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trial · primary record

LY3954068

Alzheimer Disease

PhasePhase 1
StatusRECRUITING
SponsorUnknown
Enrolment56
Primary completion2028-07
Primary endpointPart A: Number of participants with one or more Adverse Event (s) (AEs), Treatment Emergent Adverse Events (TEAEs) and Serious Adverse Event(s) (SAEs) considered by the investigator to be related to study drug administration
Registry IDNCT06297590

Provenance

  • Source: ClinicalTrials.gov
  • Fetched at: 2026-10-29T14:35:13.665Z
  • Licence class: attribution-required
  • Verdict: primary-source
  • Entity id: NCT06297590

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