A Study Evaluating Efficacy and Safety of Gepotidacin Compared With Ceftriaxone Plus Azithromycin in the Treatment of Uncomplicated Urogenital Gonorrhea

  • STATUS
    Recruiting
  • End date
    Sep 8, 2023
  • participants needed
    600
  • sponsor
    GlaxoSmithKline
Updated on 3 March 2021
ceftriaxone
azithromycin
gepotidacin
neisseria gonorrhoeae

Summary

This is a phase III, randomized, multicenter, open-label study which will be performed to evaluate efficacy and safety of oral Gepotidacin compared to intramuscular (IM) ceftriaxone plus oral azithromycin for the treatment of uncomplicated urogenital infection caused by Neisseria gonorrhoeae in adolescent and adult subjects. In this study, subjects will be randomly assigned to receive either oral gepotidacin or IM ceftriaxone plus oral azithromycin. Approximately 600 subjects will be randomized to receive study treatment. The duration of the study will be approximately 21 days.

Details
Condition Gonorrhea
Treatment Azithromycin, ceftriaxone, Gepotidacin
Clinical Study IdentifierNCT04010539
SponsorGlaxoSmithKline
Last Modified on3 March 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Is your age greater than or equal to 12 yrs?
Gender: Male or Female
Do you have Gonorrhea?
Do you have any of these conditions: Do you have Gonorrhea??
Do you have any of these conditions: Do you have Gonorrhea??
Do you have any of these conditions: Do you have Gonorrhea??
Do you have any of these conditions: Do you have Gonorrhea??
Do you have any of these conditions: Do you have Gonorrhea??
Do you have any of these conditions: Do you have Gonorrhea??
Do you have any of these conditions: Do you have Gonorrhea??
Do you have any of these conditions: Do you have Gonorrhea??
Do you have any of these conditions: Do you have Gonorrhea??
Subjects must be >=12 years of age at the time of signing the informed consent
Subjects having body weight of >45 kilogram (kg)
Subjects having clinical suspicion of a urogenital gonococcal infection with or without pharyngeal and/or rectal gonococcal infection and have one of the following: a prior positive culture for Neisseria gonorrhoeae from up to 5 days before screening (as long as the subject has not received any treatment for this infection) or a Gram stain (urogenital specimens only) positive or presumptive for Gram-negative intracellular diplococci from up to 5 days before screening (as long as the subject has not received any treatment for this infection) or a prior positive nucleic acid amplification test assay for Neisseria gonorrhoeae from up to 7 days before screening (as long as the subject has not received any treatment for this infection)
Subjects who are willing to avoid anal, oral, and vaginal sexual intercourse or use condoms for all forms of intercourse from the Baseline Visit through the TOC Visit
Male or female subjects having his or her original urogenital anatomy at birth
Male subject must agree to use contraception (male condoms) during intercourse from the Baseline Visit through completion of the TOC Visit
Female subject is eligible to participate if she is not pregnant, not breastfeeding, and at least 1 of the following conditions applies: Not a woman of childbearing potential (WOCBP) or WOCBP who agrees to follow the contraceptive guidance (male partners of WOCBP must use a male condom during intercourse) from the Baseline Visit through completion of the TOC Visit
Subjects who are capable of giving signed informed consent or assent, which includes compliance with the requirements and restrictions listed in the informed consent form (ICF) or assent form and in study protocol

Exclusion Criteria

Male subjects with a current diagnosis of epididymitis and/or orchitis at the time of the Baseline Visit
Subject who is suspected or confirmed to have a Chlamydia trachomatis infection and per the investigator's judgement standard-of-care treatment for this infection cannot be safely postponed until the TOC Visit
Subject has a body mass index >=40 kilogram per square meter (kg/m^2) or has a body mass index >=35.0 kg/m^2 and is experiencing obesity-related health conditions such as high blood pressure or diabetes
Subject has a history of sensitivity to the study treatments, or components thereof, or a history of a drug (including erythromycin and any macrolide or ketolide drug) or other allergy that, in the opinion of the investigator or medical monitor, contraindicates his or her participation
Subject is immunocompromised or has altered immune defenses that may predispose the subject to a higher risk of treatment failure and/or complications. For example, subjects with diabetes, renal transplant recipients, subjects with clinically significant persistent granulocytopenia (absolute neutrophil count <1000 per microliter [L]) and subjects receiving immunosuppressive therapy, including corticosteroid therapy (>40 mg per day prednisolone or equivalent for >1 week, >=20 mg per day prednisolone or equivalent for >2 weeks, or prednisolone or equivalent >=10 mg per day for >6 weeks). Subjects with a known cluster of differentiation 4 (CD4) count of <200 cells per cubic millimeter (cells/mm^3) should not be enrolled
Subject has a medical condition that requires medication that may be impacted by inhibition of acetylcholinesterase, such as, poorly controlled asthma or chronic obstructive pulmonary disease at the Baseline Visit and, in the opinion of the investigator, not stable on current therapy, acute severe pain, uncontrolled with conventional medical management, active peptic ulcer disease, Parkinson disease, Myasthenia gravis, a history of seizure disorder requiring medications for control (this does not include a history of childhood febrile seizures) or subject has any surgical or medical condition (active or chronic) that may interfere with drug absorption, distribution, metabolism, or excretion of the study treatment (For example., ileostomy or malabsorption syndrome)
Subject has known anuria, oliguria, or severe impairment of renal function (creatinine clearance <30 milliliter per minute [mL/min] or clinically significant elevated serum creatinine as determined by the investigator)
Subject in the judgment of the investigator, would not be able or willing to comply with the protocol or complete study follow-up
Subject has a serious underlying disease that could be imminently life threatening, or the subject is unlikely to survive for the duration of the study period
Subject has congenital long QT syndrome or known prolongation of corrected QT interval (QTc)
Subject has uncompensated heart failure
Subject has severe left ventricular hypertrophy
Subject has a family history of QT prolongation or sudden death
Subject has a recent history of vasovagal syncope or episodes of symptomatic bradycardia or bradyarrhythmia within the last 12 months
With the exception of azithromycin study treatment, the subject is taking QT-prolonging drugs or drugs known to increase the risk of torsades de pointes (TdP) per the [www.crediblemeds.org](http://www.crediblemeds.org/) "Known Risk of TdP" category at the time of his or her Baseline Visit, which cannot be safely discontinued from the Baseline Visit to the TOC Visit; or the subject is taking a strong cytochrome P450 enzyme 3A4 (CYP3A4) inhibitor or a strong P-glycoprotein (P-gp) inhibitor
For any subject >=12 to <18 years, the subject has an abnormal electrocardiogram (ECG) reading
The subject has a QTc >450 millisecond (msec) or a QTc >480 msec for subjects with bundle-branch block
Subject has a documented or recent history of uncorrected hypokalemia within the past 3 months
Subject has a known history of cholestatic jaundice or hepatic dysfunction associated with prior use of azithromycin
Subject has a known alanine aminotransferase (ALT) value >2 times upper limit of normal (ULN)
Subject has a known bilirubin value >1.5 times ULN (isolated bilirubin >1.5 times ULN is acceptable if bilirubin is fractionated and direct bilirubin <35%)
Subject has a current or chronic history of liver disease, or known hepatic or biliary abnormalities (with the exception of Gilbert's syndrome or asymptomatic gallstones), including symptomatic viral hepatitis or moderate-to-severe liver insufficiency (Child Pugh class B or C)
Subject has been previously enrolled in this study or has previously been treated with Gepotidacin
Subject has participated in a clinical trial and has received an investigational product within 30 days or 5 half-lives, whichever is longer
Subject has any of the following gonococcal infections that require a different dose or duration of treatment: suspected or confirmed pelvic inflammatory disease or suspected or confirmed gonococcal arthritis or suspected or confirmed gonococcal conjunctivitis or suspected or confirmed gonococcal endocarditis or other evidence of disseminated gonococcal infection
Subject has received any antibacterial therapy for the treatment of a gonococcal infection within 14 days before the Baseline Visit
Subject has received any systemic, topical, or intravaginal antibiotics or any systemic antifungals within 7 days before the Baseline Visit
Subject must not use St John's wort or ergot derivatives from within 14 days before the Baseline Visit through the TOC Visit
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