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  3. FDA approves GSK & Spero Therapeutics' Tebipenem HBr?
FDA approves GSK & Spero Therapeutics' Tebipenem HBr?

FDA approves GSK & Spero Therapeutics' Tebipenem HBr?

5.0% (24u)Health & MedicineOne-Off6d
PolymarketPolymarketBeschikbaarheid controlerenGeen KYC2% kosten
Huidige impliciete kans
Ja
Ja 67%-0.1%
Marktkwaliteit

44 / 100

Lage kwaliteit
24u volume

€ 18,7

Liquiditeit

€ 1,9K

Lage liquiditeit
Bied / Laat

65.0% / 68.0%

Spread

4.6%

Gematigde spread
Marktdata

Bijgewerkt 5 minuten geleden

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

Trends

Uitkomst24uKans

Gekozen uitkomst

Yes67%

Regels

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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Regels

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