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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00624052
Other study ID # 1235.8
Secondary ID
Status Completed
Phase Phase 3
First received February 5, 2008
Last updated May 13, 2014
Start date March 2008

Study information

Verified date May 2014
Source Boehringer Ingelheim
Contact n/a
Is FDA regulated No
Health authority Australia: Responsilble Ethics CommitteeAustria: Federal Office for Safety in Health CareBulgaria: Bulgarian Drug Agency, BG-1504 SofiaCzech Republic: State Institute for Drug Control (SUKL), CZ-100 41 Prague 10Great Britain: MHRAIreland: Irish Medicines BoardItaly: Comitato Etico della prov. Di FerraraNew Zealand: Multicentre Ethics Committee/MedsafeRussia: Ministry of Healthcare and Social Development of Russian Federation, MoscowSlovakia: SUKL (state institute for drug control), SK-825 08 Bratislava 26Spain: Agencia Española del Medicamento y Productos Sanitarios (AEMPS)Ukraine: Ministry of Health Care of Ukraine (MoH of Ukraine)
Study type Interventional

Clinical Trial 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).


Recruitment information / eligibility

Status Completed
Enrollment 838
Est. completion date
Est. primary completion date June 2009
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility 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 <80% or >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.

Study Design

Endpoint Classification: Safety/Efficacy Study, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
fixed-dose combination of telmisartan 40mg+amlodipine 10mg

fixed-dose combination of telmisartan 80mg+amlodipine10mg


Locations

Country Name City State
Australia 1235.8.61005 Boehringer Ingelheim Investigational Site Elizabeth Vale South Australia
Australia 1235.8.61003 Boehringer Ingelheim Investigational Site Gosford New South Wales
Australia 1235.8.61002 Boehringer Ingelheim Investigational Site Kippa-Ring Queensland
Australia 1235.8.61004 Boehringer Ingelheim Investigational Site Liverpool New South Wales
Australia 1235.8.61001 Boehringer Ingelheim Investigational Site Milton Queensland
Austria 1235.8.43007 Boehringer Ingelheim Investigational Site Eggenburg
Austria 1235.8.43006 Boehringer Ingelheim Investigational Site Hainburg a.d. Donau
Austria 1235.8.43001 Boehringer Ingelheim Investigational Site Wien
Austria 1235.8.43002 Boehringer Ingelheim Investigational Site Wien
Austria 1235.8.43003 Boehringer Ingelheim Investigational Site Wien
Bulgaria 1235.8.35912 Boehringer Ingelheim Investigational Site Bourgas
Bulgaria 1235.8.35902 Boehringer Ingelheim Investigational Site Sofia
Bulgaria 1235.8.35903 Boehringer Ingelheim Investigational Site Sofia
Bulgaria 1235.8.35904 Boehringer Ingelheim Investigational Site Sofia
Bulgaria 1235.8.35905 Boehringer Ingelheim Investigational Site Sofia
Bulgaria 1235.8.35906 Boehringer Ingelheim Investigational Site Sofia
Bulgaria 1235.8.35907 Boehringer Ingelheim Investigational Site Sofia
Bulgaria 1235.8.35910 Boehringer Ingelheim Investigational Site Sofia
Bulgaria 1235.8.35911 Boehringer Ingelheim Investigational Site Sofia
Czech Republic 1235.8.42002 Boehringer Ingelheim Investigational Site Benatky nad Jizerou
Czech Republic 1235.8.42006 Boehringer Ingelheim Investigational Site Brno
Czech Republic 1235.8.42001 Boehringer Ingelheim Investigational Site Plzen
Czech Republic 1235.8.42003 Boehringer Ingelheim Investigational Site Praha 5
Czech Republic 1235.8.42004 Boehringer Ingelheim Investigational Site Pribram
Czech Republic 1235.8.42005 Boehringer Ingelheim Investigational Site Slany
Czech Republic 1235.8.42007 Boehringer Ingelheim Investigational Site Strakonice
Ireland 1235.8.35304 Boehringer Ingelheim Investigational Site Birr
Ireland 1235.8.35305 Boehringer Ingelheim Investigational Site Carrigtowhill
Ireland 1235.8.35303 Boehringer Ingelheim Investigational Site Gorey, Co. Wexford
Ireland 1235.8.35306 Boehringer Ingelheim Investigational Site Mallow
Ireland 1235.8.35301 Boehringer Ingelheim Investigational Site New Ross
Italy 1235.8.39002 Boehringer Ingelheim Investigational Site Broni (pv)
Italy 1235.8.39006 Boehringer Ingelheim Investigational Site Coppito (AQ)
Italy 1235.8.39001 Boehringer Ingelheim Investigational Site Ferrara
New Zealand 1235.8.64003 Boehringer Ingelheim Investigational Site Dunedin
New Zealand 1235.8.64002 Boehringer Ingelheim Investigational Site Otahuhu, Auckland
New Zealand 1235.8.64001 Boehringer Ingelheim Investigational Site Tauranga
Russian Federation 1235.8.70004 Boehringer Ingelheim Investigational Site Moscow
Russian Federation 1235.8.70005 Boehringer Ingelheim Investigational Site Moscow
Russian Federation 1235.8.70006 Boehringer Ingelheim Investigational Site Moscow
Russian Federation 1235.8.70007 Boehringer Ingelheim Investigational Site Moscow
Russian Federation 1235.8.70008 Boehringer Ingelheim Investigational Site Moscow
Russian Federation 1235.8.70009 Boehringer Ingelheim Investigational Site Moscow
Russian Federation 1235.8.70010 Boehringer Ingelheim Investigational Site St. Petersburg
Russian Federation 1235.8.70011 Boehringer Ingelheim Investigational Site St. Petersburg
Russian Federation 1235.8.70012 Boehringer Ingelheim Investigational Site St. Petersburg
Slovakia 1235.8.42103 Boehringer Ingelheim Investigational Site Dolny Kubin
Slovakia 1235.8.42106 Boehringer Ingelheim Investigational Site Kralovsky Chmlec
Slovakia 1235.8.42104 Boehringer Ingelheim Investigational Site Liptovsky Mikulas
Slovakia 1235.8.42102 Boehringer Ingelheim Investigational Site Povazska Bystrica
Slovakia 1235.8.42105 Boehringer Ingelheim Investigational Site Presov
Slovakia 1235.8.42101 Boehringer Ingelheim Investigational Site Trencin
Slovakia 1235.8.42107 Boehringer Ingelheim Investigational Site Vrable
Spain 1235.8.34008 Boehringer Ingelheim Investigational Site Badalona
Spain 1235.8.34010 Boehringer Ingelheim Investigational Site Badalona
Spain 1235.8.34009 Boehringer Ingelheim Investigational Site Barcelona
Spain 1235.8.34001 Boehringer Ingelheim Investigational Site Jerez de la Frontera (Cádiz)
Spain 1235.8.34006 Boehringer Ingelheim Investigational Site L'Hospitalet de Llobregat (Barcelona)
Spain 1235.8.34003 Boehringer Ingelheim Investigational Site Madrid
Spain 1235.8.34004 Boehringer Ingelheim Investigational Site Madrid
Spain 1235.8.34012 Boehringer Ingelheim Investigational Site Mataró
Spain 1235.8.34002 Boehringer Ingelheim Investigational Site Oviedo
Spain 1235.8.34005 Boehringer Ingelheim Investigational Site Santa Coloma de Gramanet
Spain 1235.8.34011 Boehringer Ingelheim Investigational Site Santa Coloma de Gramanet
Ukraine 1235.8.38010 Boehringer Ingelheim Investigational Site Dnepropetrovsk
Ukraine 1235.8.38001 Boehringer Ingelheim Investigational Site Kharkov
Ukraine 1235.8.38003 Boehringer Ingelheim Investigational Site Kharkov
Ukraine 1235.8.38008 Boehringer Ingelheim Investigational Site Kharkov
Ukraine 1235.8.38011 Boehringer Ingelheim Investigational Site Kharkov
Ukraine 1235.8.38004 Boehringer Ingelheim Investigational Site Kiev
Ukraine 1235.8.38006 Boehringer Ingelheim Investigational Site Kiev
Ukraine 1235.8.38012 Boehringer Ingelheim Investigational Site Kiev
Ukraine 1235.8.38013 Boehringer Ingelheim Investigational Site Kiev
Ukraine 1235.8.38002 Boehringer Ingelheim Investigational Site Lvov
Ukraine 1235.8.38005 Boehringer Ingelheim Investigational Site Odessa
Ukraine 1235.8.38009 Boehringer Ingelheim Investigational Site Odessa
Ukraine 1235.8.38007 Boehringer Ingelheim Investigational Site Zaporozhye
United Kingdom 1235.8.44010 Boehringer Ingelheim Investigational Site Bexhill on Sea
United Kingdom 1235.8.44008 Boehringer Ingelheim Investigational Site Blackpool
United Kingdom 1235.8.44016 Boehringer Ingelheim Investigational Site Blackpool
United Kingdom 1235.8.44011 Boehringer Ingelheim Investigational Site Burbage
United Kingdom 1235.8.44007 Boehringer Ingelheim Investigational Site Chestfield, Whitstable
United Kingdom 1235.8.44005 Boehringer Ingelheim Investigational Site Chorley
United Kingdom 1235.8.44002 Boehringer Ingelheim Investigational Site Edgbaston, Birmingham
United Kingdom 1235.8.44009 Boehringer Ingelheim Investigational Site Ely
United Kingdom 1235.8.44001 Boehringer Ingelheim Investigational Site Fowey
United Kingdom 1235.8.44003 Boehringer Ingelheim Investigational Site Glasgow
United Kingdom 1235.8.44012 Boehringer Ingelheim Investigational Site Penzance
United Kingdom 1235.8.44013 Boehringer Ingelheim Investigational Site Plymouth
United Kingdom 1235.8.44004 Boehringer Ingelheim Investigational Site Reading
United Kingdom 1235.8.44015 Boehringer Ingelheim Investigational Site St. Austell
United Kingdom 1235.8.44006 Boehringer Ingelheim Investigational Site Whitstable

Sponsors (1)

Lead Sponsor Collaborator
Boehringer Ingelheim

Countries where clinical trial is conducted

Australia,  Austria,  Bulgaria,  Czech Republic,  Ireland,  Italy,  New Zealand,  Russian Federation,  Slovakia,  Spain,  Ukraine,  United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Trough Seated Diastolic Blood Pressure (DBP) Control The number of patients who reached the target DBP of <90mmHg End of study (34 weeks or last value on treatment) No
Secondary Trough Seated Systolic Blood Pressure (SBP) Control The number of patients who reached the target SBP of >=140mmHg End of study (34 weeks or last value on treatment) No
Secondary Change From Baseline to End of Study in Trough Seated Diastolic Blood Pressure Change from baseline to the end of study in trough DBP. Baseline is defined as visit 3 of trial 1235.6 Baseline is defined as visit 3 of study NCT00553267 and end of study as 34 weeks or last value on treatment No
Secondary Change in DBP From Last Available Trough in NCT00553267 to Last Available Trough in NCT00624052 The difference between the last available troughs represents the additional reduction in DBP in this study Last available trough in NCT00553267 to end of study (34 weeks or last value on treatment) No
Secondary Change From Baseline to End of Study in Trough Seated Systolic Blood Pressure Change from baseline to the end of study in trough SBP. Baseline is defined as visit 3 of trial 1235.6 Baseline is defined as visit 3 of study NCT00553267 and end of study as 34 weeks or last value on treatment No
Secondary Change in SBP From Last Available Trough in NCT00553267 to Last Available Trough in NCT00624052 The difference between the last available troughs represents the additional reduction in SBP in this study Last available trough in NCT00624052 to end of study (34 weeks or last value on treatment) No
Secondary Trough Seated DBP Response The number of patients who reach the target DBP of <90mmHg or had a reduction in DBP >= 10mmHg End of study (34 weeks or last value on treatment) No
Secondary Trough Seated SBP Response The number of patients who reach the target SBP of <140mmHg or had a reduction in SBP >= 15 mmHg End of study (34 weeks or last value on treatment) No
Secondary Trough BP Normality Classes The number of patients who reach predefined BP categories End of study (34 weeks or last value on treatment) No
Secondary Time to First Additional Antihypertensive Time from first intake of medication to first intake of an antihypertensive other than the study drug up to 34 weeks No
Secondary Number of Patients Requiring Additional Antihypertensive Therapy to Achieve DBP Control The number of patients with DBP control (DBP>=90 mmHg). Last trough DBP measurement before taking additional antihypertensive compared to last trough DBP taken on treatment up to 34 weeks No
Secondary Additional Reduction in DBP by Use of Additional Antihypertensive Therapy Difference in trough DBP from last visit before add-on therapy and last visit during NCT00624052 up to 34 weeks No
Secondary Additional Reduction in SBP by Use of Additional Antihypertensive Therapy Difference in trough SBP from last visit before add-on therapy and last visit during NCT00624052 up to 34 weeks No
Secondary Trough DBP Control Pre- and Post- Uptitration The number of patients with DBP control (DBP<90 mmHg). Last trough DBP measurement before uptitration to telmisartan 80mg and amlodipine 10mg compared to first trough DBP taken after uptitration. Uptitration could be based DBP>90 or investigator opinion. up to 34 weeks No
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