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Diabetes MellitusPhase 3NCT03869931

Effects of Fenofibrate Therapy in Diabetic Nephropathy

A Phase 3 study testing Fenofibrate in people with Diabetes Mellitus and Diabetic Nephropathies, run by Singapore General Hospital at 1 site in Singapore.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Diabetic nephropathy (DN) is a common cause of end-stage renal disease (ESRD) and accounts for nearly half of all new patients starting dialysis in Singapore, the country with the highest rates of DN in the Asia-Pacific region. Read more about this study

Who is it for?
Ages 21 to 100 years
Conditions the study is for
Diabetes Mellitus, Diabetic Nephropathies
What is being tested?
Fenofibrate
Could I receive a placebo?
No, everyone receives an active treatment
How many people
300 participants
Where
1 siteSingapore
Study dates
8 Mar 2019to 30 Apr 2021
Phase
Phase 3
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 21 to 100 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Man or woman between 21 and 100 years of age
  • Type 2 diabetes mellitus Increased urine protein excretion as defined as:
  • More than one measurement in the past 1-year with urine microalbumin/creatinine ratio (ACR) > 3.3 mg/mmol creatinine, or urine total protein/creatinine ratio (PCR) > 0.2 g/urine creatinine, or creatinine clearance between 30-60 ml/min
  • More than one measurement in the past 1-year with urine microalbumin/creatinine ratio (ACR) > 3.3 mg/mmol creatinine or urine total protein/creatinine ratio (PCR) > 0.2 g/urine creatinine
  • Known diabetes duration > 3 months
  • HbA1c < 9%(within 3 months prior to enrolment)
Show all 9Show fewer
  • No change in dose of diabetes medications by more than two-fold or new agents added within the previous 3 months
  • No change in dose of lipid-lowering medications by more than two-fold or new agents added within the previous 3 months
  • Capable of providing informed consent

Who cannot join

  • Type 1 diabetes mellitus
  • Known intolerance or allergic to statins
  • Known intolerance or allergic to fenofibrate
  • Known intolerance or allergic to peanut oil or soybean lecithin or related products
  • Concurrent use of fibrates
  • Concurrent use Colchicine
Show all 44Show fewer
  • Concurrent use Nicotinic Acid
  • Concurrent use Cyclosporine
  • Concurrent use Tacrolimus
  • Concurrent use Amodiaquine
  • Concurrent use Bile acid sequestrants
  • Concurrent use Chenodiol
  • Concurrent use Ciprofibrate
  • Oral anticoagulants: vitamin K antagonist (e.g. warfarin), factor Xa inhibitors (eg. rivaroxaban, apixaban and dabigatran)
  • Concurrent use Anti-obesity medications (e.g. phentermine, orlistat)
  • Concurrent use Systemic steroids (e.g. prednisolone, hydrocortisone, dexamethasone)
  • Hepatitis B
  • Hepatitis C
  • Autoimmune hepatitis
  • Hemochromatosis
  • Previous pancreatitis
  • Serum alanine aminotransferase or aspartate aminotransferase above 2x upper limit of normal
  • Serum creatinine kinase above upper limit of normal
  • Creatinine clearance < 30 ml/min
  • Renal replacement therapy
  • Presence of any non-DN renal glomerular disease
  • Any previous organ transplantation
  • Previous bariatric surgery
  • Gallbladder disease
  • Untreated hypothyroidism
  • Untreated thyrotoxicosis
  • Hemoglobin < 10 g/L
  • Any leukopenia
  • Any thrombocytopenia)
  • Cancer within the last 5 years (except basal cell carcinoma)
  • Medical condition likely to limit survival to less than 3 years
  • Currently participation in another clinical trial
  • Pregnancy, or currently trying to become pregnant
  • Nursing mothers
  • Hospitalization within 1 month prior to enrolment
  • Alcohol intake > 1 unit per day for women or > 2 units per day for men
  • Any factors likely to limit adherence to interventions
  • Any ongoing acute medical illness
  • Failure to obtain informed consent from participant

Trial locations and contacts

1 site in 1 country.

Singapore1 site, 1 recruiting
  • Singapore General Hospital

    Singapore, 169856

    Hong Chang Tan, MBBS, MMed, +65-63214658, tan.hong.chang@sgh.com.sg

    Vieon Wu, 98295942, vieon.wu.aini@sgh.com.sg

    Recruiting

Other trials in Singapore

About this study

Official title: Effects of Fenofibrate Administration in Patients With Diabetic Nephropathy

Diabetic nephropathy (DN) is a common cause of end-stage renal disease (ESRD) and accounts for nearly half of all new patients starting dialysis in Singapore, the country with the highest rates of DN in the Asia-Pacific region. Despite the scale of the problem, little progress has been made in our understanding of the pathogenesis of the disorder and no new therapies have been offered.

The investigators have conducted a metabolomics study of human diabetic nephropathy that revealed evidence for alterations in mitochondrial fuel metabolism in patients with the disease, a finding also reported in other recent studies of human DN. Based on this finding the investigators believe that dysregulated mitochondrial fuel oxidation is a major driver of diabetic nephropathy.

Read more

Fenofibrate is an agonist of peroxisome-proliferator activating receptor (ppar)-alpha that is approved for the treatment of hypercholesterolaemia and hypertriglyceridemia alone or combined in patients unresponsive to dietary and other non-drug therapeutic measures. Fenofibrate is also indicated for the reduction in the progression of diabetic retinopathy in patients with type 2 diabetes and existing diabetic retinopathy. Presently fenofibrate is not indicated for the treatment of diabetic nephropathy.

The investigators hypothesize that treatment with fenofibrate, taken orally at 300mg per day or 100mg per day for 30 days will lead to significant changes in the circulating metabolomics patterns in patients with DN. The investigators propose to administer the drug for a period of 30 days and will perform a comprehensive analysis of the state of fuel metabolism in these patients before, and after the administration of fenofibrate using targeted metabolomics and other approaches. Fundal photography, Optical Coherence Tomography (OCT) and Optical Coherence Tomography Angiography (OCTA) will also be performed at baseline and post-treatment. A total of 300 subjects will be recruited from Singapore General Hospital (SGH) Diabetes and Metabolic Centre. Our goal is to discover key changes in fuel metabolism in DN patients receiving fenofibrate.

Read the detailed description

In this single-centre, open label study, 300 adults with DN will be recruited over 3 years. Following screening and baseline metabolic evaluations, eligible subjects will be treated with fenofibrate for 30-days and re-assessed.

4.1 Study Visits and Procedures Subjects will have their written informed consent taken during Visit 1 at the SGH Clinical Trials Research Centre (CTRC) and undergo screening and baseline assessments. Eligible subjects will return within the next 14 days for the initiation of study drug (Visit 2). The post-treatment and final visit (Visit 3) will take place 30 ± 7 days after Visit 2. Details of study visits are described in Table 1 (Refer study protocol).

4.1.1 VISIT 1: Informed Consent and Screening Interested patients will be scheduled for their first study visit (Visit 1) at SGH CTRC. Written informed consent will be taken by the principal or co-investigators assigned by the PI. After consent has been taken, study procedures in Table 1 will be performed. Subject will be given a sample copy of the treatment diary to familiarize them with the method to record study drug intake.

At the end of Visit 1, subjects will head over to Singapore Eye Research Institution (SERI) or Singapore National Eye Centre (SNEC)) for eye tests as mentioned in the following paragraphs.

Fundus Photography, conventional OCT and Assessment and grading of diabetic retinopathy (DR). The presence and severity of Diabetic Retinopathy (DR) or Diabetic Macular Edema (DME) will be assessed from digital fundus photographs and OCT. Following pupillary dilation, 7-field ETDRS photography using a non-mydriatic 45º fundus cameras will be obtained for each eye. The modified Wisconsin protocol will be used for DR grading. DR will be considered present if any characteristic lesion as defined by the ETDRS severity scale is present: microaneurysms (MA), hemorrhages, cotton wool spots, intraretinal microvascular abnormalities (IRMA), hard exudates (HE), venous beading, and new vessels. For each eye, a retinopathy severity score will be assigned according to a scale modified from the Airlie House classification system. Macular edema is defined by hard exudates in the presence of MA and blot hemorrhage within 1 disc diameter from the foveal center or presence of focal photocoagulation scars in the macular area. Clinically significant macular edema (CSME) is considered present when the macular edema involved is within 500 mm of the foveal center or if focal photocoagulation scars are present in the macular area. DR is categorized as minimal non-proliferative DR (level 20), mild non-proliferative DR (level 35), moderate non-proliferative DR (level 43 through 47), severe Non-proliferative Diabetic Retinopathy (NPDR) (level 53), and proliferative retinopathy (>60). Vision-threatening retinopathy is defined as the presence of severe NPDR, Proliferative Diabetic Retinopathy (PDR), or CSME. Presence of DME (centre involving and non centre involving) and central retinal thickness will also be assessed on OCT.

Ultrawide field (UWF) imaging Stereoscopic 200-degree-field ultrawide field images of each subject will be obtained using the Optos P200MA instrument. Unlike traditional fundus cameras, Optos imaging relies on proper eye positioning by the imager and correct patient fixation on a target, rather than the imager viewing the retinal structures for focus. The UWF200 images are centered on the fovea, covering approximately 25% and 82%, respectively, of the retinal area, including the optic disc, macula, and major vascular arcades. Grading of UWF imaging will be performed using the ETDRS protocol to determine the presence and severity of the following lesions: hemorrhages, microaneurysms, or both (H/Ma); intraretinal microvascular abnormalities (IRMA); venous beading (VB); cotton wool spots; hard exudates; retinal thickening; new vessels on the disc; new vessels elsewhere (NVE) on the retina; preretinal hemorrhage; vitreous hemorrhage; and traction retinal detachment. This test will be optional.

Optical Coherence Tomography (OCT) and Optical Coherence Tomography Angiography (OCTA) Spectral Domain Optical Coherence Tomography and optical coherence tomographic angiography will be performed in both eyes to obtain scans of the macular, macular thickness, retinal nerve fiber thickness optic disc, and optic nerve head.

4.1.2 Initiation of Study Drug

The PI or Co-Is assigned by the PI, will review screening results to determine whether subjects are eligible to continue with the study. Eligible subjects will be prescribed the study drug, fenofibrate (Trolip®). Fenofibrate is to be taken orally for 30 days, and the dose of fenofibrate will be adjusted based on the estimated CrCl during Visit 1 as below.

CrCl (ml/min) Fenofibrate Dosage > 60 300mg/day 30-59 100 mg/day < 30 Contraindicated

Study drug and subject treatment diary will be delivered to the subjects via a third party delivery service within 14 days from Visit 1. Alternatively, subjects can also return to the hospital to collect their study drug and drug diary. They will also be given a treatment diary to record the intake of study drug.

On the day of medication delivery or collection, the clinical research coordinator at SGH will call the subject to confirm that they have received the study drug. Subjects should not take the study drug until instructed by the clinical research coordinator. The clinical research coordinator will also check with subject if there is any change in their medication intake and is well feeling well before intake of the study drug.

They will be reminded to record intake of study drug into their treatment diary

4.1.3 VISIT 2: 4-Week Post-Treatment Visit

Visit 2 will take place 30 ± 7 days from the first dose of study drug. Subjects who are still on the study drug should continue take the study drug on the morning of Visit 2 with plain water. Subjects will be assessed to quantify changes in metabolic fuel utilization after treatment with fenofibrate. These changes are determined based on metabolomic profiling of acyl-carnitines, organic acids and amino acids and the eye tests.

SAMPLE COLLECTION

Up to a total of 47 ml (~3.2 tablespoons) of blood and 90 ml (~6.0 tablespoons) of urine will be collected for the entire study. During Visit 1 (Screening), approximately 25 ml (~1.7 tablespoons) of blood and 30 ml (~2.0 tablespoon) of urine will be collected. During Visit 2 (Dosing visit), 30 ml of urine will be collected and during Visit 3 (post-treatment \& final visit), approximately 22ml (~1.5 tablespoon) of blood and 30 ml (~2.0 tablespoon) of urine will be collected.

Subjects who developed drug-related adverse reactions may require additional blood and urine taken for clinical assessment.

LABORATORY MEASUREMENTS

  1. Blood Chemistry Screening and standard laboratory tests including full blood count, Potassium, Creatinine. alanine transaminase, aspartate transaminase, β-human chorionic gonadotropin, creatinine kinase (CK), lipid panel, glucose and HbA1c will be measured in the clinical laboratory using standard methods.
  2. Metabolomic Profiling Metabolomic profiling of lipids, acylcarnitines (ACs), organic acids and ketones will be measured using liquid and gas chromatography and tandem mass spectrometry (LC-MS/MS and Gas Chromatography-MS/MS) at the Duke-National University of Singapore metabolomics laboratory.

ACs represent intermediaries of metabolic fuel oxidation and provides a "snap-shot" of in vivo metabolism at the cellular level. The measurement of the various long-, intermediate-chain ACs provide an indicator of fatty acid oxidation efficiency. Ceramides are toxic lipid intermediaries that are implicated in the pathogenesis of insulin resistance. Lactate, pyruvate, succinate, fumarate, malate, alpha-ketoglutarate and citrate are organic acids involved in tricarboxylic acid cycle activity. Beta hydroxybutyrate is a ketone which will also be measured with the organic acids.

  1. Urine Protein Excretion

Urine ACR and PCR will be performed to quantify urine protein excretion.

Being tested
Fenofibrate
Keywords
Fenofibrate, Diabetic Nephropathy, Metabolomics
Medical subject headings
Diabetes Mellitus, Diabetic Nephropathies

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • FenofibrateDrug

    Fenofibrate 100 mg or 300 mg (according to CrCl)

Study groups in NCT03869931
Study groupRoleWhat they receive
FenofibrateExperimental(Refer to intervention)
Receives: Drug: Fenofibrate

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Serum concentration of palmitoylcarnitine following 30 days of fenofibrate treatment

    Percentage change in serum concentration of palmitoylcarnitine following 30 days of fenofibrate treatment compared to baseline

    Measured: Baseline and after 30 days of treatment

  2. Serum concentration of acetylcarnitine following 30 days of fenofibrate treatment

    Percentage change in serum concentration of acetylcarnitine following 30 days of fenofibrate treatment compared to baseline

    Measured: Baseline and after 30 days of treatment

  3. Serum concentration of leucine following 30 days of fenofibrate treatment

    Percentage change in serum concentration of leucine following 30 days of fenofibrate treatment compared with baseline

    Measured: Baseline and after 30 days of treatment

  4. Serum concentration of isoleucine following 30 days of fenofibrate treatment

    Percentage change in serum concentration of isoleucine following 30 days of fenofibrate treatment compared with baseline

    Measured: Baseline and after 30 days of treatment

  5. Serum concentration of valine following 30 days of fenofibrate treatment

    Percentage change in serum concentration of valine following 30 days of fenofibrate treatment compared with baseline

    Measured: Baseline and after 30 days of treatment

  6. Triglyceride concentration following 30 days of fenofibrate treatment

    Absolute change in serum triglyceride (mmol/L) concentration following 30 days of fenofibrate treatment with baseline

    Measured: Baseline and after 30 days of treatment

Secondary outcomes (1)
  1. Change in ETDRS scale following 30 days of fenofibrate treatment

    Change in ETDRS scale following 30 days of fenofibrate treatment

    Measured: Baseline and after 30 days of treatment

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted11 Mar 2019
  2. Study start8 Mar 2019
  3. Primary completion30 Apr 2021 (estimated)
  4. Study completion30 Apr 2021 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 3
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Model description
In this single-centre, open label study, 300 adults with DN will be recruited over 3 years. Following screening and baseline metabolic evaluations, eligible subjects will be treated with fenofibrate for 30-days and re-assessed.
Masking
None (open label)
Enrolment
300 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03869931
Sponsor's protocol ID
SGHDN001
Status last verified
Dec 2020
First submitted
28 Feb 2019
Last updated
14 Dec 2020
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Ansquer JC, Foucher C, Rattier S, Taskinen MR, Steiner G; DAIS Investigators. Fenofibrate reduces progression to microalbuminuria over 3 years in a placebo-controlled study in type 2 diabetes: results from the Diabetes Atherosclerosis Intervention Study (DAIS). Am J Kidney Dis. 2005 Mar;45(3):485-93. doi: 10.1053/j.ajkd.2004.11.004.

    PubMed 15754270
  • Keech A, Simes RJ, Barter P, Best J, Scott R, Taskinen MR, Forder P, Pillai A, Davis T, Glasziou P, Drury P, Kesaniemi YA, Sullivan D, Hunt D, Colman P, d'Emden M, Whiting M, Ehnholm C, Laakso M; FIELD study investigators. Effects of long-term fenofibrate therapy on cardiovascular events in 9795 people with type 2 diabetes mellitus (the FIELD study): randomised controlled trial. Lancet. 2005 Nov 26;366(9500):1849-61. doi: 10.1016/S0140-6736(05)67667-2.

    PubMed 16310551
  • Liu JJ, Ghosh S, Kovalik JP, Ching J, Choi HW, Tavintharan S, Ong CN, Sum CF, Summers SA, Tai ES, Lim SC. Profiling of Plasma Metabolites Suggests Altered Mitochondrial Fuel Usage and Remodeling of Sphingolipid Metabolism in Individuals With Type 2 Diabetes and Kidney Disease. Kidney Int Rep. 2016 Dec 16;2(3):470-480. doi: 10.1016/j.ekir.2016.12.003. eCollection 2017 May.

    PubMed 29142974
  • Teo CHY, Lin MT, Lee IXY, Koh SK, Zhou L, Goh DS, Choi H, Koh HWL, Lam AYR, Lim PS, Mehta JS, Kovalik JP, Coffman TM, Tan HC, Liu YC. Oral Peroxisome Proliferator-Activated Receptor-alpha Agonist Enhances Corneal Nerve Regeneration in Patients With Type 2 Diabetes. Diabetes. 2023 Jul 1;72(7):932-946. doi: 10.2337/db22-0611.

    PubMed 36445944

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing Fenofibrate in people with Diabetes Mellitus and Diabetic Nephropathies, run by Singapore General Hospital at 1 site in Singapore.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 9 inclusion and 44 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 14 Dec 2020. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Singapore. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Vieon Wu, BSc (9829 5942, vieon.wu.aini@sgh.com.sg), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Serum concentration of palmitoylcarnitine following 30 days of fenofibrate treatment (time frame: Baseline and after 30 days of treatment). The study lists 6 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT03869931, which also lists 4 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 14 Dec 2020.

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