A First-in-Human Safety and Efficacy Study of ALN-CFB, a Small Interfering RNA (siRNA) Targeting Complement Factor B, in Adult Participants With Paroxysmal Nocturnal Hemoglobinuria With Persistent Anemia on a C5 Inhibitor

Last updated:
2026-10-03
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View trial details

Overview

Official protocol title:

A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, FIRST-IN-HUMAN STUDY OF THE SAFETY, TOLERABILITY, PHARMACOKINETICS, AND PRELIMINARY EFFICACY OF ALN-CFB, AN INVESTIGATIONAL SIRNA THERAPEUTIC AGAINST COMPLEMENT FACTOR B, IN PARTICIPANTS WITH PAROXYSMAL NOCTURNAL HEMOGLOBINURIA AND PERSISTENT ANEMIA ON APPROVED C5-INHIBITOR THERAPY

Intervention/treatment:
ALN-CFB (ALN-1725763)
Medical condition:
PAROXYSMAL NOCTURNAL HEMOGLOBINURIA
Protocol code:
ALN-CFB-PNH-2468
Control number:
296898
Status:
Recruiting
Approved:
May 07, 2025
Trial phase:
Phase 1, Phase 2
For more information:
ClinicalTrials.gov - NCT07187401
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
18 Years and older
Accepts healthy volunteers: No

Contacts and locations

Contact
Name
Clinical Trials Administrator
Role
CONTACT
Phone:
844-734-6643
Sponsor
REGENERON PHARMACEUTICALS INC

Locations

Ontario

Toronto General Hospital
Toronto, Ontario, M5G 2C4
Recruiting
Name
Christopher Patriquin
Role
CONTACT
Phone:
416-340-3111
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