Evidence map›Paper›PMID 40759594›Full record

ArticleThe world journal of men's health2026

Efficacy and Safety of Mirabegron and Tamsulosin Combination Therapy Compared to Tamsulosin Monotherapy for Lower Urinary Tract Symptoms Due to Benign Prostatic Hyperplasia: Results of a Multicenter, Randomized, Double-Blind, Phase III Clinical Trial.

Sung Chul Kam, Yu Seob Shin, Doo Sang Kim, Won Ki Lee, Deok Hyun Han, Phil Hyun Song, Sung Hoo Hong, Young Seop Chang, Tae Hwan Kim, Sung Tae Cho and 9 more

Abstract read
In one paragraph

Article in The world journal of men's health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

19 authors.

Sung Chul Kam *Department of Urology, Gyeongsang National University College of Medicine and lnstitute of Health Sciences of Gyeongsang National University, Jinju, Korea.ORCID https://orcid.org/0000-0001-5403-3623
Yu Seob Shin *Department of Urology, Jeonbuk National University Medical School, Research Institute of Clinical Medicine of Jeonbuk National University-Biomedical Research Institute of Jeonbuk National University Hospital, Jeonju, Korea.ORCID https://orcid.org/0000-0002-1126-3821
Doo Sang KimDepartment of Urology, Soonchunhyang University Cheonan Hospital, Soonchunhyang University School of Medical, Cheonan, Korea.ORCID https://orcid.org/0000-0001-6405-1294
Won Ki LeeDepartment of Urology, Hallym University Chuncheon Sacred Heart Hospital, Hallym University School of Medical, Chuncheon, Korea.ORCID https://orcid.org/0000-0001-7172-0636
Deok Hyun HanDepartment of Urology, Sungkyunkwan University School of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-9962-802X
Phil Hyun SongDepartment of Urology, Yeungnam University College of Medicine, Daegu, Korea.ORCID https://orcid.org/0000-0002-3801-258X
Sung Hoo HongDepartment of Urology, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID https://orcid.org/0000-0002-1952-4010
Young Seop ChangDepartment of Urology, Baekje General Hospital, Daejeon, Korea.ORCID https://orcid.org/0009-0002-8254-1435
Tae Hwan KimDepartment of Urology, Kyungpook National University School of Medicine, Daegu, Korea.ORCID https://orcid.org/0000-0003-4924-4826
Sung Tae ChoDepartment of Urology, Hallym University Kangnam Sacred Heart Hospital, Seoul, Korea.ORCID https://orcid.org/0000-0002-4691-6159
Sung Yul ParkDepartment of Urology, Hanyang University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-9777-9238
Jae Hyun BaeDepartment of Urology, Korea University Ansan Hospital, Ansan, Korea.ORCID https://orcid.org/0000-0001-9862-3545
Kyung Jin ChungDepartment of Urology, Gachon University Gil Medical Center, Incheon, Korea.ORCID https://orcid.org/0000-0003-0153-7814
Joon Hwa NohDepartment of Urology, Kwangju Christian Hospital, Kwangju, Korea.ORCID https://orcid.org/0009-0007-6796-9421
Kang Su ChoDepartment of Urology, Prostate Cancer Center, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-3500-8833
Tae Nam KimDepartment of Urology, Pusan National University Hospital, Pusan National University School of Medicine, Biomedical Research Institute, Busan, Korea.ORCID https://orcid.org/0000-0002-0379-2790
Zhao LuoDepartment of Urology, Shenzhen Qianhai Taikang Hospital, Shenzhen, China.ORCID https://orcid.org/0009-0005-7807-6296
Won Sik HamDepartment of Urology and Urological Science Institute, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0003-2246-8838
Tae Hyo KimDepartment of Urology, Dong-A University Hospital, Dong-A University School of Medical, Busan, Korea. dockim0927@hanmail.net.ORCID https://orcid.org/0000-0002-5994-7878

Funding

Kyung Dong Pharmaceutical, Co, Ltd
6 · The paper itself

Abstract

purposeThis study aimed to evaluate the efficacy and safety of mirabegron and tamsulosin combination therapy compared to tamsulosin monotherapy in benign prostatic hyperplasia (BPH) patients with lower urinary tract symptoms (LUTS). MATERIALS AND

methodsThis phase 3, randomized, double-blind, placebo-controlled clinical trial evaluated the efficacy and safety of mirabegron/tamsulosin combination therapy versus tamsulosin monotherapy in men with LUTS. The trial, conducted across 25 centers from July 2021 to October 2023. Eligible participants were randomly assigned to either the combination or monotherapy group for 12 weeks. Primary efficacy endpoints included changes in total urinary frequency score (TUFS) and International Prostate Symptom Scores (IPSS), with secondary endpoints evaluating various urinary symptoms and changes in post void residual volume (PVR), maximum urinary flow rate (Qmax), and quality of life scores. Safety assessments included adverse events, PVR, Qmax, vital signs, electrocardiogram, and laboratory tests.

resultsA total of 795 participants were randomized to monotherapy (n=397) and combination therapy (n=398) groups. After 12 weeks, 342 in the monotherapy and 339 in the combination therapy group completed the study, with no significant baseline differences. The combination therapy group showed a greater improvement in TUFS (-11.28) and IPSS (-10.85) scores compared to monotherapy (-8.30 and -9.85, respectively) with significant differences (p<0.0001, p=0.0325). Combination therapy showed significant improvements in storage symptoms and voiding diary variables, including daytime frequency, urgency, and incontinence, compared to monotherapy. The incidence of treatment-emergent adverse events was similar between the groups (13.10%

conclusionsCombination therapy with mirabegron and tamsulosin is more effective than monotherapy in improving LUTS in patients with BPH, particularly storage symptoms, with a comparable safety profile. A fixed-dose combination formulation in the future may further improve patient adherence and quality of life.

Indexed as

Lower urinary tract symptomsMirabegronProstatic hyperplasiaTamsulosinUrinary bladder, overactive

Identifiers

PMID40759594
PMCPMC13036245

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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.