EICHORCondition: Heart Failure, Systolic · Sponsor: Intra-Cellular Therapies, Inc.
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This is a Phase I/II randomized, double-blind, placebo-controlled, single rising dose study in patients with systolic heart failure to evaluate the safety and tolerability of ITI-214.
This description comes directly from the study's public registry record.
No contact information is available for this study as per the public registry record.
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| Johns Hopkins University | Baltimore, Maryland, United States | — |
| Duke Clinical Research Institute | Durham, North Carolina, United States | — |
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Source record: clinicaltrials.gov/study/NCT03387215