drugset / Trial / NCT03101878

Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Ionis AGT-LRx in Healthy Volunteers

NCT03101878 ↗

Phase 1 Completed 62 enrolled Ionis Pharmaceuticals, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose is to assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of IONIS AGT-LRx in up to 82 Healthy Volunteers

Timeline

Start
2017-04-05
Primary completion
2018-03-29
Completion
2018-08-01

Drugs

EvaluationDrugModalityDoseRoute
Subject IONIS-AGT-LRx Antisense oligonucleotide — Subcutaneous

Indications

No indication recorded.