Evidence map›Paper›PMID 35020038›Full record

Trial reportArchives of osteoporosis2022

Efficacy of Yigu® versus Aclasta® in Chinese postmenopausal women with osteoporosis: a multicenter prospective study.

Mei Li, Qun Cheng, Ya-Nan Huo, Ai-Jun Chao, Liang He, Qing-Yun Xue, Jin Xu, Shi-Gui Yan, Hui Jin, Zhen-Lin Zhang and 5 more

Open access · hybridAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Archives of osteoporosis, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 40% of its field
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

2 citing papers in PubMed, 1 synthesis or guideline pooled it, 3 citations in OpenAlex.

  1. Pooled it
  2. Article
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

15 authors at 14 institutions in 1 country.

Mei LiDepartment of Endocrinology, Peking Union Medical College Hospital, Beijing, China.
Qun ChengDepartment of Osteoporosis and Bone Disease, Huadong Hospital Affiliated To Fudan University, Shanghai, China.
Ya-Nan HuoDepartment of Endocrinology, Jiangxi People's Hospital, Jiangxi, China.
Ai-Jun ChaoDepartment of Cadre Ward, Tianjin Hospital, Tianjin, China.
Liang HeOrthopedics Department, Beijing Jishuitan Hospital, Beijing, China.
Qing-Yun XueDepartment of Orthopedics, Beijing Hospital, Beijing, China.
Jin XuDepartment of Endocrinology, Shandong Provincial Hospital, Jinan, China.
Shi-Gui YanDepartment of Orthopaedic Surgery, The Second Affiliated Hospital, School of Medicine, Zhejiang University, Zhejiang, China.
Hui JinDepartment of Endocrinology, The Affiliated Zhongda Hospital of Southeast University, Nanjing, China.
Zhen-Lin ZhangDepartment of Osteoporosis and Bone Diseases, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.
Jian-Hua LinDepartment of Orthopedic Surgery, The First Affiliated Hospital of Fujian Medical University, Fuzhou, China.
Xiao-Lan JinDepartment of Endocrinology, General Hospital of People's Liberation Army Chengdu Military Region, Chengdu, China.
You-Jia XuOrthopaedic Department, The 2nd Affiliated Hospital of Suzhou University, Suzhou, China.
Feng LiuDepartment of Geriatric, The First Municipal People's Hospital of Guangzhou, Guangzhou, China.
Wei-Bo XiaDepartment of Endocrinology, Peking Union Medical College Hospital, Beijing, China. xiaweibo8301@163.com.
Peking Union Medical College Hospital · CNBeijing Hospital · CNBeijing Jishuitan Hospital · CNChengdu Military General Hospital · CNFirst Affiliated Hospital of Fujian Medical University · CNFudan University · CNGuangzhou Medical University · CNJiangxi Provincial People's Hospital · CNSecond Affiliated Hospital of Zhejiang University · CNShandong Provincial Hospital · CNShanghai Sixth People's Hospital · CNSoochow University · CNTianjin Hospital · CNZhongda Hospital Southeast University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Zoledronic acid (ZOL) is a therapy inhibiting bone resorption. In this study, generic ZOL (Yigu®) showed its clinical efficacy consistency with original ZOL (Aclasta®) in Chinese postmenopausal women with osteoporosis. This study provides a practical basis for the application of Yigu® in Chinese population.

introductionYigu® has been approved its bioequivalence to Aclasta®. However, the clinical efficacy and safety of Yigu® have not been evaluated yet. Here, we compared the effectiveness and safety between Yigu® and Aclasta® in Chinese postmenopausal women with osteoporosis and assessed the efficacy of intravenous infusion of ZOL.

methodsThis was a randomized open-label, active-controlled study in postmenopausal women with osteoporosis of 14 clinical centers in China. Postmenopausal women with osteoporosis were recruited and randomized to receive a single infusion of 5 mg Yigu® or Aclasta®. The primary endpoint was the percentage change in bone mineral density (BMD) at lumbar spine after 12 months of treatment and was assessed for equivalence. The secondary endpoint was the percentage change in BMD at proximal femur after 12 months. Additional secondary endpoints were percentage changes in BMD at the above sites after 6 months of treatment and changes in bone turnover biomarkers during ZOL treatment. Safety was also evaluated and compared between two groups.

resultsA total of 458 postmenopausal women with osteoporosis were enrolled (n = 227, Yigu®; n = 231, Aclasta®). The mean percentage change in the BMD had no statistical difference at the lumbar spine (5.32% vs 5.18%), total hip (2.72% vs 2.83%), and femoral neck (2.37% vs 2.81%) between Yigu® and Aclasta® groups after 12 months of treatment. The mean difference of BMD change at the lumbar spine after 12 months between two groups was 0.15% (95% CI: - 0.71 to 1.00, equivalence margin: - 1.5%, 1.5%), demonstrating the treatments were equivalent. Meanwhile, the decreases in the P1NP and β-CTX showed no difference between two groups after 14 days and 6 and 12 months of treatment. As regards the whole sample, BMD significantly increased after 12 months of treatment. Also, serum C-terminal telopeptide of type 1 collagen (β-CTX) and procollagen 1 N-terminal peptide (P1NP) significantly decreased at each visit period. The overall adverse events were comparable and quite well between two groups.

conclusionIntravenous infusion of zoledronic acid achieved the potent anti-resorptive effects which led to significant increase in BMD of Chinese postmenopausal women with osteoporosis. Yigu® was equivalent to Aclasta® with respect to efficacy and safety.

Indexed as

Bone Density Conservation AgentsOsteoporosisOsteoporosis, PostmenopausalBone DensityDiphosphonatesDouble-Blind MethodFemaleHumansPostmenopauseProspective StudiesBone Density Conservation AgentsDiphosphonatesBMDP1NPPostmenopausal osteoporosisZoledronic acidβ-CTX

Identifiers

PMID35020038
PMCPMC8755672
OpenAlexW4205175894

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.