New AntiBiotic Treatment Options for Uncomplicated Anogenital GOnorrhoea (NABOGO)

• ClinicalTrials.gov Identifier: NCT03294395
• Recruitment Status: Completed
• First Posted: September 27, 2017
• Last Update Posted: August 6, 2021
• Sponsor: Public Health Service of Amsterdam
• Collaborator: Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
• Information provided by (Responsible Party): Henry J.C. de Vries, Public Health Service of Amsterdam

Tracking Information

• First Submitted Date: September 18, 2017
• First Posted Date: September 27, 2017
• Last Update Posted Date: August 6, 2021
• Actual Study Start Date: September 18, 2017
• Actual Primary Completion Date: June 5, 2020 (Final data collection date for primary outcome measure)

Current Primary Outcome Measures (submitted: September 22, 2017)

Proportion of participants with treatment success in each study arm for the included anatomic infection [ Time Frame: 7-14 days after treatment ]

Proportion of participants with treatment success in each study arm using a molecular test (Nucleic acid amplification test, NAAT). Treatment succes is defined as a negative test of cure (NAAT) 7-14 days after treatment.

• Original Primary Outcome Measures: Same as current

Current Secondary Outcome Measures (submitted: April 8, 2019)

• Proportion of participants with treatment success in each study arm at all anatomical infection sites [ Time Frame: 7-28 days after treatment ]
  Proportion of participants with treatment success in each study arm using a molecular test (Nucleic acid amplification test, NAAT). Treatment succes is defined as a negative test of cure (NAAT) 7-28 days after treatment.
• Incidence of treatment-emergent adverse events [ Time Frame: until 30 days after treatment ]
  The incidence, type and severity of treatment-related adverse events as assessed by CTCAE v4.0 will be measured.
• Antimicrobial susceptibility of Ng-strains to study antibiotics [ Time Frame: Day 0 (before treatment) - 28 (after treatment) ]
  The in vitro antimicrobial susceptibility (in MIC) of the experimental and reference treatment will be measured in all Ng strains collected at all infected anatomical sites of each participant at inclusion and in case of a positive test of cure.
• Blood plasma concentration of ceftriaxone, ertapenem and gentamicin in a subset of 60 NABOGO participants [ Time Frame: within 24 hours after treatment administration ]
  The blood plasma concentration will be measured 1 times within the first 24 hours after treatment administration. With these measurements the investigators will estimate the population pharmacokinetics of ceftriaxone, ertapenem and gentamicin.
• Duration of symptoms after treatment [ Time Frame: 1-30 days after treatment ]
  All participants are asked to report their symptoms daily in a diary, this will be evaluated at the follow-up visit (7-14 days after treatment) and at the online evaluation questionnaire (30 days after treatment). The mean duration of all symptoms after treatment will be measured for all study antibiotics.
• Clinical and demographic predictors for treatment failure [ Time Frame: until 7-14 days after treatment ]
  The investigators will measure if demographic (e.g. gender, HIV status) and clinical factors (e.g. anatomical location, duration of symptoms before treatment) are associated with treatment failure (treatment failure is defined as any case in which the participant received escape medication).
• Blood plasma concentration of ceftriaxone, ertapenem and fosfomycin in 60 healthy volunteers [ Time Frame: 24 hours ]
  Healthy volunteers will be randomly assigned to one of the three antibiotics. After administration of the antibiotic, the blood plasma concentration will be measured 4 times within the first 24 hours. With these measurements the investigators will estimate the population pharmacokinetics of ceftriaxone, ertapenem and fosfomycin.

Original Secondary Outcome Measures (submitted: September 22, 2017)

• Proportion of participants with treatment success in each study arm at all anatomical infection sites [ Time Frame: 7-28 days after treatment ]
  Proportion of participants with treatment success in each study arm using a molecular test (Nucleic acid amplification test, NAAT). Treatment succes is defined as a negative test of cure (NAAT) 7-28 days after treatment.
• Incidence of treatment-emergent adverse events [ Time Frame: until 30 days after treatment ]
  The incidence, type and severity of treatment-related adverse events as assessed by CTCAE v4.0 will be measured.
• Antimicrobial susceptibility of Ng-strains to study antibiotics [ Time Frame: Day 0 (before treatment) - 28 (after treatment) ]
  The in vitro antimicrobial susceptibility (in MIC) of the experimental and reference treatment will be measured in all Ng strains collected at all infected anatomical sites of each participant at inclusion and in case of a positive test of cure.
• Blood plasma concentration of antibiotics in a subset of 160 participants (40 participants per study antibiotic) [ Time Frame: within 24 hours after treatment ]
  The blood plasma concentration will be measured 1-3 times within the first 24hours after treatment in approximately 40 participants for each study antibiotic. With these measurements the investigators will estimate the population pharmacokinetics of each antibiotic. Subsequently the maximal plasma concentration and the area under the curve will be asessed.
• Duration of symptoms after treatment [ Time Frame: 1-30 days after treatment ]
  All participants are asked to report their symptoms daily in a diary, this will be evaluated at the follow-up visit (7-14 days after treatment) and at the online evaluation questionnaire (30 days after treatment). The mean duration of all symptoms after treatment will be measured for all study antibiotics.
• Clinical and demographic predictors for treatment failure [ Time Frame: until 7-14 days after treatment ]
  The investigators will measure if demographic (e.g. gender, HIV status) and clinical factors (e.g. anatomical location, duration of symptoms before treatment) are associated with treatment failure (treatment failure is defined as any case in which the participant received escape medication).

• Current Other Pre-specified Outcome Measures: Not Provided
• Original Other Pre-specified Outcome Measures: Not Provided

Descriptive Information

• Brief Title: New AntiBiotic Treatment Options for Uncomplicated Anogenital GOnorrhoea
• Official Title: New Antibiotic Treatment Options for Uncomplicated Anogenital Gonorrhoea Infections - a Double-blind Randomized Controlled Non-inferiority Trial

Brief Summary

This study evaluates the efficacy of three experimental antibiotics in the treatment of uncomplicated anogenital gonorrhoea. Participants will be randomized to one of four study arms and will receive either one of the three experimental antibiotics (ertapenem, fosfomycin and gentamicin) or the current standard antibiotic (ceftriaxone). Both the study team and the participant are blinded to the administered treatment. This enables the investigators to compare the eradication capacity and safety of the experimental antibiotics with the standard treatment.

*Following the advise of the DSMB based on a planned interim analysis, in October 2018 one study arm (fosfomycin 6g PO) was dropped and the randomized clinical trial was continued with three treatment arms (ceftriaxone 500mg IM, ertapenem 1000mg IM and gentamicin 5mg/kg IM) and without the oral placebo.

Detailed Description

Antimicrobial resistance (AMR) to extended spectrum cephalosporins (ESC) among Neisseria gonorrhoeae (Ng) is a major public health concern. With no alternative antimicrobial treatment options for gonorrhoea and only a few new drugs in the development pipeline, it is important to test existing antibiotics for their efficacy in gonorrhoea treatment. This project aims to identify new treatment modalities for uncomplicated gonorrhoea using the registered drugs ertapenem, fosfomycin and gentamicin. This trial is a double blind randomized clinical non-inferiority trial with four treatment arms. 108 participants are randomly assigned to each study arm . Participants will receive either ceftriaxone 500mg intramuscularly (IM) or ertapenem 1000mg IM or gentamicin 5mg/kg IM with a maximum of 400mg (in two doses) supplemented with an oral placebo, or receive fosfomycin 6g oral suspension supplemented with an intramuscular placebo. The bacterial eradication capacity of the study antimicrobials at the included infection site is measured 7-14 days after treatment, using an RNA-based Nucleic Acid Amplification Test (NAAT).

*Following the advise of the DSMB based on a planned interim analysis, in October 2018 one study arm (fosfomycin 6g PO) was dropped and the randomized clinical trial was continued with three treatment arms (ceftriaxone 500mg IM, ertapenem 1000mg IM and gentamicin 5mg/kg IM) and without the oral placebo.

• Study Type: Interventional
• Study Phase: Phase 3

Study Design

Allocation: Randomized
Intervention Model: Parallel Assignment
Intervention Model Description:

A double-blind randomized clinical trial with non-inferiority design

*since October 2018 one study arm (fosfomycin) has been dropped. In a subset of these participants the plasma concentration of ceftriaxone, ertapenem and gentamicin is measured.

An open-label randomized substudy evaluating the pharmacokinetics of ceftriaxone ertapenem and fosfomycin in 60 healthy volunteers (this number is in addition to the 346 NABOGO participants with gonorrhea)

Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Masking Description:

All participants receive either intramuscular treatment and if applicable intramuscular placebo. Both particpant and care provider are blind to the regimen.

Primary Purpose: Treatment

• Condition: Gonorrhea

Intervention

• Drug: Ertapenem 1000 MG
  single dose 1000mg intramuscular injection
  Other Name: Invanz
• Drug: Fosfomycin Oral Suspension
  single dose 6g oral suspension
  Other Name: Monuril
• Drug: Gentamicin Sulfate, Injectable
  single dose 5mg/kg (maximum 400mg) intramuscular injection
  Other Name: no other names
• Drug: Ceftriaxone
  single dose 500mg intramuscular injection
  Other Name: no other names

Study Arms

• Active Comparator: Ceftriaxone im
  Current standard treatment. Ceftriaxone 500mg (single intramuscular dose) + placebo (single oral dose)
  Intervention: Drug: Ceftriaxone
• Experimental: Ertapenem im
  Ertapenem 1000mg (single intramuscular dose) + placebo (single oral dose)
  Intervention: Drug: Ertapenem 1000 MG
• Experimental: Fosfomycin po
  Fosfomycin oral suspension 6g (single oral dose) + placebo (single intramuscular dose)
  Intervention: Drug: Fosfomycin Oral Suspension
• Experimental: Gentamicin im
  Gentamicin sulfate, injectable 5mg/kg (single intramuscular dose) + placebo (single oral dose)
  Intervention: Drug: Gentamicin Sulfate, Injectable

• Publications *: de Vries HJC, de Laat M, Jongen VW, Heijman T, Wind CM, Boyd A, de Korne-Elenbaas J, van Dam AP, Schim van der Loeff MF; NABOGO steering group. Efficacy of ertapenem, gentamicin, fosfomycin, and ceftriaxone for the treatment of anogenital gonorrhoea (NABOGO): a randomised, non-inferiority trial. Lancet Infect Dis. 2022 May;22(5):706-717. doi: 10.1016/S1473-3099(21)00625-3. Epub 2022 Jan 19.

Recruitment Information

• Recruitment Status: Completed
• Actual Enrollment (submitted: April 8, 2019): 346
• Original Estimated Enrollment (submitted: September 22, 2017): 548
• Actual Study Completion Date: June 5, 2020
• Actual Primary Completion Date: June 5, 2020 (Final data collection date for primary outcome measure)

Eligibility Criteria

Inclusion criteria main study

• 18 years or older

• Anorectal, cervical/vaginal or urethral Ng infection, diagnosed by the following:

  • Ng-positive Gram-stained smear (intracellular Gram-negative diplococci and leukocytes) and/or
  • Positive for Ng by nucleic acid amplification test (NAAT) (Aptima Combo 2) and/or
  • Positive for Ng by culture
• Provide samples from the included infection site for NAAT and direct culture immediately before treatment
• Willing to abstain from anal, vaginal and oral sex until the test of cure (TOC)-visit, or use condoms during sex
• Willing and able to return for a TOC-visit 7-14 days after treatment
• Provide informed consent
• Accept intramuscular injections

Exclusion criteria main study

Pre-randomisation:

• Suspicion of a complicated Ng infection based on signs and/or symptoms indicating pelvic inflammatory disease (PID), epididymitis, prostatitis or gonococcal arthritis*
• Another (sexually transmitted) infection or a suspicion of another infection for which systemic antimicrobial therapy is indicated
• Pregnancy, having a wish to become pregnant or breastfeeding (tested at inclusion visit)
• Not able to read/understand Dutch or English

• HIV infection if:

  • Newly diagnosed HIV infection (upon the inclusion visit) and/or
  • CD4+ cell-count <200 cells/μL (as reported by the patient)
• Known allergy or adverse reactions to ceftriaxone, ertapenemor gentamicin
• Known renal impairment (based on estimated GFR using Cockroft and Gault formula using serum creatinin measured with a point-of-care (POC) test; cut off value renal impairment eGFR ≤ 50 ml/min)
• Known liver cirrhosis (based on history)
• Known congestive heart failure (based on history)
• Known myasthenia gravis
• Known hearing loss or balance disorder, confirmed by an ear-nose-throat (ENT)-doctor or for which an ENT doctor has been consulted and a diagnostic process is still in progress (based on history)

• Concurrent use of any of the following medication:

  • systemic antibacterial antimicrobials other than nitrofurantoin or metronidazole
  • systemic immunosuppressive drugs
  • systemic valproic acid
• Use of any antimicrobial therapy other than nitrofurantoin or metronidazole in the two weeks prior to study enrollment (based on history)
• Previous enrollment in the study
• Concurrent participation in other non-observational medical research*
• Unlikely to adhere to the study protocol

Post-randomisation:

Exclusion of participants from the modified intention to treat analysis (mITT):

• Negative result of Ng NAAT of sample collected on T0 (the day of treatment). This could be the case in the following situations:

  1. Negative NAAT in spite of positive gram stain.
  2. Positive NAAT on pre-study visit but spontaneous clearance of the infection in the time period between first test and return visit for treatment (=study inclusion visit). A novel sample for NAAT will be collected on the study inclusion visit just before administration of treatment; if these results are Ng-negative a participant will be excluded of mITT.
• Loss to follow-up, i.e. no study visit TOC 7-14 days after treatment administration.

Exclusion from per protocol analysis (PP):

• Exclusion of mITT
• Use of non-study related antibiotics after inclusion and prior to TOC visit
• Condomless sexual contact with the primary anatomical gonorrhea site involved after inclusion and prior to TOC visit
• Other protocol violations

Inclusion criteria PK substudy (healthy volunteers):

• 18 years or older
• Provide informed consent

Exclusion criteria PK substudy (healthy volunteers)

Pre-randomisation:

• Pregnancy, having a wish to become pregnant or breastfeeding (tested at inclusion visit)
• Not able to read/understand Dutch or English
• Known allergy or adverse reactions to ceftriaxone, ertapenem, or fosfomycin.
• Known renal impairment (based on estimated GFR using Cockroft and Gault formula using serum creatinin measured with a point-of-care (POC) test; cut off value renal impairment eGFR ≤ 50 ml/min)
• Known liver cirrhosis (based on history)

• Concurrent use of any of the following medication:

  • systemic valproic acid
  • systemic metoclopramide
• Use of any systemic antimicrobial therapy other than nitrofurantoin or metronidazole in the two weeks prior to study enrollment (based on history)
• Concurrent participation in other non-observational medical research (apart from NABOGO RCT)
• Unlikely to adhere to the study

Sex/Gender

• Sexes Eligible for Study: All

• Ages: 18 Years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: Yes
• Contacts: Contact information is only displayed when the study is recruiting subjects
• Listed Location Countries: Netherlands

Administrative Information

• NCT Number: NCT03294395
• Other Study ID Numbers: NABOGO
• Has Data Monitoring Committee: Yes

U.S. FDA-regulated Product

• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No

IPD Sharing Statement

• Plan to Share IPD: Undecided

• Current Responsible Party: Henry J.C. de Vries, Public Health Service of Amsterdam
• Original Responsible Party: Same as current
• Current Study Sponsor: Public Health Service of Amsterdam
• Original Study Sponsor: Same as current
• Collaborators: Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

Investigators

• Principal Investigator: Henry JC de Vries, PhD, MD; Public Health Service of Amsterdam

• PRS Account: Public Health Service of Amsterdam
• Verification Date: July 2021