Evidence map›Paper›PMID 42332828›Full record

Trial reportArthritis research & therapy2026

Safety, tolerability, pharmacokinetics, and pharmacodynamics of ABP-671 in healthy participants and patients with hyperuricemia and gout: a proof-of-concept study.

Jin Wang, Lan Zhang, Ullrich Schwertschlag, Jingfei Li, Yan Yang, Adam W Jin, Roy J Wu, Chaoying Hu, Dongfang Shi

Abstract readRandomized Controlled TrialClinical Trial, Phase IClinical Trial, Phase II
PubMed Publisher
In one paragraph

Trial report in Arthritis research & therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Jin WangPhase I Clinical Research Unit, Xuanwu Hospital Capital Medical University, Beijing, 100053, China.
Lan ZhangPhase I Clinical Research Unit, Xuanwu Hospital Capital Medical University, Beijing, 100053, China.
Ullrich SchwertschlagAtom Therapeutics Co., Ltd, Hangzhou, Zhejiang, 310018, China.
Jingfei LiAtom Therapeutics Co., Ltd, Hangzhou, Zhejiang, 310018, China.
Yan YangAtom Therapeutics Co., Ltd, Hangzhou, Zhejiang, 310018, China.
Adam W JinAtom Therapeutics Co., Ltd, Hangzhou, Zhejiang, 310018, China.
Roy J WuAtom Therapeutics Co., Ltd, Hangzhou, Zhejiang, 310018, China.
Chaoying HuPhase I Clinical Research Unit, Xuanwu Hospital Capital Medical University, Beijing, 100053, China. hucarol@126.com.
Dongfang ShiAtom Therapeutics Co., Ltd, Hangzhou, Zhejiang, 310018, China. williamshi3777@atombp.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis proof-of-concept study evaluated the safety, tolerability, pharmacokinetics, and pharmacodynamics of ABP-671, a novel URAT1 inhibitor, in healthy participants and in patients with hyperuricemia and gout.

methodsThis single-center, randomized, double-blind, placebo-controlled phase I/IIa clinical trial consisted of two parts: a single ascending dose study (SAD) in healthy participants (0.5, 1, 3, and 6 mg, with two participants receiving placebo and six participants receiving ABP-671 tablets per dose cohort), and a multiple ascending dose (MAD) study in patients with hyperuricemia and gout (1, 2, 4, 6 and 12 mg daily, with two patients receiving placebo and seven patients receiving ABP-671 tablets per cohort).

resultsThirty-two and 45 Chinese participants were enrolled in the SAD and MAD studies, respectively. In the SAD and MAD studies, eight (25.0%) and 24 (53.3%) participants reported treatment-emergent adverse events (TEAEs), respectively; there were no serious AEs (SAEs), and no grade ≥ 3 TEAEs. In the MAD study, the maximum mean serum urate decrease from baseline in patients with gout was 17.7% (placebo), 56.4% (1 mg QD), 58.1% (2 mg QD), 69.4% (4 mg QD), 77.0% (6 mg QD), and 79.2% (12 mg QD), respectively. The maximum mean serum urate decrease from baseline in serum urate in patients with hyperuricemia was 19.9% (placebo), 50.1% (1 mg QD), 64.1% (2 mg QD), 73.2% (4 mg QD), 81.2% (6 mg QD), and 82.1% (12 mg QD), respectively.

conclusionsABP-671 had an acceptable safety profile in Chinese healthy participants and patients with hyperuricemia and gout. ABP-671 reduced serum urate levels in a dose-dependent manner.

trial registrationhttps://chinadrugtrials.org.cn (No. CTR20211668) .

Indexed as

GoutGout SuppressantsHyperuricemiaAdultDose-Response Relationship, DrugDouble-Blind MethodFemaleHealthy VolunteersHumansMaleMiddle AgedOrganic Anion TransportersOrganic Cation Transport ProteinsProof of Concept StudyUric AcidYoung AdultGout SuppressantsOrganic Anion TransportersOrganic Cation Transport ProteinsSLC22A12 protein, humanUric AcidABP-671GoutPharmacodynamicsPharmacokineticsSafetyURAT1 inhibitor

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.