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Double-blind study of VAA489 in patients with essential hypertension (factorial study)

Double-blind study of VAA489 in patients with essential hypertension (factorial study)

Status
Unknown
Phases
Phase 3
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT2080220350
Enrollment
1404
Registered
2007-02-13
Start date
2007-02-13
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertension

Interventions

Sponsors

Novartis Pharma K.K.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria - Essential hypertension - Outpatients - Male or female aged 20 to 80 years old Exclusion criteria - Secondary hypertension or suspected of having secondary hypertension - A history of malignant hypertension - Severe hypertension - Significant heart, renal, hepatic diseases or significant cerebrovascular disorder Other protocol-defined inclusion/exclusion criteria may apply

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Primary Outcomes: Change from baseline in mean sitting diastolic blood pressure at 8 weeks. Secondary Outcomes: Change from baseline in mean sitting systolic blood pressure (MSSBP) at trough at 8 weeks.; Responder rate for achieving MSDBP < 90 mmHg or a = 10 mmHg decrease compared to baseline.; Diastolic control rate for achieving MSDBP < 90mmHg.; Blood pressure control rate for achieving MSDBP <90 mmHg and MSSBP <140 mmHg.

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026