NotablePrimary and study completion pushed from Jan 2028 to Oct 2028
Enrollment reduced: 127 → 90 participants
Eligibility criteria expanded, about 34 words
Study description expanded, about 2 words
MinorSite details revised at 10 of 14 sitesv17
MinorEligibility criteria expanded, about 50 words
Site contacts updated at 1 of 14 sites
v16
MinorSite details revised at 1 of 14 sitesv15
MinorRe-verified, no change to tracked fieldsv14
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MinorStudy sites: 13 to 14v13
MinorSite details revised at 1 of 13 sitesv12
MinorSite contacts updated at 1 of 13 sitesv11
MinorStudy sites: 14 to 13v10
MinorStudy sites: 13 to 14v9
MinorEligibility criteria expanded, about 36 wordsv8
MinorSecondary endpoints: 4 to 6v7
MinorSite contacts updated at 1 of 13 sitesv6
NotablePrimary endpoints revised (4)v5Show 4 more changesShow less
Primary and study completion dates: Nov 2027 to Jan 2028
Eligibility criteria revised
Secondary endpoints revised (4)
Study sites revised (13)
MinorStudy sites: 2 to 13v4
MinorRe-verified, no change to tracked fieldsv3
NotableTrial status: Not Yet Recruiting to Recruiting
Primary and study completion dates: May 2028 to Nov 2027
Start date changed from estimate of Feb 2025 to Feb 18, 2025
Site details revised at 2 of 2 sites
v2
MinorStudy First Submitted
Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The purpose of this study is to generate evidence of the safety, tolerability, and pharmacokinetics/pharmacodynamics of IV LY4006896 compared with placebo in healthy participants and participants with Parkinson's disease.