A Phase Ib Study of Extending Relugolix Dosing Intervals Through Addition of the CYP3A4 and Pg-P Inhibitor Itraconazole or Ritonavir in Prostate Cancer Patients
试验速览
- 阶段
- 1 期
- 状态
- 招募中
- 入组人数
- 100
- 试验地点
- 1
- 主要终点
- Testosterone Suppression of Participants as Assessed by Testosterone Levels
研究概览
简要总结
Researchers leading this study hope to learn about the safety of combining the study drug relugolix with another study drug called itraconazole or ritonavir in prostate cancer. This study is for individuals who have advanced prostate cancer and plans to have medical castration (the use of medications or chemicals to lower hormone production in the testicles). Your participation in this research will last up to 1 month.
The purpose of this research is to gather information on the safety and effectiveness of relugolix in combination with ritonavir or itraconazole. The goal of this research is to find out if combining two medications (relugolix and itraconazole or relugolix and ritonavir) could possibly lead to using less relugolix, which is an expensive drug.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Single (Participant)
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- Male
- 接受健康志愿者
- 否
入选标准
- •Must have histologically or cytologically confirmed prostate cancer with plans to start medical castration therapy.
- •Age 18 or older. Because no dosing or adverse event data are currently available on the use of relugolix in combination with itraconazole or ritonavir in patients <18 years of age, children are excluded from this study.
- •Eastern Cooperative Oncology Group performance status ≤2 (Karnofsky ≥60%)
- •Participants must satisfy the following laboratory criteria:
- •Testosterone > 200 ng/dl
- •QTc within normal limits
- •Aspartate Transferase (AST)/alanine transaminase (ALT) < 3x upper limit of normal
- •Ability to take oral medication and be willing to adhere to the medication regimen.
- •Ability to understand and the willingness to sign a written informed consent document.
排除标准
- •Need for combination systemic therapy for prostate cancer including docetaxel and/or second-generation androgen receptor pathway targeted agents (i.e. abiraterone, enzalutamide, apalutamide, darolutamide, etc).
- •Concurrent therapy with strong interacting drugs with CYP3A4 and P-gp (See Appendix list of strong inhibitors or inducers) due to concerning possible drug-drug interactions with itraconazole, ritonavir and relugolix. Potential drug-drug interactions will also be reviewed by study investigators prior to enrollment.
- •History of allergic reactions attributed to compounds of similar chemical or biologic composition to relugolix, itraconazole or ritonavir.
- •Patients receiving treatment with another investigational drug or other intervention within 3 expected half-lives of the agent.
- •Serious or uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, unstable angina pectoris, or psychiatric illness/social situations that would limit compliance with study requirements.
- •New York Heart Association Class III of IV congestive heart failure
- •Known gastrointestinal malabsorption.
- •Active psychiatric illness/social situations that would limit compliance with protocol requirements.
研究组 & 干预措施
Study Group 1
All study participants will receive a starting dose of relugolix (360 mg in the form of three 120 mg tablets) on Day 1 of the 29-day drug administration period. After Day 1, you will receive relugolix on its own or relugolix combined with another medication called itraconazole or ritonavir. The combination of medications you receive, the dosage for each medication, and when you take each medication will be based on the study group you are enrolled in.
Study Group 1 will receive:
- Relugolix (360 mg) on Day 1
- Relugolix (120 mg) on Days 2-7
干预措施: Relugolix Pill (Drug)
Study Group 2a
All study participants will receive a starting dose of relugolix (360 mg in the form of three 120 mg tablets) on Day 1 of the 29-day drug administration period. After Day 1, you will receive relugolix on its own or relugolix combined with another medication called itraconazole or ritonavir. The combination of medications you receive, the dosage for each medication, and when you take each medication will be based on the study group you are enrolled in.
Study Group 2a will receive:
- Relugolix (360 mg) on Day 1
- Relugolix (120 mg) on Days 2-7
- Itraconazole (200 mg) on Days 1-14
干预措施: Relugolix Pill (Drug)
Study Group 2a
All study participants will receive a starting dose of relugolix (360 mg in the form of three 120 mg tablets) on Day 1 of the 29-day drug administration period. After Day 1, you will receive relugolix on its own or relugolix combined with another medication called itraconazole or ritonavir. The combination of medications you receive, the dosage for each medication, and when you take each medication will be based on the study group you are enrolled in.
Study Group 2a will receive:
- Relugolix (360 mg) on Day 1
- Relugolix (120 mg) on Days 2-7
- Itraconazole (200 mg) on Days 1-14
干预措施: Itraconazole (Drug)
Study Group 2b
All study participants will receive a starting dose of relugolix (360 mg in the form of three 120 mg tablets) on Day 1 of the 29-day drug administration period. After Day 1, you will receive relugolix on its own or relugolix combined with another medication called itraconazole or ritonavir. The combination of medications you receive, the dosage for each medication, and when you take each medication will be based on the study group you are enrolled in.
Study Group 2b will receive:
- Relugolix (360 mg) on Day 1
- Relugolix (120 mg) on Days 2-7
- Ritonavir (100 mg tablets taken by mouth) on Days 1-14
干预措施: Relugolix Pill (Drug)
Study Group 2b
All study participants will receive a starting dose of relugolix (360 mg in the form of three 120 mg tablets) on Day 1 of the 29-day drug administration period. After Day 1, you will receive relugolix on its own or relugolix combined with another medication called itraconazole or ritonavir. The combination of medications you receive, the dosage for each medication, and when you take each medication will be based on the study group you are enrolled in.
Study Group 2b will receive:
- Relugolix (360 mg) on Day 1
- Relugolix (120 mg) on Days 2-7
- Ritonavir (100 mg tablets taken by mouth) on Days 1-14
干预措施: Ritonavir (Drug)
Study Group 3a
All study participants will receive a starting dose of relugolix (360 mg in the form of three 120 mg tablets) on Day 1 of the 29-day drug administration period. After Day 1, you will receive relugolix on its own or relugolix combined with another medication called itraconazole or ritonavir. The combination of medications you receive, the dosage for each medication, and when you take each medication will be based on the study group you are enrolled in.
Study Group 3a will receive:
- Relugolix (360 mg) on Day 1
- Relugolix (120 mg) on Days 2-4
- Itraconazole (200 mg tablets taken by mouth) on Days 1-14
干预措施: Relugolix Pill (Drug)
Study Group 3a
All study participants will receive a starting dose of relugolix (360 mg in the form of three 120 mg tablets) on Day 1 of the 29-day drug administration period. After Day 1, you will receive relugolix on its own or relugolix combined with another medication called itraconazole or ritonavir. The combination of medications you receive, the dosage for each medication, and when you take each medication will be based on the study group you are enrolled in.
Study Group 3a will receive:
- Relugolix (360 mg) on Day 1
- Relugolix (120 mg) on Days 2-4
- Itraconazole (200 mg tablets taken by mouth) on Days 1-14
干预措施: Itraconazole (Drug)
Study Group 3b
All study participants will receive a starting dose of relugolix (360 mg in the form of three 120 mg tablets) on Day 1 of the 29-day drug administration period. After Day 1, you will receive relugolix on its own or relugolix combined with another medication called itraconazole or ritonavir. The combination of medications you receive, the dosage for each medication, and when you take each medication will be based on the study group you are enrolled in.
Study Group 3b will receive:
- Relugolix (360 mg) on Day 1
- Relugolix (120 mg) on Days 2-4
- Ritonavir (100 mg) on Days 1-14
干预措施: Relugolix Pill (Drug)
Study Group 3b
All study participants will receive a starting dose of relugolix (360 mg in the form of three 120 mg tablets) on Day 1 of the 29-day drug administration period. After Day 1, you will receive relugolix on its own or relugolix combined with another medication called itraconazole or ritonavir. The combination of medications you receive, the dosage for each medication, and when you take each medication will be based on the study group you are enrolled in.
Study Group 3b will receive:
- Relugolix (360 mg) on Day 1
- Relugolix (120 mg) on Days 2-4
- Ritonavir (100 mg) on Days 1-14
干预措施: Ritonavir (Drug)
结局指标
主要结局
Testosterone Suppression of Participants as Assessed by Testosterone Levels
时间窗: 1 month post start of treatment
To determine whether the addition of itraconazole and ritonavir to relugolix sustains testosterone suppression as assessed by participant testosterone levels.
次要结局
- Decrease in Relugolix Levels(1 month post start of treatment)
- Reduction in Prostate-Specific Antigens Levels of Participants After Study Treatment(1 month post start of treatment)
- Rate of Reported Adverse Events Among Participants(1 month post start of treatment)