Trials / Completed
CompletedNCT03350451
An Extension Study of an Investigational Drug, Lumasiran (ALN-GO1), in Participants With Primary Hyperoxaluria Type 1
A Phase 2, Multicenter, Open-Label, Extension Study to Evaluate the Long-Term Administration of ALN-GO1 in Patients With Primary Hyperoxaluria Type 1
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 20 (actual)
- Sponsor
- Alnylam Pharmaceuticals · Industry
- Sex
- All
- Age
- 6 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to evaluate the long-term safety and tolerability of lumasiran in participants with Primary Hyperoxaluria Type 1.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Lumasiran | Multiple doses of lumasiran by SC injection |
Timeline
- Start date
- 2018-04-04
- Primary completion
- 2023-02-07
- Completion
- 2023-02-07
- First posted
- 2017-11-22
- Last updated
- 2024-04-25
- Results posted
- 2024-04-25
Locations
9 sites across 5 countries: France, Germany, Israel, Netherlands, United Kingdom
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT03350451. Inclusion in this directory is not an endorsement.