Resistance Training and Rapamycin to Enhance Bone Formation in Postmenopausal Women (StrongBone)

Odense University Hospital

Status and phase: Not yet enrolling; Phase 2

Conditions: Osteopenia; Healthy; Osteoporosis Risk

Treatments: Drug: Placebo; Other: Resistance training; Drug: Everolimus

Study type: Interventional

Funder types: Other

Identifiers

NCT07191353

2024-520372-10-00

Details and patient eligibility

About

The aim of the present clinical trial is to examine the effects of everolimus, resistance training, or their combination on bone and muscle health formation in elderly women aged 60-75 years. The main questions it aims to answer are:

Can rapamycin's analog (Everolimus), resistance training, or their combination, enhance bone formation and muscle functions in elderly women compared to non-treatment controls.

Participants will be randomized 1:1:1:1 to one of the following treatment regimens:

• Oral everolimus 5 mg once a week.
• Oral placebo once a week.
• Oral everolimus 5 mg once a week plus resistance training RT 1 hour, 3 times weekly.
• Oral placebo once a week plus resistance training RT 1 hour, 3 times weekly.

During the study there will be a total of 5-7 visits, where the participants will undergo the following:

• Blood samles
• DXA-, HRpQCT- (only Odense Universitetshospital) and MRI-scans
• Muscle- and bone biopsies
• Quality of life questionnaires
• Testing of muscle funtion
• Metabolic studies of muscle and bone protein turnover using labelling with deuturated water

Enrollment: 148 estimated patients

Sex: Female

Ages: 60 to 75 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Women aged 60-75 years old, any ethnicity.
• Participants with T- score between < 1.0 and > -2.5 measured by DXA scan within 6 months of the first day of the study.
• Adequate cognitive function to be able to give informed consent.

Exclusion criteria

• Osteoporosis and fracture history

  • Participants with osteoporosis (defined by DXA scan < 6 months old: low bone mass, T-score < -2.5 or hip fracture or clinical compression fracture of the spine).
  • History of low energy fractures within last 6 months. Health conditions limiting exercise
  • Health conditions that could limit walking and weightbearing exercise (for instance recent surgery, mobility limitation)
  • Participants with impaired wound healing or history of a chronic open wound Bone metabolism disorders
  • Primary hyperparathyroidism.
  • Known vitamin D deficiency (<25 nM) (re-test after substitution acceptable).
  • Known disorders affecting bone metabolism, e.g., uncontrolled thyrotoxicosis, severe renal impairment (eGFR < 30) or impaired 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.

Medication use and health conditions

• Use of anabolic steroids in the previous year.
• Use of antiresorptive therapy in the previous year.
• Known medication/supplements affecting bone in the previous year.
• Diabetes type 1 and 2.
• Heart failure similar to NYHA Class IV.
• Treatment with drugs known to affect cytochrome P450 3A due to its role in everolimus metabolism, excluding strong CYP3A4 inhibitors or inducers, while allowing weak and intermediate inhibitors or inducers. Patients on the following drugs will be excluded from the trial: Ketoconazole, Itraconazole, Posaconazole, Voriconazole, Telithromycin, Clarithromycin, Nedazodone, Ritonavir, Atazanavir, Saquinavir, Darunavir, Indinavir, Nelfinavir, Rifampicin, Dexamethasone, Carbamazepine, phenobarbital, Phenytoin, Efavirenz and Nivirapine.
• History of coagulopathy or medical condition requiring long-term anticoagulation.

Blood disorders and other health concerns

• Anemia - Hg < 5,59 mmol/L, Leukopenia - white blood cells (WBC) < 3,5 x 10⁹/L, Neutropenia absolute neutrophil count < 2,0 x 10⁹/L, or Platelet count - platelet count < 125 x 10⁹/L.
• Insufficiently treated 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.

Immunosuppressive and current cancer Treatment

• Scheduled for immunosuppressant therapy for transplant or scheduled to undergo chemotherapy or any other treatment for malignancy
• Any form of clinically relevant primary or secondary immune dysfunction or deficiency Cardiovascular and heart conditions
• Unstable ischemic heart disease.

Allergies

• Known allergy to rapamycin or rapalogs. Language limitations
• The study will exclude participants with inability to speak and understand Danish and with inability to cooperate.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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148 participants in 4 patient groups, including a placebo group

Everolimus

Experimental group

Description:

Oral everolimus 5 mg once a week

Treatment:

Drug: Everolimus

Everolimus and resistance training

Experimental group

Description:

Oral everolimus 5 mg once a week plus resistance training RT 1 hour, 3 times weekly

Treatment:

Drug: Everolimus

Other: Resistance training

Placebo

Placebo Comparator group

Description:

Oral placebo once a week

Treatment:

Drug: Placebo

Placebo and resistance training

Placebo Comparator group

Description:

Oral placebo once a week plus resistance training RT 1 hour, 3 times weekly

Treatment:

Other: Resistance training

Drug: Placebo