FDAAPP / ONE TIME
No resting orders on this market.
Important information: 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: Complete Response Letters (CRLs) indicating the application cannot be approved in its current form Approvable letters that require additional actions before approval Tentative approvals pending patent or exclusivity expiration FDA requests for additional information or studies Extension of Prescription Drug User Fee Amendments dates Approval for compassionate use or expanded access programs only Emergency Use Authorization (EUA) without full approval Approval only for export or for use outside the United States If the FDA issues a Complete Response Letter before Jun 1, 2026, the market will resolve to No unless the FDA subsequently approves camizestrant for HR+/HER2- advanced breast cancer with ESR1 mutation after addressing the CRL concerns and before Jun 1, 2026. If the FDA convenes an Advisory Committee that votes against approval but the FDA approves camizestrant for HR+/HER2- advanced breast cancer with ESR1 mutation anyway before Jun 1, 2026, the market will resolve to Yes. If camizestrant for HR+/HER2- advanced breast cancer with ESR1 mutation receives accelerated approval that is later withdrawn before Jun 1, 2026, the market will resolve based on whether the initial accelerated approval occurred after Issuance (Yes), regardless of the subsequent withdrawal. If the drug sponsor withdraws the application before FDA action and before Jun 1, 2026, the market will resolve to No immediately.
Resolves Yes if the FDA approves camizestrant for HR+/HER2- advanced breast cancer with ESR1 mutation for marketing before Jun 1, 2026, 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: Complete Response Letters (CRLs) indicating the application cannot be approved in its current form Approvable letters that require additional actions before approval Tentative approvals pending patent or exclusivity expiration FDA requests for additional information or studies Extension of Prescription Drug User Fee Amendments dates Approval for compassionate use or expanded access programs only Emergency Use Authorization (EUA) without full approval Approval only for export or for use outside the United States If the FDA issues a Complete Response Letter before Jun 1, 2026, the market will resolve to No unless the FDA subsequently approves camizestrant for HR+/HER2- advanced breast cancer with ESR1 mutation after addressing the CRL concerns and before Jun 1, 2026. If the FDA convenes an Advisory Committee that votes against approval but the FDA approves camizestrant for HR+/HER2- advanced breast cancer with ESR1 mutation anyway before Jun 1, 2026, the market will resolve to Yes. If camizestrant for HR+/HER2- advanced breast cancer with ESR1 mutation receives accelerated approval that is later withdrawn before Jun 1, 2026, the market will resolve based on whether the initial accelerated approval occurred after Issuance (Yes), regardless of the subsequent withdrawal. If the drug sponsor withdraws the application before FDA action and before Jun 1, 2026, the market will resolve to No immediately.