €

Liquidité

1,7 k €

Faible liquidité
Achat / Vente

78.0% / 80.0%

Spread

2.6%

Spread serré
Données du marché

Mis à jour il y a 6 minutes

4 juin 26, 20:0429 juin 26, 0:00

Tendances

Résultat24hProbabilité

Résultat choisi

Yes79%

Règles

As of market creation, the FDA's expected decision date for the specified application is June 29, 2026.

Polymarket
  • This market will resolve to "Yes" if the U.S.
  • Food and Drug Administration (FDA) grants full or conditional approval for Unicycive's Oxylanthanum carbonate as a treatment for hyperphosphatemia in CKD patients on dialysis by July 13, 2026, 11:59 PM ET.
  • Otherwise, this market will resolve to "No."
  • An approval is defined as: For new drugs: FDA issuance of an approval letter for a New Drug Application (NDA) or Biologics License Application (BLA) For already-marketed drugs seeking new indications: FDA approval of a supplemental NDA (sNDA) or supplemental BLA (sBLA) for the specific indication referenced For generic drugs: FDA approval of an Abbreviated New Drug Application (ANDA) For biosimilars: FDA approval of a 351(k) application
  • The following constitute qualifying approvals: Standard approval (traditional approval based on clinical benefit), Accelerated approval (based on surrogate endpoints), Approval with Risk Evaluation and Mitigation Strategy (REMS), Approval with restricted distribution or indication limitations, except compassionate use/expanded access programs

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Actifs dans ces sujets

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Règles

As of market creation, the FDA's expected decision date for the specified application is June 29, 2026.

Polymarket
  • This market will resolve to "Yes" if the U.S.
  • Food and Drug Administration (FDA) grants full or conditional approval for Unicycive's Oxylanthanum carbonate as a treatment for hyperphosphatemia in CKD patients on dialysis by July 13, 2026, 11:59 PM ET.
  • Otherwise, this market will resolve to "No."
  • An approval is defined as: For new drugs: FDA issuance of an approval letter for a New Drug Application (NDA) or Biologics License Application (BLA) For already-marketed drugs seeking new indications: FDA approval of a supplemental NDA (sNDA) or supplemental BLA (sBLA) for the specific indication referenced For generic drugs: FDA approval of an Abbreviated New Drug Application (ANDA) For biosimilars: FDA approval of a 351(k) application
  • The following constitute qualifying approvals: Standard approval (traditional approval based on clinical benefit), Accelerated approval (based on surrogate endpoints), Approval with Risk Evaluation and Mitigation Strategy (REMS), Approval with restricted distribution or indication limitations, except compassionate use/expanded access programs