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Completed Phase 3 Interventional

Evaluation of Repeat Administration of Purified Poloxamer 188

ClinicalTrials.gov ID: NCT02449616

Public ClinicalTrials.gov record NCT02449616. 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 Oct 20, 2026, 10:51 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

Evaluation of Repeat Administration of Purified Poloxamer 188 in Vaso-Occlusive Crisis of Sickle Cell Disease (EPIC-E): An Open-Label Safety Extension Trial Assessing Repeat Administration of MST-188 (Purified Poloxamer 188) Injection in Subjects With Sickle Cell Disease Experiencing Vaso Occlusive Crisis

Brief summary

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

The purpose of this study is to evaluate the safety of repeat administration of MST-188 during vaso-occlusive crisis of sickle cell disease. Additionally, this study will evaluate the development of acute chest syndrome during VOC and re-hospitalization for recurrence of VOC.

Study identification

NCT ID
NCT02449616
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Mast Therapeutics, Inc.
Industry
Enrollment
16 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
4 Years to 65 Years
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 2015 (Type not available)
Primary completion
Sep 2016 (Actual)
Completion
Not listed
Last update posted
Oct 28, 2016

Started 2015

United States locations

U.S. sites
9
U.S. states
8
U.S. cities
9
Facility City State ZIP Site status
Rady Children's Hospital San Diego California — —
Children's Hospital of Southwest Florida Fort Myers Florida 33908 —
Joe Dimaggio Children's Hospital Hollywood Florida 33021 —
Ann and Robert H. Lurie Children's Hospital of Chicago Chicago Illinois — —
University of Iowa Children's Hospital Iowa City Iowa — —
Our Lady of the Lake Children's Hospital Baton Rouge Louisiana 70808 —
Rutgers University New Brunswick New Jersey — —
Medical University of South Carolina Charleston South Carolina — —
T. C. Thompson Children's Hospital Chattanooga Tennessee — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02449616, 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 Oct 28, 2016 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02449616 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →