The Fenofibrate And Microvascular Events in Type 1 Diabetes Eye.
PHASE3ACTIVE_NOT_RECRUITING
The purpose of this study is to evaluate the potential benefits of 145 mg of daily fenofibrate in adults with type 1 diabetes mellitus and pre-existing non-proliferative diabetic retinopathy.
Study details:
Diabetes is the most common cause of adult onset blindness. Irreversible vision loss is a most feared complication of diabetes. Fenofibrate is a blood fat lowering drug available in Australia and has been shown to reduce eye damage in people with Type 2 diabetes by 35-40%, and to prevent eye damage in Type 1 diabetic animal models.
This study will evaluate the potential benefits of oral Fenofibrate 145mg once daily for average 36 months in 450 adults with Type 1 diabetes mellitus who are at high risk of eye damage.
Eligibility criteria
Researchers look for people who fit a certain description, called eligibility criteria. See if you qualify.
Inclusion criteria
- Men or non-pregnant women (on acceptable contraception) with T1D according to standard criteria: T1D defined as either (1) T1D diagnosed below 40 years of age and insulin therapy commencing within one year of T1D diagnosis, or (2) T1D diagnosed before, at or after 40 years of age along with: i) Documented history of ketoacidosis, and/or ii) Documented history of very low or undetectable C-peptide (fasting <200 nmol/L or 0.2 pmol/L), and/or iii) Documented history of T1D related autoantibody/ies (anti-Glutamic acid decarboxylase, anti-A2, anti-ZnT8).
- Age 18 years or over;
- Estimated glomerular filtration rate (eGFR) must exceed 30 ml/min/1.73m2;
- Must have at least one eligible eye with non-proliferative retinopathy (ETDRS score 35-53 inclusive) confirmed by current retinal photography within the last 3 months (irrespective of prior laser therapy). Note: Any eye having undergone prior pan-retinal laser therapy is not eligible, but prior focal, macular or grid laser does not exclude that eye from eligibility.;
- All types of insulin therapy, with no restriction by level of HbA1c;
- Willing and able to comply with all study requirements, including treatment, assessment and clinic visit attendances;
- Able to personally read and understand the Participant Information and Consent Form and provide written, signed and dated informed consent to participate in the study.
Exclusion criteria
- Definite indication for or contraindications to fibrate treatment (Other lipid drugs [e.g. statins, ezetimibe, fish oils] are allowed.);
- Need for bilateral intra-ocular treatment or laser photocoagulation therapy within the next 3 months (this exclusion only applies to retinal laser photocoagulation treatment to the posterior pole i.e. laser correction of corneas for short-sightedness is NOT an exclusion criterion);
- Prior bilateral pan-retinal photocoagulation (PRP) treatment for diabetic retinopathy;
- Prior bilateral intra-ocular injection(s) within the last 6 months;
- Bilateral cataract surgery within the last 6 months;
- Planned bilateral cataract surgery within the next 12 months;
- History of any other non-diabetic eye disease that is or is likely to affect bilateral vision;
- History of photosensitive skin rash or myositis;
- Abnormal thyroid function (untreated);
- Liver function tests exceeding 3x upper limit of normal (ULN);
- Persistent elevated unexplained blood creatinine phosphokinase level above normal range;
- Documented fasting triglycerides (TG) levels >6.5 mmol/L;
- History of pancreatitis, deep vein thrombosis (DVT) or pulmonary embolism;
- Use of investigational drugs in the prior 8 weeks;
- Any unstable condition in last 3 months including active sepsis, diabetic ketoacidosis;
- Myocardial infarction (MI), unstable angina, stroke or heart failure within last 6 months;
- Diagnosed cancer with ongoing treatment or prognosis anticipated at <5 years;
- Any obstacle to regular follow-up including scheduled clinic attendances;
- Prior or planned organ transplantation (including islet cells) with subsequent continued immunosuppression therapy.
Eligibility
Age eligible for study : NA
Healthy volunteers accepted : No
Gender eligible for study: ALL
Things to know
Study dates
Study start:
Primary completion:
Study completion finish:
Study type
TREATMENT
Phase
- PHASE3
Study ID
NCT01320345
Intervention or treatment
DRUG: Fenofibrate
DRUG: Inert lactose placebo
Conditions
- Type 1 Diabetes Mellitus
- Diabetic Retinopathy
- Diabetic Nephropathies
You may be eligible to participate in this trial based on your search. Check eligibility by answering some questions.
Research sites nearby
Closest Location:
Canberra Hospital
Select from list below to view details:
Canberra Hospital
Garran, Australian Capital Territory, Australia
Royal Prince Alfred Hospital
Camperdown, New South Wales, Australia
Concord Repatriation General Hospital
Concord, New South Wales, Australia
Garvan Institute of Medical Research
Darlinghurst, New South Wales, Australia
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Who is running the clinical trial?
UoS
University of Sydney
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
| Participant Group/Arm | Intervention/Treatment |
|---|---|
EXPERIMENTAL: Fenofibrate
| Drug: Fenofibrate |
PLACEBO_COMPARATOR: Placebo
| Drug: Inert lactose placebo |
What is the study measuring?
Primary Outcome
| Measure | Description | Time Frame |
|---|---|---|
| Occurrence of clinical significant retinopathy progression. | Comprising 2-step progression of ETDRS score (to at least moderately severe grade), clinically significant macular oedema, need for laser surgery, need for intraocular anti-VEGF or corticosteroid therapy or vitrectomy, adjudicated to be for diabetic retinopathy (DR) | As reported throughout the study and/or annual eye assessment post-randomisation |
Secondary Outcome
| Measure | Description | Time Frame |
|---|---|---|
| The individual components of the primary endpoint | Clinically significant retinopathy progression, 2-step progression of ETDRS score | At baseline, 12 m post-randomisation, 24 m post-randomisation and the end of study visit (which is on average 36 months post-randomisation). |
| Occurrence of clinically significant macula oedema (CSME). | Occurrence of clinically significant macula oedema (CSME) per standard ophthalmological assessment or laser therapy. | As reported throughout the study |
| Need for laser surgery for DR | Need for laser surgery for DR | As reported throughout the study |
| Need for intraocular anti-VEGF or corticosteroid injection or vitrectomy | Need for intraocular anti-VEGF or corticosteroid injection or vitrectomy for DR | As reported throughout the study |
| Visual acuity. | Visual acuity using ETDRS/LogMar or Snellen Chart | At baseline, 12 m post-randomisation, 24 m post-randomisation and the end of study visit (which is on average 36 months post-randomisation). |
| Macular volume and thickness | Macular volume and thickness by Optical Coherence Tomography (OCT) | At baseline, 12 m post-randomisation, 24 m post-randomisation and the end of study visit (which is on average 36 months post-randomisation). |
| Albuminuria. | Albuminuria measured as urinary albumin:creatinine ratio. | At baseline, 12 m post-randomisation, 24 m post-randomisation, the end of study visit (which is on average 36 months post-randomisation) and wash-out visit. |
| Estimated glomerular filtration rate. | Estimated glomerular filtration rate using Modification of Diet in Renal Disease (MDRD) formula. | At study completion and washout visit |
| Peripheral neuropathy status | Peripheral neuropathy status assessed by temperature \& vibration sensation and monofilament test. | At baseline, 12 m post-randomisation, 24 m post-randomisation and the end of study visit (which is on average 36 months post-randomisation). |
| Autonomic neuropathy. | Autonomic neuropathy (QTc and R-R intervals) on annual ECGs. | At baseline, 12 m post-randomisation, 24 m post-randomisation and the end of study visit (which is on average 36 months post-randomisation). |
| Total cardiovascular events. | Total cardiovascular events including myocardial infarction, stroke, sudden cardiac death, hospitalisation for acute coronary syndrome or any revascularisation events. | As reported throughout the study. |
| Frequency of foot ulcer and non-traumatic amputation. | Foot ulcer and/or non-traumatic amputation are reported by site during the study. | As reported throughout the study |
Are you running this trial?If you're a clinic or sponsor, you can claim this study.
References
Clinical Trials Gov: The Fenofibrate And Microvascular Events in Type 1 Diabetes Eye.Other trials to consider
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