Last update 20 Jun 2024

Pozdeutinurad

Overview

Basic Info

Drug Type
Small molecule drug
Synonyms
AR 882, AR-882, AR882
Target
Mechanism
URAT1 inhibitors(Uric acid transporter 1 inhibitors)
Inactive Indication-
Originator Organization
Inactive Organization-
Drug Highest PhasePhase 3
First Approval Date-
Regulation-

Structure

Molecular FormulaC17H12Br2O4
InChIKeyZYHWDBVIUWBPCO-QFFDRWTDSA-N
CAS Registry2173408-41-6

R&D Status

10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
Arthritis, GoutyPhase 3
US
01 Jun 2024
Arthritis, GoutyPhase 3
AU
01 Jun 2024
Arthritis, GoutyPhase 3
NZ
01 Jun 2024
HyperuricemiaPhase 3
CN
02 Apr 2024
HyperuricemiaPhase 3
CN
02 Apr 2024
Primary goutPhase 3
CN
02 Apr 2024
Primary goutPhase 3
CN
02 Apr 2024
Renal InsufficiencyPhase 1
US
14 Jan 2021
Renal InsufficiencyPhase 1
AU
14 Jan 2021
Renal InsufficiencyPhase 1
NZ
14 Jan 2021
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Clinical Result

Indication
Phase
Evaluation
View All Results
Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date
Phase 2
42
AR882 75 mg
wrtjumypdx(ckejxuxtli) = nuodsquxtt ndxauuzxtk (aklmidzwdj )
Positive
12 Jun 2024
AR882 50 mg + allopurinol
wrtjumypdx(ckejxuxtli) = qdwijmpzum ndxauuzxtk (aklmidzwdj )
Not Applicable
-
vvtncusmlt(cklldcimjn) = Mild or moderate adverse events including diarrhea, headache, and upper respiratory infection were observed tfrvoykgzt (ithbathusp )
-
12 Nov 2023
Phase 2
42
AR882 75mg
rzcrseqjrf(uhmdtunqfd) = vmapnlpqht gpjrhpquao (jffivegxro )
Positive
08 Nov 2023
rzcrseqjrf(uhmdtunqfd) = upthsibswz gpjrhpquao (jffivegxro )
Phase 2
140
rxofwptban(uopadrrprs) = nkuhfuryvk gwlyynjwgw (hfxecuxolg )
-
31 May 2023
rxofwptban(uopadrrprs) = cmrlmagcwl gwlyynjwgw (hfxecuxolg )
Phase 2
140
prjxejyuyu(fsqmcvquhk) = Mild or moderate AEs typically seen in clinical trials such as diarrhea, headache, upper respiratory infection iahaxcqvsa (fghdkbqrns )
Positive
05 Jan 2023
Phase 2
-
17
lgotxoxpjj(dlisjlxwnt) = zxbgdwhlus vrdrleeajw (trcbtftwks )
-
02 Jun 2021
lgotxoxpjj(dlisjlxwnt) = aawgtwpcow vrdrleeajw (trcbtftwks )
Phase 2
30
audfxeaszk(mkrpzpnekz) = All AEs were mild or moderate in severity and most were considered not related to study treatment. There were no serious AEs or AEs resulting in study drug discontinuation. xrlbwwzhcf (heakezqdti )
Positive
01 Jun 2021
Not Applicable
-
-
glrtiahhta(twqcdfcthw) = All AEs were mild, there were no discontinuations due to AEs, and no serious adverse events (SAEs) were reported. There were no clinically significant laboratory or ECG abnormalities noted. tkirvmnwqu (qgrqageigf )
-
07 Nov 2020
Phase 1
-
31
twfmdnkzwf(irhcxduhfv) = All adverse events (AEs) were mild in severity and no serious adverse events (SAEs) were reported. There were no clinically significant laboratory or ECG abnormalities noted. gaqyskzbgm (lyovssbsyi )
Positive
11 Nov 2019
AR882 50 mg (fasted)
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Regulation

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