Evidence map›Paper›PMID 40135354›Full record

Trial reportActa dermato-venereologica2025

Safety, Pharmacokinetics, and Efficiency of JS005, a Novel Anti-interleukin-17A Monoclonal Antibody, in Healthy Chinese Adults and Patients with Moderate to Severe Psoriasis.

Lin Cai, Huichen Liu, Zhanglei Mu, Xiaohua Tao, Litao Zhang, Chunlei Zhang, Yumei Li, Guoqiang Zhang, Furen Zhang, Xiuqin Dong and 8 more

Abstract readMulticenter StudyRandomized Controlled TrialClinical Trial, Phase I
In one paragraph

Trial report in Acta dermato-venereologica, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors.

Lin Cai *Peking University People's Hospital, Beijing, China.
Huichen Liu *Phase I Clinical Trial Ward, Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Zhanglei MuPeking University People's Hospital, Beijing, China.
Xiaohua TaoZhejiang Provincial People's Hospital, Hangzhou, China.
Litao ZhangTianjin Academy of Traditional Chinese Medicine Affiliated Hospital, Tianjin, China.
Chunlei ZhangPeking University Third Hospital, Beijing, China.
Yumei LiAffiliated Hospital of Jiangsu University, Zhenjiang, China.
Guoqiang ZhangThe First Hospital of Hebei Medical University, Shijiazhuang, China.
Furen Zhang
Xiuqin DongGuangdong Provincial People's Hospital, Guangzhou, China.
Chengxin LiChinese PLA General Hospital, Beijing, China.
Aijun ChenThe First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Zhuning WuShanghai Junshi Biosciences, Shanghai, China.
Yuxian ZhuShanghai Junshi Biosciences, Shanghai, China.
Mengqi ZhangShanghai Junshi Biosciences, Shanghai, China.
Jiangnian Liu
Aiming LiDepartment of Clinical Pharmacology, Beijing Luhe Hospital, Capital Medical University, Beijing, China. liaimin53@163.com.
Jianzhong ZhangPeking University People's Hospital, Beijing, China. rmzjz@126.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

JS005 is a novel anti-IL-17A monoclonal antibody. A Phase Ia study (Study 1) in healthy adults, followed by a Phase Ib/II study (Study 2) in patients with moderate to severe plaque psoriasis (PsO), were designed to evaluate the safety, efficacy, and pharmacokinetic characteristics of JS005. Study 1 was a double-blind, randomized, placebo-controlled, single dose-escalation (15, 60, 150, 300, and 600 mg) study. Forty healthy participants were enrolled. Study 2 consisted of a dose-escalation (60, 150, 300, or 600 mg) phase Ib, and a multicentre, double-blind, placebo-controlled phase II administering JS005 150, 300 mg, or placebo once weekly from week 0 to 4 and once every 4 weeks from week 5 to 12. Forty and 143 patients were enrolled in phases Ib and II, respectively. The exposure of JS005 increased linearly with dosage, while the treatment-emergent adverse events did not show this trend. JS005 was well tolerated in both populations. In phase II of Study 2, the proportion of patients with at least a 75% improvement in the Psoriasis Area and Severity Index at week 12 was significantly higher in each JS005 group than in the placebo group (p < 0.001 for all comparisons). JS005 was highly effective in PsO patients.

Indexed as

Antibodies, MonoclonalAntibodies, Monoclonal, HumanizedDermatologic AgentsInterleukin-17PsoriasisAdolescentAdultChinaDose-Response Relationship, DrugDouble-Blind MethodEast Asian PeopleFemaleHealthy VolunteersHumansMaleMiddle AgedAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedDermatologic AgentsIL17A protein, humanInterleukin-17

Identifiers

PMID40135354
PMCPMC11977408

What OpenQuestion holds

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Registered trials

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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.