Safety and Efficacy of Isomyosamine in Reducing Inflammation and Treating Muscle Loss in Older Adults After Hip or Thigh Bone Fractures

Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age60-85
SponsorTNF Pharmaceuticals, Inc.

About this trial

This Phase II clinical study investigates the safety and effectiveness of a new drug, Isomyosamine, in patients with sarcopenia or frailty, conditions associated with aging and muscle weakness. Isomyosamine is a promising oral medication that reduces inflammation by targeting cytokines like TNF-α and IL-6, which are linked to these conditions. Previous studies have shown it is well-tolerated and may help improve muscle strength, mobility, and healing after hip fractures. This trial aims to determine its potential benefits in reducing inflammation and improving recovery in elderly patients.

Eligibility criteria

Qualifiers

Age 60 to 85 years of age

Non-complex, non-comminuted fracture of the femoral head, femoral neck, or acetabulum due to an accidental (non-neurologic or cardiovascular) fall

Concomitant medication limited to treatment for chronic conditions

The ability to give informed consent and comply with study procedures

Disqualifiers

Receiving immunotherapy for cancer or solid organ transplantation

Complex or comminuted fracture or fracture of multiple long bones

Regular treatment for chronic disease including chronic renal failure, chronic heart failure (CHF) cerebrovascular disease including stroke, rheumatoid arthritis, or polymyalgia rheumatica

Chronic kidney disease (estimated glomerular filtration rate [eGFR] <60 mL/min)

Trial design

Treatments tested in this trial

  • Isomyosamine 250mg
  • Placebo 250 mg

Treatment groups

60 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators