A Study of Safety, PK, & PD of ISIS 416858 Administered Subcutaneously to Patients With End-Stage Renal Disease on Hemodialysis

Last updated:
2026-07-11
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View trial details

Overview

Official protocol title:

A PHASE 2, RANDOMIZED, DOUBLE BLIND, PLACEBO CONTROLLED STUDY OF THE SAFETY, PHARMACOKINETICS, AND PHARMACODYNAMICS OF MULTIPLE DOSES OF ISIS 416858 (ISIS-FXIRX AN ANTISENSE INHIBITOR OF FACTOR XI), ADMINISTERED SUBCUTANEOUSLY TO PATIENTS WITH END-STAGE RENAL DISEASE ON HEMODIALYSIS

Intervention/treatment:
ISIS 416858
Medical condition:
END STAGE RENAL DISEASE
Protocol code:
ISIS 416858-CS4
Control number:
186334
Status:
Closed
Approved:
August 11, 2015
Trial phase:
Phase 2
For more information:
ClinicalTrials.gov - NCT02553889
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
18 Years to 80 Years
Accepts healthy volunteers: No

Contacts and locations

Contact
Sponsor
IONIS PHARMACEUTICALS INC

Locations

Alberta

Ionis Investigative Site
Edmonton, Alberta, T6G 2P4

Nova Scotia

Ionis Investigative Site
Halifax, Nova Scotia, B3H 1V8

Ontario

Ionis Investigative Site
Hamilton, Ontario, L8N 4A6
Ionis Investigative Site
London, Ontario, N6A 5W9
Ionis Investigative Site
Toronto, Ontario, M5B 1W8
Ionis Investigative Site
Toronto, Ontario, M9N 1N8

Quebec

Ionis Investigative Site
Montreal, Quebec, H2X 0A9
Ionis Investigative Site
Montreal, Quebec, H4J 1C5
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