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AZ

azithromycin (Azimac)

✓ Approved

Beijing Holley-Cotec Pharma · 小分子 · 小分子

什么是 azithromycin?

azithromycin 是一种小分子,由Beijing Holley-Cotec Pharma研发。该药已获批,用于治疗相关适应症,给药途径:Oral (PO)。

药物档案

商品名Azimac
公司Beijing Holley-Cotec Pharma
药物类别小分子
给药途径Oral (PO)
状态Approved

治疗适应症

azithromycin 针对 8 个适应症,涉及 3 个治疗领域。

治疗领域疾病/病症分期
Infections and infestationsLower respiratory tract infection✓ Approved
Infections and infestationsOtitis media✓ Approved
Infections and infestationsSinusitis✓ Approved
Infections and infestationsTonsillitis✓ Approved
Infections and infestationsUrinary tract infection✓ Approved

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相关研究文献

PubMedThe Journal of antimicrobial chemotherapy2026-08-04

Antimicrobial resistance in Neisseria gonorrhoeae isolates at the Bangrak STIs Center, Bangkok, Thailand and WGS of antimicrobial-resistant isolates, 2018-23.

Paopang Porntip P, Sangprasert Pongsathorn P, Golparian Daniel D, Girdthep Natnaree N et al.

Antimicrobial resistance (AMR) in Neisseria gonorrhoeae is a global public health concern, particularly due to increasing resistance to the last remaining monotherapy, ceftriaxone, in several Asian countries. We examined the AMR of gonococcal isolates obtained at the Bangrak STIs Center, Bangkok, Thailand in 2018-23, and used WGS on isolates resistant to ceftriaxone, cefixime and/or azithromycin. Genital and extragenital swabs from males, females and transgender women were cultured. Etest (five antimicrobials) and EUCAST breakpoints (v16.0), or disc diffusion method (ciprofloxacin) were used to determine AMR. WGS was performed using Illumina NextSeq 550. In 2018-23, 765 gonococcal isolates from 739 patients were cultured. Resistance to ceftriaxone, cefixime, azithromycin, tetracycline and ciprofloxacin was 0.5%, 0.8%, 1.7%, 83.7% and 95.7%, respectively. Ceftriaxone-resistant isolates, all resistant also to cefixime, were first detected in 2023 (n = 3, 1.2%). Additional cefixime-resistant isolates were found in 2022 (n = 2, 1.4%). Azithromycin-resistant isolates first emerged in 2020 (n = 1, 0.9%) and increased to nine (3.7%) isolates in 2023. All ceftriaxone-resistant isolates contained penA-60.001, but cefixime resistance was additionally caused by penA-34.019 and penA-10.001. All azithromycin-resistant isolates had 23S rRNA mutations and/or mosaic/semi-mosaic MtrD (subunit of the MtrCDE efflux pump). Resistance to ceftriaxone, cefixime and azithromycin has emerged in gonococcal strains circulating in Bangkok, Thailand, and resistance appears to be increasing. Resistance to these last options for monotherapy or dual therapy emphasize the need for strengthened national culture-based and genomic surveillance to prevent the spread of MDR and XDR strains in Thailand and globally, and implementation of the novel oral treatments, i.e. zoliflodacin and gepotidacin.

PMID 42550164
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PubMedFrontiers in pediatrics2026-08-04

Case Report: Intestinal mycobacterium abscessus infection in a child.

Zhang Linlin L, Huang Dixi D, Song Jie J, Zhao Tianming T et al.

The diagnosis and treatment of Mycobacterium abscessus infections present significant challenges, especially in the rare cases of extrapulmonary involvement in pediatric patients. These cases are characterized by diagnostic difficulties, limited therapeutic options, scarce clinical experience, and a lack of evidence-based treatment guidelines. This article reports on a 6-year-old child who experienced fever and abdominal pain. Metagenomic next-generation sequencing (mNGS) facilitated the rapid and accurate identification of Mycobacterium abscessus as the causative pathogen. Under a standardized full-course protocol, an individualized therapy regimen (that includes Imipenem, Azithromycin, and Linezolid) led to favorable clinical outcomes. Through the analysis of this successfully treated case, we aim to derive clinical insights and identify potential limitations, with the goal of exploring effective diagnostic and therapeutic approaches for pediatric patients with non-tuberculous mycobacterial (NTM) infections in the future.

PMID 42548723
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PubMedChronic obstructive pulmonary diseases (Miami, Fla.)2026-08-03

Erratum.

This corrects the article "Rationale and Design of the Roflumilast or Azithromycin to Prevent COPD Exacerbations Clinical Trial" in Volume 13, Issue 1, pp 17-28.

PMID 42545984
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PubMedAntimicrobial agents and chemotherapy2026-08-03

In vitro activity of zoliflodacin against Neisseria gonorrhoeae collected in the United States from 2020 to 2022.

McLeod Sarah M SM, Moussa Samir H SH, Hackel Meredith M, Au Carmen C et al.

Zoliflodacin is a first-in-class spiropyrimidinetrione, oral, single-dose antibacterial recently approved by the US FDA for treatment of uncomplicated urogenital gonorrhea. Isolates of Neisseria gonorrhoeae (n = 322) collected in the United States in 2020-2022 by the Centers for Disease Control and Prevention, as well as two ceftriaxone-resistant isolates, were tested for susceptibility to zoliflodacin. All isolates were susceptible to zoliflodacin with MIC50/90 values of 0.12 µg/mL. Zoliflodacin activity was consistent over time and against ceftriaxone-, ciprofloxacin-, and tetracycline-resistant and azithromycin-non-susceptible isolates.

PMID 42545106
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PubMedClinical and experimental dermatology2026-08-02

Pulsed Azithromycin for the Treatment of Dacomitinib Induced Skin Toxicity in Patient with Tetracycline Intolerance - A Case Report.

Ho Wei W, Chen Yi-Ming YM, Lin Mong-Wei MW, Liao Yu-Qing YQ et al.

Skin toxicities like paronychia and acneiform rash are common side effects of epidermal growth factor receptor tyrosine kinase inhibitors (EGFR TKI) and significantly impact patients' quality of life. Tetracycline antibiotics are the recommended first-line treatment but can cause side effects, leading to intolerance and untreated toxicities, highlighting needs for alternative therapies. We present a case of stage IV EGFR-mutated non-small cell lung cancer (NSCLC) treated with the second-generation EGFR TKI, dacomitinib. The patient developed grade 3 skin toxicities and was subsequently treated with azithromycin after demonstrating intolerance to tetracycline antibiotics. Azithromycin was administered using various dosing strategies, and we found 500 mg every other day might be the most effective regimen for treating EGFR-TKI-induced acneiform rash. However, this approach appeared to be less effective in managing paronychia.

PMID 42541756
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PubMedMedicine2026-07-31

Efficacy of azithromycin sequential therapy combined with montelukast in the treatment of pediatric mycoplasma pneumonia: A meta-analysis.

Wu Mingming M, Chen Kan K, Yu Haihong H

Mycoplasma pneumoniae pneumonia (MPP) stands as a predominant cause of community-acquired respiratory infections in children. With the increasing prevalence of macrolide-resistant Mycoplasma pneumoniae strains, the therapeutic efficacy of azithromycin monotherapy has become a growing concern in clinical practice. Montelukast sodium, a selective leukotriene receptor antagonist, has emerged as a promising adjunctive agent, as it can effectively alleviate airway inflammation and reduce airway hyperresponsiveness. This meta-analysis was designed to systematically evaluate the efficacy and safety of azithromycin sequential therapy combined with montelukast in the management of pediatric MPP. A comprehensive literature search was conducted across PubMed, Embase, Web of Science Core Collection, Wanfang Data, Variant Impact Predictor database, and Chinese National Knowledge Infrastructure from the establishment of each database up to November 2025. Eligible studies were randomized controlled trials (RCTs) that compared azithromycin sequential monotherapy with azithromycin sequential therapy plus montelukast in pediatric patients diagnosed with MPP. Primary outcome measures included overall clinical efficacy, resolution time of key clinical symptoms (cough, wheezing, pulmonary rales, and fever), and the incidence of adverse events. Thirty-six RCTs involving 3450 pediatric patients (1726 in the combination group and 1724 in the azithromycin group) met the inclusion criteria. Compared with azithromycin sequential therapy, combination therapy significantly improved overall clinical efficacy (odds ratio = 4.75, 95% confidence interval [CI]: 3.70-6.10). The addition of montelukast also shortened the resolution time of cough (mean difference [MD] = -3.63, 95% CI: -4.27 to -2.99), wheezing (MD = -1.48, 95% CI: -1.82 to -1.14), pulmonary rales (MD = -2.06, 95% CI: -2.54 to -1.57), and fever (MD = -1.43, 95% CI: -1.89 to -0.96). No significant difference in adverse event rates was observed between groups. Azithromycin sequential therapy combined with montelukast may provide additional therapeutic benefits for the treatment of pediatric MPP, characterized by higher overall clinical efficacy and more rapid resolution of clinical symptoms, without a statistically significant increase in short-term adverse events. Despite the encouraging findings, the included studies were predominantly single-center trials with moderate methodological quality. Therefore, well-designed, large-scale, multicenter RCTs are urgently needed to validate these results and provide more reliable evidence for guiding clinical decision-making.

PMID 42536509
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