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  1. Marchés de Prédiction
  2. Health & Medicine
  3. FDA approves GSK & Spero Therapeutics' Tebipenem HBr?
FDA approves GSK & Spero Therapeutics' Tebipenem HBr?

FDA approves GSK & Spero Therapeutics' Tebipenem HBr?

5.0% (24h)Health & MedicineOne-Off6j
PolymarketPolymarketVérifier la disponibilitéSans KYC2% de frais
Probabilité implicite actuelle
Oui
Oui 67%-0.1%
Qualite du marche

44 / 100

Faible qualité
Volume 24h

18,7 €

Liquidité

1,9 k €

Faible liquidité
Achat / Vente

65.0% / 68.0%

Spread

4.6%

Spread modéré
Données du marché

Mis à jour il y a 5 minutes

4 juin 26, 19:3518 juin 26, 0:00

Tendances

Résultat24hProbabilité

Résultat choisi

Yes67%

Règles

As of market creation, the FDA's expected decision date for the specified application is June 18, 2026.

Polymarket
  • This market will resolve to "Yes" if the U.S.
  • Food and Drug Administration (FDA) grants full or conditional approval for GSK & Spero Therapeutics's Tebipenem HBr as a treatment for complicated urinary tract infections (cUTIs), including pyelonephritis by July 2, 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 18, 2026.

Polymarket
  • This market will resolve to "Yes" if the U.S.
  • Food and Drug Administration (FDA) grants full or conditional approval for GSK & Spero Therapeutics's Tebipenem HBr as a treatment for complicated urinary tract infections (cUTIs), including pyelonephritis by July 2, 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