Literature DB >> 35441200

The Design and Rationale of a Phase 2b, Randomized, Double-Blinded, and Placebo-Controlled Trial to Evaluate the Safety and Efficacy of Lomecel-B in Older Adults with Frailty.

K Yousefi1, K N Ramdas, J G Ruiz, J Walston, H Arai, E Volpi, A B Newman, C Wang, B Hitchinson, L McClain-Moss, L Diaz, G A Green, J M Hare, A A Oliva.   

Abstract

BACKGROUND: Frailty in older adults is a rapidly growing unmet medical need. It is an aging-related syndrome characterized by physical decline leading to higher risk of adverse health outcomes.
OBJECTIVES: To evaluate the efficacy of Lomecel-B, an allogeneic medicinal signaling cell (MSC) formulation, in older adults with frailty.
DESIGN: This multicenter, randomized, parallel-arm, double-blinded, and placebo-controlled phase 2b trial is designed to evaluate dose-range effects of Lomecel-B for frailty on physical functioning, patient-reported outcomes (PROs), frailty status, and biomarkers.
SETTING: Eight enrolling clinical research centers, including the Miami Veterans Affairs Medical Center. PARTICIPANTS: Target enrollment is 150 subjects aged 70-85 years of any race, ethnicity, or gender. Enrollment criteria include a Clinical Frailty Score of 5 ("mild") or 6 ("moderate"), a 6MWT of 200-400 m, and serum tumor necrosis factor-alpha (TNF-α) ≥2.5 pg/mL. INTERVENTION: A single intravenous infusion of Lomecel-B (25, 50, 100, or 200 million cells) or placebo (N=30/arm). Patients are followed for 365 days for safety, and the efficacy assessments performed at 90, 180, and 270 days. MEASUREMENTS: The primary endpoint is change in 6MWT in the Lomecel-B-treated arms versus placebo at 180 days post-infusion. Secondary and exploratory endpoints include change in: 6MWT and other physical function measures at all time points; PROs; frailty status; cognitive status; and an inflammatory biomarkers panel. A pre-specified sub-study examines vascular/endothelial biomarkers. Safety is evaluated throughout the trial.
RESULTS: The trial is conducted under a Food and Drug Administration Investigational New Drug (IND), with Institutional Review Board approval, and monitoring by an NIH-appointed independent Data Safety Monitoring Board.
CONCLUSION: This clinical trial investigates the use of a regenerative medicine strategy for frailty in older adults. The results will further the understanding of the potential for Lomecel-B in the geriatric condition of frailty.

Entities:  

Keywords:  6-minute walk test; Frailty; medicinal signaling cell; mesenchymal stem cells; physical function

Mesh:

Substances:

Year:  2022        PMID: 35441200     DOI: 10.14283/jfa.2022.2

Source DB:  PubMed          Journal:  J Frailty Aging        ISSN: 2260-1341


  3 in total

1.  Endpoints for geroscience clinical trials: health outcomes, biomarkers, and biologic age.

Authors:  Steven R Cummings; Stephen B Kritchevsky
Journal:  Geroscience       Date:  2022-10-19       Impact factor: 7.581

2.  Potential of Stem Cell-Based Therapy to Restore Function in Aging Systems: Are We There Yet?

Authors:  Joshua M Hare; Isabel Beerman
Journal:  J Gerontol A Biol Sci Med Sci       Date:  2022-07-05       Impact factor: 6.591

3.  Challenges in the Development of Drugs for Sarcopenia and Frailty - Report from the International Conference on Frailty and Sarcopenia Research (ICFSR) Task Force.

Authors:  M Cesari; R Bernabei; B Vellas; R A Fielding; D Rooks; D Azzolino; J Mariani; A A Oliva; S Bhasin; Y Rolland
Journal:  J Frailty Aging       Date:  2022
  3 in total

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