Evaluate the Safety and Tolerability, as Well as the Pharmacokinetic and Pharmacodynamic Profiles of Single and Multiple Doses of Eplontersen Administered Subcutaneously to Healthy Volunteers and Patients With Hereditary Transthyretin-Mediated Amyloido…

Last updated:
2026-07-25
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View trial details

Overview

Official protocol title:

A PHASE 1/2 STUDY TO EVALUATE THE SAFETY, TOLERABILITY, PHARMACOKINETICS, AND PHARMACODYNAMICS OF ION-682884, AN ANTISENSE INHIBITOR OF TRANSTHYRETIN PRODUCTION, IN HEALTHY VOLUNTEERS AND PATIENTS WITH HEREDITARY TRANSTHYRETIN-MEDIATED AMYLOIDOSIS

Intervention/treatment:
ION-682884
Medical condition:
AMYLOIDOSIS
Protocol code:
ION-682884-CS1
Control number:
220514
Status:
Closed
Approved:
October 24, 2018
Date Completed:
Trial phase:
Phase 1, Phase 2
For more information:
ClinicalTrials.gov - NCT03728634
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
18 Years to 65 Years
Accepts healthy volunteers: Yes

Contacts and locations

Contact
Name
Ionis Pharmaceuticals, Inc.
Organization
Ionis Pharmaceuticals, Inc.
Phone:
800-679-4747
Sponsor
IONIS PHARMACEUTICALS INC

Locations

Ontario

Bio Pharma Services, Inc.
Toronto, Ontario, M9L 3A2

Results

See the results from the trial NCT03728634. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
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