Injection drug users (IDUs) often develop acute bacterial skin and skin structure infections (ABSSSI) and use emergency departments as their primary source for medical care.
A post hoc subgroup analysis of two randomized trials examined the efficacy and safety of tedizolid in the treatment of ABSSSI in IDUs. IDUs (n = 389) were identified from two pooled phase 3 trials (NCT01170221, NCT01421511) in patients with ABSSSI (n = 1333). Patients were randomly assigned to tedizolid phosphate (200 mg once daily, 6 days) or linezolid (600 mg twice daily, 10 days). Primary endpoint was ≥ 20% reduction in lesion area from baseline at 48 –72 h. Secondary endpoints included investigator-assessed clinical and microbiological response at the post-therapy evaluation (PTE).
Wound infection was more common in IDUs (52.2%), while cellulitis/erysipelas was more common in non-IDUs (55.9%). Most infections were due to Staphylococcus aureus (IDUs, 75.2%; non-IDUs, 85.6%), while oral pathogens were more prevalent in IDUs. Early clinical success rates for tedizolid and linezolid were 82.5% and 79.6% in IDUs and 81.3% and 79.3% for non-IDUs, respectively; responses at PTE were similar. Microbiological response per pathogen was similar between treatment groups. Rates of treatment-emergent adverse events (AEs) in IDUs were comparable between tedizolid (46.2%) and linezolid (47.8%) arms, while lower incidence of gastrointestinal AEs was observed with tedizolid (20.3%) than with linezolid (25.1%).
Efficacy and safety of tedizolid and linezolid in the treatment of ABSSSI was similar in IDUs and non-IDUs, supporting the use of oxazolidinones in treating ABSSSIs in IDUs.
Merck & Co., Inc., Kenilworth, NJ, USA.
Acute bacterial skin and skin structure infections (ABSSSI) are among the most common reasons for visits to the emergency department . One group at particularly high risk for ABSSSI is injection drug users (IDUs) [2,3,4,5]. The high incidence and the high rate of recurrence of ABSSSI in this population are likely due to frequent, repeated injections, injection method (subcutaneous injection), and/or drug mixture (cocaine and heroin, often with contaminants). The lack of aseptic injection methods, including the practice of needle licking, contaminates the injection site and increases the risk for skin infections [2, 3, 5, 6]. Subcutaneous injection has been strongly associated with the development of purulent infections and cellulitis due to the localized introduction of contaminants, irritants, and bacteria directly into the tissue [7, 8]. Injection of cocaine and heroin may also increase the risk for ABSSSI because it induces localized irritation and tissue reaction that promote the development of infections .
Among IDUs, the most commonly identified causative pathogens for ABSSSI are Staphylococcus aureus—including methicillin-resistant S. aureus (MRSA) [3, 4, 9, 10]—and streptococcal species . However, the bacteriology of ABSSSI in IDUs can be diverse and polymicrobic with infections from nontraditional pathogens—such as those present in the oral flora—commonly seen [4, 10].
Injection drug users often use emergency departments as their primary source for medical care, with ABSSSI a leading reason for presentation [2, 4]. Physicians may be faced with many challenges when treating IDUs including poor compliance, delays in seeking medical care, and recurring infections [2, 3, 7]. Additionally, many IDUs have comorbid mental health illnesses and hepatitis C or HIV coinfection, which may complicate treatment options (e.g., limited mental capacity, immunosuppression, adherence to therapy) [2, 11,12,13]. Given the numerous challenges associated with treating ABSSSI in IDUs, better understanding of patient and disease characteristics and clinical outcomes in IDUs compared with non-IDUs may help guide the best treatment option for this patient population.
Tedizolid, the active moiety of tedizolid phosphate, is a novel oxazolidinone antibacterial with potent activity against a wide range of Gram-positive pathogens, including MRSA and vancomycin-resistant enterococci [14,15,16]. Two phase 3 trials, ESTABLISH-1 and ESTABLISH-2, demonstrated the noninferior efficacy of tedizolid (200 mg daily for 6 days) compared with linezolid (600 mg twice daily for 10 days) in patients with ABSSSI [17, 18]. This post hoc subgroup analysis, using pooled data from the two phase 3 ABSSSI clinical trials, aims to assess the safety and efficacy of tedizolid and linezolid in IDUs and non-IDUs.
Study Design and Setting
All procedures followed were in accordance with the ethical standards of the responsible committee on human experimentation (institutional and national) and with the Helsinki Declaration of 1964, as revised in 2013. Informed consent was obtained from all patients for being included in the study. The study was conducted in accordance with the principles of Good Clinical Practice and was approved by the appropriate institutional review boards and regulatory agencies. ESTABLISH-1 and ESTABLISH-2 were randomized, double-blind, double-dummy, multicenter, multinational, noninferiority, phase 3 clinical trials in patients with ABSSSI. Patients had to have suspected or documented Gram-positive infection from baseline Gram stain or culture to be included in the study. Patients with cellulitis/erysipelas or abscess were not enrolled if there was suspected Gram-negative involvement. Concomitant Gram-negative coverage was only allowed with infected wounds. Methods and results of the individual studies and pooled analysis have been previously published [17,18,19]. These trials are registered at ClinicalTrials.gov (NCT01170221 and NCT01421511).
Selection of Participants
The trials enrolled patients older than 18 years (ESTABLISH-1) or older than 12 years (ESTABLISH-2) with ABSSSI (cellulitis/erysipelas, wound infection or major cutaneous abscess). Full details of patient eligibility criteria have been published [17, 18]. The pooled intent-to-treat (ITT) population from both clinical trials was classified into IDU and non-IDU subgroups based on injection drug use, and all endpoints were evaluated between these groups. Patients who disclosed that they were current or recent users of injection drugs at screening were included in the IDU subpopulation.
Patients received 200 mg tedizolid phosphate once daily for 6 days or 600 mg linezolid twice daily for 10 days. Patients in ESTABLISH-1 received oral drug. Patients in ESTABLISH-2 received intravenous treatment for 1 day and could subsequently be switched to oral drug at the investigator’s discretion if they met two or more of the following criteria: no increase from baseline in primary lesion area, temperature lower than 37.7 °C, no worsening of local signs and symptoms, or improvement of local signs and symptoms at the primary infection site.
Methods and Measurements
Baseline assessments were performed within 24 h before the first dose of study drug (day 1). Patients were evaluated on day 1, day 2, 48–72 h after the first dose, day 7, and day 11 [end-of-treatment (EOT) visit]; at the post-therapy evaluation (PTE) visit (7–14 days after the EOT visit); and at the late follow-up (LFU) visit (18–25 days after the EOT visit). Intravenous treatment was delivered in a health care setting, but patients were permitted to take oral study drug at home.
Bacterial pathogens were identified from a blood culture or from culture of a microbiological sample obtained from the primary lesion site by needle aspiration, biopsy, deep swab, incision or other surgical techniques. Pathogens (genus and species) were identified by the central laboratory; local laboratory data were used if central laboratory data were not available.
The primary endpoint was a ≥ 20% reduction in lesion area [length × width of erythema, edema or induration (in ESTABLISH-1; only erythema was used to determine lesion size)] without receipt of rescue antibiotics. Early clinical response was assessed 48–72 h after the first dose of study drug; patients who had received nonstudy systemic antibacterial agents for any reason within 72 h of the first dose were considered nonresponders, per US Food and Drug Administration guidelines . A key secondary endpoint was late response, which involved investigator-assessed clinical response at the PTE [7–14 days after the end of therapy (EOT; 11 days after the start of study drug)], per European Medicines Agency guidelines .
Microbiological response per pathogen at EOT and PTE was also analyzed. A favorable microbiological response was defined as eradication (absence of original baseline pathogens) and presumed eradication (no source specimen to culture in a patient assessed by the investigator as a clinical success).
Safety evaluations included adverse events (AEs), clinical laboratory assessments, vital signs, electrocardiograms, and physical examination.
The ITT population included all randomly assigned patients. Patients with missing data and patients who did not receive study drug were defined as having an indeterminate response and were considered nonresponders for the primary efficacy endpoint. The microbiological ITT (MITT) population included patients with ≥ 1 Gram-positive ABSSSI pathogen isolated at baseline. The clinically evaluable (CE) population included all patients in the ITT analysis set who complied with the protocol and had no major violations. The CE population at PTE (CE-PTE) included patients who completed the study through the PTE assessment without any concomitant systemic antibiotic therapy or other confounding events or factors. The microbiologically evaluable at PTE (ME-PTE) population included all patients in the MITT analysis set who were also in the CE-PTE analysis set. The microbiologically evaluable at end-of-therapy (ME-EOT) population included all patients in the MITT and clinically evaluable at end of therapy (CE-EOT) populations. The safety population included all patients from the MITT population who received ≥ 1 dose of the study drug.
Summaries included frequency and percentages for categorical data, frequency and median for ordinal data, and frequency, mean, standard deviation, and median, minimum and maximum, for quantitative data. Version 9.2 (or higher) of SAS statistical software package was used to provide all summaries and statistical analyses. For both primary and secondary outcomes, 95% confidence intervals (CIs) were adjusted for the study and were calculated using the methodology of Miettinen and Nurminen  to determine the differences in response rates between tedizolid and linezolid treatment arms.
Characteristics of Study Subjects
A total of 1333 patients (664 treated with tedizolid and 669 treated with linezolid) made up the ITT population. Approximately 30% of the pooled ITT population were IDUs: 27.6% (183/664) were in the tedizolid group and 30.8% (206/669) were in the linezolid group. Fewer IDUs were elderly (aged ≥ 65 years) (Table 1). Overall, IDUs had a lower incidence of traditional systemic signs and symptoms of infection than non-IDUs, including fever [4.9% (19/389) vs. 31.8% (300/944)], abnormal white blood cell count [36.8% (143/389) vs. 48.4% (457/944)], systemic inflammatory response syndrome [SIRS; 8.2% (32/389) vs. 27.4% (259/944)], and immature neutrophils [1.3% (5/389) vs. 11.4% (108/944)], respectively. Lymphadenopathy, however, was more prevalent in IDUs [94.3% (367/389)] than in non-IDUs [72.1% (681/944)]. Risk factors, including poor living conditions [11.3% (44/389) vs. 3.2% (30/944)] and previous ABSSSI lesion [33.4% (130/389) vs. 16.9% (160/944); Table 1], respectively, were more common in IDUs than in non-IDUs. Hepatitis C and concurrent secondary skin infection were approximately nine times [73.8% (287/389) vs. 7.9% (75/944)] and three times [27.0% (105/389) vs. 8.6% (81/944)] more prevalent in IDUs than in non-IDUs, respectively (Table 1). However, the incidence of each of these comorbidities was similar between the tedizolid and linezolid treatment groups for both IDUs and non-IDUs (Table 1).
The distribution of ABSSSI types differed between IDUs and non-IDUs in both treatment groups. Wound infections, often injection-site infections, were the most common ABSSSI in IDUs [tedizolid, 50.8% (93/183); linezolid, 53.4% (110/206)], whereas, in non-IDUs, cellulitis/erysipelas was more prevalent [tedizolid, 54.5% (262/481); linezolid, 57.5% (266/463); Table 1].
Patients who used injection drugs presented with a more diverse spectrum of baseline pathogens, including organisms not traditionally associated with ABSSSI, and more frequently had polymicrobial Gram-positive infections (Table 2). Among IDUs and non-IDUs, the most common baseline pathogen was S. aureus [75.2% (212/282) and 85.6% (459/536), respectively]; the prevalence of methicillin-resistant and methicillin-susceptible S. aureus was similar between IDUs [39.6% (84/212) and 60.8% (129/212), respectively] and non-IDUs [44.2% (203/459) and 56.0% (257/459), respectively]. However, Streptococcus anginosus Group [17% (48/282) in IDUs and 1.9% (10/536) in non-IDUs] and streptococcal species that generally form part of the oral flora [including S. mitis, S. salivarius, S. sanguinis, and S. viridans Group; 10.3% (29/282) vs. 0.0% in non-IDUs] were more frequently observed in patients who used injection drugs (Table 2). Infections due to S. pyogenes were more frequent in non-IDUs [9.7% (52/536)] than IDUs [0.4% (1/282)].
Early clinical response rates in the ITT population at the 48- to 72-h visits were similar in IDUs treated with tedizolid [82.5% (151/183)] or linezolid [79.6% (164/206); Fig. 1]. For IDUs, the treatment difference between tedizolid and linezolid was 2.9% (95% CI − 4.9, 10.7). Similarly, for non-IDUs, early clinical response was comparable between tedizolid-treated patients [81.3% (391/481)] and linezolid-treated patients [79.3% (367/463)] (Fig. 1). Early response rates did not differ between IDUs and non-IDUs (Fig. 1).
In the ITT population, the rates of clinical success based on investigator assessment of clinical response at the PTE visit were similar between IDUs and non-IDUs treated with tedizolid [83.1% (152/183) and 88.1% (424/481), respectively] or linezolid [84.0% (173/206) and 88.1% (408/463), respectively] (Fig. 2a). The treatment difference between tedizolid and linezolid was − 0.9% (95% CI − 8.3, 6.5) for IDUs. Clinical success rates in the CE-PTE population were also comparable between IDUs treated with tedizolid and linezolid (Fig. 2b), with a treatment difference of − 1.0% (95% CI − 6.8, 4.2) in IDUs. Similar clinical success rates were observed for IDUs and non-IDUs at the PTE visit in both the ITT (83.1–88.1%) and the CE-PTE (93.4–96.1%) populations (Fig. 2a, b).
Rates of favorable microbiological response per baseline pathogen at the EOT visit for the MITT and ME-EOT populations are presented in Table 3. Rates were generally similar between both treatment groups in IDUs and non-IDUs from the MITT and ME-EOT populations at EOT (Fig. 3a, b). Microbiological response to S. anginosus was lower for tedizolid than for linezolid in IDUs from the MITT population at EOT. However, at the PTE visit, high response rates were observed with both treatments in IDUs and non-IDUs (> 80% positive response in the MITT population and > 90% positive response in the ME-PTE population) (Fig. 3c, d).
The incidence of treatment-emergent adverse events (TEAEs) was slightly elevated in IDUs compared with non-IDUs. TEAEs occurred in 46.2% (84/182) of tedizolid patients and 47.8% (97/203) of linezolid patients who used injection drugs; in non-IDUs, 41.5% (199/480) of tedizolid patients and 41.2% (189/459) of linezolid patients reported experiencing any TEAE (Table 4). TEAEs under the grouping “infections and infestations” were more common among IDUs than non-IDUs, particularly new, secondary abscess or cellulitis. In the tedizolid group, 8.2% (15/182) of IDUs and 4.2% (20/480) of non-IDUs experienced secondary abscess; 4.4% (8/182) and 1.9% (9/480), respectively, had secondary cellulitis. Results were similar in the linezolid group: 6.9% (14/203) and 2.6% (12/459) of IDUs and non-IDUs, respectively, had secondary abscess and 3.4% (7/203) and 1.5% (7/459), respectively, had secondary cellulitis.
Among the most frequently reported TEAEs (≥ 2%), gastrointestinal (GI) disorders (including nausea, vomiting, and diarrhea) were most common and were higher in the linezolid arm in both IDUs and non-IDUs. GI TEAEs in IDUs were reported in 20.3% (37/182) of the tedizolid group compared with 25.1% (51/203) of the linezolid group, which was slightly higher than rates reported in non-IDUs [tedizolid, 14.4% (69/480); linezolid, 22.0% (101/459)]. Three deaths occurred during the study; one of those who died was a patient actively using injection drugs. This patient developed septic shock with multiorgan failure and died 46 days after receiving the final dose of tedizolid. All deaths were considered unrelated to the study drug .
ABSSSI is a leading reason that IDUs seek medical treatment [2, 4]. Treatment of this patient group frequently rests with emergency physicians as many IDUs utilize emergency departments as their primary source of medical care [2, 4]. Effective antibacterial treatment relies heavily on the appropriateness of initial therapy and first-line treatment in the emergency department is critical to ensuring successful outcomes in this patient population.
In this post hoc subgroup analysis from two phase 3 clinical trials of tedizolid, IDUs overall had fewer traditional systemic signs and symptoms of infection (fever, abnormal white blood cell counts, SIRS, and immature neutrophils) than non-IDUs. However, lymphadenopathy, hepatitis C, poor living conditions, and past ABSSSI lesions were more prevalent in IDUs, consistent with reported conditions known to be common in this population [7, 13, 23, 24]. The higher incidence of secondary skin infections and hepatitis C is unsurprising given that IDUs repeatedly inject into various anatomic sites which all have the potential for infection.
The distribution of ABSSSI types differed between IDUs and non-IDUs. As would be expected from repeated injections, more than half of IDUs had wound infections, whereas non-IDUs predominantly had cellulitis/erysipelas, similar to what was observed in the overall ITT population . It is possible that some infections in IDUs classified as cellulitis/erysipelas or abscess were related to an injection site and might therefore be considered wound infections or vice versa.
The majority of ABSSSI in both IDUs and non-IDUs were due to S. aureus. However, infections in IDUs were associated with a more diverse range of bacterial species not typically causative of ABSSSI, specifically those of the oral flora. These species increase the risk for infection from oral streptococcal and Gram-positive anaerobic species [6, 7]. The findings from this study are consistent with previous reports that found S. aureus to be the predominant causative pathogen in ABSSSI with oral pathogens constituting higher proportions among IDUs [4, 10].
Despite differences in baseline patient and clinical characteristics, treatment outcomes in both IDUs and non-IDUs were comparable with tedizolid and linezolid at both the early evaluation and the PTE. Early clinical response approximated 80% for IDUs and non-IDUs in both treatment arms. This rate was similar to that observed in the overall, pooled ITT population, as reported . Investigator-assessed clinical response at PTE was also comparable between treatment arms and IDU/non-IDU patient populations. Similarities in clinical outcomes suggest that complicating factors associated with injection drug use did not greatly impact the efficacy profile of tedizolid or linezolid in treating ABSSSI. The microbiological response of IDUs was also generally similar to that of non-IDUs in the MITT and ME populations, despite the greater diversity of pathogens in the IDU group and regardless of treatment arm. At EOT and PTE, high response rates were observed for both treatments in IDUs, and > 90% of pathogens were eradicated or presumed eradicated with either treatment in both IDUs and non-IDUs in the ME population.
Overall, tedizolid and linezolid were well tolerated in IDUs, although the rate of TEAEs was slightly higher in IDUs than in non-IDUs. In both treatment groups, IDUs experienced secondary abscesses and secondary cellulitis more often than non-IDUs, although this could be associated with new infections caused by repeated needle use in other locations. GI disorders also occurred at a higher frequency in IDUs, with a numerically greater incidence in the linezolid group than in the tedizolid group, consistent with safety results observed in the overall ITT population . These GI TEAEs generally occurred within the first 6 days of treatment. As such, they were likely the result of pharmacologic differences between linezolid and tedizolid and not a result of the shorter course of therapy with tedizolid phosphate .
The high-risk lifestyle of IDUs, often coupled with increased rates of reinfection and concomitant mental health issues, makes compliance a major concern in this treatment population [2, 11, 13, 25]. In a systematic review of patient adherence to oral antibacterials, medical compliance was higher in patients prescribed once-daily, short-course oral therapy than in patients prescribed longer and more frequent regimens . The convenience and effectiveness of a once-daily, short-course oral treatment such as tedizolid phosphate may be particularly beneficial in this population. Reducing pill burden has the potential to increase treatment compliance and optimize outcomes in a real-world setting. IDUs may also be at risk for serotonin syndrome, a potentially life-threatening reaction caused by overactivation of the serotonergic system . Many cases of serotonin syndrome are caused by unintended drug–drug interactions, and it is known that some drugs of abuse can lead to serotonin toxicity . Tedizolid may be less likely to cause serotonin syndrome than linezolid, though further research is required to support this hypothesis [28, 29].
Several limitations should be considered when evaluating the results of this study. This was a post hoc subgroup analysis of a patient subpopulation and might have lacked sufficient power to detect differences between IDUs and non-IDUs. The study relied on self-reporting of injection drug use, which might have been subject to underreporting. In addition, the two treatment groups within the IDU and non-IDU subgroups might not have been balanced with respect to all prognostic factors.
In summary, although IDUs present with treatment challenges not typically seen in non-IDUs, clinical outcomes were similar for both patient populations. Both tedizolid and linezolid were well tolerated; however, fewer GI AEs were associated with tedizolid treatment. This study showed that short-course, 6-day treatment with tedizolid was as effective as 10 days of linezolid in treating ABSSSI in IDUs, which suggests that tedizolid (including exclusively oral treatment) is a suitable treatment option in this complex patient population.
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This work was supported by Merck & Co., Inc., Kenilworth, NJ, USA. This support included funding for the clinical trials as well as journal processing fees. In collaboration with the authors, employees of the study sponsor were involved in study design, data analysis, interpretation of results, and review of the manuscript. All authors had full access to all of the data in this study and take complete responsibility for the integrity of the data and accuracy of the data analysis.
Medical Writing and Editorial Assistance
Editorial and medical writing assistance in the preparation of this manuscript was provided by Sally Mitchell, PhD (Apothecom, Yardley, PA). Support for this assistance was funded by Merck & Co., Inc., Kenilworth, NJ, USA.
All named authors meet the International Committee of Medical Journal Editors (ICMJE) criteria for authorship for this manuscript, take responsibility for the integrity of the work as a whole, and have given final approval to the version to be published.
Gregory J. Moran was involved in drafting the manuscript, data acquisition, interpretation of the results and critical review and revision of the manuscript for important intellectual content. Carisa De Anda was involved in drafting the manuscript, study conception and design, data analysis, interpretation of the results and critical review and revision of the manuscript for important intellectual content. Anita F. Das was involved in drafting the manuscript, study conception and design, data analysis, interpretation of the results and critical review and revision of the manuscript for important intellectual content. Sinikka Green was involved in drafting the manuscript, data acquisition, interpretation of the results and critical review and revision of the manuscript for important intellectual content. Purvi Mehra was involved in drafting the manuscript, data acquisition and critical review and revision of the manuscript for important intellectual content. Philippe Prokocimer was involved in drafting the manuscript, study conception and design, interpretation of the results and critical review and revision of the manuscript for important intellectual content. All authors provided final approval of the version to be published. All authors agree to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.
Presented at IDWeek, October 8–12, 2014, Philadelphia, PA, USA.
Gregory J. Moran reports receiving grant support from Trius Therapeutics (now Merck & Co., Inc.) during the conduct of the study; he also reports receiving grants and consultancy fees from Allergan. Carisa De Anda is a current employee of Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Kenilworth, NJ, USA and may hold stock in the company. Philippe Prokocimer is a current employee of AntibioTx A/S, San Diego, CA, USA and a past employee of Merck & Co., Inc., Kenilworth, NJ, USA. Anita F. Das is a current employee of ADStat, Guerneville, CA, USA and was an employee of InClin and a consultant to Cubist Pharmaceuticals (now Merck & Co., Inc.) at the time this study was conducted and was compensated for supporting this research; she is also a consultant to Achaogen, Cempra, Cerexa, Contrafect, Durata, Melinta, Nabriva, Paratek, Tetraphase, Theravance, Wockhardt and Zavante. Sinikka Green and Purvi Mehra have nothing to disclose.
Compliance with Ethics Guidelines
All procedures followed were in accordance with the ethical standards of the responsible committee on human experimentation (institutional and national) and with the Helsinki Declaration of 1964, as revised in 2013. Informed consent was obtained from all patients for being included in the study. The ESTABLISH-1 and ESTABLISH-2 (ClinicalTrials.gov numbers NCT01170221 and NCT01421511) phase 3 studies received institutional review board approval.
Merck & Co., Inc.’s data sharing policy, including restrictions, is available at http://engagezone.merck.com/ds_documentation.php. Requests for access to the study data can be submitted through the EngageZone site or via email to email@example.com.
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Moran, G.J., De Anda, C., Das, A.F. et al. Efficacy and Safety of Tedizolid and Linezolid for the Treatment of Acute Bacterial Skin and Skin Structure Infections in Injection Drug Users: Analysis of Two Clinical Trials. Infect Dis Ther 7, 509–522 (2018). https://doi.org/10.1007/s40121-018-0211-4