Project Details
Description
The purpose of this study is to evaluate the efficacy and safety of lumasiran in children and adults with primary hyperoxaluria type 1 (PH1).
| Acronym | ILLUMINATE-A |
|---|---|
| Status | Finished |
| Effective start/end date | 27/11/18 → 12/01/24 |
Collaborative partners
- Alnylam Pharmaceuticals (lead)
Keywords
- PH1
- Primary Hyperoxaluria
- RNAi Therapeutic
- siRNA
- AGT
- Oxalate
- Hyperoxaluria
- Kidney Diseases
- Urologic Diseases
- Female Urogenital Diseases
- Female Urogenital Diseases and Pregnancy Complications
- Urogenital Diseases
- Male Urogenital Diseases
- Carbohydrate Metabolism, Inborn Errors
- Inborn Genetic Diseases
- Metabolic Diseases
- Renal Agents
- Lumasiran
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