Efficacy and Safety of SIL-8301 for Control of Hemolysis in a Uniform Sickle Cell Disease Endotype

Last updated:
2026-09-12
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View trial details

Overview

Official protocol title:

A MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO DETERMINE EFFICACY AND SAFETY OF SIL-8301 IN SICKLE CELL DISEASE (SCD) PATIENTS WITH A PREDOMINANTLY HEMOLYTIC PHENOTYPE

Intervention/treatment:
SENICAPOC (SIL-8301)
Medical condition:
SICKLE CELL DISEASE
Protocol code:
SIL-8301-001
Control number:
301325
Status:
Recruiting
Approved:
September 24, 2025
Trial phase:
Phase 2
For more information:
ClinicalTrials.gov - NCT07282210
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
16 Years to 35 Years
Accepts healthy volunteers: No

Contacts and locations

Contact
Name
Head of Clinical Operations
Role
CONTACT
Phone:
(978) 245-7397
Sponsor
BIOSSIL INC.

Locations

Ontario

The Hospital for Sick Children
Toronto, Ontario
RECRUITING
University Health Network, Toronto General Hospital
Toronto, Ontario
NOT_YET_RECRUITING

Quebec

Centre Hospitalier de l'Université de Montréal (CHUM)
Montreal, Quebec
NOT_YET_RECRUITING
McGill University Health Centre
Montreal, Quebec
NOT_YET_RECRUITING
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