A Study to Investigate Outcomes With Elecoglipron Compared With Placebo in Adult Participants With Chronic Kidney Disease.

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18+
SponsorAstraZeneca

About this trial

This is a Phase III, randomized, double-blind, parallel-group, placebo-controlled multicenter study to investigate outcomes with elecoglipron compared with placebo in participants with CKD with and without T2DM who are on background SGLT2i (dapagliflozin) as GDMT and other SoC treatments for CKD.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adults with confirmed CKD; UACR ≥30 mg/g and eGFR ≥20 mL/min/1.73 m² within specified ranges.

On stable, patient maximum tolerated, labeled daily dose of ACEI or ARB for ≥4 weeks at least 28 days before screening.

Disqualifiers

BMI <23 kg/m² at screening

History of type 1 diabetes mellitus

HbA1c ≥10% (86 mmol/mol) at screening

Currently receiving, or anticipated to receive, therapeutic intervention for diabetic retinopathy and/or macular edema.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Elecoglipron

    Drug

    Elicoglipron tablet

  • Placebo

    Drug

    Placebo tablet

Treatment groups

7,000 Participants
are divided into 2 treatment groups
Group A: ElecoglipronExperimental treatment 1 intervention
Group B: PlaceboActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

To evaluate the effect of elecoglipron compared with placebo in reducing the risk of the composite of ≥ 50% sustained decline in eGFR, ESKD, or all-cause mortality

Time to the first occurrence of any component of this composite: * ≥ 50% sustained decline in eGFR * ESKD defined as sustained eGFR \< 10 mL/min/1.73 m2, or Chronic dialysis treatment, or Receiving a renal transplant * All-cause mortality

Time frame
Event-driven, trial is estimated to be up to 4.5 years

Secondary outcomes

1

To evaluate the effect of elecoglipron compared with placebo in reducing the risk of the composite of ≥ 50% sustained decline in eGFR, ESKD, or CV and renal death

Time to the first occurrence of any component of this composite: * ≥ 50% sustained decline in eGFR * ESKD defined as: Sustained eGFR \< 10 mL/min/1.73 m2, or Chronic dialysis treatment, or Receiving a renal transplant * CV and renal death

Time frame
Event-driven, trial is estimated to be up to 4.5 years
2

To evaluate the effect of elecoglipron compared with placebo in reducing the risk of composite of all-cause mortality, MI, or stroke

Time to the first occurrence of any component of this composite: * All-cause mortality * MI * Stroke

Time frame
Event-driven, trial is estimated to be up to 4.5 years
3

To evaluate the effect of elecoglipron compared with placebo in reducing the risk of MACE (CV death, MI, or stroke)

Time to the first occurrence of any component of this composite: * CV and renal death * MI * Stroke

Time frame
Event-driven, trial is estimated to be up to 4.5 years
4

To evaluate the effect of elecoglipron compared with placebo in reducing the risk of all-cause mortality

Time to death from any cause

Time frame
Event-driven, trial is estimated to be up to 4.5 years

Other outcomes

Sponsors and contacts

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