Linezolid for Syphilis Pilot Study
Primary Purpose
Syphilis
Status
Not yet recruiting
Phase
Early Phase 1
Locations
Study Type
Interventional
Intervention
Group C, Linezolid 5
Group B, Linezolid 10d
Group A, Penicillin
Sponsored by
About this trial
This is an interventional treatment trial for Syphilis focused on measuring Linezolid, Treponema pallidum, Penicillin, Early Syphilis
Eligibility Criteria
Inclusion Criteria:
- 16 years of age or older
- Diagnosed cases of primary, secondary, or early latent syphilis with RPR titer ≥1:8 within 3 weeks prior to enrollment
- Able to provide informed consent
- For PLHIV: on treatment for HIV-infection and most recent viral load <200 copies/mL or most recent CD4 T-cell count >350 cells/mL
Exclusion Criteria:
- Pregnancy or a positive pregnancy test on the day of enrollment
- Participants who receive certain psychotropic medications, e.g., MAO inhibitors, SNRIs, SSRIs
- Patients showing signs and symptoms of neurosyphilis
- Serofast RPR titer
- Recent (<7 days) or concomitant antimicrobial therapy with azithromycin, doxycycline, ceftriaxone, cefixime, or other beta lactam antibiotics (e.g. amoxicillin)
- Linezolid or penicillin allergy
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
Active Comparator
Arm Label
Linezolid 5 Day
Linezolid 10 Day
Benzathine Penicillin G
Arm Description
Oral Linezolid 600mg, taken twice a day for 5 days
Oral linezolid 600mg, taken twice a day for 10 days
Single intramuscular injection of 2.4 million units of benzathine penicillin G
Outcomes
Primary Outcome Measures
Response to Treatment
Percentage of linezolid participants with a 4-fold decrease or greater in the serum RPR titer by 180 days after treatment
Secondary Outcome Measures
Treponema pallidum susceptibility
Determine the Minimum Inhibitory Concentration (MIC) and Minimum Bactericidal Concentration (MBC) of linezolid against 6 historical and 3 clinical isolated strains
Full Information
NCT ID
NCT05548426
First Posted
September 16, 2022
Last Updated
October 25, 2022
Sponsor
University of Southern California
Collaborators
Universidad Peruana Cayetano Heredia, The University of Texas Health Science Center, Houston
1. Study Identification
Unique Protocol Identification Number
NCT05548426
Brief Title
Linezolid for Syphilis Pilot Study
Official Title
Pilot Study of Linezolid for Early Syphilis Treatment
Study Type
Interventional
2. Study Status
Record Verification Date
October 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
April 2023 (Anticipated)
Primary Completion Date
March 2025 (Anticipated)
Study Completion Date
March 2025 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Southern California
Collaborators
Universidad Peruana Cayetano Heredia, The University of Texas Health Science Center, Houston
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
Yes
5. Study Description
Brief Summary
The two specific aims are: AIM 1: To evaluate the efficacy of linezolid compared to benzathine penicillin G in the treatment of syphilis. AIM 2: Evaluate the susceptibility of Treponema pallidum historical and novel strains to linezolid.
Detailed Description
This will be a randomized, open-label, non-comparative, adaptive pilot trial to evaluate the efficacy of two linezolid oral dosing schemes (600mg orally, twice a day, for five or ten days) compared to the current recommendation for the treatment of syphilis, benzathine penicillin G (single dose of 2.4 million units) in participants with and without HIV infection. In total, 60 participants will be enrolled across 2 clinical sites in Peru. Participants will participate in follow-ups to monitor clinical outcomes and serological response (RPR titer) at 1 month, 3 months, and 6 months. The investigators will also test linezolid against several types of syphilis strains in the lab to evaluate the microbicidal activity of linezolid in treating early syphilis. Study findings may identify an efficacious alternative syphilis treatment to penicillin that is effective for people living with HIV. Study findings may also help address the crisis of penicillin shortages, difficulty in administration, and offer options for those with penicillin allergy.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Syphilis
Keywords
Linezolid, Treponema pallidum, Penicillin, Early Syphilis
7. Study Design
Primary Purpose
Treatment
Study Phase
Early Phase 1
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Linezolid 5 Day
Arm Type
Experimental
Arm Description
Oral Linezolid 600mg, taken twice a day for 5 days
Arm Title
Linezolid 10 Day
Arm Type
Experimental
Arm Description
Oral linezolid 600mg, taken twice a day for 10 days
Arm Title
Benzathine Penicillin G
Arm Type
Active Comparator
Arm Description
Single intramuscular injection of 2.4 million units of benzathine penicillin G
Intervention Type
Drug
Intervention Name(s)
Group C, Linezolid 5
Intervention Description
Oral Linezolid 600mg, taken twice a day for 5 days
Intervention Type
Drug
Intervention Name(s)
Group B, Linezolid 10d
Intervention Description
Oral Linezolid 600mg, taken twice a day for 10 days
Intervention Type
Drug
Intervention Name(s)
Group A, Penicillin
Intervention Description
Standard of care benzathine penicillin G, one intramuscular injection, 2.4MU
Primary Outcome Measure Information:
Title
Response to Treatment
Description
Percentage of linezolid participants with a 4-fold decrease or greater in the serum RPR titer by 180 days after treatment
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Treponema pallidum susceptibility
Description
Determine the Minimum Inhibitory Concentration (MIC) and Minimum Bactericidal Concentration (MBC) of linezolid against 6 historical and 3 clinical isolated strains
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
16 years of age or older
Diagnosed cases of primary, secondary, or early latent syphilis with RPR titer ≥1:8 within 3 weeks prior to enrollment
Able to provide informed consent
For PLHIV: on treatment for HIV-infection and most recent viral load <200 copies/mL or most recent CD4 T-cell count >350 cells/mL
Exclusion Criteria:
Pregnancy or a positive pregnancy test on the day of enrollment
Participants who receive certain psychotropic medications, e.g., MAO inhibitors, SNRIs, SSRIs
Patients showing signs and symptoms of neurosyphilis
Serofast RPR titer
Recent (<7 days) or concomitant antimicrobial therapy with azithromycin, doxycycline, ceftriaxone, cefixime, or other beta lactam antibiotics (e.g. amoxicillin)
Linezolid or penicillin allergy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jeffrey D Klausner, MD MPH
Phone
(415) 876-8901
Email
jdklausner@med.usc.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jeffrey D Klausner, MD MPH
Organizational Affiliation
University of Southern California
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
No IPD will be shared with other researchers
Learn more about this trial
Linezolid for Syphilis Pilot Study
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