Rx-BBIO-2705 · May 8, 2027 sponsor target
Will the FDA approve Encaleret for autosomal dominant hypocalcemia type 1 (ADH1)?
Sponsor update lists encaleret for ADH1 under Priority Review with a May 8, 2027 FDA target.
Open outcome workspaceA PDUFA goal date is not an approval determination or a trading cutoff. Application scope, delays and invalid-result terms require reviewed rules.
2 publications1 exact-program1 related5 context / correction notes
Publication and retrieval dates are shown separately. Market rules determine which evidence can resolve an outcome.
Sponsor update lists encaleret for ADH1 under Priority Review with a May 8, 2027 FDA target.
Sponsor describes encaleret as an orally administered small molecule targeting the calcium-sensing receptor.
Registry identifies the associated compound, condition and sponsor; trial completion is separate from FDA action.
This research candidate has no onchain question, committed rule hash or funded pool.
These terms require review and cannot resolve a market.
RESEARCH DRAFT / NOT FINAL RULES / NOT COMMITTED Program: Encaleret Sponsor: BridgeBio Pharma Indication under review: autosomal dominant hypocalcemia type 1 (ADH1) Event: FDA marketing-approval decision Sponsor target: 2027-05-08 (date only, not a trading cutoff) YES: FDA approval of the exact application, formulation and eligible indication, established under a reviewed evidence hierarchy. Exact application/label scope requires review. NO: The approved market terms must specify treatment of a Complete Response Letter, withdrawal, extension and no decision by cutoff. No automatic NO outcome is inferred from the sponsor target date. INVALID: The approved terms must specify erroneous dates, ambiguous identity, unsupported evidence and withdrawal handling. No policy has been committed for this candidate. Cutoff and timezone: UNSET / OWNER APPROVAL REQUIRED. Evidence: FDA approval letter or other authoritative FDA record; sponsor disclosures require the corroboration specified in final rules. Oracle: assertion, dispute bond, liveness and final settlement require separately reviewed deployment settings. This draft cannot resolve a market or pay a claim. Publish reviewed canonical bytes and their keccak256 commitment before listing.
No question ID, approved deadline or UMA assertion exists for this research candidate. Sandbox claims have no redemption rights.