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Completed Phase 3 Interventional Results available

Phase III Trial With Caplacizumab in Patients With Acquired Thrombotic Thrombocytopenic Purpura

ClinicalTrials.gov ID: NCT02553317

Public ClinicalTrials.gov record NCT02553317. 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 Jul 21, 2026, 6:50 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 Phase III Double-blind, Randomized, Parallel Group, Multicenter Placebo-controlled Trial to Study the Efficacy and Safety of Caplacizumab in Patients With Acquired Thrombotic Thrombocytopenic Purpura

Study identification

NCT ID
NCT02553317
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Ablynx, a Sanofi company
Industry
Enrollment
145 participants

Conditions and interventions

Interventions

  • Caplacizumab Biological
  • Placebo Biological

Biological

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
Oct 31, 2015
Primary completion
Jul 31, 2017
Completion
Jul 31, 2017
Last update posted
Apr 4, 2023

2015 – 2017

United States locations

U.S. sites
19
U.S. states
13
U.S. cities
18
Facility City State ZIP Site status
Investigator Site Birmingham Alabama 35249
Investigator Site Los Angeles California 90033
Investigator Site Atlanta Georgia 30322
Investigator Site Boston Massachusetts 02114
Investigator Site St Louis Missouri 63110
Investigator Site Rochester New York 14642
Investigator Site Rochester New York 55905
Investigator Site Valhalla New York 10595
Investigator Site Chapel Hill North Carolina 27599
Investigator Site Durham North Carolina 27710
Investigator Site Winston-Salem North Carolina 27157
Investigator SIte Cleveland Ohio 44195
Investigator Site Columbus Ohio 43210
Investigator Site Oklahoma City Oklahoma 73104
Investigator Site Pittsburgh Pennsylvania 15213
Investigator Site Charleston South Carolina 29425
Investigator Site Greenville South Carolina 27834
Investigator Site Houston Texas 77030
Investigator Site Salt Lake City Utah 84112

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 82 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02553317, 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 4, 2023 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02553317 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →