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  1. Mercados de Predicción
  2. Health & Medicine
  3. FDA approves Viridian Therapeutics' Veligrotug?
FDA approves Viridian Therapeutics' Veligrotug?

FDA approves Viridian Therapeutics' Veligrotug?

8.5% (24h)Health & MedicineOne-Off18d
PolymarketPolymarketComprobar disponibilidadSin KYC2% de comisión
Probabilidad implícita actual
Sí
Sí 69%-0.1%
Calidad del mercado

49 / 100

Baja calidad
Volumen 24h

22,4 €

Liquidez

1,3 mil €

Baja liquidez
Compra / Venta

68.0% / 70.0%

Spread

2.9%

Spread estrecho
Datos de mercado

Actualizado hace 4 minutos

4 jun 26, 20:0430 jun 26, 0:00

Tendencias

Resultado24hProbabilidad

Resultado elegido

Yes69%

Reglas

As of market creation, the FDA's expected decision date for the specified application is June 30, 2026.

Polymarket
  • This market will resolve to "Yes" if the U.S.
  • Food and Drug Administration (FDA) grants full or conditional approval for Viridian Therapeutics's Veligrotug as a treatment for thyroid eye disease by July 14, 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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Activos en estos temas

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Reglas

As of market creation, the FDA's expected decision date for the specified application is June 30, 2026.

Polymarket
  • This market will resolve to "Yes" if the U.S.
  • Food and Drug Administration (FDA) grants full or conditional approval for Viridian Therapeutics's Veligrotug as a treatment for thyroid eye disease by July 14, 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