NCT Number: NCT01970215
TA-8995: Its Use in Patients With Mild Dyslipidaemia (TULIP)
The primary objective of this study is to evaluate the efficacy of different doses of TA-8995, a cholesteryl ester transfer protein (CETP) inhibitor, on the elevation of high-density lipoprotein cholesterol (HDL-C) and reduction of low-density lipoprotein cholesterol (LDL-C), alone and in combination with statin therapy.
The secondary objectives of this study are to determine the safety and tolerability of TA-8995 in patients with mild dyslipidaemia.
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Notify MeKey information
Conditions
Age range
18 year–75 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 2
Primary location
H:S Amager Hospital, Copenhagen, Denmark
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Fasting LDL-C levels >2.5 mmol/L and <4.5 mmol/L, HDL-C levels <1.8 mmol/L and >0.8 mmol/L, and TG levels <4.5 mmol/L after run in or washout of existing therapies
- Not on lipid-altering therapy at screening or on lipid-altering treatment regimens at screening
Exclusion criteria
- Body mass index >32 kg/m2;
- Participation in another clinical study involving an investigational or marketed drug within 30 days prior to enrolment (Visit 2);
- Any clinical manifestation of atherosclerotic vascular disease;
- Diagnosis of type 1 diabetes;
- Uncontrolled type 2 diabetes: haemoglobin A1c >8%;
- Uncontrolled hypertension: sitting systolic blood pressure >160 mmHg and/or sitting diastolic blood pressure >90 mmHg;
- History of hyperaldosteronism;
- Active muscle disease or persistent creatine kinase concentration >3 × the upper limit of normal (ULN). One retest will be allowed after 1 week to verify the result;
Treatment and study plan
atorvastatin
DrugRosuvastatin
DrugTA-8995 0mg (placebo)
DrugPlacebo Statin
DrugPrimary outcomes
-
The co-primary efficacy endpoints are the percentage changes in both HDL-C and LDL-C levels at Week 12 compared to baseline.
Time frame: 12 weeks
Sponsors and collaborators
Lead sponsor
Xention Ltd
Industry
Registry information
Official study title
A Multi-Centre, Randomised, Double-Blind, Placebo-Controlled, Parallel-Group Study of TA-8995 in Patients With Mild Dyslipidaemia, Alone and In Combination With Statin Therapy
Acronym: TULIP
Important dates
- Study start
- 2013
- Primary completion
- 2014
- Study completion
- 2014
- First posted
- Oct 28, 2013
- Registry last updated
- Aug 21, 2014
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
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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