RecruitingPhase 2NCT05758246

Senolytics To slOw Progression of Sepsis (STOP-Sepsis) Trial


Sponsor

University of Minnesota

Enrollment

220 participants

Start Date

Aug 23, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

The long-term goal is to test the clinical efficacy of senolytic therapies to reduce progression to and severity of sepsis in older patients. The central hypothesis is that a threshold burden of SnCs predisposes to a SASP mediated dysfunctional response to PAMPs, contributing to a disproportionate burden of sepsis in older patients. The study hypothesizes timely treatment with fisetin will interrupt this pathway. A multicenter, randomized, adaptive allocation clinical trial to identify the most efficacious dose of the senolytic fisetin to reduce the composite cardiovascular, respiratory, and renal sequential organ failure assessment score at 1 week, and predict the probability of success of a definitive phase III clinical trial.


Eligibility

Min Age: 65 Years

Inclusion Criteria5

  • Age >=65 years
  • Primary diagnosis of acute infection (per investigator judgment)
  • SOFA >1
  • Admission order to the hospital
  • Expected length of stay >=48 hours (per investigator judgment)

Exclusion Criteria13

  • Admission to the ICU
  • Vasopressors, mechanical ventilation, or dialysis
  • Comfort care only
  • Total bilirubin >3X or AST/ALT >4x upper limit of normal
  • eGFR < 25 ml/ min/ 1.73 m2
  • Hemoglobin <7 g/dL; white blood cell count ≤ 2,000/mm3; absolute neutrophil count ≤1 x 10\^9/;, or platelet count ≤ 40,000/μL
  • Known HIV, Hepatitis B, or Hepatitis C
  • Invasive fungal infection (per investigator judgment)
  • Uncontrolled effusions or ascites (per investigator judgment)
  • New/active invasive cancer except non-melanoma skin cancers
  • Known hypersensitivity or allergy to Fisetin.
  • Active treatment with potential drug-drug interactions
  • Enrolled in another sepsis clinical trial

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Interventions

DRUGFisetin-dose 1

20mg/kg once a day for one day.

DRUGFisetin-dose 2

20mg/kg once a day for two days

DRUGPlacebo

Placebo treatment


Locations(10)

University of Florida

Gainesville, Florida, United States

University of Iowa

Iowa City, Iowa, United States

Ridges

Burnsville, Minnesota, United States

Southdale

Edina, Minnesota, United States

M Health Fairview St. John's

Maplewood, Minnesota, United States

St. John's

Maplewood, Minnesota, United States

University of Minnesota

Minneapolis, Minnesota, United States

HCMC

Minneapolis, Minnesota, United States

UMMC

Minneapolis, Minnesota, United States

University of Mississippi Medical Center

Jackson, Mississippi, United States

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NCT05758246


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