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Safety, Pharmacokinetics, and Efficacy of AT 1501 in Patients Undergoing Kidney Transplant

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NCT05027906 · readout ≤ 165 d

Sponsored by Eledon Pharmaceuticals (industry) · ELDN — their whole pipeline →.

Phase
Phase 1/2
Status
Recruiting
Study type
Interventional
Design
Na · None · Treatment
Enrollment
48estimated
Sites
9
Countries
Australia, Brazil, Canada +2

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
Start2022-02-18actualWhen the study began enrolling
Primary completionJan 2027estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionJan 2027estimatedThe whole study's end, after follow-up
First posted2021-08-30actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-06-29actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Prevention of Rejection in Kidney Transplant

Intervention

  • Drug: AT-1501

Primary outcomes

what the primary-completion date above is the date OF
Safety Incidences
measured Through study completion, an average up to 20 months
Pharmacokinetic- PK profile
measured Day 1 and at steady state Month 3
Pharmacokinetic- Area under the plasma concentration
measured Day 1 and at steady state Month 3
Pharmacokinetic- Cmax
measured Day 1 and at steady state Month 3
Pharmacokinetic- Tmax
measured Day 1 and at steady state Month 3
Pharmacokinetic- Ke
measured Day 1 and at steady state Month 3
Pharmacokinetic- (t1/2)
measured Day 1 and at steady state Month 3
Pharmacokinetic- CL
measured Day 1 and at steady state Month 3
Pharmacokinetic- (Vdss)
measured Day 1 and at steady state Month 3

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