Study of Dose Confirmation and Safety of Crizanlizumab in Pediatric Sickle Cell Disease Patients

Last updated:
2026-07-11
Language and content disclaimer

The content and search results on this site are collected from or provided by third parties. As such some of the information may only be available in the language originally submitted by the sponsor of the trial. Learn more about the information on the search portal.

Linking to Non-Government of Canada Websites

Links to websites not under the control of the Government of Canada, including those to our social media accounts, and to clinical trial records in international registries are provided solely for the convenience of our website visitors. We are not responsible for the accuracy, currency or reliability of the content of such websites. The Government of Canada does not offer any guarantee in that regard and is not responsible for the information found through these links, nor does it endorse the sites and their content.

Visitors should also be aware that information offered by non-Government of Canada sites to which this website links is not subject to the Privacy Act or the Official Languages Act and may not be accessible to persons with disabilities. The information offered may be available only in the language(s) used by the sites in question. With respect to privacy, visitors should research the privacy policies of these non-government websites before providing personal information.

View trial details

Overview

Official protocol title:

A PHASE 2, MULTICENTER, OPEN-LABEL STUDY TO ASSESS APPROPRIATE DOSING AND TO EVALUATE SAFETY OF CRIZANLIZUMAB, WITH OR WITHOUT HYDROXYUREA/HYDROXYCARBAMIDE, IN SEQUENTIAL, DESCENDING AGE GROUPS OF PEDIATRIC SICKLE CELL DISEASE PATIENTS WITH VASO-OCCLUSIVE CRISIS

Intervention/treatment:
CRIZANLIZUMAB (SEG101)/ HYDROXYUREA
Medical condition:
SICKLE CELL DISEASE
Protocol code:
CSEG101B2201
Control number:
221186
Status:
Closed
Approved:
November 16, 2018
Date Completed:
Trial phase:
Phase 2
For more information:
ClinicalTrials.gov - NCT03474965
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
2 Years to 17 Years
Accepts healthy volunteers: No

Contacts and locations

Contact
Name
Study Director
Organization
Novartis Pharmaceuticals
Phone:
+ 1 862 778 8300
Sponsor
NOVARTIS PHARMACEUTICALS CANADA INC

Locations

Quebec

Novartis Investigative Site
Montreal, Quebec, H3T 1C5

Results

See the results from the trial NCT03474965. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
Did you find what you were looking for?