drugset / Trial / NCT04522180

A Study to Assess the Safety, Tolerability, and Efficacy of IONIS-GHR-LRx Administered in Patients With Acromegaly

NCT04522180 ↗

Phase 2 Completed 34 enrolled Ionis Pharmaceuticals, Inc.
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study was to determine the safety, tolerability, and efficacy of IONIS-GHR-LRx subcutaneous (SC) injection as monotherapy in patients with acromegaly.

Timeline

Start
2021-01-04
Primary completion
2022-07-15
Completion
2023-05-04

Drugs

EvaluationDrugModalityDoseRoute
Subject GHR-LRX Antisense oligonucleotide 120 mg Subcutaneous
Subject GHR-LRX Antisense oligonucleotide 160 mg Subcutaneous

Indications