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Low-Dose TEL/AML/CHTD SPC Versus Standard-Dose TEL in Hypertension: Phase III RCT

delete2026-04-01
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PRE
AI
L
Lee, Cheol Whan
J
Jong‐Hwa Ahn
K
K Lim
I
IL SUK SOHN
S
Sung, Ki-Chul
K
Kye Hun Kim
J
Jang Ho Bae
S
S Hong
W
W Jang
S
Sang Ho Jo
H
Han, Seung Hwan
K
Kim, Ji Bak
C
Chan Joo Lee
J
Ju-Hee Lee
N
N K Kim
E
Eun Joo Cho
S
Sung, Jung-Hoon
H
Hyo-Suk Ahn
S
S Y Kim
J
Jinho Shin Shin
S
Suk Min Seo
W
Weon Kim
C
Chang-Gyu Park
DOI:10.1161/HYPERTENSIONAHA.125.25810delete
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Abstract

Abstract

En 中文
BACKGROUND: Although low-dose triple single-pill combination therapies show promising efficacy and safety, studies comparing them to standard-dose monotherapies remain limited. This phase III, randomized, double-blind trial evaluated the efficacy and safety of a low-dose single-pill combination of telmisartan, amlodipine, and chlorthalidone versus standard-dose telmisartan monotherapy in patients with essential hypertension. METHODS: After a 4-week placebo run-in period, 314 eligible subjects were randomized to either receive telmisartan/amlodipine/chlorthalidone 20/2.5/6.25 mg or telmisartan 40 mg for 8 weeks. The primary efficacy end point was the change in mean sitting systolic blood pressure from baseline to week 8, with noninferiority assessed in the per-protocol set (PPS), followed by superiority testing in the full analysis set using a gatekeeping approach to control for type I error. RESULTS: At week 8, the combination group demonstrated significant mean sitting systolic blood pressure reduction compared with monotherapy in the per-protocol set analysis (least squares mean difference, -3.8 mm Hg [95% CI: -6.7 to -0.9]; P=0.01), establishing its noninferiority. Furthermore, the superiority of the combination therapy was confirmed in the full analysis set (LS mean difference, -4.0 mm Hg [95% CI, -6.8 to -1.3]; P<0.01). Mean sitting diastolic BP, BP normalization rates, and response rates also favored the combination group at weeks 4 and 8 (all P<0.01). Subgroup analyses showed consistent efficacy across clinical strata, including age and prior antihypertensive treatment. The incidence of adverse events was comparable between groups, with no serious drug-related events reported. CONCLUSIONS: Low-dose triple single-pill combination of telmisartan/amlodipine/chlorthalidone demonstrated superior BP-lowering efficacy with well-tolerated and comparable safety to standard-dose telmisartan monotherapy.
Keywords:
amlodipine
antihypertensive agents
blood pressure
chlorthalidone
hypertension
telmisartan

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Hypertension cover
Hypertension
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