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Is NCT04320173 results overdue?

Yes — results are overdue. Primary completion was 2017-03-22; the FDAAA-801 reporting deadline (2018-03-22) passed 3013 days ago and no results are posted on ClinicalTrials.gov.

Adhesion Performance Study of Lidocaine Topical System 1.8% Compared to Lidocaine Patch 5% and Lidocaine Medicated Plaster 5% in Healthy, Adult, Human Subjects

NCT IDNCT04320173 ↗
SponsorScilex Pharmaceuticals, Inc. (INDUSTRY)
Public issuerScilex Holding Co — SCLX (CIK 0001820190) best-effort name match, 95% conf — verify on EDGAR ↗
PhasePHASE1
StatusCOMPLETED
Primary completion2017-03-22 (ACTUAL)
Reporting deadline2018-03-22 (completion + 365d)
Days overdue3013
Results postedNo — check results tab ↗
FDA-regulateddrug: yes, device: no
ProvenanceFlagged overdue on 2026-06-21 · SHA-256 436af01d197e0ba7… (hash-chained, tamper-evident)

Source of record: ClinicalTrials.gov NCT04320173. 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 →