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Gent for Pharyngeal Gonorrhea (GC)

Primary Purpose

Pharyngeal Gonococcal Infection

Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
gentamicin 360mg IM
Sponsored by
University of Washington
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pharyngeal Gonococcal Infection focused on measuring gonorrhea, pharynx, treatment, gentamicin

Eligibility Criteria

16 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Persons diagnosed with pharyngeal gonorrhea who are not yet treated

Exclusion Criteria:

  • Age less than 16 years
  • Receipt of antibiotics in ≤30 days
  • Known allergy to any aminoglycoside
  • History of renal disease (including diagnosis of solitary kidney, chronic renal insufficiency, renal cell carcinoma etc),
  • Use of concurrent nephrotoxic drugs or muscle relaxants
  • History of diabetes
  • History of hearing loss or tinnitus
  • Concurrent infection with syphilis or chlamydia
  • Pregnancy and/or nursing
  • Unable to return for a follow-up visit 4-7 days (+/- 1 day).
  • Study team's discretion

Sites / Locations

  • Public Health -- Seattle & King County STD Clinic

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Single Arm

Arm Description

Men who have sex with men (MSM) with pharyngeal gonorrhea will be treated with 360mg intramuscular gentamicin x 1.

Outcomes

Primary Outcome Measures

Cure Rate Defined as the Percentage of Persons With Pharyngeal Gonorrhea Treated With Gentamicin 360mg IM Who Have a Negative Culture 4-7 Days Following Treatment
Negative Pharyngeal Culture

Secondary Outcome Measures

Renal Safety
Measured by a percent change in serum creatinine from baseline to test of cure (4-7 days following treatment)
Tolerability of the Injection Gentamicin 360mg IM x 1
Participant reported pain scale, with 1 being little to no pain, and 10 being the worst pain ever.
Peak Gentamicin Levels
serum gentamicin concentration
Gentamicin Minimal Inhibitory Concentration (MIC)
laboratory defined MIC of infecting strain of N. gonorrhoeae at enrollment visit determined by agar dilution

Full Information

First Posted
July 3, 2018
Last Updated
July 24, 2020
Sponsor
University of Washington
Collaborators
National Institute of Allergy and Infectious Diseases (NIAID)
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1. Study Identification

Unique Protocol Identification Number
NCT03632109
Brief Title
Gent for Pharyngeal Gonorrhea (GC)
Official Title
Gentamicin for Pharyngeal Gonorrhea - A Demonstration Study
Study Type
Interventional

2. Study Status

Record Verification Date
July 2020
Overall Recruitment Status
Terminated
Why Stopped
Efficacy
Study Start Date
September 17, 2018 (Actual)
Primary Completion Date
March 12, 2019 (Actual)
Study Completion Date
March 12, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Washington
Collaborators
National Institute of Allergy and Infectious Diseases (NIAID)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The Centers for Disease Control and Prevention has identified antimicrobial-resistant (AMR) Neisseria gonorrhoeae (NG) as one of the nation's top three urgent AMR threats. Since the advent of antibiotics in the 1930s, NG has developed resistance to every first-line antibiotic. Parenteral third-generation cephalosporins are now the only class of drug with consistent efficacy against NG. New therapies are urgently needed. Although some novel antimicrobials are under development, reevaluating older drugs is another option for quickly identifying additional treatments for gonorrhea. We propose a demonstration study to test a single dose of gentamicin for the treatment of pharyngeal gonorrhea. We chose to focus on pharyngeal gonorrhea because these infections are common, play an important role in fostering gonococcal resistance, and are harder to eradicate than genital infections. Although gentamicin is 91% efficacious for genital NG, its efficacy at the pharynx may be less since streptomycin, another aminoglycoside previously used to treat gonorrhea, was not effective for pharyngeal NG. It is unknown if streptomycin's poor efficacy is indicative of limitations of aminoglycosides as a class. We plan to enroll 60 men who have sex with men in a demonstration study to be conducted at the Seattle & King County STD Clinic to test the efficacy of 360 mg of gentamicin given intramuscularly for pharyngeal gonorrhea. Secondary objectives include determining the ideal pharmacodynamic criterion (comparing in vitro minimal inhibitory concentrations (MIC) of NG to peak gentamicin serum levels), estimating resistance induction among treatment failures, and assessing the tolerability of 360 mg of IM gentamicin. Objectives The proposed study aims to evaluate the efficacy of a single intramuscular (IM) dose of gentamicin in the treatment of pharyngeal gonorrhea. Secondary objectives include documenting the efficacy stratified by minimal inhibitory concentration (MIC) compared with the gentamicin peak level in order to estimate a pharmacodynamic criterion. We will also attempt to determine whether gentamicin monotherapy induces antimicrobial resistance among treatment failures. Lastly, we will evaluate the tolerability of 360 mg of IM gentamicin, stratified by subject weight (i.e. weight based dosing). The specific aims are: Determine the proportion of persons whose pharyngeal gonococcal infections are cured with a single dose of 360mg gentamicin intramuscularly alone. Evaluate the renal safety and tolerability of 360mg IM of gentamicin. Document mean peak gentamicin levels following 360mg IM of gentamicin stratified by weight. Estimate the best pharmacodynamics criterion (i.e. peak/MIC ratio) for pharyngeal gonorrhea treated with gentamicin using individual and mean peak gentamicin levels and NG isolate MIC. Among treatment failures, conduct exploratory analyses comparing pre- and post-treatment MIC for evidence of induced resistance.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pharyngeal Gonococcal Infection
Keywords
gonorrhea, pharynx, treatment, gentamicin

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
13 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Single Arm
Arm Type
Experimental
Arm Description
Men who have sex with men (MSM) with pharyngeal gonorrhea will be treated with 360mg intramuscular gentamicin x 1.
Intervention Type
Drug
Intervention Name(s)
gentamicin 360mg IM
Intervention Description
360mg IM of gentamicin
Primary Outcome Measure Information:
Title
Cure Rate Defined as the Percentage of Persons With Pharyngeal Gonorrhea Treated With Gentamicin 360mg IM Who Have a Negative Culture 4-7 Days Following Treatment
Description
Negative Pharyngeal Culture
Time Frame
4-7 days (+/- 1 day) after treatment
Secondary Outcome Measure Information:
Title
Renal Safety
Description
Measured by a percent change in serum creatinine from baseline to test of cure (4-7 days following treatment)
Time Frame
4-7 days (+/- 1 day) after treatment
Title
Tolerability of the Injection Gentamicin 360mg IM x 1
Description
Participant reported pain scale, with 1 being little to no pain, and 10 being the worst pain ever.
Time Frame
4-7 days (+/- 1 day) after treatment
Title
Peak Gentamicin Levels
Description
serum gentamicin concentration
Time Frame
at 30, 45, or 60 minutes post dose
Title
Gentamicin Minimal Inhibitory Concentration (MIC)
Description
laboratory defined MIC of infecting strain of N. gonorrhoeae at enrollment visit determined by agar dilution
Time Frame
baseline/enrollment visit
Other Pre-specified Outcome Measures:
Title
Exploratory Study: Look for Evidence of Induced Resistance
Description
Among treatment failures, compare pre-treatment and post-treatment minimal inhibitory concentrations (MIC)
Time Frame
4-7 days (+/- 1 day) after treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Persons diagnosed with pharyngeal gonorrhea who are not yet treated Exclusion Criteria: Age less than 16 years Receipt of antibiotics in ≤30 days Known allergy to any aminoglycoside History of renal disease (including diagnosis of solitary kidney, chronic renal insufficiency, renal cell carcinoma etc), Use of concurrent nephrotoxic drugs or muscle relaxants History of diabetes History of hearing loss or tinnitus Concurrent infection with syphilis or chlamydia Pregnancy and/or nursing Unable to return for a follow-up visit 4-7 days (+/- 1 day). Study team's discretion
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lindley A Barbee, MD, MPH
Organizational Affiliation
University of Washington
Official's Role
Principal Investigator
Facility Information:
Facility Name
Public Health -- Seattle & King County STD Clinic
City
Seattle
State/Province
Washington
ZIP/Postal Code
98104
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
31712813
Citation
Barbee LA, Soge OO, Morgan J, Leclair A, Bass T, Werth BJ, Hughes JP, Golden MR. Gentamicin Alone Is Inadequate to Eradicate Neisseria Gonorrhoeae From the Pharynx. Clin Infect Dis. 2020 Nov 5;71(8):1877-1882. doi: 10.1093/cid/ciz1109.
Results Reference
derived

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Gent for Pharyngeal Gonorrhea (GC)

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