Pegloticase

Treatment for Gout

Typical Dosage: 8 mg IV every two weeks

Effectiveness
90%
Safety Score
45%
Clinical Trials
18
Participants
2K

Comparative Safety Scale(Higher is safer)

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45
DangerousModerateSafe
Treatment Details
Dosage Range
8 mg IV every two weeks
Time to Effect
24 hours (sUA reduction), weeks-months (clinical benefits)
Treatment Duration
6-12 months
Evidence Quality
MODERATE
Number Needed to Treat (NNT)
2(Treat 2 patients to see 1 additional successful outcome)
Number Needed to Harm (NNH)
4(Treat 4 patients to see 1 additional serious adverse event)
Confidence Score
80%confidence in effectiveness data
Health Economics
Annual Cost of Care
Drug Cost:$234,000
Monitoring:$15,000
Side Effect Mgmt:$7,000
Total Annual:$256,000
Cost-Effectiveness Analysis
Cost-Effectiveness Rating
POOR
ICER
$350,000/QALY
QALYs Gained
1
Outcome-Based Costs
Cost per Responder
$568,889
Cost per Remission
$731,429
Comparison vs Conventional management (refractory gout)
Cost Difference
+$250,000/year
More expensive
QALY Difference
+0.80 QALYs
Better outcomes
Dominance
No dominance
Pegloticase Outcomes

for Gout

Efficacy Outcomes
Overall Effectiveness
+90%
Response Rate
+45%
Remission Rate
+35%
Common Side Effects
Infusion reactions
+40%
Gout flares (initiation)
+25%
Nausea
+15%
Antibody formation (loss of efficacy)
+30%

WARNING: LIMITED TRIALS AVAILABLE

You can search for trials, but you probably can't join any because the 1% Treaty hasn't passed yet. Most trials are severely limited by lack of funding and bureaucratic barriers. Help change this!

Active Clinical Trials
2 active trials recruiting for Pegloticase in Gout

A Double-blind, Randomized Controlled Trial to Investigate the Efficacy, Safety, and Pharmacokinetics of Pegloticase Administration Via Subcutaneous and Intravenous Routes Both With Methotrexate in Participants With Uncontrolled Gout

NCT07388498RECRUITINGPHASE3
View Study
270 participants
INTERVENTIONAL
Tustin, United States +36 more
Started: Feb 9, 2026

Evaluation of Efficacy and Safety of AR882 and XOI Co-administration in Uricase Treatment Failed Patients

NCT07116746RECRUITINGPHASE2
View Study
25 participants
INTERVENTIONAL
Margate, United States +7 more
Started: Dec 3, 2025
Completed Clinical Trials
17 completed trials for Pegloticase in Gout

Pegylated Recombinant Mammalian Uricase (PEG-uricase) as Treatment for Refractory Gout

NCT00111657COMPLETEDPHASE2
View Study
30 participants
INTERVENTIONAL
Durham, United States
Started: Dec 1, 2004

A Trial to Investigate the Non-inferiority of Pegloticase Administered Every 4 Weeks (Q4W) With MTX Compared With Every 2 Weeks (Q2W) With MTX in Participants With Uncontrolled Refractory Gout

NCT06229145COMPLETEDPHASE4
View Study
262 participants
INTERVENTIONAL
Birmingham, United States +73 more
Started: Mar 18, 2024

Open-Label Extension Study for Patients Who Completed a Phase 3 Double-blind Study of PEG-uricase for Symptomatic Gout

NCT01356498COMPLETEDPHASE3
View Study
151 participants
INTERVENTIONAL
San Francisco, United States +21 more
Started: Dec 1, 2006

Tolerization Reduces Intolerance to Pegloticase and Prolongs the Urate Lowering Effect

NCT02598596COMPLETEDPHASE2
View Study
132 participants
INTERVENTIONAL
Birmingham, United States +10 more
Started: Dec 1, 2015

Safety and Efficacy Study of PEG-uricase in the Treatment of Hyperuricemic Patients With Symptomatic Gout

NCT00325195COMPLETEDPHASE3
View Study
225 participants
INTERVENTIONAL
Birmingham, United States +55 more
Started: May 1, 2006

Observational Study of the Use of Pegloticase (KRYSTEXXAĀ®) in Refractory Chronic Gout

NCT01466166COMPLETED
View Study
188 participants
OBSERVATIONAL
Birmingham, United States +66 more
Started: Nov 15, 2011

A Phase 4, Open-label Study of KRYSTEXXAĀ® (Pegloticase) Co-administered With Methotrexate (MTX) in Patients With Uncontrolled Gout (FORWARD OL)

NCT04762498COMPLETEDPHASE4
View Study
50 participants
INTERVENTIONAL
Anchorage, United States +11 more
Started: Jan 26, 2021

A Study of Persons With Gout Who Do Not Respond to or Are Allergic to Conventional Therapy

NCT00080210COMPLETEDPHASE2
View Study
40 participants
INTERVENTIONAL
Birmingham, United States +8 more
Started: Mar 1, 2004

A Study to Compare the Efficacy of SEL-212 to KRYSTEXXAĀ® in Gout Participants Refractory to Conventional Therapy

NCT03905512COMPLETEDPHASE2
View Study
170 participants
INTERVENTIONAL
Anniston, United States +42 more
Started: May 7, 2019

Infusion Duration Study To Assess Tolerability of Pegloticase Administered With a Shorter Infusion Duration in Subjects With Uncontrolled Gout Receiving Methotrexate

NCT04511702COMPLETEDPHASE4
View Study
191 participants
INTERVENTIONAL
Birmingham, United States +38 more
Started: Oct 2, 2020

Study of Pegloticase in Participants With Uncontrolled Gout Who Have Had a Kidney Transplant

NCT04087720COMPLETEDPHASE4
View Study
20 participants
INTERVENTIONAL
Birmingham, United States +7 more
Started: Sep 9, 2019

Pegloticase and Methotrexate Co-administered in Participants With Uncontrolled Gout Who Previously Failed Pegloticase Monotherapy

NCT04772313COMPLETEDPHASE4
View Study
11 participants
INTERVENTIONAL
Birmingham, United States +14 more
Started: Mar 8, 2021

REduCing Immunogenicity to PegloticasE (RECIPE) Study

NCT03303989COMPLETEDPHASE2
View Study
35 participants
INTERVENTIONAL
Birmingham, United States
Started: Jun 14, 2018

Study of KRYSTEXXAĀ® (Pegloticase) Plus Methotrexate in Participants With Uncontrolled Gout

NCT03994731COMPLETEDPHASE4
View Study
152 participants
INTERVENTIONAL
Birmingham, United States +59 more
Started: Jun 13, 2019

Study of Pegloticase (KRYSTEXXAĀ®) Plus Methotrexate in Patients With Uncontrolled Gout

NCT03635957COMPLETEDPHASE4
View Study
14 participants
INTERVENTIONAL
Anchorage, United States +5 more
Started: Sep 26, 2018

Re-exposure Study of Pegloticase Intravenous (i.v.) in Symptomatic Gout Patients

NCT00675103COMPLETEDPHASE3
View Study
7 participants
INTERVENTIONAL
Chicago, United States +3 more
Started: May 1, 2008

Recapturing Immune Tolerance to Pegloticase for the Management of Tophaceous Gout

NCT06186219COMPLETEDPHASE1
View Study
2 participants
INTERVENTIONAL
Los Angeles, United States
Started: Apr 10, 2024