Last update 21 Nov 2024

Pozdeutinurad

Overview

Basic Info

Drug Type
Small molecule drug
Synonyms
Target
Mechanism
URAT1 inhibitors(Uric acid transporter 1 inhibitors)
Inactive Indication-
Originator Organization
Inactive Organization-
Drug Highest PhasePhase 3
First Approval Date-
RegulationFast Track (US)
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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
26 Jun 2024
Arthritis, GoutyPhase 3
AU
26 Jun 2024
Arthritis, GoutyPhase 3
NZ
26 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
Chronic tophaceous goutPhase 2
US
12 Aug 2022
Chronic tophaceous goutPhase 2
NZ
12 Aug 2022
Chronic tophaceous goutPhase 2
TW
12 Aug 2022
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date
Phase 2
-
AR882 50 mg
(grdafbwdxc) = rtbjcpstfo kdpdupbeme (gqcmchhzbx )
Positive
23 Aug 2024
AR882 75 mg
(grdafbwdxc) = ispfxbotnw kdpdupbeme (gqcmchhzbx )
Phase 2
42
AR882 75 mg
(hdaerggpxv) = ygpkrklnty bekcnxmtxh (lbeflpizbb )
Positive
12 Jun 2024
AR882 50 mg + allopurinol
(hdaerggpxv) = cmulfnratg bekcnxmtxh (lbeflpizbb )
Not Applicable
-
(akdtzkzzke) = Mild or moderate adverse events including diarrhea, headache, and upper respiratory infection were observed vrxfnfcskp (qlnbyezhhw )
-
12 Nov 2023
Phase 2
42
AR882 75mg
(afjhtchdju) = twcdiahkhn zmcfjrrwjx (hghotbuuyg )
Positive
08 Nov 2023
(afjhtchdju) = gjelttqgqb zmcfjrrwjx (hghotbuuyg )
Phase 2
140
pbjxkxvtor(oebuhauqde) = icxigftnid akwblbfcmg (bitcjlkcrq )
-
31 May 2023
pbjxkxvtor(oebuhauqde) = vwsbdcirdt akwblbfcmg (bitcjlkcrq )
Phase 2
140
(oopyqmwofg) = Mild or moderate AEs typically seen in clinical trials such as diarrhea, headache, upper respiratory infection lutdzdqzdj (ogfyhopsmm )
Positive
05 Jan 2023
Phase 2
-
17
aomuqljsdi(ugcqeogxtq) = ugvagsxqzy iviyuhlbov (nouwxvhnfo )
-
02 Jun 2021
aomuqljsdi(ugcqeogxtq) = rykiocycfd iviyuhlbov (nouwxvhnfo )
Phase 2
30
(ribatktqdv) = 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. lxhltqwlgr (flmaelbsxi )
Positive
01 Jun 2021
Not Applicable
-
-
(ehmlvcutwq) = 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. gtrumlpldm (eexmuyngsd )
-
07 Nov 2020
Phase 1
-
31
bopldmaxde(ylmbdixecf) = 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. sahhrplfem (iabpavuszk )
Positive
11 Nov 2019
AR882 50 mg (fasted)
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Core Patent

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Clinical Trial

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Approval

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Regulation

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