drugset / Trial / NCT00686803

Safety Study of Subcutaneously Administered PL-3994 in Subjects With Controlled Hypertension

NCT00686803 ↗

Phase 2 Completed 21 enrolled Palatin Technologies, Inc
RandomizedParallel-groupTriple-blindTreatment

Summary

The objective of this study is to evaluate the safety, tolerability, and pharmacokinetics of subcutaneous (SC) PL-3994, relative to placebo in subjects with controlled hypertension. Including in this evaluation is the effect PL3994 has on blood pressure.

Timeline

Start
2008-04
Primary completion
2008-07
Completion
2008-07

Drugs

EvaluationDrugModalityDoseRoute
Subject PL-3994 Protein / enzyme biologic — Subcutaneous

Indications