A Randomised, Parallel-group, Open-label Phase II Trial of the Immunological Effects of Three Regimens of GX301 Vaccination in Castration-resistant Prostate Cancer Patients Who Have Achieved Response or Disease Stability With First-line Chemotherapy
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 99
- 试验地点
- 48
- 主要终点
- Incidence of adverse events
研究概览
简要总结
GX301 is an experimental therapeutic vaccine directed against human telomerase, an enzyme playing an essential role in cancer cell proliferation.
This clinical trial will test three different GX301 administration regimens in castration-resistant prostate cancer patients who have achieved response or disease stability with first-line docetaxel treatment. This is aimed at identifying an optimal vaccination regimen.
The three regimens will primarily be compared for their efficacy and safety in inducing vaccine-specific immunological responses over a period of 6 months following treatment initiation. In addition, patients will be observed for the occurrence of disease progression and for their vital status up to 24 months.
详细描述
GX301, an experimental therapeutic (anti-cancer) vaccine, is composed of four immunogenic peptides from human telomerase and two complementary adjuvants, Montanide ISA-51 VG and imiquimod.
An earlier Phase 1 study of GX301 has provided evidence of vaccine-specific immune response in a small sample of stage 4 prostate cancer patients given eight GX301 administrations over 9 weeks.
The present Phase 2, randomised, parallel-group, multicentre trial is aimed at comparing three different GX301 administration regimens in patients with progressive, castration-resistant prostate cancer who have completed a first-line docetaxel treatment and have achieved response to chemotherapy or disease stability. Primary comparisons will include regimen efficacy in inducing vaccine-specific immunological responses over a period of 6 months following randomisation; and treatment safety and tolerability over the same period.
A further study aim is to investigate whether achievement of immunological response, irrespective of the assigned GX301 regimen, is related to progression-free and/or overall survival.
Eligible patients will be randomly assigned to receive one of three GX301 vaccination regimens consisting of two, four or eight administrations, respectively, each regimen being given over a fixed 9-week period. Randomisation ratio will be 1:1:1. Randomisation will be stratified by previous cumulative exposure to docetaxel.
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
- None
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
- •Documented patient history
- •Histologically confirmed diagnosis of prostate cancer, with an available Gleason score.
- •Diagnosis of progressive, castration-resistant prostate cancer (CRPC), leading to inception of first-line chemotherapy with a docetaxel-based regimen.
- •Completion of chemotherapy with a cumulative delivered dose of 300 to 825 mg/m2 docetaxel.
- •Note: Pre-chemotherapy exposure to abiraterone and prednisone does not preclude eligibility, provided that both agents have been discontinued prior to initiation of docetaxel.
- •Current patient status
- •Ability to understand study-related patient information and provision of written informed consent for participation in the study.
- •Eastern Cooperative Oncology Group (ECOG) performance status of 0 or
- •Life expectancy of at least 6 months.
- •An interval ≥4 weeks elapsed from the last docetaxel administration.
- •Documented achievement of response or disease stability with docetaxel chemotherapy.
- •Absence of cancer-related symptoms suggesting clinical disease progression.
- •Current castrate testosterone level (≤50 ng/dL) due to current gonadotropin-releasing hormone (GnRH) agonist or antagonist therapy or past orchiectomy.
- •Haematology and blood chemistry tests within specified limits.
- •Successful recovery from acute toxicities from prior chemotherapy.
- •Confirmation from the immunology laboratory that the blood sample provided for baseline immunological tests is technically adequate.
排除标准
- •Known intolerance to Montanide or imiquimod.
- •Known presence of brain metastatic disease or spinal cord compression.
- •Radiotherapy within the past 4 weeks.
- •Concomitant presence of other primary malignancy
- •Major surgery within 4 weeks prior to randomisation.
- •Cardiovascular illness or complication which, in Investigator's judgment, compromises prognosis at 6 months or prevents the patient from following study procedures.
- •Serious uncontrolled infection.
- •Known presence of active autoimmune disease.
- •Known presence of acquired, hereditary, or congenital immunodeficiency.
- •HIV infection.
- •Current need for immunosuppressive drug therapy, including systemic corticosteroids.
- •Current need for denosumab therapy. (Patients under bisphosphonate treatment are eligible).
- •Skin disease interfering with evaluation of local tolerance of GX301 injections.
- •Participation in any interventional drug or medical device study within 30 days prior to treatment start.
结局指标
主要结局
Incidence of adverse events
时间窗: Up to Day 180
Changes from baseline in laboratory tests for immunological safety
时间窗: Days 63, 90 and 180
Achievement of immunological response
时间窗: Days 90 and 180 following randomisation
次要结局
- Changes from baseline in serum prostate-specific antigen (PSA)(Up to Day 540 or end of observation (if earlier))
- Incidence of adverse events(Up to Day 540 or end of observation (if earlier))
- Changes from baseline in laboratory tests for immunological safety(Up to Day 540 or end of observation (if earlier))
- Progression-free survival(Up to Day 540 or end of observation (if earlier))
- Overall survival(Up to Day 720)