Project Details
Description
Multicenter, open-label, single dose study to evaluate safety, tolerability and pharmacokinetics of LCZ696 followed by a 52-week randomized, double-blind, parallel group, active-controlled study to evaluate
Status | Finished |
---|---|
Effective start/end date | 1/1/16 → 9/30/21 |
Funding
- NOVARTIS PHARMACEUTICALS CORPORATION
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