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NCT Number: NCT06942182

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

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.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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
  • Body weight ≥35 kg
  • Adequate dietary intake
  • Potential subjects' intention to avoid reproductive activity will be confirmed

And one or more of the following criteria:

  • Previous history frailty or sarcopenia diagnosis using standardized tests;
  • Positive assessment for frailty or sarcopenia using standardized tests or as per clinician's judgement;
  • Previous positive assessment for elevated biomarkers of inflammation (serum IL-6 level> LOQ, TNFR1 level > LOQ, and/or TNF-alpha level > LOQ)

Exclusion criteria

  • 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)
  • Newly (< 2 weeks) diagnosed COVID-19
  • Inability or unwillingness to give written informed consent
  • History of upper/lower respiratory tract infection, requiring systemic steroids, antibiotics, and or emergency room (ER) visit or urgent care within 6 weeks of screening visit
  • History of adverse reaction or allergy to TNF inhibitor
  • History of neurological, hepatic, renal, diabetic mellitus, thyroid disorder, psychiatric, addiction or other medical conditions that may interfere with the interpretation of data or the patient's participation in the study or may increase safety concerns per investigator discretion
  • Currently under treatment by an anti-TNFα drug, such as adalimumab, etanercept, infliximab, certolizumab pegol, golimumab, and biosimilars
  • Currently under treatment by an anti-diabetic medication, including glucagon-like peptide-1 (GLP-1) drugs such as semaglutide, or any of metformin, jenuvia, or insulin
  • Unwillingness or inability to comply with study procedures, including smoking cessation
  • History of epilepsy or seizure propensity, ataxia, abnormal EEG findings, abnormal brain magnetic resonance image, or other co-morbid neurological conditions
  • Positive TB test
  • Patients who are pregnant or breastfeeding

Treatment and study plan

Isomyosamine 250mg

Drug

Isomyosamine 250 mg capsules dosed 4 times daily

Placebo 250 mg

Drug

Placebo 250 mg capsule 4 times daily

Primary outcomes

  1. Change in Short Physical Performance Battery (SPPB) Test in subjects treated with Isomyosamine or placebo

    Time frame: From enrollment to the end of treatment at 90 days

Secondary outcomes

  1. 4-meter walk test

    Time frame: From enrollment to the end of treatment at 90 days

    Change in the time taken to walk 4 meters through 90 days dosing.

  2. 6-minute walk test

    Time frame: From enrollment to the end of treatment at 90 days

    Change in the distance walked in the 6-minute walk test (m) through 90 days dosing.

  3. Grip strength

    Time frame: From enrollment to the end of treatment at 90 days

    Change in grip strength score over 90 day dosing.

  4. Effect on serum levels of biochemical markers of TNF activation

    Time frame: From enrollment to the end of treatment at 90 days

  5. Number of participants with treatment-related adverse events as assessed by CTCAE v5.0 in the Isomyosamine vs Placebo groups

    Time frame: From enrollment to the end of treatment at 90 days

Study contacts

Contact information is provided by the study sponsor or research team.

Dan Mazzucco

CONTACT

[email protected]

Sponsors and collaborators

Lead sponsor

TNF Pharmaceuticals, Inc.

Industry

Registry information

Official study title

Double Blind Placebo-Controlled Parallel Group Study Of Safety And Efficacy Of Isomyosamine In Treating Sarcopenia After Hip Or Femoral Fracture In Gerontological Population

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Apr 24, 2025
Registry last updated
Apr 24, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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