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
研究类型
注册 (估计的)
阶段
- 第四阶段
联系人和位置
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
参与标准
资格标准
适合学习的年龄
- 成人
接受健康志愿者
描述
Inclusion Criteria:
- Man with good general health status, as determined by medical history, physical examination, screening laboratory tests, vital signs (including temperature), and clinical judgment
- Age 18 to 45 years at informed consent
- Weight ≥35 kg at Screening
- Laboratory results at Screening, including FSH, LH, and total testosterone, within laboratory reference ranges
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%
- 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
- Provision of written informed consent
- Willingness to participate and comply with all aspects of the trial through the entire trial period
Exclusion Criteria:
- 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
- Prior diagnosis of male impaired fertility (including reduced fertility)
- History of antisperm antibodies
- History of radiation to the testicles
- History of clinically significant trauma to or surgery on the scrotum or testicles, including vasectomy
- Known hypersensitivity to zoliflodacin or formulation excipients
- Disorders of sperm transport including, but not limited to, retrograde ejaculation and immotile cilia syndrome
- Sexual dysfunction of a nature that would prevent sperm collection in accordance with the protocol requirements (phosphodiesterase inhibitor use is permitted)
- Uncontrolled thyroid dysfunction (e.g., untreated hypothyroidism or hyperthyroidism)
- 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
- History of major surgery or trauma within 4 weeks before Day 1 or anticipated need for major surgery during the trial
- Febrile illness within 4 weeks before Screening
- Clinically significant urinary tract infection, prostatitis, epididymitis, or STI diagnosed or treated within 4 weeks before Screening
- Genitourinary sign or symptom indicative of a current STI (urethral discharge, dysuria, or genital lesion) at Screening or Day 1
- Positive nucleic acid amplification test (NAAT) result for N gonorrhoeae at Screening
- 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
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
- 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
- Current tobacco use of ≥1 pack/day or equivalent
- Current alcohol use >5 units per week
- Known or suspected drug abuse
- A positive drug or alcohol screen result at Screening or Day 1 visit
- 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
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
出版物和有用的链接
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
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