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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 Oct 21, 2026, 1:45 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

Brief summary

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

The study was a Phase III, double-blind, placebo-controlled, randomized study to evaluate the efficacy of caplacizumab in more rapidly restoring normal platelet counts as measure of prevention of further microvascular thrombosis

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

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
Nov 2015 (Actual)
Primary completion
Aug 2017 (Actual)
Completion
Aug 2017 (Actual)
Last update posted
Apr 5, 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 5, 2023 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02553317 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →