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Last update 16 May 2025

Mupirocin

Last update 16 May 2025

Overview

R&D Status

Clinical Result

Translational Medicine

Overview

Basic Info

SummaryMupirocin, also known by its brand name CENTANY®, is a small molecule drug that works as an RNA synthetase inhibitor to treat bacterial infections. It is commonly used to treat impetigo and other skin infections caused by Gram-positive bacteria. Originally developed by GSK, Mupirocin was first approved for use in 1987. CENTANY® ointment is a topical medication used to treat impetigo by inhibiting bacterial growth and stopping the spread of infection.

Drug Type

Small molecule drug

Synonyms

Bactroban Nasal, Mupirocin (USP/INN), Mupirocin cream

+ [6]

Target

Bacterial IRS

Action

inhibitors

Mechanism

Bacterial IRS inhibitors(Bacterial isoleucyl-tRNA synthetase inhibitors)

Therapeutic Areas

Infectious DiseasesSkin and Musculoskeletal Diseases

Active Indication

ImpetigoSecondary infectionGram-Positive Bacterial Infections

Inactive Indication-

Originator Organization

GSK Plc

Active Organization

GlaxoSmithKline Australia Pty Ltd.

Nanjing Indetek Pharmaceutical Technology Co., Ltd.

Sino-American Tianjin SmithKline & French Lab., Ltd.

+ [2]

Inactive Organization

GSK Plc

License Organization-

Drug Highest PhaseApproved

First Approval Date

United States (31 Dec 1987),

Impetigo

Regulation-

Structure/Sequence

Molecular FormulaC26H44O9

InChIKeyMINDHVHHQZYEEK-HBBNESRFSA-N

CAS Registry12650-69-0

Clinical Trials associated with Mupirocin

NCT06712433

/ Not yet recruitingPhase 2IIT

Bacterial Decolonization Plus Intraoperative Indocyanine Green Angiography for Soft Tissue Sarcomas of the Lower Extremity Receiving Preoperative Radiotherapy (CONCERTO)

This trial will investigate the combination of two low-cost, non-toxic strategies to assess whether they can reduce the risk of acute major wound complications in soft tissue sarcoma of the lower extremity. Intranasal mupirocin ointment twice daily and chlorhexidine body cleanser once daily for 5 days prior to radiation therapy and repeated for 5 days every 2 weeks during radiation therapy may significantly reduce the risk of acute radiation dermatitis. That, along with use of indocyanine green (ICG) angiography at the time of wound closure.

Start Date31 Oct 2025

Sponsor / Collaborator

University of Pittsburgh

NCT06541145

/ RecruitingNot ApplicableIIT

Impact of Bacterial Decolonization on Bacterial Burden Within Maternal-infant Dyads

The goal of this study is to measure bacterial burden, specifically Staph aureus, and how it spreads between mothers and their infants. Researchers will evaluate if the amount of bacteria on their skin remains the same after mothers use a skin antisepsis treatment prior to delivering their infants. The investigators also aim to assess participant interest in and compliance with skin antisepsis treatments. The hypothesis is that increased maternal interest will align with increased treatment compliance.

Start Date21 Aug 2024

Sponsor / Collaborator

Duke University

[+1]

ChiCTR2400085012

/ RecruitingEarly Phase 1IIT

Clinical effects of photodynamic therapy with Ondapench photosensitive antibacterial powder as photosensitiser compared with mupirocin ointment in the treatment of bacterial skin infections

Start Date01 Jun 2024

Sponsor / Collaborator

Xiangya Hospital Central South University

100 Clinical Results associated with Mupirocin

100 Translational Medicine associated with Mupirocin

100 Patents (Medical) associated with Mupirocin

3,526

Literatures (Medical) associated with Mupirocin

01 Jun 2025·JOURNAL OF HAZARDOUS MATERIALS

Removal of antibiotic resistance from wastewater in aquatic ecosystems dominated by submerged macrophytes

Article

Author: Huang, Xian-Hui ; Li, Ling-Lin ; Li, Xin-Ting ; Zhang, Rong-Min ; Li, Ya-Fei ; Tan, Hui-Zhen ; Chen, Xiao-Jie ; Huang, Wen-Qing ; Xie, Jie ; Chong, Yun-Xiao ; Lian, Xin-Lei

Submerged macrophytes in constructed wetlands (CWs) can effectively improve wastewater quality. However, the effectiveness of different submerged macrophytes in removing antibiotic-resistant genes (ARGs) from wastewater remains unexplored. Additionally, wastewater loading in wetlands can fluctuate due to climate change, potentially affecting ARG removal efficiency. In this study, we systematically constructed microscale wetlands using three submerged plants: Vallisneria natans (VN), Sagittaria pygmaea (SP), and Myriophyllum spicatum (MS). Their effectiveness in ARGs removal was analyzed at hydraulic retention times (HRTs) of 0, 3, 6, and 9 days under high (HWL) and low (LWL) wastewater loading. The results indicated that under LWL conditions, all ecosystems exhibited a higher reduction rate of ARG diversity and relative abundance (RS) compared to HWL conditions. The efficiency of all ecosystems in reducing ARG diversity and abundance followed the order: MS > VN > SP. The sul resistance gene exhibited the highest RS and was degraded most rapidly in all samples. Additionally, sulfadimidine concentrations significantly decreased under LWL conditions, which was significantly correlated with sul reduction. Chemical oxygen demand, total phosphorus, total nitrogen, ammonium nitrogen, and nitrate nitrogen were identified as key factors influencing bacterial and ARG profiles. The increase in rhizobial bacteria and decrease in aerobic denitrifying bacteria likely contributed significantly to ARGs removal. This study offers new insights into ARG removal by submerged macrophytes in CWs, emphasizing the role of wastewater loading and the potential of MS in enhancing ARG degradation. These findings enhance CW design and management to mitigate ARG contamination in wastewater.

01 Jun 2025·JOURNAL OF HAZARDOUS MATERIALS

Metagenomic insights into the inhibitory effect of phytochemical supplementation on antibiotic resistance genes and virulence factors in the rumen of transition dairy cows

Article

Author: Zhao, Huiying ; Zhang, Ao ; Jiang, Linshu ; Wang, Ying ; Tan, Jian ; Zhao, Yuchao ; Li, Liuxue

Antimicrobial resistance (AMR) is a major global health concern, with the rumen microbiota of dairy cows serving as an important reservoir for antibiotic resistance genes (ARGs) and virulence factors (VFs). This study explores the impact of dietary phytochemical supplementation on the rumen resistome and virulome of transition dairy cows using metagenomic sequencing. Naringin supplementation reduced the abundance of ARGs by up to 9.0 % and VFs by up to 7.2 % during the transition period, as indicated by metagenomic analysis (P < 0.05). Clinically high-risk ARGs, including those conferring resistance to beta-lactams (mecA), tetracyclines (tetM, tetO), and aminoglycosides (rmtF), were notably downregulated (P < 0.05). Virulence factors associated with adherence, secretion systems, and toxins were also significantly decreased (P < 0.05). Naringin altered the microbial community structure, particularly reducing the abundance of Proteobacteria, a key phylum harboring ARGs and VFs. Despite inducing increased ARG-VF network complexity, naringin supplementation promoted a less pathogenic microbiome with reduced resistance potential. These findings demonstrate the potential of naringin as a natural dietary strategy to mitigate AMR by reducing the risk of ARG and VF dissemination into the environment, while supporting rumen microbiota stability in transition dairy cows.

01 May 2025·JOURNAL OF HAZARDOUS MATERIALS

Presence of high-risk ARGs with greater diversity and abundance in the rare resistome in wastewater across China

Article

Author: Zhou, Bo ; Zhang, Yu ; Wang, Yue ; Qin, Jun ; Chen, Chaoqi ; Li, Xiqing ; Huang, Jianwen

Antibiotic resistance genes (ARGs) are widely recognized as hazardous materials that pose risks to public health. The core resistome, with its low ARG diversity yet accounting for the majority of the total ARG abundance, dominating the profile of antibiotic resistance. In this study, nationwide wastewater surveillance in China using metagenomic sequencing also identified a core resistome of 117 ARGs that accounted for 69.6 % of the total abundance. The emphasis of the work was to examine the rare resistome that included 1503 ARGs outside the core resistome. The abundances of clinically relevant ARG types (e.g., β-lactams and quinolones) were significantly higher in the rare resistome compared to the core resistome. Human pathogen-related ARGs were much greater in subtype number (96 vs. 34) and significantly higher in abundance (67.0 % vs. 33.0 %) in the rare relative to the core resistome, indicating that the rare resistome was the major contributor to the human pathogen resistome. The majority of ARG types accounting for the highest proportions of the rare resistome were plasmid-originated (65.5 %-100 %). In addition, human pathogen-related ARGs also had a significantly higher proportion of plasmid sources than non-pathogen ARGs, further highlighting their importance in wastewater-based surveillance.

News (Medical) associated with Mupirocin

13 May 2025

·www.prnewswire.com

iNtRON Seeks a Strategic Partner to Explore the Promising Market for MRSA Decolonization

Aiming to Provide a Novel Solution Against Post-Operative MRSA Infections Demonstrated its Efficacy and Safety through previous Clinical Trials Company seeks global partners to co-develop toward Commercialization SEOUL, South Korea and BOSTON, May 13, 2025 /PRNewswire/ -- iNtRON Biotechnology, Inc., a biotechnology company focused on developing innovative endolysin-based new biological drug for superbugs and unmet medical needs, today announced the strategic initiative aimed at expanding the clinical applications of SAL200 and seeking a strategic partnership to target the prevention of surgical site infections (SSIs) by nasal MRSA decolonization. Methicillin-resistant Staphylococcus aureus (MRSA) remains one of the most dangerous superbugs worldwide, with rising infection rates in both hospital and community settings. Even in sterile operating environments, MRSA-related SSIs frequently originate from the patient's own nasal or skin, potentially leading to extended hospital stays, increased treatment costs, and in severe cases, serious systemic infections such as sepsis, osteomyelitis, or endocarditis. High-risk surgical patients including those undergoing implant or cardiac surgeries, or those with compromised immune systems face significantly elevated risks of MRSA infections. Although mupirocin-based nasal ointments have been used as a standard of care product for the prevention of SSI, resistance rates are continuously increasing, leaving clinicians with few effective solution. As an intravenous injection drug for infective endocarditis and bacteremia, SAL200 has already demonstrated a strong safety profile through Phase 1a/1b and Phase 2a clinical trials. Encouraged by recent feedback from key clinical experts, iNtRON is now pursuing an additional indication for SAL200 as a pre-operative MRSA nasal decolonization solution. According to recent industry reports, the global nasal decolonization market which is closely related to SSI prevention was valued at USD 1.6 billion in 2024 and is projected to grow at a CAGR of 7.5%, driven by heightened hospital infection control regulations and growing concern over antimicrobial resistance. With the strategic expansion of the clinical application of SAL200 for the promising market opportunity, iNtRON is seeking global partners to co-develop a new formulation, delivery route, and product type as a nasal or topical use, and to collaborate on preclinical and clinical studies aimed at commercialization. "As SAL200 has demonstrated its strong efficacy and safety as an I.V. injection formulation in the previous clinical studies, we believe it can be developed into a nasal or topical use formulation through a much simplified clinical trial process" said YOON Kyung Won, CEO. "We believe SAL200 can fill a critical gap in MRSA nasal decolonization, an area in urgent need of a new solution. We aim to begin clinical development for this new indication in 2025 and are confident that our novel solution will significantly advance efforts to prevent MRSA-related SSIs. We are open to all types of partnerships including co-development and licensing, and welcome discussion with those who share our vision." About iNtRON Biotechnology, Inc. iNtRON Biotechnology () is a clinical-stage biopharmaceutical company at the forefront of bacteriophage-derived technology and immune therapeutics. The company specializes in developing first-in-class and first-in-concept bio-drugs to combat infectious diseases and immune-related disorders. Since its foundation and subsequent IPO on KOSDAQ, iNtRON has focused on global R&BD collaborations and is committed to delivering innovative therapies that address urgent medical needs in infectious disease and immunotherapy. Contact Us YOON, Kyung Won (Kevin) / CEO, Vice President / [email protected] SHIN, Tae Kyu (TK) / BD Team Leader / [email protected] it is iNtRON. SOURCE iNtRON Biotechnology, Inc. WANT YOUR COMPANY'S NEWS FEATURED ON PRNEWSWIRE.COM? 440k+ Newsrooms & Influencers 9k+ Digital Media Outlets 270k+ Journalists Opted In GET STARTED

Phase 2

26 Sep 2024

·www.haleon.com

Haleon to increase stake in China JV to 88%

Haleon plc (“Haleon”) (LSE/NYSE: HLN) today announces that it has entered into an agreement to acquire an additional 33% equity interest in Tianjin TSKF Pharmaceutical Co. Ltd (“TSKF”), its joint venture in China from its partners, Tianjin Pharmaceutical Group (“TPG”) and Tianjin Pharmaceutical Da Ren Tang Group Corporation Limited (“DRTG”) for a total consideration of RMB 4,465 million (c. £0.5 billion). TSKF accounted for c. 40% of Haleon’s China revenues in FY 2023 and manufactures and/or distributes leading brands such as Fenbid, Voltaren and Bactroban. This acquisition will increase Haleon’s participation in TSKF from 55% to 88% and deliver greater control and increased strategic and operational flexibility across the business. The acquisition is expected to be funded through a combination of Haleon’s existing cash resources and new third-party Renminbi-denominated debt. Subject to customary closing conditions, including the approval of DRTG’s shareholders and applicable regulatory clearances, the transaction is expected to close end of 2024 and to be accretive to EPS. In addition, Haleon and DRTG have agreed, effective from closing of the acquisition, that Haleon would have an option to acquire and DRTG an option to sell the remaining 12% shareholding in TSKF. Brian McNamara, Chief Executive Officer of Haleon commented: "China is a key strategic market for Haleon. Over the last three years, it has delivered strong market share growth and our acquisition of a further 33% in our JV partnership is an important milestone which is both strategically and commercially compelling. It reflects our commitment to this important market, the exceptional growth potential we see in China and is fully consistent with our capital allocation priorities to drive attractive returns for shareholders and maintain a strong investment grade balance sheet.

Acquisition

13 Dec 2023

·www.businesswire.com

Ondine Successfully Raised C$4.91 Million to Support Acceleration of Its Commercial Rollout of Nasal Decolonization to Prevent Healthcare-associated Infections

VANCOUVER, Canada--( BUSINESS WIRE )--Following its successful fundraising of C$4.91 million (US$3.62), Canadian life sciences company Ondine Biomedical Inc. will continue accelerating commercialisation of its proven nasal photodisinfection technology. This cutting-edge technology replaces topical antibiotics for the prevention of healthcare-associated infections (HAIs) and kills all types of pathogens – bacteria, viruses and fungi – without causing antimicrobial resistance. The company has confirmed that it has more than doubled the number of Steriwave ® deployments in 2023 and is in discussions with more than 75 hospitals in the UK, Mexico, Spain, and Canada. The growing global focus on preventing HAIs post-surgery, coupled with the escalating challenge of antimicrobial resistance, has spurred heightened interest in Ondine’s photodisinfection technology. The deployments are in areas of major surgery, including spinal, orthopedic, and cardiovascular. The antibiotic mupirocin has been used for nasal decolonization for the prevention of HAIs since the 1980s. However, mupirocin has resistance rates of up to 81%, 2 and very poor compliance. 3 Carolyn Cross, CEO of Ondine, commented, "We have put great efforts into improving our commercial activity sales process, which has increased the speed of the average sales cycle from contact to deployment by 50%. We have appointed distributors in the UK, Spain, and Mexico and are gaining real momentum. What is particularly encouraging is that many hospitals are recommending Steriwave to other hospitals. We believe this momentum will continue to increase, and commercial sales will become more significant in 2024.” The five-minute Steriwave nasal decolonization procedure is easy to incorporate into the pre surgery procedures. It is painless and very well received by patients who are often intrigued by the process. There have been no reports of serious side effects as a result of Steriwave usage. Steriwave has been used by more than 150,000 patients, including at Vancouver General Hospital where its use has been associated with a significant reduction in HAIs across major surgeries. 4,5 As well as growing its commercial activities, the company continues to work closely with HCA – the largest hospital group in the United States – to prepare for the Phase 3 trial in circa 14 HCA hospitals as part of its Ondine’s submission to the FDA for approval. The company already has approval for Steriwave in Canada, the UK, the EU, and Mexico. Implementing nasal decolonization prior to major surgery to reduce HAIs is recommended by leading medical bodies, including the World Health Organization, 6 the Society for Healthcare Epidemiology of America (SHEA), 7 and NICE. 8 The nose is the major reservoir of pathogens and the majority of surgical site infections (SSIs) and bloodstream infections have been traced back to bacteria in the patient’s nose. 9 A patient with a surgical site infection (SSI) will, on average, spend 7 to 11 days longer in the hospital, significantly increasing costs and lengthening patients' recovery. 10 While currently focusing on nasal decolonization, Ondine’s patented photodisinfection technology will be developed to prevent and treat a wide variety of topical infections. About Ondine Biomedical Inc. Ondine Biomedical Inc. is a Canadian life science company pioneering the field of photodisinfection therapies. Ondine has a pipeline of investigational products, based on its proprietary photodisinfection platform, in various stages of development. Products beyond nasal photodisinfection include therapies for a variety of medical indications such as chronic sinusitis, ventilator-associated pneumonia, burns, and other indications. 1 Stone PW. Economic burden of healthcare-associated infections: an American perspective. Expert Rev Pharmacoecon Outcomes Res. 2009 Oct;9(5):417-22. doi: 10.1586/erp.09.53. PMID: 19817525; PMCID: PMC2827870. 2 Poovelikunnel T, Gethin G, Humphreys H. Mupirocin resistance: clinical implications and potential alternatives for the eradication of MRSA. J Antimicrob Chemother . 2015;70(10):2681-2692. doi:10.1093/jac/dkv169 3 Hansen D, Patzke PI, Werfel U, Benner D, Brauksiepe A, Popp W. Success of MRSA eradication in hospital routine: depends on compliance. Infection. 2007 Jun;35(4):260-4. doi: 10.1007/s15010-007-6273-y. Epub 2007 Jul 23. PMID: 17646910. 4 Bryce E, Wong T, Forrester L, Masri B, Jeske D, Barr K, Errico S, Roscoe D. Nasal photodisinfection and chlorhexidine wipes decrease surgical site infections: a historical control study and propensity analysis. J Hosp Infect. 2014 Oct;88(2):89-95. doi: 10.1016/j.jhin.2014.06.017. Epub 2014 Aug 1. Erratum in: J Hosp Infect. 2015 Sep;91(1):93. PMID: 25171975. 5 Moskven E, Banaszek D, Sayre E, Gara A, Bryce E, Wong T, Ailon T, Charest-Morin R, Dea N., Dvorak M, Fisher C, Kwon B, Paquette S, Street J. Effectiveness of prophylactic intranasal photodynamic disinfection therapy and chlorhexidine gluconate body wipes for surgical site infection prophylaxis in adult spine surgery. Can J Surg. 2023 Nov;66(6), E550–E560. https://doi-org.libproxy1.nus.edu.sg/10.1503/cjs.016922 6 World Health Organization. Global Guidelines for the Prevention of Surgical Site Infection. World Health Organization; 2016. Available at: https://www-who-int.libproxy1.nus.edu.sg/publications/i/item/9789241550475 . Accessed December 12, 2023. 7 Calderwood MS, Anderson DJ, Bratzler DW, et al. Strategies to prevent surgical site infections in acute-care hospitals: 2022 Update. Infect Control Hosp Epidemiol. 2023;44(5):695-720. doi:10.1017/ice.2023.67 8 National Institute for Health and Care Excellence (NICE). NICE Surgical Site Infections: Prevention and Treatment. NICE; 2019. Available at: https://www.nice.org.uk/guidance/ng125 . Accessed December 12, 2023. 9 von Eiff C, Becker K, Machka K, Stammer H, Peters G. Nasal carriage as a source of Staphylococcus aureus bacteremia. Study Group. N Engl J Med. 2001 Jan 4;344(1):11-6. doi: 10.1056/NEJM200101043440102. PMID: 11136954. 10 Seidelman JL, Mantyh CR, Anderson DJ. Surgical Site Infection Prevention: A Review. JAMA. 2023;329(3):244–252. doi:10.1001/jama.2022.24075

Phase 3Drug Approval

100 Deals associated with Mupirocin

External Link

KEGG	Wiki	ATC	Drug Bank
D01076	Mupirocin	R01AX06 D06AX09	DB00410

R&D Status

10 top approved records.

to view more data

Indication	Country/Location	Organization	Date
Secondary infection	Australia	GlaxoSmithKline Australia Pty Ltd.	03 Apr 1998
Gram-Positive Bacterial Infections	China	Sino-American Tianjin SmithKline & French Lab., Ltd.	01 Jan 1993
Impetigo	United States	GSK Plc	31 Dec 1987

Clinical Result

Indication

Phase

Evaluation

View All Results

Study	Phase	Population	Analyzed Enrollment	Group	Results	Evaluation	Publication Date


NCT02127658 (MEDiC, CTgov)	Phase 4	-	14	Hygiene education (Hygiene Education)	kfeysveikm = tnwmaffyfz pmdktakaub (ojhkhxrmdl, plrzuntcle - ylpqvcyjso) View more	-	25 Jun 2024
				Sodium Hypochlorite+Mupirocin ointment (Hygiene Education and Decolonization)	kfeysveikm = hpntvkmcme pmdktakaub (ojhkhxrmdl, iuvdfnwulr - ivynazwczu) View more
NCT03140423 (CTgov)	Phase 4	Sepsis	353,323	Mupirocin (Arm 1: Routine Care (Mupirocin/CHG))	bglqbcknuf = cjbzvklfbn ikyokbqqxe (vvrhkeadbv, kzboppwpys - hwnmroxlai) View more	-	07 Feb 2024
				Arm 2. Iodophor/CHG Decolonization (Arm 2: Iodophor/CHG Decolonization)	bglqbcknuf = pzrelqpvza ikyokbqqxe (vvrhkeadbv, bldycptamy - kcadwlbqlp) View more
NCT03883828 (ASCO2022) Manual	Phase 2/3	Radiodermatitis	76	mupirocin+Chlorhexidine gluconate	lwclrofmyr(ksqhjjzine) = ptxcthujsg ruxrnbiqls (pdbfwmnuex ) View more	Positive	08 Jun 2022
				standard of care	lwclrofmyr(ksqhjjzine) = qbcgynbzcs ruxrnbiqls (pdbfwmnuex ) View more
NCT03673956 (CTgov)	Phase 1/2	Chronic sinusitis	19	Tobramycin (Tobramycin Topical Antibiotic Nasal Saline Rinse)	ayuqgehawp = getkkjwjak qcjpjejwau (trqbhuynfe, xbymkzflkc - etimhbbsan) View more	-	20 Apr 2022
				Levofloxacin (Levofloxacin Topical Antibiotic Nasal Saline Rinse)	ayuqgehawp = lkaqbumtyy qcjpjejwau (trqbhuynfe, zjedktfmjt - ioylcrewvc) View more
NCT04218799 (CTgov)	Phase 4	Cross Infection	19	Chlorhexidine+Mupirocin	whwuojbhtm(qetmcmfqla) = ksmifgrgod oqpzxqsnuu (brlbhkwvgn, 11003) View more	-	24 Apr 2020
NCT02223520 (TREAT PARENTS, CTgov)	Not Applicable	Staphylococcus Aureus Infections \| Staphylococcus aureus bacteraemia \| Staphylococcal Infections	307	Chlorhexidine+Mupirocin (Mupirocin and Chlorhexidine)	vkhuswaibq = inbxqugipa gpsneuuxcp (xxjhfmmkgr, ltwrketcmf - fmxlonnpkb) View more	-	16 Mar 2020
				placebo cloths (Placebo Ointment and Placebo Cloths)	vkhuswaibq = urninfcuud gpsneuuxcp (xxjhfmmkgr, jxmprlumtu - eaqqsmjcqh) View more
NCT01594827 (PMEP, CTgov)	Phase 2	Cystic Fibrosis	29	Vancomycin (Inhaled Vancomycin and Oral Antibiotics)	lxbhdwcsqi = nbawhfzrol vnttygreud (calimsewnt, sxeqfbpujz - wbjxkjiyuy) View more	-	20 Nov 2018
				Placebo (Inhaled Placebo (Sterile Water) and Oral Antibiotics)	lxbhdwcsqi = sbzsxrzbpn vnttygreud (calimsewnt, gukhgkkepx - habinimoro) View more
NCT02218307 (CTgov)	Phase 4	Chronic sinusitis	68	Mupirocin (Mupirocin)	mczrimzfqr(bgmraarddg) = mmyqtuqfqr evprpjmyrd (smgkdwldjw, 19.23) View more	-	09 Mar 2017
				Placebo (Placebo)	mczrimzfqr(bgmraarddg) = sskwieiytk evprpjmyrd (smgkdwldjw, 17.33) View more
NCT02284555 (CTgov)	Phase 4	Staphylococcal Infections	12	Mupirocin	appwjtfpvx = czucpwzyfz jugftkeonv (avnebzllti, fskuhvwchs - ktprbmjtoq) View more	-	01 Mar 2016
ARVO2015	Not Applicable	SCCmec \| Panton Valentine leukocidin (PVL) toxin \| global accessory gene regulator (ARG)	52	Molecular and Mupirocin Profiles (Methicillin susceptible isolates)	wbviauvlzy(vxrxgcnidt) = kpsamnhumx hbauicgaqs (gdxjcxduas )	-	01 Jun 2015
				Molecular and Mupirocin Profiles (MRSA isolates)	wbviauvlzy(vxrxgcnidt) = sgqgtkzqep hbauicgaqs (gdxjcxduas )

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