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Study to Evaluate the Effect of a Single Oral Dose of Zoliflodacin 3 g on Testicular Function in Healthy Adult Men

A Randomized, Double-blind, Placebo-controlled Study to Evaluate the Effect of a Single Oral Dose of Zoliflodacin 3 g on Testicular Function in Healthy Adult Men

This study is a randomized, double-blind, placebo-controlled clinical trial to evaluate the effect of zoliflodacin on testicular function in healthy adult men. Participants will be screened within 21 days before randomization (Day 1), including collection of 2 semen samples (each collected after a ≥48 hours and ≤7 days ejaculation-free period). Approximately 220 participants who provide written informed consent and meet all inclusion and no exclusion criteria will be enrolled and randomized in a 1:1 fashion to receive a single dose of either zoliflodacin 3 g or placebo administered as an oral suspension on Day 1.

Each participant will be contacted by telephone at Week 1 and at Week 7 post dosing to review adverse events (AEs), concomitant medications and procedures, and genitourinary symptoms.

Each participant will return to the trial site at Week 13 for collection of 2 semen samples (each collected after a ≥48 hours and ≤7 days ejaculation-free period). A serum sample will also be collected for hormone testing (luteinizing hormone [LH], follicle-stimulating hormone [FSH], and total testosterone) at Week 13 to support biological interpretation of any decrease in sperm concentration.

Participants who do not have a ≥50% decrease from baseline in sperm concentration at Week 13 will complete the trial at Week 13 (end of trial). Participants with a ≥50% decrease from baseline in sperm concentration at Week 13 will return to the trial site at Week 26 for collection of 2 semen samples (independent ejaculates, each collected after a ≥48 hours and ≤7 days ejaculation-free period) for evaluation of the reversibility of the Week 13 finding, following completion of a one additional spermatogenic cycle post completion of dosing/drug exposure (FDA 2018) (end of trial).

All Adverse Events, medications, and procedures will be recorded from the signing of the informed consent form (ICF) through the end-of-trial visit (Week 13, Week 26, or Early Termination)

研究概览

地位

尚未招聘

条件

研究类型

介入性

注册 (估计的)

200

阶段

  • 第四阶段

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

  • 姓名:Jovana Albig, MD
  • 电话号码:+41 22 555 19 90
  • 邮箱:info@gardp.org

学习地点

      • Berlin、德国
        • Parexel EPCU
      • London、英国
        • Parexel EPCU

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人

接受健康志愿者

是的

描述

Inclusion Criteria:

  1. Man with good general health status, as determined by medical history, physical examination, screening laboratory tests, vital signs (including temperature), and clinical judgment
  2. Age 18 to 45 years at informed consent
  3. Weight ≥35 kg at Screening
  4. Laboratory results at Screening, including FSH, LH, and total testosterone, within laboratory reference ranges
  5. Semen parameters for each semen sample collected during Screening meeting the following criteria (WHO 2021):

    • sperm concentration ≥16 million/mL
    • semen volume ≥1.4 mL
    • total sperm per ejaculate ≥39 million
    • progressive motility ≥ 30%
    • sperm morphology : normal forms ≥4%
  6. Willingness to use a highly effective form of contraception with female sexual partners of reproductive potential for 3 months after the last study drug dose
  7. Provision of written informed consent
  8. Willingness to participate and comply with all aspects of the trial through the entire trial period

Exclusion Criteria:

  1. History of male reproductive health issues including, but not limited to, known hypothalamic-pituitary disorders (e.g., pituitary macroadenomas, pituitary infarction, hyperprolactinemia, panhypopituitarism), primary hypogonadism (e.g., cryptorchidism, Klinefelter's syndrome), Grade III varicocele, testicular torsion, orchitis, unilateral orchiectomy, or prostate gland pathology
  2. Prior diagnosis of male impaired fertility (including reduced fertility)
  3. History of antisperm antibodies
  4. History of radiation to the testicles
  5. History of clinically significant trauma to or surgery on the scrotum or testicles, including vasectomy
  6. Known hypersensitivity to zoliflodacin or formulation excipients
  7. Disorders of sperm transport including, but not limited to, retrograde ejaculation and immotile cilia syndrome
  8. Sexual dysfunction of a nature that would prevent sperm collection in accordance with the protocol requirements (phosphodiesterase inhibitor use is permitted)
  9. Uncontrolled thyroid dysfunction (e.g., untreated hypothyroidism or hyperthyroidism)
  10. Any chronic medical or psychiatric condition that, in the opinion of the investigator, may harm the participant or make the participant unsuitable for the trial or would prevent compliance with the trial protocol procedures
  11. History of major surgery or trauma within 4 weeks before Day 1 or anticipated need for major surgery during the trial
  12. Febrile illness within 4 weeks before Screening
  13. Clinically significant urinary tract infection, prostatitis, epididymitis, or STI diagnosed or treated within 4 weeks before Screening
  14. Genitourinary sign or symptom indicative of a current STI (urethral discharge, dysuria, or genital lesion) at Screening or Day 1
  15. Positive nucleic acid amplification test (NAAT) result for N gonorrhoeae at Screening
  16. Positive serologic test for HIV-1 or HIV-2 antibody, hepatitis B surface antigen, or hepatitis C antibody or for any other pathogen tested according to the trial site standards for blood and semen handling
  17. Use within 13 weeks before Screening of or anticipated need during the trial for a medication known to affect spermatogenesis or reproductive hormone regulation including, but not limited to, the following medications:

    • testosterone
    • gonadotropin analogues
    • anabolic steroids
    • antiandrogens (e.g., spironolactone, finasteride, dutasteride, ketoconazole)
    • 5-α reductase inhibitors
    • α-1 blockers
    • chemotherapeutic agents
    • chronic (≥90 days) use of opioids
    • other hormone-modulating medications
  18. Use within 14 days before Day 1 of a moderate or strong cytochrome P450 isoenzyme 3A4 (CYP3A4) inducer (e.g., rifampin, carbamazepine, phenytoin, St. John's Wort) or anticipated need for moderate or strong CYP3A4 inducers from Day 1 to Day 3
  19. Current tobacco use of ≥1 pack/day or equivalent
  20. Current alcohol use >5 units per week
  21. Known or suspected drug abuse
  22. A positive drug or alcohol screen result at Screening or Day 1 visit
  23. Participation in an interventional clinical study within 30 days or 5 half-lives of the study drug, whichever is longer, before Day 1 -

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:放映
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:四人间

武器和干预

参与者组/臂
干预/治疗
安慰剂比较:安慰剂
Oral suspension of matching placebo
实验性的:Zoliflodacin
Oral suspension of Zoliflodacin 3g

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Sperm concentration
大体时间:Week 13 (and potentially week 26)
Percentage of participants with a ≥50% decrease from baseline in sperm concentration (million/mL) at Week 13
Week 13 (and potentially week 26)

次要结果测量

结果测量
措施说明
大体时间
Semen Volume
大体时间:At baseline and week 13
Change in semen volume (in mL)
At baseline and week 13
Sperm count
大体时间:At Baseline and week 13
Total sperm count per ejaculate (million)
At Baseline and week 13
Progressive mobility
大体时间:At Baseline and Week 13
Sperm exhibiting active forward movement (μm/s)
At Baseline and Week 13
Morphology
大体时间:At baseline and week 13
Evaluated using Tygerberg Strict Criteria (%)
At baseline and week 13
Serum Hormones (LH)
大体时间:At Baseline and Week 13
Change in luteinizing hormone (LH), shift analysis relative to reference ranges
At Baseline and Week 13
Serum hormones (FSH)
大体时间:At Baseline and Week 13
Change in Follicle Stimulating Hormone (FSH), shift analysis relative to reference ranges
At Baseline and Week 13
Serum Hormones (Testosterone)
大体时间:At baseline and week 13
Change in Testosterone, shift analysis relative to reference ranges
At baseline and week 13

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年10月1日

初级完成 (估计的)

2027年11月1日

研究完成 (估计的)

2027年11月1日

研究注册日期

首次提交

2026年6月1日

首先提交符合 QC 标准的

2026年6月5日

首次发布 (实际的)

2026年6月10日

研究记录更新

最后更新发布 (实际的)

2026年6月10日

上次提交的符合 QC 标准的更新

2026年6月5日

最后验证

2026年6月1日

更多信息

与本研究相关的术语

其他相关的 MeSH 术语

其他研究编号

  • STI_PMR_Zoli007

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

未定

药物和器械信息、研究文件

研究美国 FDA 监管的药品

是的

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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