SBIR/STTR Research Award

Biologics for Improved Aged Muscle Function

Award identifier 08a663c357607aa757e7acec5fe1de6d8e7c3f0ede446ca715a0b8ec4f461aaeAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$254,262

Program and phase

SBIR · Phase I

Award year

2021

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
JUVENA THERAPEUTICS INC
Proposal award date
2021-09-01
Contract end date
2022-08-31
UEI
Not reported
Solicitation number
PA20-260
Topic code
NIA

Research abstract

ABSTRACTSarcopenia is the disease of muscle wasting and loss of strength associated with aging. This disease afflicts 10-25% of those over age 65, increasing andgt; 50% of those over age 80. While debilitating in its own right, muscle weakness is a major risk factor for fall injury and increases the risk of resulting disability up to 4.6-fold, resulting in an immense healthcare burden to society. 1 in 4 Americans over the age of 65 suffers a fall every year, leading to over 8 million cases requiring medical care annually, the direct costs of which exceed $50 billion to the US healthcare system. Thus, developing therapeutics to treat and reverse sarcopenia will be essential for preventing the frequent spiral into disability after injury in the elderly. While the CDC recognized sarcopenia as a reimbursable clinical indication in 2016, unfortunately, there are 0 FDA approved therapeutics available today, as no drug candidates have demonstrated both safety and efficacy. Using a proprietary ML-enabled high-throughput screening platform, Juvena Therapeutics has identified several signaling proteins secreted by human embryonic stem cells that ameliorate key cellular aspects of sarcopenia in aged muscle fibers and progenitor cells. In pilot studies, systemic or local administration of these proteins in sarcopenic, aged mice improved muscle strength and fiber size, and enhanced the regenerative capability of andquot;agedandquot; muscle stem cells. This Phase I will focus on developing variants of two of the lead candidates modified to achieve a target product profile with extended stability and wider therapeutic window required for effective clinical use and product commercialization. In Aim 1, we will: (1) add stabilization motifs to modulate stability, extending half-lives from minutes to andgt;96 hours; (2) confirm that the engineered variants maintain their regenerative properties in aged mouse and human myoblasts using validated in vitro injury-activate models of skeletal muscle regeneration; and (3) conduct pilot PK studies using 2 routes of administration (s.c. and i.v.) to inform Aim 2 in vivo efficacy studies. In Aim 2, efficacy of the modified lead candidates will be assessed in a natural sarcopenia model using aged mice. Success will be indicated by demonstrating the lead biologic produces an improvement in maximal or sustained muscle force production (strength and endurance) as a statistically significant increase in grip strength, treadmill performance, in vivo and in situ direct muscle stimulation and force measurement, improvements in muscle fiber size and reduced fibrosis. Once feasibility is demonstrated, Phase II will focus on large-scale, GMP production of sufficient material to carry out CMC, Safety/tox for IND enabling studies as well as in vivo efficacy studies. In the long term, we will expand the therapeutic applications for our regenerative proteins to include other indications associated with stem cell dysregulation with aging such as acute injury / post-operative care, osteoarthritis, and/or Amyotrophic lateral sclerosis.NARRATIVESarcopenia, the disease of muscle wasting and loss of strength caused by aging, afflicts millions of older adults, including andgt; 50% of those over the age of 80. With no FDA-approved therapeutic solutions for treating sarcopenia the direct health care costs for patient care exceed $50 billion to the US healthcare system annually. To address this unmet need Juvena Therapeutics has identified therapeutic candidates that can restore aged muscle strength, endurance, and regeneration capacities of muscle precursor to reverse sarcopenia and is proposes creating variants of two lead molecules with improved regenerative capacity, which, once feasibility is demonstrated, will provide a therapeutic option to treat sarcopenia.

Technology keywords

Not reported

Agency intelligence

Department of Health and Human Services

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