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临床试验/NCT06789900
NCT06789900招募中2 期

Targeting mTOR With Everolimus and/or Physical Training for Preventing Postmenopausal Bone Loss and Accelerated Skeletal Aging: The RapaLoad Study

Odense University Hospital1 个研究点 分布在 1 个国家目标入组 136 人开始时间: 2024年10月14日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
招募中
入组人数
136
试验地点
1
主要终点
Procollagen type 1 N-terminal propeptide (P1NP)

研究概览

简要总结

It is estimated that women lose around 20-25% of bone mass during the 5-10 years period of postmenopausal transition, and menopause is considered a major risk factor for osteoporotic fragility fracture. Currently, there is no preventive strategy to counteract these changes, and hormone replacement therapy is not considered an attractive option for many women, because of concerns related to side effects. Rapamycin, through inhibition of mTOR (the mechanistic target of Rapamycin) has been demonstrated in many preclinical animal models to extend lifespan and healthspan. The most well-established mTOR inhibitors include rapamycin (sirolimus) and its analog (also referred as rapalog). Everolimus are FDA approved and have been used for many years at a high dose as an immunosuppressant and anti-cancer drug. Exercise training has been demonstrated to counteract age-related degenerative changes in several clinical studies. The aim of this randomized clinical trial is to test the effects of treatment with oral Everolimus, exercise, or their combination as a preventive strategy for impaired musculoskeletal function in healthy postmenopausal women.

The trial will include 136 women aged 45-60 years with T-score >-3 and no history of hip, Colles' or symptomatic vertebral fractures within the last 6 months, randomized to 24 weeks of treatment with one of the following regimens:

  1. control group getting general health advice,
  2. Football fitness session group, physical training consisting of structured hybrid exercise training via the "football fitness concept" for 1hour, 2 times/ week
  3. Everolimus group receiving an oral dosage of 5 mg everolimus once a week, (4) Everolimus and football fitness session group, consisting of structured hybrid exercise training via the "football fitness concept" for 1 hour, 2 times/week combined with oral everolimus 5 mg once a week.

The primary outcome of this trial is percentage change in bone formation marker P1NP (Procollagen Type 1 propeptide) between baseline and week 24. Secondary outcomes include percentage changes in bone resorption marker CTX (cross-lined C-telopeptide of type 1 collagen), bone mineral density (BMD), bone structure as determined by high resolution CT-scanning, muscle function and postural balance. As exploratory endpoints, changes in biological age as determined by "epigenetic clocks", levels of senescence-associated secretory phenotype (SASP) as an indicator of whole-body burden of senescent cells.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
45 Years 至 60 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Postmenopausal women aged 45-60 years old as evidenced by measuring serum levels of LH and FSH and absence of menstruation for at least 1 year.
  • No history of low energy hip or vertebral fractures during the last 6 months.
  • Ability to provide informed consent.

排除标准

  • Diabetes (type 1 and 2)
  • Heart failure similar to NYHA Class IV
  • Primary hyperparathyroidism
  • Known disorders affecting bone metabolism, e.g., uncontrolled thyrotoxicosis, severe renal impairment (eGFR <20) or liver function (baseline phosphatase higher than twice upper limit (105 U/L)), active rheumatic diseases, celiac disease, severe chronic obstructive lung disease (COPD), hypopituitarism, or Cushing's disease.
  • Previous use of bone antiresorptive or bone anabolic drugs within the last 5 years.
  • Use of anabolic steroids in the previous year
  • Treatment with drugs known to affect cytochrome P450 3A due to its role in everolimus metabolism
  • History of coagulopathy or medical condition requiring long-term anticoagulation
  • Anemia - Hg < 9.0 g/dl, Leukopenia - white blood cells (WBC) < 3,500/mm3, Neutropenia absolute neutrophil count < 2,000/mm3, or Platelet count - platelet count < 125,000/mm3
  • Patients with impaired wound healing or history of a chronic open wound
  • Scheduled for immunosuppressant therapy for transplant or scheduled to undergo chemotherapy or any other treatment for malignancy
  • Untreated dyslipidemia with LDL-c > 4.9 mmol/L and family history of dyslipidemia, Total cholesterol > 9.1 mmol/L, or triglycerides > 9.9 mmol/L
  • Any form of clinically relevant primary or secondary immune dysfunction or deficiency
  • Unstable ischemic heart disease
  • Bone mineral density (BMD) measured by DXA scanning with T-score <-3
  • Known allergy to rapamycin or rapalogs
  • The study will exclude participants with inability to speak and understand Danish and with inability to cooperate or perform physical training.
  • Inability to give informed consent

研究组 & 干预措施

Everolimus and Football fitness group

Experimental

Participants will join structured hybrid exercise training via the "football fitness concept" designed for participants with little prior experience with football and it is multifaceted training incorporating endurance training, high-intensity interval training (HIIT) and strength training. The training session lasts 60 minutes, and participants will receive two training sessions per week for 24 weeks. Each session is composed of: a 15 min warm-up that includes strength and balance exercises, a 15 min period with technical pair-based drills, and a 30-min period with small-sided football drills and take an oral dose of everolimus 5 mg once a week for 24 weeks.

干预措施: Football Fitness Concept (Other)

Football fitness group

Experimental

Participants will join structured hybrid exercise training via the "football fitness concept" designed for participants with little prior experience with football and it is multifaceted training incorporating endurance training, high-intensity interval training (HIIT) and strength training. The training session lasts 60 minutes, and participants will receive two training sessions per week for 24 weeks. Each session is composed of: a 15 min warm-up that includes strength and balance exercises, a 15 min period with technical pair-based drills, and a 30-min period with small-sided football drills.

干预措施: Football Fitness Concept (Other)

Everolimus group

Experimental

Participants will take an oral dose of everolimus 5 mg once a week for 24 weeks.

干预措施: Everolimus (Afinitor®) (Drug)

Everolimus and Football fitness group

Experimental

Participants will join structured hybrid exercise training via the "football fitness concept" designed for participants with little prior experience with football and it is multifaceted training incorporating endurance training, high-intensity interval training (HIIT) and strength training. The training session lasts 60 minutes, and participants will receive two training sessions per week for 24 weeks. Each session is composed of: a 15 min warm-up that includes strength and balance exercises, a 15 min period with technical pair-based drills, and a 30-min period with small-sided football drills and take an oral dose of everolimus 5 mg once a week for 24 weeks.

干预措施: Everolimus (Afinitor®) (Drug)

结局指标

主要结局

Procollagen type 1 N-terminal propeptide (P1NP)

时间窗: Baseline and 24 weeks

Percentage change in circulating levels of bone formation marker N-terminal fragment of procollagen type 1 (P1NP) at 24 weeks as compared with baseline

次要结局

  • Bone microarchitecture, mass and geometry(Baseline, week 24)
  • Muscle fitness and postural balances (test 1)(Baseline, week 24)
  • Cardiopulmonary health (test 3)(Baseline, 24 weeks)
  • Bone resorption markers (CTX and TRAcP)(Baseline, week 2, week 4, week 12 and week 24)
  • Bone formation markers (Osteocalcin, bALP, P1NP (other time points))(Baseline, week 2, week 4, week 12 and week 24 (P1NP: week 2, week 4 and week 12))
  • Bone mineral density (BMD)(Baseline, week 24)
  • Muscle Fitness and postural balances (test 2)(Baseline, week 24)
  • Muscle fitness and postural balances (test 3)(Baseline, week 24)
  • Muscle fitness and postural balances (test 4)(Baseline, week 24)
  • Muscle fitness and postural balances (test 5)(Baseline, 24 weeks)
  • Muscle fitness and postural balances (test 6)(Baseline, week 24)
  • Muscle fitness and postural balances (test 7)(Baseline, week24)
  • Cardiopulmonary health (test 1)(Baseline, week 24)
  • Cardiopulmonary health (test 2)(Baseline, week 24)
  • Cardiopulmonary health (test 4)(Baseline, week 24)
  • Cardiopulmonary health (test 5)(Baseline, week 24)
  • Metabolic health (test 1)(Baseline, week 24)
  • Metabolic health (test 2)(Baseline, week 24)
  • Metabolic health (test 3)(Baseline, week 24)
  • Metabolic health (test 4)(Baseline, week 24)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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