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Is NCT03092232 results overdue?

Yes — results are overdue. Primary completion was 2017-07-13; the FDAAA-801 reporting deadline (2018-07-13) passed 2900 days ago and no results are posted on ClinicalTrials.gov.

Single Dose Study to Assess the Safety, Tolerability and Pharmacokinetics(PK) of PF-06865571

NCT IDNCT03092232 ↗
SponsorPfizer (INDUSTRY)
Public issuerPFIZER INC — PFE (CIK 0000078003) best-effort name match, 95% conf — verify on EDGAR ↗
PhasePHASE1
StatusCOMPLETED
Primary completion2017-07-13 (ACTUAL)
Reporting deadline2018-07-13 (completion + 365d)
Days overdue2900
Results postedNo — check results tab ↗
FDA-regulateddrug: yes, device: no
ProvenanceFlagged overdue on 2026-06-21 · SHA-256 20d40a6bb59054d1… (hash-chained, tamper-evident)

Source of record: ClinicalTrials.gov NCT03092232. The reporting requirement is FDAAA 801 (Public Law 110-85 §801) and the Final Rule, 42 CFR Part 11.

⚠ Public-record facts from ClinicalTrials.gov — not a finding of violation, fraud, or non-compliance, and not legal or investment advice. Full disclaimer →