Organization
Dicerna Pharmaceuticals
10 clinical trials
Clinical trial
A Phase 2 Open-Label Multicenter Study to Evaluate the Safety, Pharmacokinetics, and Efficacy of Nedosiran in Pediatric Patients From Birth to 11Years of Age With Primary Hyperoxaluria and Relatively Intact Renal FunctionStatus: Recruiting, Estimated PCD: 2024-12-01
Clinical trial
A Phase 2, Randomized, Double-blind, Placebo-Controlled Study Investigating Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Two Dose Levels of Belcesiran in Patients With Alpha-1 Antitrypsin Deficiency-Associated Liver DiseaseStatus: Active (not recruiting), Estimated PCD: 2023-12-08
Clinical trial
An Open-Label Roll-Over Study to Evaluate the Long-Term Safety and Efficacy of DCR-PHXC Solution for Injection (Subcutaneous Use) in Patients With Primary HyperoxaluriaStatus: , Estimated PCD: 2030-04-01
Clinical trial
A Phase 2 Open-Label Study to Evaluate the Safety and Efficacy of DCR-PHXC in Patients With Primary Hyperoxaluria Type 1 or 2 and Severe Renal Impairment, With or Without DialysisStatus: Recruiting, Estimated PCD: 2024-11-01
Clinical trial
A Phase 1 Single Ascending Dose, Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics Study of Subcutaneously Administered Belcesiran in Healthy Adult VolunteersStatus: Completed, Estimated PCD: 2021-07-06
Clinical trial
A Phase 1b, Double-blind, Placebo-controlled, Repeat-dose, Safety, Tolerability, Pharmacokinetic, and Pharmacodynamic Study of DCR-AUD in Healthy VolunteersStatus: Completed, Estimated PCD: 2023-08-22
Clinical trial
A Phase 1, Double-blind, Placebo-controlled, Single-ascending Dose, Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics Study of DCR-AUD in Healthy VolunteersStatus: Completed, Estimated PCD: 2022-12-31
Clinical trial
A Three-Part, Phase 1, Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics Study of DCR-HBVS in Healthy Volunteers and Patients With Chronic Hepatitis BStatus: Completed, Estimated PCD: 2022-07-12
Clinical trial
An Open-label, Phase 1, Dose-ranging Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Intravenous DCR-STAT3 in Adults With Refractory Solid TumorsStatus: Recruiting, Estimated PCD: 2025-07-01