Fixed-dose Combination of an Angiotensin Receptor Blocker and Thiazide Diuretic for Essential Hypertension

Trial statusNot yet recruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18+
SponsorEurofarma Laboratorios S.A.

About this trial

This is a phase III, non-inferiority, randomized, double-blind, double-dummy, active-controlled, multicenter study to compare the efficacy and safety of N0877 versus double combination with already established efficacy on systolic blood pressure (SBP) in the sitting position in the medical office in patients with SAH after 8 weeks of treatment.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Ability to confirm voluntary participation and agree to all purposes of the study, signing and dating the Informed Consent Form in two copies.

Age ≥ 18 years.

Medical office blood pressure with SBP ≥ 160 mm Hg or DBP ≥ 100 mm Hg without pharmacological treatment or which is not adequately controlled with monotherapy or with a combination of two drugs in which at least one of the drugs is not at the maximum dose.

Uncontrolled arterial hypertension (medical office BP with SBP ≥ 140 mm Hg or DBP ≥ 90 mm Hg) after at least two (02) weeks of run-in treatment.

Disqualifiers

Pregnant or lactating women.

Women in the reproductive age or of childbearing potential who do not agree to use a proven effective contraceptive method, unless they are surgically sterile or expressly declare themselves to be free from the risk of pregnancy because they do not engage in sexual practices or engage in them in a non-reproductive manner.

Medical office blood pressure with SBP ≥ 180 mm Hg or DBP ≥ 110 mm mmHg.

Resistant hypertension or secondary hypertension of any etiology (including renovascular disease, pheochromocytoma and Cushing's syndrome).

Trial design

Design model

Parallel

Treatments tested in this trial

  • N0877

    Drug

    1 tablet of N0877 and 1 tablet of Placebo of Benicar HCT®

  • Benicar HCT ® Tablets 40 mg/25 mg

    Drug

    1 tablet of Benicar HCT® and 1 tablet of Placebo of N0877

Treatment groups

292 Participants
are divided into 2 treatment groups
Group A: N0877Experimental treatment 1 intervention
Group B: Benicar HCT®Active comparator 1 intervention

Trial outcomes

Primary outcomes

1

Mean change in SBP in the sitting position at medical office at week 8 after randomization from baseline

To demonstrate the non-inferiority of the N0877 to double combination with an already established profile (olmesartan 40 mg + hydrochlorothiazide 25 mg) on systolic blood pressure (SBP) in the sitting position in the medical office in patients with SAH after 8 weeks of treatment.

Time frame
8 weeks

Secondary outcomes

Other outcomes

Sponsors and contacts

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