Executive Summary / Description
Muscle loss - spanning sarcopenia, cachexia, disuse atrophy, and GLP-1-associated muscle decline - is emerging as a priority therapeutic frontier driven by global demographic and metabolic shifts.
By 2035, over 1.5 billion people will be aged >60, and >250 million patients treated with GLP-1 agonists will be at risk of drug-induced sarcopenia, accelerating clinical urgency.
Historically managed through exercise, protein nutrition, and physical therapy, the field is now entering a biological medicine era characterized by:
- Myostatin/activin-A pathway blockade
- Selective androgen receptor modulators (SARMs)
- Mitochondrial biogenesis activators
- Anabolic peptides & myokine-based therapies
- Neuromuscular trophic modulation
- Adipomyokine axis reprogramming
- AI-driven digital muscle biomarkers & precision movement diagnostics
Drivers transforming this market: Macro Trend and its Implications
- Aging population: Exponential rise in sarcopenia burden
- GLP-1 expansion: Muscle depletion & metabolic fragility flags
- Cancer care & cachexia: Oncology supportive-care expansion
- Longevity medicine: Muscle seen as core biological organ system
- Sports performance -> medical translation: Advanced protein synthesis biology
Muscle is increasingly recognized not as a mechanical tissue but as a metabolic, endocrine, mitochondrial, and immunologic organ, producing myokines (Irisin, IL-15, Myostatin, FGF-21, GDF11) with systemic signaling effects.
Muscle mass = metabolic reserve + cognitive aging predictor + survival biomarker.
Market Outlook
Market expected to rise from ~USD 3.8B in 2024 -> USD 28-35B by 2040
Key launch inflection categories: Different Classes with Time Horizon
- SARMs 2.0 -> 2025-2027
- Myostatin/ActRIIB biologics -> 2026-2030
- Mitochondrial boosters -> 2027-2033
- Neuro-muscular circuit drugs -> 2029+
- Longevity precision exercise biologics -> 2030+
Scientific & Technology Landscape
Primary Mechanistic Axes: Biological Domain and it's Mechanism
- Muscle-growth pathway -> Myostatin inhibition, Smad signaling
- Androgen receptor -> SARMs, tissue-selective anabolics
- Mitochondria -> AMPK/PGC1a activation, mito-peptides (MOTS-C)
- Neuro-muscular -> Motor neuron trophic signaling, NMJ stabilization
- Myokine / Adipokine -> Irisin, IL-15, FGF-21, adiponectin
- Inflammation -> Cytokine blockers (IL-6, TNF-a)
- Stem Cells -> Satellite cell activation, senescence reversal
- Metabolic synergy -> Osteo-muscular endocrine cross-talk
Digital & Biometric Innovations
- Musculoskeletal digital twins
- AI gait analysis & EMG telemetry
- Ultrasound-AI muscle quality scoring
- Wearable mechano-transduction biomarkers
- CT radiomics / MRI muscle fat infiltration quantification
Modalities Profile with Example
- Monoclonal biologics -> Anti-myostatin, anti-activin (bimagrumab)
- Small molecules -> SARMs, mitophagy modulators
- Mito-peptides -> MOTS-C, Humanin
- Gene therapy -> Myostatin gene silencing
- Regenerative -> Satellite cell modulation
- Extremes emerging -> In-vivo muscle-fiber reprogramming