Sanofi-Aventis
Bridgewater, New Jersey, 08807, United States
NCT Number: NCT00562809
The purpose of this study is to assess the efficacy and safety of Irbesartan 150/12.5 mg and 300/25 mg in patients with hypertension not controlled by monotherapy.
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Notify Me18 year and older
All sexes
Interventional
Phase 4
Bridgewater, New Jersey, 08807, United States
The primary and secondary endpoints applied to sub-groups defined by age, race, diabetes, metabolic syndrome and prior HTN therapy.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Note: Female patients must be post-menopausal for one year, surgically sterilized, or using a medically accepted method of contraception (intrauterine device, oral contraceptives, barrier method with spermicide) and must agree to use an effective method of contraception throughout the study.
Exclusion criteria
150/12.5 mg tablets one or two tablets orally per day
Time frame: from baseline to week 18
Time frame: from baseline to week 18.
Time frame: from baseline to week 10
Time frame: at weeks 10 and 18
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Notify MeSanofi
Industry
A Multicenter, Open-Label Study Assessing the Efficacy and Safety of Irbesartan 150/12.5 mg and 300/25 mg in Patients With Hypertension Not Controlled by Monotherapy
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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