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SAD and MAD Study of AKB-9090 in Healthy Adult Participants

← catalyst calendar

NCT07429006 · readout ≤ 73 d

Sponsored by Akebia Therapeutics (industry) · AKBA — their whole pipeline →. With Emerald Clinical Trials.

Phase
Phase 1
Status
Recruiting
Study type
Interventional
Design
Randomized · Double · Treatment
Enrollment
70estimated
Sites
1
Country
New Zealand

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
Start2026-03-16actualWhen the study began enrolling
Primary completionOct 2026estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionDec 2026estimatedThe whole study's end, after follow-up
First posted2026-02-24actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-04-13actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Healthy Volunteers

Interventions

  • Drug: AKB-9090
  • Other: Placebo

Primary outcomes

what the primary-completion date above is the date OF
Number of participants who will report serious Treatment emergent adverse events (TEAEs) and TEAEs
measured From First Dose to Day 7
Number of Participants with Clinically Significant Changes in Physical Examinations
measured From First Dose to Day 7
Number of Participants with Clinically Significant Changes in Vital Signs
measured From First Dose to Day 7
Number of Participants with Clinically Significant Changes in 12-lead Electrocardiogram (ECG)
measured From First Dose to Day 7
Number of Participants with Clinically Significant Changes in Chemistry parameters
measured From First Dose to Day 7
Number of Participants with Clinically Significant Changes in Hematology Parameters
measured from first dose to Day 7
Number of Participants with Clinically Significant Changes in Lipid Parameters
measured From First Dose to Day 7
Number of Participants with Clinically Significant Changes in Coagulation Parameters
measured From First Dose to Day 7
Number of Participants with Clinically Significant Changes in Urinalysis Parameters
measured From First Dose to Day 7

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