A Study of CST-3056 for Neurogenic Orthostatic Hypotension

This study is looking at how a drug called CST-3056, given as an oral solution, affects people with neurogenic orthostatic hypotension (nOH). nOH is a condition where your blood pressure drops significantly when you stand up, often due to Parkinson's disease or pure autonomic failure. Researchers want to see if CST-3056 can improve symptoms and signs of nOH. You might be able to join if you are between 18 and 85 years old and have been diagnosed with symptomatic nOH. The main way they will measure success is by checking changes in your standing systolic blood pressure (the top number in a blood pressure reading) over several hours after taking the drug. The study is currently unclear about its recruitment status and plans to enroll 12 participants.

Study design
This is an interventional study, meaning participants will receive a specific treatment. It is a single-blind, dose-ranging study, meaning you won't know if you're getting CST-3056 or a placebo (an inactive substance), but the researchers will.
What's involved
You would take single oral doses of CST-3056 or placebo once daily for five days. You may need to stop certain medications for at least one day before screening and before starting the study drug.
Compensation
Not stated in the trial record.
Follow-up
Between 3-7 days after leaving the in-patient stay, you will be contacted by phone to check on your health status.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07089043

A Study in Subjects With Neurogenic Orthostatic Hypotension

Active, Not Recruiting
PHASE2Ages 18–85InterventionalTreatment
CuraSen Therapeutics, Inc.
~12 participants
Updated 2026-08-28 on ClinicalTrials.gov
What's tested:CST-3056Placebo

At a glance

Recruiting sites
0 of 5 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Change from Baseline in Standing Systolic Blood Pressure
Measured over Baseline and 1, 2, 3, and 4 hours post-dose on Days 1 to 4
Neurogenic Orthostatic Hypotension

NCT07089043

Where you'd take part

This study runs at 5 sites. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • CuraSen Investigational Site

    Scottsdale, Arizonano site contact published

  • CuraSen Investigational Site

    Farmington Hills, Michiganno site contact published

  • CuraSen Investigational Site

    Eatontown, New Jerseyno site contact published

  • CuraSen Investigational Site

    New York, New Yorkno site contact published

  • CuraSen Investigational Site

    Nashville, Tennesseeno site contact published

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

  • Chief Medical Officer · STUDY_DIRECTOR · CuraSen Therapeutics, Inc.

This trial hasn't published a contact. View it on ClinicalTrials.gov

  • Change from Baseline in Standing Systolic Blood PressureBaseline and 1, 2, 3, and 4 hours post-dose on Days 1 to 4

    Baseline is defined as the pre-dose measurement on Day 1