Nafamostat Efficacy in Phase 3 Registrational CRRT Study

Last updated: October 13, 2025
Sponsor: Talphera, Inc
Overall Status: Active - Recruiting

Phase

N/A

Condition

Kidney Failure

Renal Failure

Kidney Disease

Treatment

Placebo (0.9% NaCl)

Niyad (nafamostat mesylate)

Clinical Study ID

NCT06150742
NYD301
  • Ages 18-80
  • All Genders

Study Summary

A prospective, randomized, placebo-controlled clinical study to investigate the safety and efficacy of Niyad (nafamostat mesylate) for anticoagulation of extracorporeal blood circulating through a dialysis filter in patients undergoing CRRT who cannot tolerate heparin or are at higher risk for bleeding.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Patients requiring CRRT or undergoing CRRT initiated within the prior 48 hours

  • Patients who cannot tolerate heparin or are at high risk of bleeding

Exclusion

Exclusion Criteria:

  • Patients weighing less than 50 kg

  • Patients receiving systemic anticoagulation

  • Patients with active bleeding

Study Design

Total Participants: 70
Treatment Group(s): 2
Primary Treatment: Placebo (0.9% NaCl)
Phase:
Study Start date:
August 15, 2024
Estimated Completion Date:
December 31, 2025

Study Description

Patients in intensive care units with acute kidney injury are often too frail to undergo the rapid fluid shifts that accompany intermittent hemodialysis. Continuous renal replacement therapy (CRRT) allows a more gentle continual dialysis, more similar to regular kidney function. Anticoagulation of the CRRT circuit can reduce clotting of the filter, which can lead to less filter changes and possibly less transfusions. Niyad (nafamostat mesylate), an anticoagulant with an ultra-short half-life of 8 minutes, is approved for use in South Korea and Japan for anticoagulation of the CRRT circuit. For patients who cannot tolerate heparin or who are at a high risk of bleeding, nafamostat may be an optimal anticoagulant to infuse into the CRRT circuit as the short half-life should minimize patient exposure. The primary objective of this study is to measure the anticoagulation efficacy of Niyad in the CRRT circuit versus placebo. Evaluation of the safety of Niyad in patients undergoing CRRT versus placebo will also be performed.

Connect with a study center

  • UCLA

    Los Angeles, California 90095
    United States

    Site Not Available

  • University of California Los Angeles

    Los Angeles 5368361, California 5332921 90095
    United States

    Active - Recruiting

  • AdventHealth

    Orlando 4167147, Florida 4155751 32804
    United States

    Site Not Available

  • Henry Ford Health

    Detroit 4990729, Michigan 5001836 48202
    United States

    Active - Recruiting

  • University of New Mexico

    Albuquerque, New Mexico 87131
    United States

    Site Not Available

  • University of New Mexico

    Albuquerque 5454711, New Mexico 5481136 87131
    United States

    Active - Recruiting

  • Mt Sinai

    New York, New York 10029
    United States

    Site Not Available

  • Northwell Health

    Great Neck 5119218, New York 5128638 11021
    United States

    Active - Recruiting

  • Mount Sinai

    New York 5128581, New York 5128638 10029
    United States

    Active - Recruiting

  • Wake Forest

    Winston-Salem, North Carolina 27157
    United States

    Site Not Available

  • Children's Hospital Medical Center

    Cincinnati, Ohio 45229
    United States

    Site Not Available

  • Cincinnati Children's Hospital Medical Center

    Cincinnati 4508722, Ohio 5165418 45229
    United States

    Active - Recruiting

  • University of Pittsburgh Medical Center

    Pittsburgh 5206379, Pennsylvania 6254927 15213
    United States

    Active - Recruiting

  • Medical University of South Carolina

    Charleston 4574324, South Carolina 4597040 29425
    United States

    Active - Recruiting

  • Baylor University Medical Center

    Dallas 4684888, Texas 4736286 75246
    United States

    Active - Recruiting

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