PMID- 20678674 OWN - NLM STAT- MEDLINE DCOM- 20101122 LR - 20220409 IS - 1879-114X (Electronic) IS - 0149-2918 (Linking) VI - 32 IP - 7 DP - 2010 Jul TI - Triple therapy with olmesartan medoxomil, amlodipine besylate, and hydrochlorothiazide in adult patients with hypertension: The TRINITY multicenter, randomized, double-blind, 12-week, parallel-group study. PG - 1252-69 LID - 10.1016/j.clinthera.2010.07.008 [doi] AB - BACKGROUND: Patients with hypertension may require a combination of > or =2 antihypertensive agents to achieve blood pressure (BP) control. OBJECTIVE: The aim of this study was to determine whether a triple combination of olmesartan medoxomil (OM), amlodipine besylate (AML), and hydrochlorothiazide (HCTZ) had a clinically significant benefit compared with dual combinations of the individual components in patients with moderate to severe hypertension. METHODS: This was a multicenter, randomized, doubleblind, parallel-group study in which triple combination treatment with OM 40 mg + AML 10 mg + HCTZ 25 mg was compared with dual combinations of the individual components-OM 40 mg/AML 10 mg in fixed-dose combination, OM 40 mg/HCTZ 25 mg in fixed-dose combination, and AML 10 mg + HCTZ 25 mg-in patients aged > or =18 years who had a mean seated BP > or =140/100 mm Hg or > or =160/90 mm Hg. The study consisted of a 3-week washout period with no study medication and a 12-week double-blind treatment period. In the first 2 weeks of the double-blind treatment period, all patients were randomized to receive dual combination treatment or placebo. All patients assigned to a dual combination treatment group continued the assigned treatment until week 4, and all patients assigned to placebo were switched at week 2 to receive 1 of the dual combination treatments until week 4. At week 4, patients either continued dual combination treatment or switched to triple combination treatment until week 12. The primary end point was the change in seated diastolic BP (SeDBP) from baseline to week 12; SeDBP reduction of > or =2 mm Hg was considered a clinically significant benefit. Secondary efficacy end points included the change in seated systolic BP (SeSBP) at week 12 and the percentages of patients achieving BP targets of <140/90 mm Hg, <120/80 mm Hg, SeSBP <140 mm Hg, and SeDBP <90 mm Hg at week 12. The tolerability of the treatments was also evaluated based on adverse events (AEs), clinical laboratory evaluations (chemistry, hematology, and urinalysis), physical examinations, and 12-lead ECGs. RESULTS: The 2492 randomized patients (52.9% male, 66.8% white, 30.4% black) had a mean (SD) age of 55.1 (10.9) years and a mean weight of 96.0 (22.9) kg. Diabetes was present in 15.5% of the population, chronic cardiovascular disease in 9.1%, and chronic kidney disease in 4.1%. At baseline, the mean SeBP was 168.5/100.9 mm Hg. At week 12, triple combination treatment was associated with significantly greater least squares mean reductions in SeBP compared with the dual combinations (SeDBP: -21.8 vs -15.1 to -18.0 mm Hg, respectively [P < 0.001]; SeSBP: -37.1 vs -27.5 to -30.0 mm Hg [P < 0.001]). A significantly higher proportion of patients receiving triple combination treatment reached BP targets compared with the dual combinations at week 12 (P < 0.001). The proportions of patients reaching the BP target of <140/90 mm Hg at week 12 was 69.9% in the triple combination treatment group and 52.9%, 53.4%, and 41.1% in the treatment groups receiving OM 40 mg/AML 10 mg, OM 40 mg/HCTZ 25 mg, and AML 10 mg + HCTZ 25 mg, respectively (P < 0.001, triple combination vs each dual combination). The incidence of treatment-emergent AEs (TEAEs) was 58.4% for triple combination treatment and 51.7% to 58.9% for the dual combinations; most TEAEs were mild or moderate in severity. The most common TEAEs in the triple combination treatment group were dizziness (9.9%), peripheral edema (7.7%), and headache (6.4%). In total, 52 patients (2.3%) discontinued the study due to TEAEs-6 (1.0%) in the OM 40 mg/AML 10 mg group, 12 (2.1%) in the OM 40 mg/HCTZ 25 mg group, 11 (2.0%) in the AML 10 mg + HCTZ 25 mg group, and 23 (4.0%) in the OM 40 mg + AML 10 mg + HCTZ 25 mg group. Thirty-two patients (1.4%)-4 (0.7%), 5 (0.9%), 5 (0.9%), and 18 (3.1%) in the respective treatment groups-discontinued the study due to drug-related TEAEs. CONCLUSIONS: In these adult patients with moderate to severe hypertension, triple combination treatment with OM 40 mg + AML 10 mg + HCTZ 25 mg was associated with significant BP reductions compared with dual combinations of the individual components. All treatments were generally well tolerated. ClinicalTrials. gov identifier: NCT00649389. CI - 2010 Excerpta Medica Inc. All rights reserved. FAU - Oparil, Suzanne AU - Oparil S AD - University of Alabama at Birmingham, 35294-0007, USA. suzanne.oparil@ccc.uab.edu FAU - Melino, Michael AU - Melino M FAU - Lee, James AU - Lee J FAU - Fernandez, Victor AU - Fernandez V FAU - Heyrman, Reinilde AU - Heyrman R LA - eng SI - ClinicalTrials.gov/NCT00649389 PT - Comparative Study PT - Journal Article PT - Multicenter Study PT - Randomized Controlled Trial PT - Research Support, Non-U.S. Gov't PL - United States TA - Clin Ther JT - Clinical therapeutics JID - 7706726 RN - 0 (Antihypertensive Agents) RN - 0 (Drug Combinations) RN - 0 (Imidazoles) RN - 0 (Tetrazoles) RN - 0J48LPH2TH (Hydrochlorothiazide) RN - 1J444QC288 (Amlodipine) RN - 6M97XTV3HD (Olmesartan Medoxomil) SB - IM MH - Adult MH - Aged MH - Amlodipine/administration & dosage/adverse effects/*therapeutic use MH - Antihypertensive Agents/administration & dosage/adverse effects/therapeutic use MH - Blood Pressure/drug effects MH - Double-Blind Method MH - Drug Combinations MH - Drug Therapy, Combination MH - Female MH - Follow-Up Studies MH - Humans MH - Hydrochlorothiazide/administration & dosage/adverse effects/*therapeutic use MH - Hypertension/*drug therapy/physiopathology MH - Imidazoles/administration & dosage/adverse effects/*therapeutic use MH - Male MH - Middle Aged MH - Olmesartan Medoxomil MH - Severity of Illness Index MH - Tetrazoles/administration & dosage/adverse effects/*therapeutic use EDAT- 2010/08/04 06:00 MHDA- 2010/12/14 06:00 CRDT- 2010/08/04 06:00 PHST- 2010/06/14 00:00 [accepted] PHST- 2010/08/04 06:00 [entrez] PHST- 2010/08/04 06:00 [pubmed] PHST- 2010/12/14 06:00 [medline] AID - S0149-2918(10)00235-3 [pii] AID - 10.1016/j.clinthera.2010.07.008 [doi] PST - ppublish SO - Clin Ther. 2010 Jul;32(7):1252-69. doi: 10.1016/j.clinthera.2010.07.008.