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Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of EV-077 in Type 2 Diabetic Subjects

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ClinicalTrials.gov Identifier: NCT01551381
Recruitment Status : Terminated (Interim review indicated that the dose selected was too high for diabetics)
First Posted : March 12, 2012
Last Update Posted : June 17, 2013
Information provided by (Responsible Party):
Evolva SA

Brief Summary:

The principal objective of this study is to evaluate the safety and tolerability of repeated doses of EV-077-3201-2TBS given to diabetic subjects over a 4 week treatment period. The secondary aim of this initial Phase IIa study is to evaluate the effect of multiple oral doses of EV-077-3201-2TBS on platelet function, vascular function, vascular inflammation, vascular oxidative stress, renal function and a selection of exploratory parameters and biomarkers in type 2 diabetic subjects, as well as multiple dose pharmacokinetics in diabetic subjects.

In order to ensure the safety of the diabetic subjects, initial parts of the study will evaluate the safety and tolerability of EV-077-3201-2TBS. In Part A, the safety of different doses EV-077-3201-2TBS will be investigated in healthy subjects treated for 4 weeks. In parallel, Part B will investigate potential interactions between EV-077-3201-2TBS and ASA in healthy subjects. Part C will then investigate the safety, pharmacokinetics and pharmacodynamics of EV-077-3201-2TBS in type 2 diabetic subjects with and without concomitant ASA therapy.

Condition or disease Intervention/treatment Phase
Type 2 Diabetes Drug: EV-077 Drug: Placebo Phase 2

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 33 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double (Participant, Investigator)
Primary Purpose: Treatment
Official Title: Double-blind, Controlled Study in Healthy and Type 2 Diabetic Subjects to Assess Safety, Tolerability and Pharmacokinetics of 28 Days EV-077 Treatment, and the Effects on Platelet Function, Vascular Inflammation and Oxidative Stress.
Study Start Date : January 2012
Actual Primary Completion Date : May 2012
Actual Study Completion Date : May 2012

Resource links provided by the National Library of Medicine

Arm Intervention/treatment
Experimental: EV-077
Oral administration
Drug: EV-077
twice daily oral administration
Other Name: EV-077-3201-2TBS

Placebo Comparator: Placebo
Oral administration
Drug: Placebo
twice daily oral administration

Primary Outcome Measures :
  1. Platelet aggregation [ Time Frame: 8 days ]
    Measured at Day 8 by Multiplate® with arachidonic acid as the agonist

Secondary Outcome Measures :
  1. Platelet aggregation [ Time Frame: Days 1, 2, 8, 15, 22 and 29 ]
    Measured at multiple time points by Multiplate (using arachidonic acid, collagen, U-46619 and ADP as agonists) and the Born method (using arachidonic acid, collagen and ADP as agonists)

  2. Vascular inflammatory state [ Time Frame: Baseline, 2 weeks and 4 weeks ]
    Changes from baseline in markers of platelet function, vascular function, vascular inflammation and vascular oxidative stress

  3. Diabetic state [ Time Frame: Baseline, 2 weeks and 4 weeks ]
    Change from baseline in fasting plasma glucose and HbA1c

  4. Renal function [ Time Frame: Baseline, 2 weeks and 4 weeks ]
    Change from baseline in urinary albumin excretion, creatinine clearance and exercise-induced microalbuminuria

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Ages Eligible for Study:   18 Years to 70 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Male or female subjects aged 18 to 70 years inclusive. (NB. All females must be of non-reproductive potential, i.e. post-menopausal, post-hysterectomy, bilateral tubal ligation or bilateral oophorectomy).
  • Body mass index (BMI) between 25.0 and 40.0 kg/m2 (both inclusive).
  • Subjects with type 2 diabetes mellitus according to American Diabetes Association (ADA) definition for a duration of at least 3 years, on a stable therapy with oral anti-diabetic drugs (OAD) or with insulin, with or without one or two OADs or a glucagon like peptide-1 (GLP-1) agonist, or glitazones. Stable baseline therapy is defined as unchanged dose regimen for at least 3 months before administration of the study drug.
  • HbA1c ≥ 6.0 and ≤ 9.0 %.
  • History of hyperlipidaemia, with either elevated LDL cholesterol (>140 mg/dL) without therapy, or treatment with statins (NB. Patients on statin therapy must have a 2 week wash-out before they can enter the study).
  • History of hypertension, either with systolic blood pressure levels between 140 to 160 mmHg without treatment, or treatment with ACE inhibitors or ARB, which should be stable over the previous 3 months.

Exclusion Criteria:

  • Abnormal and clinically significant ECG at screening.
  • Donation of any blood or plasma in the past month or in excess of 500 mL within the 12 weeks preceding screening.
  • Intake of paracetamol within 7 days before start of treatment.
  • Surgery or trauma with significant blood loss within the last 3 months before administration of study drug.
  • Smokers (negative cotinine test required).
  • Clinically significant abnormal laboratory test results during the screening as judged by the Investigator (one retest within a week is permitted, the last result being conclusive).
  • Increased risk of bleeding, e.g. subjects with a history of deep cerebral bleeding or known defects of haemostasis with increased risk of bleeding, as judged by the Investigator.
  • History of or presence of clinically significant diseases such as cancer, clinically significant cardiovascular, respiratory, metabolic, renal, hepatic, gastrointestinal, endocrinological, haematological, dermatological, venereal, neurological, psychiatric diseases, other major disorders as judged by the Investigator, or significant secondary diabetic complications, such as but not limited to clinically relevant peripheral neuropathy, retinopathy, diabetic foot ulcers, as judged by the Investigator.
  • Supine blood pressure at screening, after resting for 5 min, of > 160 mmHg systolic or > 95 mmHg diastolic (excluding white-coat hypertension; therefore, if a repeat measurement on a second screening visit shows values within the range, the subject can be included in the trial).
  • Type 1 diabetes mellitus.
  • Intake of anti-inflammatory drugs except ASA (dose 75-125mg/day stable for the previous 3 months) within 14 days before start of treatment. Steroid therapy other than topical application is not allowed.
  • Any treatment with diuretics (hydrochlorothiazide is allowed)
  • Liver enzymes (ALT and AST) more than 1.5 times the upper limit of normal.
  • Any contraindication for a therapy with ASA such as allergy to ASA, including asthma, acute gastric ulcers, haemorrhagic diathesis, renal or liver insufficiency, or heart failure.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01551381

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Profil Institut für Stoffwechselforschung GmbH
Neuss, Germany
Sponsors and Collaborators
Evolva SA
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Principal Investigator: Thomas Jax, MD Profil Institut für Stoffwechselforschung GmbH, Germany
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Responsible Party: Evolva SA
ClinicalTrials.gov Identifier: NCT01551381    
Other Study ID Numbers: EV077/C005
2011-003808-20 ( EudraCT Number )
First Posted: March 12, 2012    Key Record Dates
Last Update Posted: June 17, 2013
Last Verified: June 2013
Keywords provided by Evolva SA: