Droxidopa to Increase Mean Arterial Pressure in Decompensated Cirrhosis Patients With Acute Kidney Injury

Status: Recruiting
Location: See location...
Intervention Type: Other, Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

This study tests whether a medication called droxidopa can help improve blood flow to the kidneys in people with liver cirrhosis who develop kidney problems while in the hospital. When someone with cirrhosis experiences kidney injury, having better blood pressure can help their kidneys recover. Droxidopa is an oral medication that may help raise blood pressure without requiring intensive care or invasive treatments. The study will compare droxidopa to a placebo (inactive pill) in 75 people hospitalized with cirrhosis and kidney injury. Participants will take either droxidopa or placebo pills for 28 days and be monitored for an additional 30 days. Researchers will measure changes in blood pressure and kidney function to determine if droxidopa is effective and safe for these patients. This research could identify a new treatment option for a serious complication of liver disease.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 70
Healthy Volunteers: f
View:

• Ability to provide informed consent by subject or legally authorized representative

• Consent to blood and urine collection for biomarker analysis

• Ability to take oral medications

• At least 18 years of age

• Hospitalized at Columbia University Irving Medical Center

• Child-Pugh Score ≥ B7 cirrhosis (documented by imaging, biopsy, or clinical evidence)

• KDIGO Stage 1 AKI or greater, defined as:

• ≥0.3 mg/dL increase in serum creatinine within 48 hours OR

• ≥50% increase in serum creatinine from outpatient baseline

• Mean arterial pressure ≤85 mmHg averaged over 24 hours prior to randomization

• For women of childbearing potential: negative pregnancy test and agreement to use effective contraception

Locations
United States
New York
Columbia University Irving Medical Center
RECRUITING
New York
Contact Information
Primary
Giuseppe Cullaro, MD, MAS
gc2576@cumc.columbia.edu
2123050914
Time Frame
Start Date: 2025-05-27
Estimated Completion Date: 2027-12-31
Participants
Target number of participants: 75
Treatments
Experimental: Droxidopa
Participants in this arm will receive oral droxidopa capsules at an initial dose of 100 mg three times daily, titrated in 100 mg increments every 24 hours based on blood pressure response and tolerability, up to a maximum dose of 300 mg three times daily. Doses will be given approximately 4 hours apart during daytime hours for a total treatment duration of 28 days.
Placebo_comparator: Placebo
Participants in this arm will receive matched placebo capsules following the same dosing schedule and titration protocol as the experimental arm. Placebo capsules will be identical in appearance to droxidopa capsules with the same over-encapsulation process to maintain blinding. Doses will be given three times daily for a total treatment duration of 28 days.
Related Therapeutic Areas
Sponsors
Leads: Giuseppe Cullaro, MD

This content was sourced from clinicaltrials.gov