2026-06-10 15:09 UTC
Market snapshot
Vol 130 calls·Liq 94 XP·Ends Jan 1 UTC
Answer options
BinaryWhy it matters
Each new FDA nod for CRISPR expands the map of treatable genetic disease; 2026 approvals would signal whether the platform is moving beyond sickle cell into broader in vivo and ex vivo indications.
Resolution criteria
Resolves YES if the US FDA grants marketing approval in calendar year 2026 for a CRISPR or CRISPR-based gene-editing therapy for at least one disease indication not covered by any prior FDA-approved gene-editing product. Clinical holds or filings without approval resolve NO.
https://www.fda.gov/Timing
expiresAt: 2027-01-01T04:59:59.000Z
votingClosesAt: 2026-12-31T04:59:59.000Z
votingLockMinutesBeforeDue: = 1440 minutes
eventStart: 2026-12-31T05:59:59.000Z
Expires 2027-01-01 04:59 UTC
Metadata
53%
0.0%
Will the FDA approve a CRISPR gene-editing therapy for a new disease in 2026?
Vol 130 calls·Liq 94 XP·Ends Jan 1 UTC
Will the FDA approve a CRISPR gene-editing therapy for a new disease in 2026?
Vol 130 calls·Liq 94 XP·Ends Jan 1 UTC
53%
0.0%