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Phase 3 N=838 Treatment

26-week Open Study of telmisartan40mg+amlodipine10mg or telmisartan80mg+amlodipine10 mg in Hypertension

Hypertension

Enrolled (actual)
838
Serious AEs
1.2%
Results posted
Mar 2010
Primary outcome: Primary: Trough Seated Diastolic Blood Pressure (DBP) Control — 201; 402; 72; 70 patients

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
fixed-dose combination of telmisartan 40mg+amlodipine 10mg (Drug); fixed-dose combination of telmisartan 80mg+amlodipine10mg (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Boehringer Ingelheim
Primary completion
Jun 2009

Outcome Measures

OutcomeResultp-value
PRIMARY
Trough Seated Diastolic Blood Pressure (DBP) Control
201; 402; 72; 70; 15; 34
SECONDARY
Trough Seated Systolic Blood Pressure (SBP) Control
179; 366; 70; 51; 37; 70
SECONDARY
Change From Baseline to End of Study in Trough Seated Diastolic Blood Pressure
-13.41; -13.36; -11.52; -10.64
SECONDARY
Change in DBP From Last Available Trough in NCT00553267 to Last Available Trough in NCT00624052
-4.36; -4.97; -5.51; -5.43
SECONDARY
Change From Baseline to End of Study in Trough Seated Systolic Blood Pressure
-14.76; -15.93; -14.85; -12.44
SECONDARY
Change in SBP From Last Available Trough in NCT00553267 to Last Available Trough in NCT00624052
-4.73; -6.02; -6.55; -5.61
SECONDARY
Trough Seated DBP Response
201; 405; 71; 73; 13; 29
SECONDARY
Trough Seated SBP Response
190; 401; 75; 69; 24; 33
SECONDARY
Trough BP Normality Classes
12; 20; 5; 3; 70; 146
SECONDARY
Time to First Additional Antihypertensive
91.9
SECONDARY
Number of Patients Requiring Additional Antihypertensive Therapy to Achieve DBP Control
27; 67; 94; 4; 23; 27
SECONDARY
Additional Reduction in DBP by Use of Additional Antihypertensive Therapy
-6.79
SECONDARY
Additional Reduction in SBP by Use of Additional Antihypertensive Therapy
-7.79
SECONDARY
Trough DBP Control Pre- and Post- Uptitration
306; 168; 474; 18; 90; 108

Summary

The primary objective of this trial is to assess the efficacy and safety of the fixed dose combinations telmisartan 40mg/amlodipine 10mg (T40/A10) or telmisartan 80mg/amlodipine 10mg (T80/A10) during open-label treatment for at least six months. An additional objective is to assess the efficacy and safety of concomitant administration of either T40/A10 or T80/A10 with any other therapies commonly used in the treatment of hypertension. The primary endpoint is the proportion of patients achieving DBP control (defined as mean seated DBP < 90 mmHg at trough i.e. approximately 24 hours after last dose of study treatment) at six months of treatment or at last trough observation during the treatment period (i.e. last trough observation carried forward).

Eligibility Criteria

Inclusion Criteria

  • diagnosis of essential hypertension

Exclusion Criteria

  • pregnancy, breast-feeding, unwilling to use effective contraception (if female of child-bearing potential).
  • development of any condition in the preceding trial that could be worsened by telmisartan 40mg/amlodipine 10mg (T40/A10) or telmisartan 80mg/amlodipine 10mg (T80/A10).
  • discontinuation from the preceding trial.
  • known or suspected secondary hypertension.
  • mean seated systolic blood pressure (SBP) >= 180 mmHg and/or mean seated diastolic blood pressure (DBP) >= 120 mmHg at any visit.
  • any clinically significant hepatic impairment or severe renal impairment bilateral renal artery stenosis or renal artery stenosis in a solitary kidney or post post-renal transplant.
  • clinically relevant hyperkalaemia.
  • uncorrected volume or sodium depletion.
  • primary aldosteronism.
  • hereditary fructose or lactose intolerance.
  • symptomatic congestive heart failure.
  • patients who have previously experienced symptoms characteristic of angioedema during treatment with angiotensin converting enzyme (ACE) inhibitors or angiotensin receptor blockers (ARBs).
  • any new drug or alcohol dependency since signing consent of the preceding trial.
  • concurrent participation in another clinical trial or any investigational therapy since completing the preceding trial.
  • hypertrophic obstructive cardiomyopathy, hemodynamically relevant stenosis of the aortic or mitral valve.
  • known allergic hypersensitivity to any component of the formulations under investigation. [Includes known hypersensitivity to telmisartan or other ARBs or amlodipine or other dihydropyridine calcium channel blockers (CCBs).] non-compliance with study medication (defined as 120%) during the preceding trial.
  • administration of ARBs or dihydropyridine CCBs (apart from trial medication). any other clinical condition which, in the opinion of the investigator, would not allow safe completion of the protocol and safe administration of telmisartan and amlodipine.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00624052). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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