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Terminated Phase 2Phase 3 Interventional Results available

Selepressin Evaluation Programme for Sepsis-Induced Shock - Adaptive Clinical Trial

ClinicalTrials.gov ID: NCT02508649

Public ClinicalTrials.gov record NCT02508649. 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 Sep 2, 2026, 4:51 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 Double-blind, Randomised, Placebo-Controlled, Phase 2b/3 Adaptive Clinical Trial Investigating the Efficacy and Safety of Selepressin as Treatment for Patients With Vasopressor-dependent Septic Shock

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a double-blind, randomised, placebo-controlled, two-part adaptive clinical trial. The trial is designed to investigate the efficacy and safety of multiple dosing regimens of selepressin and to confirm the efficacy and safety of one dosing regimen in treatment of adult patients with septic shock requiring vasopressor.

Study identification

NCT ID
NCT02508649
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2, Phase 3
Lead sponsor
Ferring Pharmaceuticals
Industry
Enrollment
868 participants

Conditions and interventions

Conditions

Interventions

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
Jun 30, 2015
Primary completion
Oct 2, 2017
Completion
Feb 25, 2018
Last update posted
Apr 5, 2021

2015 – 2018

United States locations

U.S. sites
17
U.S. states
13
U.S. cities
16
Facility City State ZIP Site status
Memorial Hospital Colorado Springs Colorado 80909
Eastern Idaho Regional Medical Center Idaho Falls Idaho 83404
Rush University Medical Center Chicago Illinois 60612
Northshore University Healthsystem Research Institute Evanston Illinois 60201
Stormont Vail Health Care Topeka Kansas 66604
Baystate Medical Center Springfield Massachusetts 01199
Henry Ford Hospital Detroit Michigan
HealthPartners Speciality Clinics Saint Paul Minnesota 55101
University of Nebraska Medical Center Omaha Nebraska 68198
Cooper University Hospital Camden New Jersey 08103
Wake Forest University School of Medicine Winston-Salem North Carolina 27157
Ohio State University Columbus Ohio 43210-1252
Remington Davis Inc Columbus Ohio 43215
St Vincent Mercy Medical Center Toledo Ohio 43608
University of Oklahoma Health Sciences Center Oklahoma City Oklahoma
Temple University Hospital Philadelphia Pennsylvania
University of Pittsburgh Medical Center Pittsburgh Pennsylvania

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 4 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02508649, 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 Apr 5, 2021 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02508649 live on ClinicalTrials.gov.

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