KalshiVerificar disponibilidadeKYC obrigatório2% de taxaProbabilidade implícita atualBefore Jan 1, 2027 17%-11.0%Líder entre 5 opções
Qualidade do mercado
28 / 100
Baixa qualidadeVolume 24h
5,1 €
Liquidez
73,8 €
Baixa liquidezCompra / Venda
16.0% / 19.0%
Spread
18.8%
Spread amploDados do mercado
Atualizado há 7 minutos
14/05/26, 2:001/01/27, 4:59
Tendências
Resultado escolhido
Before Jan 1, 202717%
Também disponível em Polymarket
FDA approves Retatrutide this year?
1.0%6m
-0.0%12%
+0.0%89%
52 • Qualidade médiaSpread amploLiquidez média
Volume total493,2 mil €
Volume 24h238,8 €
POLYMARKETRegras
If the FDA approves retatrutide (LY3437943) for marketing before Jan 1, 2027, then the market resolves to Yes.
- 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 approvals that trigger the Payout Criterion:
- 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
- The following do NOT constitute approvals:
Os dados de comparação são apenas informativos. Preços e liquidez podem variar.
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If the FDA approves retatrutide (LY3437943) for marketing before Jan 1, 2027, then the market resolves to Yes.
- 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 approvals that trigger the Payout Criterion:
- 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
- The following do NOT constitute approvals: