Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT06602453 · ClinicalTrials.gov registry record · Phase 2

A Study to Evaluate the Efficacy and Safety of GDC-8264 in Preventing Cardiac Surgery-Associated Acute Kidney Injury (AKI) and Major Adverse Kidney Events (MAKE)

A Phase 2 study, sponsored by Genentech.

Terminated
Registry status
Phase 2
Development phase
67
Enrollment target

NCT06602453: Clinical Trial Phase 2 study, sponsored by Genentech.

NCT06602453 is a Phase 2 study that was terminated before completion, run by Genentech. The registered enrollment target is 67 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (50% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT06602453, a Phase 2 study, was terminated before completion, sponsored by Genentech.

TERMINATED
Registry status
Phase 2
Development phase
67 participants
Enrollment target

Study Summary

The aim of this study is to evaluate the efficacy and safety of GDC-8264 compared with placebo in participants undergoing cardiac surgery who are determined to be at moderate to high risk of developing AKI and subsequent MAKE at 90 days after surgery (MAKE90). The study will be performed in two parts- Part 1 and Part 2.

Interventions

  • DRUG Placebo
  • DRUG GDC-8264

Trial Details

FieldValue
Enrollment Target 67 participants
Start Date 2025-01-17
Est. Completion 2026-03-03
Phase Phase 2
Genentech

332 total trials

Why NCT06602453 stopped before completion

NCT06602453 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 67 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (50% lower).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT06602453 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06602453 about?

NCT06602453 is a clinical study titled "A Study to Evaluate the Efficacy and Safety of GDC-8264 in Preventing Cardiac Surgery-Associated Acute Kidney Injury (AKI) and Major Adverse Kidney Events (MAKE)". The aim of this study is to evaluate the efficacy and safety of GDC-8264 compared with placebo in participants undergoing cardiac surgery who are determined to be at moderate to high risk of developing AKI and subsequent MAKE at 90 days after surgery (MAKE90). The study will be performed in two part...

What is the current status of trial NCT06602453?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 67 participants. The study started on 2025-01-17. Estimated completion is 2026-03-03.

What interventions are being tested in trial NCT06602453?

The interventions under investigation include: Placebo (DRUG), GDC-8264 (DRUG).

Who is sponsoring clinical trial NCT06602453?

This trial is sponsored by Genentech, which has 332 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06602453's enrollment target sits among peer trials

67 974th of 2000 higher than 1,026 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT03213002 · 67 participants · Phase 1

    Oral Capecitabine and Temozolomide (CAPTEM) for Newly Diagnosed GBM

  • NCT04115163 · 67 participants · Phase 2

    Biologically Optimized Infusion Schedule of Gemcitabine and Nab-Paclitaxel for the Treatment of Metastatic Pancreatic Cancer

  • NCT04315324 · 67 participants · Phase 1

    Study to Test OBI-3424 in Patients With T-Cell Acute Lymphoblastic Leukemia (T-ALL) or T-Cell Lymphoblastic Lymphoma (T-LBL)

  • NCT04532424 · 67 participants · NA

    Transcranial Magnetic Stimulation for Restricted and Repetitive Behavior in ASD

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT06602453, the US trial registry maintained by the National Library of Medicine. NCT06602453 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.