Intensive Urate Lowering Therapy of Febuxostat Compared to Allopurinol on Cardiovascular Risk in Patients With Gout

Gout Clinical Trial

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Official title:

The Effect of Intensive Urate Lowering Therapy (ULT) With Febuxostat in Comparison With Allopurinol on Cardiovascular Risk in Patients With Gout Using Surrogate Markers: a Randomized, Controlled Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02500641
• Other study ID #: MEIN/14/FEB-PWV/001
• Secondary ID: 2014-005567-33
• Status: Completed
• Phase: Phase 4
• Start date: August 17, 2015
• Est. completion date: May 10, 2017

Study information

• Verified date: March 2019
• Source: Menarini International Operations Luxembourg SA
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

There is a mounting and clear association between hyperuricaemia, gout and the presence of traditional cardiovascular (CV) risk factors and CV event-equivalent conditions such as chronic kidney disease, metabolic syndrome, and diabetes. Gout is associated with increased risk of CV events such as myocardial infarction and CV death. Furthermore hyperuricaemia is clearly associated with an increased arterial stiffness, a marker of pre-clinical atherosclerosis. Carotid-femoral pulse wave velocity (PWV) is the "gold standard" measurement of arterial stiffness and it is considered, in this trial, as a valid surrogate endpoint with clearly established relevance to predict cardiovascular disease (CVD) clinical outcome In this randomised trial conducted on adult subjects with a history of gout, we use surrogate endpoints to investigate the efficacy of febuxostat compared with allopurinol to predict (CVD) clinical outcome.

Eligible subjects were randomised in a 1:1 ratio to the following treatment groups:

• Test product: febuxostat 80 mg or 120 mg once daily (120 mg daily, if serum urate was >6 mg/dL after 2 weeks of treatment at 80 mg daily).

• Active comparator: allopurinol 100 mg once daily (up to a maximum dose of 600 mg daily escalated in 100 mg increments every 2 weeks, if serum urate acid (sUA) was >6 mg/dL after 2 weeks of treatment at the previous dose).

The study duration was 39 weeks, which included the:

• Run-in/screening period: 1 week (extendable up to a maximum of 30 days according to variability of sUA levels);

• Treatment period: 36 weeks;

• Safety follow-up period: 2 weeks.

Description:

The study physician, responsible for randomization and drug supply handling, is unblinded to study medications and therefore will not be involved in the main efficacy evaluations of each patient randomized in the study.

Conversely, the study physician/s responsible for the main efficacy evaluation (Pulse Wave Velocity) will be blind to study treatments.

Key efficacy variables will be performed by an independent centralized laboratory.

Trial was conducted in a detailed and orderly manner in accordance with established research principles, International Conference on Harmonization (ICH), Good Clinical Practice (GCP) Guidelines and with Clinical Research Organization (CRO) Standard Operating Procedures (SOPs). As part of a concerted effort to fulfill these obligations, the authorised CRO study monitor visited investigative sites prior to and during the trial in addition to maintaining telephone and written communication. Data from each subject were reviewed and source verified as the study progressed.

In accordance with audit plans, this trial may have been selected for audits. The investigators committed to permit independent audits by auditors assigned by the Sponsor at a reasonable notice. Audits included, but were not limited to, drug supply, presence of required documents, the informed consent process, protection of rights and well-being of subjects and verification of Electronic case report form (eCRF) entries against source documents.

Regulatory authorities worldwide had the right to inspect the investigative sites during or after the trial. In such cases, the investigators were required to contact the Sponsor immediately and to fully cooperate with the inspectors.

Copies of written correspondence between the investigators, CRO, Sponsor, Competent Authorities, Institutional Review Board (IRB) and Independent Ethic Committee (IEC) are on file with the Sponsor and investigators.

Adverse events were according to the Medical Dictionary for Regulatory Activities (MedDRA, version 18.0) thesaurus.

Statistical analysis were conducted according the Statistical Analysis Plan (SAP) describing the analytical principles and statistical techniques employed in order to address the objectives specified in the Protocol.

A Data Management Plan was present for missing data, to address situations where variables are reported as missing, unavailable, non-reported, uninterpretable, or considered missing because of data inconsistency or out-of-range results.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 196
• Est. completion date: May 10, 2017
• Est. primary completion date: May 10, 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Male or female patients 18 years and older;

2. History of gout, flare free in the 4 weeks prior to study entry

3. History of crystal (joint liquid) proven diagnosis or anamnestic diagnosis of gout according to Wallace at el. To be eligible, a subject had to present at least 6 of the following 12 clinical, laboratory, and x-ray phenomena:

1. Maximum inflammation developed within 1 day, 2. More than one attack of acute arthritis,

3. Monoarticular arthritis attack, 4. Redness observed over joints, 5. First metatarsophalangeal (MTP) pain or swelling, 6. Unilateral first MTP joint attack, 7. Unilateral tarsal joint attack, 8. Suspected or proven tophus, 9. Hyperuricemia, 10. Asymmetric swelling within a joint on a X ray, 11. Subcortical cysts without erosions on X ray, 12. Negative organisms on culture of joint fluid; 4. Naive to ULT or previously treated with ULT, but with no ULT treatment in the last 1 month prior to study entry and only if reason for ULT interruption was not due to safety concerns.

5. Patients at study entry have elevated serum urate level >8 mg/dl. 6. Overall Cardiovascular (CV) risk based on the scoring proposed by the Joint Task Force of the European Society of Cardiology and other European Societies on cardiovascular disease prevention in clinical practice between 5 and 15-% (inclusive). Patients with diabetes mellitus type 2 could be included in the study if their CV risk score is calculated as =7%.

7. Allowed concomitant medications should be maintained stable during the last 2 weeks before randomisation

Exclusion Criteria:

1. Severe chronic renal failure (creatinine clearance < 30 ml/min)

2. Hepatic failure

3. Active liver disease or hepatic dysfunction, defined as both alanine aminotransferase (ALT) and aspartate aminotransferase (AST) >2 times the upper limit of normal.

4. Diabetes mellitus type1

5. Life-threatening co-morbidity or with a significant medical condition and/or conditions that would interfere with the treatment, the safety or the compliance with the protocol

6. Diagnosis of, or receiving treatment for malignancy (excluding basalioma skin cancer) in the previous 5 years

7. Patients who have experienced either myocardial infarction or stroke

8. Patients with inflammatory based arthritis (e.g.: rheumatoid arthritis, etc.)

9. Patients with congestive heart failure, New York Heart Association (NYHA) Class III or IV

10. Patients with untreated/uncontrolled thyroid function

11. Patients with clinically severe peripheral arterial disease

12. Concomitant administration of any of the following: azathioprine, mercaptopurine, theophylline, meclofenamate, sulfinpyrazone, trimethoprim-sulfamethoxazole, cyclophosphamide, benzbromarone, pyrazinamide, captopril and enalapril (for Allopurinol), tegafur, pegloticase and tacrolimus.

13. Hypersensitivity to any one of the active substances or to any of the excipients

14. Any contraindication to febuxostat or allopurinol (with reference to the summary of product characteristics).

15. Subject is unable to take either of the protocol-required gout flare prophylactic medications (NSAID or colchicine) due to contraindications or intolerance, e.g. hypersensitivity, active gastric ulcer disease, renal impairment and/or changes in liver enzymes

16. Participation in another trial of an investigational drug or device within 30 days prior to screening, or prior treatment with investigational product(s)

17. Women of childbearing potential (WOCBP), including peri-menopausal women who have had a menstrual period within 1 year, not willing to use highly effective method of birth control throughout the study period and for 4 weeks after study completion defined as a method which results in a failure rate of less than 1% per year such as:

• combined (estrogen and progestogen containing) hormonal contraception associated with inhibition of ovulation (oral, intravaginal, transdermal),

• progestogen-only hormonal contraception associated with inhibition of ovulation (oral, injectable, implantable),

• intrauterine device (IUD),

• intrauterine hormone-releasing system (IUS),

• bilateral tubal occlusion,

• vasectomised partner (provided that partner is the sole sexual partner of the trial participant and that the vasectomised partner has received medical assessment of the surgical success),

• sexual abstinence;

18. Severe psychiatric disorders/neurological disorders

19. Severe concurrent pathology, including terminal illness (cancer, AIDS, etc)

20. Abuse of alcohol, analgesics, or psychotropic drugs

21. Inability or unwillingness, in the investigator's opinion, to follow study procedures including, but not limited to the ability to obtain adequate PWV/Pulse Wave Analysis (PWA) recordings. Special attention was made to any physical abnormalities which could affect quality of PWV/PWA measurement:

• Neck region- neck flexibility and accessibility of carotid artery,

• Upper arm and thigh region- exclude any abnormalities which would prevent adequate placement of the cuff;

22. Inability or unwillingness to issue the informed consent

Related Conditions & MeSH terms

• Gout

Intervention

Drug:
• Febuxostat 80/120mg/day
Starting dose and dose regimen of Febuxostat : the initial daily dose is 80 mg. In case the patient has the serum urate concentration > 6 mg/dl after 2 weeks of treatment the dose will be escalated to 120 mg and if tolerated will be maintained for the duration of the study.
• Allopurinol 100 up to 600mg/day
Starting dose and dose regimen of allopurinol : the initial daily allopurinol dose is 100 mg, to be increased by 100 mg every 2 weeks in patients with serum urate concentration >6 mg/dl. The maximum daily dose of allopurinol achievable in the study will depend on kidney function and tolerability, but will not exceed 600 mg.
• Colchicine
Colchicine 0.5 mg tablets.To prevent flares in the initial stages of treatment, patients will be treated for at least 6 months with colchicine 0.5 - 1 mg QD
• Naproxen
Naproxen sodium 550 mg film coated tablets. In case of colchicine intolerance patients will be treated for at least 6 months with Naproxen 550 mg BID and Omeprazole (20-40 mg once daily), if indicated to be used.
• Omeprazole
Omeprazole 20 mg capsules, co-administered to patients for gastric protection.

Locations

Country	Name	City	State
Germany	Medizinische Klinik und Poliklinik III/Rheumatologie Universitätsklinikum "Carl Gustav Carus" Der Technischen Universität	Dresden
Italy	Presidio Ospedaliero San Filippo e Nicola Università degli Studi dell'Aquila U.O.C Geriatria e Lungodegenza Geriatrica	Avezzano	L'Aquila
Italy	Azienda Ospedaliero-Universitaria Policlinico Sant'Orsola-Malpighi	Bologna
Italy	Ospedale Policlinico SS. Annunziata Università degli Studi "G. d'Annunzio". Dipartimento di Medicina e Scienze dell'Invecchiamento.	Chieti
Italy	Ospedale San Salvatore U.O.C. Medicina Interna e Nefrologia Dipartimento MeSVA Università degli Studi dell'Aquila	Coppito	L'Aquila
Netherlands	Reade Clinic	Amsterdam
Poland	Gdanskie Centrum Zdrowia Sp.z o.o.	Gdansk
Poland	Specjalistyczna Praktyka Lekarska Piotr Kubalski	Grudziadz
Poland	Centrum Medyczne Pratia Katowice	Katowice
Poland	Centrum Medyczne Plejady	Kraków
Poland	Krakowski Szpital Specjalistyczny im. Jana Pawla II w Krakowie	Kraków
Poland	Specjalistyczny Gabinet Dermatologiczno-Kosmetyczny	Kraków
Poland	Oddzial Kardiologiczny, WSS im. W. Bieganskiego w Lodzi	Lódz
Poland	Polimedica	Lódz
Poland	Pratia S,A	Warsaw
Poland	Reumatika- Centrum Reumatologii	Warsaw
Romania	Clinica Medicala Data Plus SRL	Bucharest
Romania	Institutul Clinic Fundeni	Bucharest
Romania	S.C. Centrul Medical Sana S.R.L.	Bucharest
Romania	S.C. Cardiomed S.R.L.	Craiova
Romania	Cabinet Medical Medicina Interna	Timisoara
Romania	Institutul de Boli Cardiovasculare Clinica de Cardiologie si Recuperare Cardiovasculara	Timisoara
Serbia	Institut za kardiovaskularne bolesti Dedinje	Belgrade
Serbia	Institut za reumatologiju	Belgrade
Serbia	Klinicko-bolnicki centar "Bežanijska kosa" Klinika za imunologiju i alergologiju	Belgrade
Serbia	Vojnomedicinska akademija Klinika za reumatologiju	Belgrade

Sponsors (1)

Lead Sponsor	Collaborator
Menarini International Operations Luxembourg SA

Countries where clinical trial is conducted

Germany,  Italy,  Netherlands,  Poland,  Romania,  Serbia, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Pulse Wave Velocity	Comparison of the effects of Febuxostat and Allopurinol on Pulse Wave Velocity (PWV) after 36 weeks of treatment.	36 weeks of treatment