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A Study to Evaluate the Efficacy and Safety of LY06006 in Postmenopausal Women With Osteoporosis at High Risk for Fracture

2021年9月17日 更新者:Luye Pharma Group Ltd.

A Randomized, Double-blind, Placebo-controlled, Parallel-group, Multicenter Study to Evaluate the Efficacy and Safety of LY06006 in Postmenopausal Women With Osteoporosis at High Risk for Fracture

A multicenter, randomized, double-blind, placebo-controlled phase III clinical study will be conducted to evaluate the efficacy and safety of LY06006 in the treatment of postmenopausal women with osteoporosis at high risk for fracture, as well as an exploratory population pharmacokinetic analysis of LY06006.

研究概览

地位

招聘中

干预/治疗

详细说明

It is a multicenter, randomized, double-blind, placebo-controlled phase III clinical trial.

Primary Objective:

To evaluate the efficacy of LY06006 in the treatment of postmenopausal women with osteoporosis at high risk for fracture.

Secondary Objectives:

To evaluate the safety of LY06006. To evaluate the immunogenicity of LY06006. Population pharmacokinetic analysis of LY06006.

研究类型

介入性

注册 (预期的)

448

阶段

  • 第三阶段

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

研究联系人备份

学习地点

    • Shanghai
      • Shanghai、Shanghai、中国、200233
        • 招聘中
        • Shanghai Sixth People's Hospital
        • 接触:
        • 首席研究员:
          • Zhenlin Zhang, doctor
        • 副研究员:
          • Jiemei Gu, doctor

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

50年 至 85年 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

女性

描述

Inclusion Criteria:

  1. Postmenopausal woman, ages ≥50 to ≤85 years.≥3 years postmenopausal, which can be≥3 years of spontaneous amenorrhea or ≥3 years post-surgical bilateral oophorectomy. If < 60 years of age and had hysterectomy but ovarian retention, require follicle stimulating hormone (FSH) levels ≥40U/L.

    Exclusion Criteria:

  2. Low BMD (BMD absolute value consistent with a T-score≤-2.5 and >-4.0 at either the lumbar spine or total hip). The BMD equivalents by T-score thresholds for each DXA scanner manufacturer are provided below.
  3. Have at least one of the following risk factors:

    1. history of fragility fracture
    2. parental history of hip fracture
    3. low body weight (BMI≤19kg/m2)
    4. elderly (age≥65y)
    5. current smoker
  4. Voluntarily signed written informed consent

Exclusion criteria

  1. Bone/metabolic disease:

    1. Any metabolic bone disease, e.g., osteomalacia or osteogenesis imperfecta,
    2. Paget's disease
    3. Cushing's disease
    4. Hyperprolactinemia
    5. Hypopituitarism
    6. Acromegaly
    7. Current hyperparathyroidism or hypoparathyroidism by medical record.
    8. Current hyperthyroidism or hypothyroidism (allowed if having normal hormone level on thyroid hormone replacement therapy or 5.5μIU/mL<thyroid-stimulating hormone (TSH) level≤10.0μIU/mL, but the serum thyroxine (T4) is within the normal range.
    9. Malabsorption syndrome or any gastrointestinal disorders associated with malabsorption, for example Crohn's Disease and chronic pancreatitis.
    10. Hypocalcemia or hypercalcemia, or serum albumin corrected blood calcium level is not within the normal range of the laboratory;
    11. Vitamin D deficiency: 25 hydroxy vitamin D (25OHD) level <20 ng/mL. (allowed 200,000 units of vitamin D2 injection (trade name: Futai®) once during the screening period, and re-test the 25OHD level once. Those with 25OHD level ≥20 ng/mL can be included
    12. Others such as rheumatoid arthritis, gout, multiple myeloma and so on.
  2. Subjects with a history of greater than 2 vertebral fractures.
  3. Malignancy within the 5 years before enrollment (except fully resected cutaneous basal cell or squamous cell carcinoma, cervical or breast ductal carcinoma in situ).
  4. Severe renal disease, creatinine clearance <30mL/min
  5. Liver or biliary diseases:

    1. Cirrhosis of the liver;
    2. Biliary tract abnormalities (except asymptomatic gallstones);
    3. Positive Hepatitis C virus (HCV) antibody;
    4. Positive hepatitis B surface antigen (HBsAg) test with the peripheral blood hepatitis B virus deoxyribonucleic acid (HBV DNA) titer test ≥1×103 copies/mL (if positive HBsAg with the peripheral blood HBV DNA titer test <1× 103 copies/mL, the subject is eligible for selection if the investigator believes that the subject is in a stable phase of chronic hepatitis B and will not increase the risk of the subject,;
    5. Alkaline phosphatase <lower limit of normal (LLN); alkaline phosphatase or total bilirubin ≥ 1.5 times the upper limit of normal (ULN); serum aspartate aminotransferase (AST) ≥ 2.0×ULN; serum alanine Acid aminotransferase (ALT) ≥2.0×ULN;
  6. Oral/Dental Diseases

    1. Prior history or current evidence of osteomyelitis or osteonecrosis of the jaw.
    2. Active dental or jaw condition which requires oral surgery.
    3. Planned invasive dental procedure.
    4. Non-healed dental or oral surgery.
  7. DXA measurements:

    1. Less than two lumbar vertebrae evaluable for DXA measurements.
    2. Height, weight, or girth that could preclude accurate DXA measurements.
  8. Administration of the following medications:

    1. RANKL inhibitor, fluoride or strontium salt or intravenous bisphosphonate within the past 5 years;
    2. Oral bisphosphonates, allowed if patients had the following conditions :

      • Cumulative use> 3 months but <3 years: ≥ 6 months before the last medication was taken from the screening visit;
      • Cumulative use ≤3 months;
    3. parathyroid hormone (PTH) or parathyroid hormone analogs (PTHa) within 6 weeks before screening, such as teriparatide; anabolic hormones or testosterone; glucocorticoids (equivalent to> 5 mg/day strength Pine> 10 days); systemic hormone replacement therapy; selective estrogen receptor modulators (SERMs), such as raloxifene; tibolone; calcitonin; active vitamin D and its analogs; other bone active drugs including anticonvulsants (except benzodiazepines) and heparin; long-term systemic use of ketoconazole, androgens, corticotropin, cinacalcet, aluminum, lithium, protease inhibitors, methotrexate, Gonadotropin releasing hormone agonist;
  9. Positive human immunodeficiency virus (HIV) antibody.
  10. Self-reported alcohol or drug abuse [defined as drinking an average of 14 units or more of alcoholic beverages per week in the 3 months before screening (1 unit = 350 mL of beer, or 45 mL of liquor, or 150 mL of wine)]
  11. Known allergy to the treatment drugs used in the research protocol, including allergy to the test drugs
  12. Have received any other experimental drug treatment or prior participation in another interventional clinical trial within 3 months before screening
  13. Other severe acute or chronic diseases, psychiatric disorder or abnormal laboratory tests, etc., in the opinion of the investigator, not suitable for participating in this research.

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:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:双倍的

武器和干预

参与者组/臂
干预/治疗
实验性的:LY06006 60mg

injection

Interventions:

Drug: LY06006 Injection; Dietary Supplement: Elemental Calcium; Dietary Supplement: Vitamin D

60 mg/1 ml, once every 6 months administered subcutaneously, two injections in total
其他名称:
  • recombinant human monoclonal anti-RANKL antibody injection
安慰剂比较:Placebo

injection

Interventions:

Drug: Placebo; Dietary Supplement: Elemental Calcium; Dietary Supplement: Vitamin D

60 mg/1 ml, once every 6 months administered subcutaneously, two injections in total
其他名称:
  • recombinant human monoclonal anti-RANKL antibody injection

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
Percent Change in Bone Mineral Density (BMD) at the Lumbar Spine
大体时间:Baseline and Month 12
Percent Change From Baseline in Bone Mineral Density (BMD) at the Lumbar Spine at Month 12
Baseline and Month 12

次要结果测量

结果测量
措施说明
大体时间
Percent Change in Bone Mineral Density (BMD) at the Lumbar Spine
大体时间:Baseline and Month 6
Percent Change From Baseline in BMD at the Lumbar Spine at Month 6
Baseline and Month 6
Percent Changes in total hip BMD
大体时间:Baseline,Month 6 and Month 12
Percent Changes in total hip BMD from baseline at 6 and 12 months of treatment
Baseline,Month 6 and Month 12
Percent Changes in femoral neck BMD
大体时间:Baseline,Month 6 and Month 12
Percent Changes in femoral neck BMD from baseline at 6 and 12 months of treatment
Baseline,Month 6 and Month 12
Percent Changes in trochanteric BMD
大体时间:Baseline,Month 6 and Month 12
Percent Changes in trochanteric BMD from baseline at 6 and 12 months of treatment
Baseline,Month 6 and Month 12
Percent Change in Serum Carboxy-terminal Cross-linking Telopeptide of Type I Collagen (s-CTX) From Baseline
大体时间:Baseline, Month 1, Month 6 and Month 12
Percent Change From Baseline in Serum Carboxy-terminal Cross-linking Telopeptide of Type I Collagen (s-CTX) From Baseline at Month 1, Month 6, and Month 12
Baseline, Month 1, Month 6 and Month 12
Percent Change in Serum Procollagen Type I N Propeptideserum (s-PINP) From Baseline
大体时间:Baseline, Month 1, Month 6 and Month 12
Percent Change From Baseline in Serum Procollagen Type I N Propeptideserum (s-PINP) From Baseline at Month 1, Month 6, and Month 12
Baseline, Month 1, Month 6 and Month 12

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。

调查人员

  • 首席研究员:Zhenlin Zhang, doctor、Shanghai 6th People's Hospital

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 (实际的)

2019年6月30日

初级完成 (预期的)

2021年9月30日

研究完成 (预期的)

2021年12月31日

研究注册日期

首次提交

2021年4月20日

首先提交符合 QC 标准的

2021年9月17日

首次发布 (实际的)

2021年9月29日

研究记录更新

最后更新发布 (实际的)

2021年9月29日

上次提交的符合 QC 标准的更新

2021年9月17日

最后验证

2021年9月1日

更多信息

与本研究相关的术语

其他研究编号

  • LY06006/CT-CHN-302

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

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