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Long-term Treatment of Gout: New Opportunities for Improved Outcomes.



* Make a presumptive diagnosis of gout based on history and physical examination

* Individualize and modify urate-lowering therapy based on best evidence to achieve treatment goals


Family physicians and clinicians who wish to gain increased knowledge and greater competency regarding primary care management of the long-term treatment of gout.


As a continuing medical education provider accredited by the Accreditation Council for Continuing Medical Education (ACCME), Primary Care Education Consortium (PCEC) requires any individual in a position to influence educational content to disclose any financial interest or other personal relationship with any commercial interest. This includes any entity producing, marketing, reselling or distributing health care goods or services consumed by, or used on, patients. Mechanisms are in place to identify and resolve any potential conflict of interest prior to the start of the activity. In addition, any discussion of off-label, experimental, or investigational use of drugs or devices will be disclosed by the faculty.

Paul P. Doghramji, MD discloses that he is on the advisory board for Iron wood Pharmaceuticals, Inc. and owns stock in Pfizer, Inc.

Gregory Scott, PharmD, RPh and Angela Cimmino, PharmD, editorial support, disclose they have no real or apparent conflicts of interest to report.

Michael Hanak, MD, CME Reviewer, discloses that he has no real or apparent conflicts of interest to report.


This activity is sponsored by Primary Care Education Consortium


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Release Date: 1 August 2018

Expiration Date: 31 July 2019



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This article is supported by an educational grant from Ironwood Pharmaceuticals, Inc.


1. An adult male presenting with pain in the foot and instep

2. A postmenopausal female presenting with wrist pain and stiffness

3. A young, thin male presenting with severe pain in the midfoot, similar to what his father and brother experience.

The underlying cause of pain in all 3 of these patients is undiagnosed gout, demonstrating different presentations of gout.

This article will discuss some of the key questions and clinical challenges encountered in the long-term primary care management of patients with gout.


Gout is an independent predictor of premature death and is associated with a high frequency of comorbidities, many with a prevalence 2 to 3 times higher than among people without gout: hypertension, chronic kidney disease (CKD), obesity, type 2 diabetes, nephrolithiasis, cardiac disease (including coronary artery disease, heart failure, and atrial fibrillation), dyslipidemia, stroke, peripheral arterial disease, and sleep apnea. (13)


Based on an estimated prevalence of gout of 3.9% (8.3 million) and hyperuricemia (ie, serum uric acid [sUA] level >7.0 mg/dL in men and >5.7 mg/dL in women) of 21.4% (43.3 million) among US adults, approximately 1 in 5 people with hyperuricemia develop symptoms of gout. (4) Although the prevalence of hyperuricemia is similar among men (21.2%) and women (21.6%), the prevalence of gout is approximately 3 times higher in men than in women (5.9% and 2% of adults in the United States, respectively); the disparity between sexes lessens after menopause. (5) The overall prevalence of gout increases with age, from 3.3% in adults over the age of 40 years to 9.3% in adults over the age of 70 years. (4) Family history may also play a small role.


A 37-year-old male with obesity (body mass index, 33 kg/[m.sub.2]) presents with a painful, swollen big toe. He has a family history of gout (father, brother). sUA is 7.3 mg/dL.


An acute gout attack (flare) is typically monoarthritic early in the disease and peaks within hours, manifesting as a severely inflamed joint that is red, hot, swollen, and tender to the touch or movement. (6) The attack is self-limiting, with symptoms resolving within about 2 weeks, although ongoing joint damage during intercritical asymptomatic periods usually occurs due to continuing monosodium urate (MSU) crystal deposition and inflammation. (7) An acute attack most commonly manifests in the lower extremities, particularly the first metatarsophalangeal joint (podagra) in men, whereas the elbow, wrist, and hands are more likely to be affected in women. (6,8) The reduced solubility of urate at lower temperatures may account for the occurrence of gout at peripheral joints, which are cooler than central-axis joints. (9) Involvement of more than (1) joint is more common as disease progresses. (6)


The most important component of the differential diagnosis of acute gout is septic arthritis, although the incidence of septic arthritis is much lower. In addition, the onset of septic arthritis is more insidious, and patients with septic arthritis tend to be quite sick with fever, rash, or other signs of systemic illness, and typically require hospitalization. (8,10)

Synovial fluid aspiration and identification of MSU crystals by polarized light microscopy is the gold standard of gout diagnosis. (6) However, an adequate clinical analysis is sufficient for diagnosis in most cases, so this test is often not required. (11) Combined with intra-articular corticosteroid injection, joint aspiration provides immediate and lasting pain relief for many patients. (6,8) Radiography is not useful in early gout because small erosions and tophi are difficult to detect, but such lesions are detectable in chronic gout. (6) Although not commonly done, ultrasonography is useful in early gout to distinguish between active and inactive tophi. (6)

The absence of hyperuricemia is inadequate alone to rule out a gout diagnosis because the sUA level may drop to normal during a gout attack. Therefore, even though it is reasonable to measure sUA during an attack, the sUA level should be measured again several weeks after the flare has resolved. (10) It should be kept in mind that each laboratory calculates its own sUA threshold for hyperuricemia, so a "normal" sUA level may, nevertheless, reflect levels in joint tissues that are above ~6.8 mg/dL necessary for MSU crystal deposition. (7) Most labs these days will also list, "sUA desirable level for gout treatment: <6.0 mg/dL."

Hyperuricemia and gout should be considered red flags for metabolic syndrome and cardiovascular disease. Therefore, additional evaluation includes a comprehensive metabolic panel (eg, blood glucose and hemoglobin Alc levels and kidney and liver function) and a lipid panel, as well as clinical screening for associated comorbidities and cardiovascular risk factors (eg, obesity, hypertension, smoking). (12,13)


A diagnosis of gout is confirmed. A plan is developed to begin a nonsteroidal anti-inflammatory drug for acute treatment for the flare. Once the flare has resolved, urate-lowering therapy will be initiated.


Monosodium urate crystal formation is reversible, and crystals will dissolve when the sUA level drops below the limit of solubility (~6.8 mg/dL). This will result in the disappearance of gout flares and a reduction in the size and number of tophi. (12,14) The lower the sUA

level, the faster the crystal deposits (and tophi) resolve. Therefore, the goal of long-term gout management is to lower the sUA level below the limit of solubility. (14) In addition, the management of patients with gout should include prevention and treatment of associated cardiovascular and other diseases. (3)


According to both the American College of Rheumatology (ACR) guidelines and the European League Against Rheumatism (EULAR) recommendations, the target sUA goal for urate-lowering therapy (ULT) is <6 mg/dL for all gout patients. A lower sUA target (<5 mg/dL) to facilitate faster dissolution of crystals is recommended for patients with severe gout (tophi, chronic arthropathy, frequent attacks) until total crystal dissolution and resolution of gout are achieved. (12,15)

Appropriately treated gout, with maintenance of sUA below target levels, markedly reduces the frequency of gout flares and the size and number of tophi and improves quality of life (QoL). (12) Inadequate treatment that fails to maintain sUA below target levels is associated with recurrent flares, further joint damage, and subsequent loss of mobility, functional impairment, and decreased QoL. (11)


The American College of Radiology guidelines recommend monitoring sUA every 2 to 5 weeks during ULT titration (see "How is each of the approved ULTs initiated and titrated?," on page S23), then every 6 months once the sUA target level is achieved. (15)


Evidence from randomized, blinded studies is lacking regarding alteration of lifestyle factors translating into improved outcomes in patients with gout. However, diet, exercise, and weight loss have been associated with a modest reduction in the sUA level in some clinical trials; therefore, every patient should be encouraged to make such changes as best as possible. (12,15) Lifestyle management (eg, reducing excess body weight, regular exercise, smoking cessation, and avoiding excessive alcohol and sugar-sweetened drinks) has a greater role in reducing the risk and optimizing management of life-threatening comorbidities in patients with gout. (12,13,15)


Available US Food and Drug Administration (FDA)-approved options for lowering sUA include xanthine oxidase inhibitors (allopurinol and febuxostat) that prevent production of uric acid; a uricosuric agent (probenecid) that increases uric acid output in urine; and a uric acid-specific enzyme (pegloticase) that converts uric acid to allantoin. Another recently approved uricosuric agent, lesinurad, inhibits the function of transporter proteins (urate transporter 1 and organic anion transporter 4) involved in uric acid reabsorption in the kidney. (6,16)

Fenofibrate, losartan, and atorvastatin are not FDA-approved for gout but act as uricosurics and can therefore be used to treat gout comorbidities or in association with xanthine oxidase inhibitors. (6) There has been limited study of rasburicase, an injectable approved for tumor lysis, in the treatment of tophaceous gout. (16)


In a patient diagnosed with gout (and who has normal renal function), allopurinol, 300 mg daily, is initiated after resolution of an acute flare. sUA is reduced from 8.6 mg/dL to 7.2 mg/dL after 9 months of treatment. Clinical decision points:

* Should the dosage of allopurinol be increased or should a non-xanthine oxidase inhibitor be initiated?

* If the patient's estimated glomerular filtration rate is 35 ML/min/1.73 kg/[m.sup.2], would this impact the decision between uptitrating and adding a second agent?


Guidelines recommend a xanthine oxidase inhibitor as first-line therapy. (15) Allopurinol is most commonly used due to its low cost, extensive clinical experience, and relatively good safety and efficacy profile. (8,13)

For patients who do not achieve the target sUA level with optimized allopurinol therapy, the next-step choice is primarily a consideration of patient-specific factors, physician and patient choice, and cost. In the author's experience, a good option is using medications with different mechanisms of action because this provides further lowering of sUA while enabling the use of lower dosages of individual medications, thereby reducing the incidence and severity of dosage-related adverse events.

The xanthine oxidase inhibitor febuxostat, 80 mg/d or 120 mg/d (the latter an investigational dose but recommended by ACR and EULAR when needed) has demonstrated superior urate-lowering efficacy compared with allopurinol at a fixed dosage of 300 mg/d (table). (12,17-19) Although ACR guidelines do not give preference to allopurinol or febuxostat, EULAR and other international guidelines recommend that febuxostat be used in patients who are intolerant of, or do not respond to, an adequate dosage of allopurinol. (12,13,15) Febuxostat has been associated with cutaneous reactions, but data do not support any cross-reactivity with allopurinol. (12) Liver function abnormalities and a slightly higher incidence of cardiovascular thromboembolic events may occur. (20)

Guidelines also recommend adding a uricosuric agent (lesinurad or probenecid) or switching to a uricosuric agent (probenecid) if the sUA target level cannot be reached by an appropriate dosage of a xanthine oxidase inhibitor or when a xanthine oxidase inhibitor is not tolerated. (12,13,15) The efficacy of probenecid in combination with allopurinol in such patients has been demonstrated in a few small trials. (21) However, probenecid is not recommended in patients with a creatinine clearance <50 mL/minute or uric acid urolithiasis. (15)

Lesinurad is approved only as add-on therapy to a xanthine oxidase inhibitor. (16) In large, randomized clinical trials, lesinurad in combination with either allopurinol or febuxostat has demonstrated greater efficacy than either of the xanthine oxidase inhibitors as monotherapy (table). (18,19,22-25) Lesinurad has been associated with a transient elevation of serum creatinine and kidney stones, the incidence of which is higher if taken without a xanthine oxidase inhibitor.

Pegloticase can be considered in patients with crystal-proven severe, debilitating chronic tophaceous gout and poor QoL, in whom the sUA target level cannot be reached with any other available drug at the maximal dosage (including combination therapy). (12) Pegloticase is an IV medication that must be given at an appropriately trained infusion center because there is a risk of anaphylaxis.

The table summarizes results of key clinical trials for ULT agents approved in the United States. (18,19,22-25)


A treat-to-target approach should be utilized, whereby ULT is initiated and intensified as needed to achieve and maintain the target sUA level <6 mg/dL, or [less than or equal to]5 mg/dL in certain patients (eg, those with tophi), as discussed. (12,15) Because initiation of ULT is associated with gout flares for approximately the first 6 months, prophylactic use of anti-inflammatory therapy (eg, colchicine or a nonsteroidal anti-inflammatory drug) is recommended during that time frame. (13)


In patients with normal kidney function, allopurinol is initiated at a low dosage (100 mg/d) and increased by 100 mg/d increments every 2 to 4 weeks if required, to reach the uricemic target. (12) A reduced initial dose, eg, 50 mg/d, and a daily dose of 200 mg is suggested in patients with a creatinine clearance of 10 to 20 mL/minute. This approach can minimize the risk of a severe cutaneous hypersensitivity reaction (eg, Stevens-Johnson syndrome) as well as an acute gout flare. (12) In approximately 30% to 50% of patients with normal kidney function, 300 mg/d is the most commonly used dosage of allopurinol. Because 300 mg/d does not achieve the target sUA level of <6 mg/dL in more than 50% of patients with gout, guidelines recommend dosage escalation when needed to reach the sUA target. (15) Dosages of 600 to 800 mg/d have a 75% to 80% success rate in achieving an sUA level <6 mg/dL. (12) Dosages >300 mg/d are given in divided doses to avoid gastrointestinal side effects. In patients with renal impairment, EULAR guidelines recommend adjusting the allopurinol dosage downward due to the risk of serious cutaneous adverse events. (12) ACR guidelines, however, recommend increasing allopurinol until the sUA target level is reached in these patients, while monitoring for drug toxicity. (9) The ACR recommendation is based on several small series of patients in which no increased incidence of severe reactions was demonstrated in patients whose allopurinol dosages were progressively titrated above those recommended, based on creatinine clearance and the level of renal impairment. (6,18,19,26-28)


Febuxostat is approved by the FDA at a starting dosage of 40 mg/d, uptitrated to 80 mg/d if patients do not achieve an sUA level <6 mg/dL after 2 weeks. (20) ACR guidelines suggest up titration to as much as 120 mg/d (an investigational dosage) if necessary to achieve the target sUA level. (15)


The initial dosage of probenecid is 250 mg twice daily, uptitrated weekly to 1 g twice daily, based on the sUA level. (6) Patients must be counseled to hydrate well due to the risk of urolithiasis. (15) Probenecid is not recommended for patients with a creatinine clearance <50 mL/min, due to lack of data on long-term safety and efficacy in stage 3 CKD. (15)


Lesinurad is indicated at a dosage of 200 mg/d as add-on therapy to allopurinol or febuxostat. (16) Lesinurad should not be initiated in patients with a creatinine clearance <45 mL/min; renal function should be evaluated prior to initiation and periodically thereafter. (16) Lesinurad is available as a 200 mg tablet and as a combination tablet of 200 mg of lesinurad with either 200 mg or 300 mg of allopurinol, which may improve patient adherence and lessen the risk of lesinurad being inadvertently taken without allopurinol. (16,29)


Pegloticase must be administered under supervision at an infusion center, due to the high risk of serious allergic reaction, including anaphylaxis. (30) Pegloticase is administered as an 8-mg IV infusion every 2 weeks, and should not be combined with other urate-lowering medications. (30)


Because Harriet has not reached the sUA target of <6.0 mg/dL and she is tolerating allopurinol, the decision is made to increase the dosage of allopurinol to 200 mg twice daily and recheck the sUA level in 2 weeks.


Gout is a common disorder that is associated with significant patient morbidity, as well as with comorbidities such as CKD, diabetes, and various cardiovascular disorders. Diagnosis is often based on history and physical examination, with confirmation by joint aspiration when necessary. Lifestyle management generally provides modest reduction of the sUA level. Several urate-lowering medications have been approved for chronic therapy. Allopurinol is typically used as first-line therapy. When combination therapy is required to achieve the target sUA level, the choice is generally based on patient-specific factors, physician and patient choice, and cost.


Dr. Doghramji discloses that he is on the advisory board for Ironwood Pharmaceuticals, Inc.; and owns stock in Pfizer Inc.


Editorial support was provided by Gregory Scott, PharmD, RPh, and Angela Cimmino, PharmD. The author was responsible for all content and editorial decisions.


This article is sponsored by Primary Care Education Consortium and supported by funding from Ironwood Pharmaceuticals, Inc.


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(2.) Zhang Y, Peloquin CE. Dubreuil M, et al. Sleep apnea and the risk of incident gout: A population-based, body mass index-matched cohort study. Arthritis Rheumatol. 2015;67(12):3298-3302.

(3.) Zhu Y, Pandya BI, Choi HK. Comorbidities of gout and hyperuricemia in the US general population: NHANES 2007-2008. Am J Med. 2012;125(7):679-687.el.

(4.) Zhu Y, Pandya BJ, Choi HK. Prevalence of gout and hyperuricemia in the US general population: the National Health and Nutrition Examination Survey 2007-2008. Arthritis Rheum. 2011;63(10):3136-3141.

(5.) MacFarlane LA, Kim SC. Gout: a review of nonmodifiable and modifiable risk factors. Rheum Dis Clin North Am. 2014;40(4):581-604.

(6.) Ragab G, Elshahaly M, Bardin T. Gout: An old disease in new perspective--A review. J Adv Res. 2017;8(5):495-511.

(7.) Ruoff G, Edwards NL. Overview of serum uric acid treatment targets in gout: Why less than 6 mg/dL? Postgrad Med. 2016;128(7):706-715.

(8.) Doghramji PP. Hot topics in primary care: Update on the recognition and management of gout: More than the great toe. J Fam Pract. 2015:64(12 Suppl):S31-S36.

(9.) Roddy E. Revisiting the pathogenesis of podagra: why does gout target the foot? J Foot Ankle Res. 2011;4(1):13.

(10.) Roddy E. Gout: presentation and management in primary care. In: Hands On: Reports on the Rheumatic Diseases: Series 6, No 9. Derbyshire, UK: Arthritis Research UK; 2011: 1-6.

(11.) Doherty M, Jansen TL, Nuki G, et al. Gout: why is this curable disease so seldom cured? Ann Rheum Dis. 2012;71(11):1765-1770.

(12.) Richette P, Doherty M, Pascual E, et al. 2016 updated EULAR evidence-based recommendations for the management of gout. Ann Rheum Dis. 2017;76(1):29-42.

(13.) Sivera F, Andres M, Carmona L, et al. Multinational evidence-based recommendations for the diagnosis and management of gout: integrating systematic literature review and expert opinion of a broad panel of rheumatologists in the 3e initiative. Ann Rheum Dis. 2014;73(2):328-335.

(14.) Keenan RT. Limitations of the current standards of care for treating gout and crystal deposition in the primary care setting: a review. Clin Ther. 2017;39(2):430-441.

(15.) Khanna D, Fitzgerald JD, Khanna PP, et al. 2012 American College of Rheumatology guidelines for management of gout. Part 1: systematic nonpharmacologic and pharmacologic therapeutic approaches to hyperuricemia. Arthritis Care Res (Hoboken). 2012;64(10):1431-1446.

(16.) Zurampic [package insert], Wilmington, DE: AstraZeneca; 2016.

(17.) Becker MA, Schumacher HR, Espinoza LR, et al. The urate-lowering efficacy and safety of febuxostat in the treatment of the hyperuricemia of gout: the CONFIRMS trial. Arthritis Res Ther. 2010;12(2):R63.

(18.) Becker MA, Schumacher HR Jr., Wortmann RL, et al. Febuxostat compared with allopurinol in patients with hyperuricemia and gout. N Engl J Med. 2005:353(23): 2450-2461.

(19.) Schumacher HR, Jr., Becker MA, Wortmann RL, et al. Effects of febuxostat versus allopurinol and placebo in reducing serum urate in subjects with hyperuricemia and gout: a 28-week, phase III, randomized, double-blind, parallel-group trial. Arthritis Rheum. 2008;59(11):1540-1548.

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(22.) Dalbeth N, Jones G, Terkeltaub R, et al. Lesinurad, a selective uric acid reabsorption inhibitor, in combination with febuxostat in patients with tophaceous gout: Findings of a phase III clinical trial. Arthritis Rheumatol. 2017;69(9):1903-1913.

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Paul P. Doghramji, MD, FAAFP, Family Physician, Collegeville Family Practice, Medical Director of Health Services, Ursinus College, Collegeville, Pennsylvania
TABLE Key studies of urate-lowering therapy (18,19,22-25)

* Study/author                Treatment
* Baseline sUA level
* Prior treatment
* FACT/Becker (18)            52 weeks

* Mean sUA, 9.8-9.9 mg/dL     ALP 300 mg/d (n=253)
* ALP (44% of subjects)       FBX 80 mg/d (n=256)
                              FBX 120 mg/d (n=251)

* APEX/Schumacher (19)        28 weeks
* Mean sUA, 9.85 mg/dL        ALP 300 mg/d (n=268) (b)
* ALP (~1/3 of subjects)      FBX 80 mg/d (n=267)
                              FBX 120 mg/d (n=269)
                              FBX 240 mg/d (n=134)
                              PBO (n=134)

* CLEAR 1/Saag (23)           12 months

* sUA, [greater than or       PBO/ALP (n=201)
  equal to]6.5 mg/dL          LSN 200 mg/d +ALP (n=201)
* ALP [greater than or        LSN 400 mg/d + ALP (n=201)
  equal to]300 mg/d
  ([greater than or equal
  to]200 mg/d in patients
  with moderate renal
  impairment) and
  [greater than or equal
  to]22 gout flares
  during the previous year
* CRYSTAL/Dalbeth (22)        12 months
* ULT-naive: sUA, [greater    PBO/FBX 80 mg/d (n=109)
  than or equal to]8 mg/      LSN 200 mg/d + FBX 80 mg/d (n=106)
  dL; ULT                     LSN 400 mg/d + FBX 80 mg/d (n=109)
  treated: sUA, [greater
  than or equal to 6 mg/dL

* Open label study/           Stage 1: 2 months
  Reinders (24)
* N/A                         ALP 200-300 mg/d (based on renal
* Benzbromarone               function) (n=32)
                              Stage 2: >2 months
                              Probenecid 1000 mg/d, added to ALP in
                              patients failing to attain sUA <0.3
                              mmol/L (c) (n=14)
* CO405/Sundy (25)            6 months
* sUA, 9.4-10.4 mg/dL         Group 1: Pealoticase 8 ma biweekly
* Intolerant or refractory    (n=43)
  to ALP                      Group 2: Pealoticase 8 mq monthly
                              Group 3: PBO (n=20)

* C0406/Sundy (25)            6 months
* sUA, 9.5-9.8 mg/dL          Group 1: Pealoticase 8 ma biweekly
* Intolerant or refractory    (n=42)
  to ALP                      Group 2: Pealoticase 8 ma monthly
                              Group 3: PBO (n=23)

* Study/author                Primary efficacy result
* Baseline sUA level
* Prior treatment
* FACT/Becker (18)            Percentage of patients with sUA <6 mg/
                              dL at last
* Mean sUA, 9.8-9.9 mg/dL     3 monthly measurements
* ALP (44% of subjects)       ALP 300 mg/d: 21%
                              FBX 80 mg/d: 53% (P<.001) (a)
                              FBX 120 mg/d: 62% (P<.001) (a)
* APEX/Schumacher (19)        Percentage of patients with sUA <6 mg/
* Mean sUA, 9.85 mg/dL        dL at last 3 monthly measurements
* ALP (~1/3 of subjects)      ALP 300 mg/d: 22%
                              FBX 80 mg/d: 48% (P[less than or equal
                              to].05) (a)
                              FBX 120 mg/d: 65% (P[less than or equal
                              to].05) (a)
                              FBX 240 mg/d: 69% (P[less than or equal
                              to].05) (a) PBO: 0%
* CLEAR 1/Saag (23)           Percentage of patients with sUA <6
                              mg/dL at
* sUA, [greater than or       6 months
  equal to]6.5 mg/dL          PBO/ALP: 27.9%
* ALP [greater than or        LSN 200 mg/d + ALP: 54.2% (P<.0001) (a)
  equal to]300 mg/d           LSN 400 mg/d + ALP: 59.2% (P<.0001) (a)
  ([greater than or equal
  to]200 mg/d in patients
  with moderate renal
  impairment) and
  [greater than or equal
  to]22 gout flares
  during the previous year
* CRYSTAL/Dalbeth (22)        Percentage of patients with sUA <5 mg/
* ULT-naive: sUA, [greater    dL by month 6
  than or equal to]8 mg/      PBO/FBX 80 mg/d: 46.8%
  dL; ULT                     LSN 200 mg/d + FBX 80 mg/d: 56.6%
  treated: sUA, [greater      (P=.13) (a)
  than or equal to 6 mg/dL    LSN 400 mg/d + FBX 80 mg/d: 76.1 %
                              (P<.0001) (a)

* Open label study/           Percentage of patients attaining sUA
  Reinders (24)               <0.3 mmol/L (c)
* N/A                         Stage 1
* Benzbromarone               ALP monotherapy: 25%
                              Stage 2
                              ALP plus probenecid: 86%

* C0405/Sundy (25)            Percentage of patients with sUA <6 mg/dL
* sUA, 9.4-10.4 mg/dL         [greater than or equal to]80% of the
* Intolerant or refractory    time at Month 3 and Month 6
  to ALP                      Group 1: 47% (95% CI, 31%-62%)
                              Group 2: 20% (95% CI. 9%-35%)
                              Group 3: 0

* CO406/Sundy (25)            Percentage of patients achieving sUA
* sUA, 9.5-9.8 mg/dL          <6 mg/dL [greater than or equal to]80%
* Intolerant or refractory    of the time at Month 3 and Month 6
  to ALP                      Group 1: 38% (95% CI, 24%-54%)
                              Group 2: 49% (95% CI, 33%-65%)
                              Group 3: 0

(a) Compared with allopurinol-based arm.

(b) 10 subjects received 100 mg/d and 258 subjects received 300 mg/d,
Based on renal function.

(c) SUA, 0.3 mmol/L = ~5.0 mg/dL.

Abbreviations: ALP, allopurinol; CI, confidence interval; FBX,
febuxostat; LSN, lesinurad; PBO, placebo; sUA, serum uric acid.
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Author:Doghramji, Paul P.
Publication:Journal of Family Practice
Article Type:Report
Geographic Code:1USA
Date:Aug 1, 2018
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