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Completed Phase 3 Interventional

Effect of RBT-1 on Reducing the Risk of Post-Operative Complications in Subjects Undergoing Cardiac Surgery

ClinicalTrials.gov ID: NCT06021457

Public ClinicalTrials.gov record NCT06021457. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 9:47 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Effect of RBT-1 on Reducing the Risk of Post-Operative Complications in Subjects Undergoing Cardiac Surgery

Study identification

NCT ID
NCT06021457
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Renibus Therapeutics, Inc.
Industry
Enrollment
454 participants

Conditions and interventions

Interventions

  • RBT-1 Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 16, 2023
Primary completion
Jun 16, 2025
Completion
Jun 16, 2025
Last update posted
Jul 31, 2025

2023 – 2025

United States locations

U.S. sites
31
U.S. states
18
U.S. cities
30
Facility City State ZIP Site status
Research Site Huntsville Alabama 35801
Research Site La Jolla California 92037
Research Site San Francisco California 94107
Research Site Stanford California 94305
Research Site Washington D.C. District of Columbia 20011
Research Site Atlantis Florida 33462
Research Site Gainesville Florida 32608
Research Site Athens Georgia 30606
Research Site Atlanta Georgia 30342
Research Site Fort Wayne Indiana 46804
Research Site Indianapolis Indiana 46202
Research Site Indianapolis Indiana 46237
Research Site Kansas City Kansas 66160
Research Site Boston Massachusetts 02115
Research Site Ann Arbor Michigan 48109
Research Site Lansing Michigan 48879
Research Site Midland Michigan 48670
Research Site Royal Oak Michigan 48703
Research Site Rochester Minnesota 55905
Research Site St Louis Missouri 63310
Research Site Flushing New York 11355
Research Site Raleigh North Carolina 27610
Research Site Winston-Salem North Carolina 27157
Research Site Cleveland Ohio 44106
Research Site Toledo Ohio 43606
Research Site Charleston South Carolina 29466
Research Site Nashville Tennessee 37203
Research Site Dallas Texas 75390
Research Site Houston Texas 77030
Research Site San Antonio Texas 78229
Research Site Charlottesville Virginia 22903

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 10 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06021457, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 31, 2025 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06021457 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →