drugset / Trial / NCT00272961

A Study Of Different Doses Of TBC3711 In Patients With Uncontrolled High Blood Pressure Already Taking Medications For High Blood Pressure.

NCT00272961 ↗

Phase 2 Terminated 60 enrolled Pfizer
RandomizedParallel-groupDouble-blindTreatment

Summary

The study was to determine the safe and effective dose of TBC3711 in patients with uncontrolled high blood pressure while already taking blood pressure medications.

Timeline

Start
2006-01
Primary completion
2008-08
Completion
2008-08

Outcome

Mixed primary results

Stopped: “See termination reason in detailed description.”

registry analysis (superiority or other test); Placebo vs TBC3711 10 mg; p = 0.044; LS Mean Difference 5.62 (95% CI 0.17 to 11.08); ANCOVA NCT00272961 ↗

registry analysis (superiority or other test); Placebo vs TBC3711 50 mg; p = 0.970; LS Mean Difference 0.21 (95% CI -11.16 to 11.59); ANCOVA NCT00272961 ↗

registry analysis (superiority or other test); Placebo vs TBC3711 100 mg; p = 0.0269; LS Mean Difference 224.89 (95% CI 27.5 to 422.3); ANCOVA NCT00272961 ↗

registry analysis (superiority or other test); Placebo vs TBC3711 50 mg; p = 0.2274; LS Mean Difference 114.77 (95% CI -75.2 to 304.8); ANCOVA NCT00272961 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject TBC3711 Unknown 10 mg —
Subject TBC3711 Unknown 50 mg —
Subject TBC3711 Unknown 100 mg —
Subject TBC3711 Unknown 200 mg —