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临床试验/NCT04983940
NCT04983940已完成4 期

Patient Satisfaction After Switching to Oral Testosterone Undecanoate in Men Currently on Testosterone Therapy

University of Miami1 个研究点 分布在 1 个国家目标入组 41 人开始时间: 2021年6月18日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
41
试验地点
1
主要终点
Hypogonadal Symptoms as Measured by qADAM Questionnaire

研究概览

简要总结

The purpose of this research study is to evaluate patient satisfaction with an oral testosterone agent, Jatenzo, compared to other forms of testosterone therapy.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • Voluntarily sign and date the study consent form(s) which have been approved by an Institutional Review Board (IRB). Written consent must be obtained prior to the initiation of any study procedures.
  • Males between 18 and 65 years of age.
  • Documented diagnosis of testosterone deficiency.
  • Prior treatment with testosterone therapy at the time of enrollment with adequate control of low testosterone symptoms. Serum total testosterone < 300 ng/dL on 2 measurements prior to the initiation of testosterone therapy. Patients must have completed an adequate washout period following prior testosterone therapy (4 weeks for gels and injection based therapies and 16 weeks for subcutaneous pellets).
  • Judged to be in good general health as determined by the principal investigator based upon the results of a medical history, physical examination, vital signs, laboratory profile and a 12-lead electrocardiogram (ECG).

排除标准

  • History of significant sensitivity or allergy to androgens or product excipients.
  • Clinically significant findings in the pre-study examinations including abnormal breast examination requiring follow-up or abnormal ECG.
  • Abnormal prostate digital rectal examination (DRE) with palpable nodule(s) or International Prostate Symptom Score (I-PSS) score > 19 points.
  • Body mass index (BMI) ≥ 40 kg/m
  • Clinically significant abnormal laboratory value, in the opinion of the investigator, in serum chemistry, hematology, or urinalysis including but not limited to:
  • Baseline hemoglobin > 16 g/dL
  • Hematocrit < 35% or > 50%
  • Poorly controlled blood pressure as defined by Systolic Blood Pressure (SBP) >150 or Diastolic Blood Pressure (DBP) > 90 on two separate measurements
  • Concurrent use of any prohibited medications that can affect testosterone levels or metabolism.
  • History of seizures or convulsions, including febrile, alcohol or drug withdrawal seizures.
  • History of any clinically significant illness, infection, or surgical procedure within 4 weeks prior to study drug administration.
  • History of stroke or myocardial infarction within the past 5 years.
  • History of, or current or suspected, prostate or breast cancer.
  • History of, or current or suspected, pituitary abnormality.
  • History of diagnosed, severe, untreated, obstructive sleep apnea.
  • History of abuse of alcohol or any drug substance in the opinion of the investigator within the previous 2 years.
  • Receipt of any investigational product within 4 weeks or within 5 half-lives prior to the start of treatment.
  • Inability to understand and provide written informed consent for the study.
  • Considered by the investigator or the sponsor-designated physician, for any reason, that the subject is an unsuitable candidate to receive Jatenzo

研究组 & 干预措施

Jatenzo Arm

Experimental

Participants in this group will receive Jatenzo for 26 consecutive weeks.

干预措施: Jatenzo (Drug)

结局指标

主要结局

Hypogonadal Symptoms as Measured by qADAM Questionnaire

时间窗: Up to 6 months

Quantitative Androgen Deficiency in the Aging Male (qADAM) has a total score ranges between 10 (most symptomatic) and 50 (least symptomatic).

Patient Satisfaction as Measured by TSQM-9 (Global Satisfaction Domain)

时间窗: Up to 6 months

Treatment Satisfaction Questionnaire for Medication (TSQM-9) has three domains (Global, Convenience, and Effectiveness), each with a total score ranging from 0 to 100 with the higher score indicating higher patient satisfaction.

次要结局

  • Serum Testosterone Levels(Up to 6 months)
  • Serum Estradiol Levels(Up to 6 months)
  • Hematocrit Levels(Up to 6 months)
  • PSA Levels Measured in ng/mL(Up to 6 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Ranjith Ramasamy, MD

Associate Professor

University of Miami

研究点 (1)

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