drugset / Trial / NCT03548415

Safety, Tolerability, and Efficacy of IONIS-GHR-LRx in Participants With Acromegaly Being Treated With Long-acting Somatostatin Receptor Ligands

NCT03548415

Phase 2 Completed 43 enrolled Ionis Pharmaceuticals, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study was to assess the safety, tolerability, and efficacy of IONIS-GHR-LRx in up to 60 participants with acromegaly.

Timeline

Start
2018-09-13
Primary completion
2021-02-18
Completion
2021-04-02

Drugs

EvaluationDrugModalityDoseRoute
Subject IONIS GHR-LRx Antisense oligonucleotide 60 mg Subcutaneous
Subject IONIS GHR-LRx Antisense oligonucleotide 80 mg Subcutaneous
Subject IONIS GHR-LRx Antisense oligonucleotide 120 mg Subcutaneous
Subject IONIS GHR-LRx Antisense oligonucleotide 160 mg Subcutaneous

Indications