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A Master Protocol Study (LY900028) of Multiple Intervention-Specific-Appendices (ISAs) in Participants With Chronic Pain

← catalyst calendar

NCT05986292 · readout ≤ 254 d

Sponsored by Eli Lilly and Company (industry) · LLY — their whole pipeline →.

Phase
Phase 2
Status
Recruiting
Study type
Interventional
Design
Randomized · Double · Screening
Enrollment
10,000estimated
Sites
64
Countries
Puerto Rico, United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2020-01-30actualWhen the study began enrolling
Primary completionApr 2027estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionApr 2027estimatedThe whole study's end, after follow-up
First posted2023-08-14actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-06-23actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Osteoarthritis, Knee
  • Diabetic Neuropathic Pain
  • Chronic Low-back Pain

Interventions

  • Drug: LY3016859 ISA
  • Drug: LY3556050 ISA
  • Drug: LY3526318 ISA
  • Drug: LY3857210 ISA
  • Drug: Placebo Oral
  • Drug: Placebo

Primary outcome

what the primary-completion date above is the date OF
Number of Participants Who Were Allocated to Each ISA
measured Baseline, Up to Week 8

Posted documents

hosted by the registry — we link, never re-serve
Study Protocolposted 2020-12-11 · 6.0 MB · Prot_005.pdf

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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