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Phase 2 N=302 Randomized Double-blind Treatment

Safety, Tolerability, and Efficacy of MK-7655 (Relebactam) + Imipenem/Cilastatin Versus Imipenem/Cilastatin Alone for Treating Complicated Urinary Tract Infection (cUTI) (MK-7655-003)

Urinary Tract Infections · Pyelonephritis

Enrolled (actual)
302
Serious AEs
3.4%
Results posted
May 2019
Primary outcome: Primary: Percentage of Participants With a Favorable Microbiological Response at Completion of IV Study Therapy — 95.5; 98.6; 98.7 Percentage of Participants — p=0.005

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Relebactam 250 mg (Drug); Relebactam 125 mg (Drug); imipenem/cilastatin 500 mg (Drug); Placebo to relebactam (Drug); Ciprofloxacin (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Merck Sharp & Dohme LLC
Primary completion
Jul 2015

Outcome Measures

OutcomeResultp-value
PRIMARY
Percentage of Participants With a Favorable Microbiological Response at Completion of IV Study Therapy
95.5; 98.6; 98.7 0.005 sig
PRIMARY
Percentage of Participants With an Elevated Aspartate Aminotransferase (AST) or Alanine Aminotransferase (ALT) Laboratory Value That Was Greater Than or Equal to 5 Times the Upper Limit of Normal (ULN)
1.0; 1.0; 0 0.315
PRIMARY
Percentage of Participants With Elevated AST or ALT Laboratory Values ≥ 3 Times the ULN, as Well as Elevated Total Bilirubin ≥ 2 Times the ULN, and Alkaline Phosphatase Values That Were < 2 Times the ULN
0; 0; 0 > 0.999
PRIMARY
Percentage of Participants With at Least 1 Adverse Event (AE)
28.3; 29.3; 30.0
PRIMARY
Percentage of Participants With Any Serious Adverse Event (SAE)
3.0; 1.0; 3.0
PRIMARY
Percentage of Participants With Any Drug-related AE
10.1; 9.1; 9.0
PRIMARY
Percentage of Participants With a Drug-related SAE
1.0; 0; 1.0
PRIMARY
Percentage of Participants Who Discontinued IV Study Therapy Due to an AE
3.0; 1.0; 2.0
PRIMARY
Percentage of Participants Who Discontinued IV Study Therapy Due to a Drug-related AE
2.0; 1.0; 1.0
PRIMARY
Percentage of Participants With Specific AEs With Incidence of >= 4 Participants in One Treatment Group
5.1; 2.0; 4.0; 4.0; 6.1; 4.0
SECONDARY
Percentage of Participants With a Favorable Microbiological Response at Completion of IV Study Therapy Who Had Imipenem-resistant, Gram-negative cUTI Infections.
100.0; 100.0; 100.0
SECONDARY
Percentage of Participants With a Favorable Microbiological Response at Early Follow-up
61.5; 68.1; 70.4
SECONDARY
Percentage of Participants With a Favorable Clinical Response at Completion of IV Study Therapy
97.1; 98.7; 98.8
SECONDARY
Percentage of Participants With a Favorable Clinical Response at Early Follow-up
89.1; 91.8; 93.4
SECONDARY
Percentage of Participants With a Favorable Clinical Response at Late Follow-up
88.7; 87.3; 88.2
SECONDARY
Percentage of Participants With a Favorable Microbiological Response at Late Follow-up
68.3; 65.2; 62.5

Summary

The purpose of this study is to evaluate the efficacy, safety and tolerability of adding 125 mg or 250 mg doses of MK-7655 (relebactam) to imipenem/cilastatin in adults 18 years or older with complicated urinary tract infection (cUTI). The primary hypothesis is that the relebactam + imipenem/cilastatin treatment regimen is non-inferior to imipenem/cilastatin with respect to the proportion of participants with a favorable microbiological response at completion of intravenous (IV) study therapy.

Eligibility Criteria

Inclusion Criteria

  • Clinically suspected and/or bacteriologically documented cUTI or acute

pyelonephritis judged by the investigator to be serious (requiring hospitalization and treatment with IV antibiotic therapy)

  • Pyuria, determined by a midstream clean-catch (MSCC) or catheterized

(indwelling or straight catheter) urine specimen with greater than or equal to 10 white blood cells (WBCs) per high-power field (hpf) on standard examination of urine sediment or greater than or equal to 10 WBCs/mm3 in unspun urine

  • One positive urine culture within 48 hours of enrollment

Exclusion Criteria

  • Complete obstruction of any portion of the urinary tract (requiring a

permanent indwelling urinary catheter or instrumentation), a known ileal loop, or intractable vesico-ureteral reflux

  • A temporary indwelling urinary catheter is in place and cannot be removed at study entry.
  • Perinephric or intrarenal abscess or known or suspected prostatitis
  • Uncomplicated UTI
  • Any history of recent accidental trauma to the pelvis or urinary tract
  • Any amount of effective antibiotic therapy after obtaining the urine culture for admission to this study and prior to the administration of the first dose of IV study therapy
  • An infection which has been treated with greater than 24 hours of systemic antibiotic therapy known to be effective against the presumed or documented etiologic pathogen(s) within the 72-hour period immediately prior to consideration for entry into the study
  • History of serious allergy, hypersensitivity (e.g., anaphylaxis), or any

serious reaction to carbapenem antibiotics, any cephalosporins, penicillins, or other beta (β)-lactam agents

  • History of serious allergy, hypersensitivity (e.g., anaphylaxis), or any serious reaction to other beta-lactam inhibitors (e.g., tazobactam, sulbactam, clavulanic acid)
  • History of a seizure disorder
  • Currently being treated with valproic acid or has received treatment with

valproic acid in the 2 weeks prior to screening.

  • Rapidly progressive or terminal illness unlikely to survive the approximately 6 to 8 week study period
  • Pregnant or expecting to conceive, breast feeding, or plans to breast feed

during the study

  • A response to all study therapy (IV study therapy or subsequent oral

ciprofloxacin) within the timeframe of treatment specified in this protocol is

considered unlikely.

  • Concurrent infection that would interfere with evaluation of response to

the study antibiotics

  • Need for concomitant systemic antimicrobial agents in addition to those

designated in the various study treatment groups (use of vancomycin, daptomycin, or linezolid is allowed for certain infections)

  • cUTI due to a confirmed fungal pathogen
  • Currently receiving immunosuppressive therapy, including use of high-dose

corticosteroids

  • Prior recipient of a renal transplantation
  • Laboratory abnormalities as specified in protocol
  • History of any other illness that, in the opinion of the investigator, might

confound the results of the study or pose additional risk in administering the study drug

  • Currently participating in, or has participated in, any other clinical study

involving the administration of investigational or experimental medication (not

licensed by regulatory agencies) at the time of presentation or during the previous 30 days prior to screening or is anticipated to participate in such a clinical study during the course of this trial

  • Estimated or actual creatinine clearance of <5 mL/minute, or is currently undergoing hemodialysis
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01505634). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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