The “Sarcopenia - Pipeline Insight, 2025” report provides comprehensive insights about 18+ companies and 20+ pipeline drugs in Sarcopenia pipeline landscape. It covers the pipeline drug profiles, including clinical and nonclinical stage products. It also covers the therapeutics assessment by product type, stage, route of administration, and molecule type. It further highlights the inactive pipeline products in this space.
The pathophysiology of sarcopenia involves a combination of muscle protein imbalance, mitochondrial dysfunction, neuromuscular degradation, and increased inflammatory cytokines. A decline in anabolic hormones, such as testosterone and growth hormone, coupled with an increase in catabolic processes, accelerates muscle degradation. Additionally, insulin resistance and chronic low-grade inflammation contribute to muscle atrophy and impaired regeneration. The loss of type II muscle fibers, which are responsible for quick and powerful movements, further exacerbates functional impairment.
Diagnosis of sarcopenia typically relies on criteria that assess muscle mass, strength, and physical performance. Common diagnostic tools include dual-energy X-ray absorptiometry (DXA) or bioelectrical impedance analysis (BIA) for muscle mass evaluation, handgrip strength tests for muscle strength, and gait speed measurements for functional assessment. The European Working Group on Sarcopenia in Older People (EWGSOP) and other international bodies have developed guidelines to standardize diagnosis and classification, which helps in identifying individuals at risk and guiding clinical management.
Treatment and prevention strategies for sarcopenia focus on resistance exercise, adequate protein intake, and potential pharmacological interventions. Strength training remains the most effective intervention for improving muscle mass and function, while ensuring sufficient dietary protein - especially leucine-rich sources - supports muscle synthesis. Emerging therapeutic approaches include myostatin inhibitors, selective androgen receptor modulators (SARMs), and anti-inflammatory agents, though none have yet been widely approved for clinical use. As the global population ages, addressing sarcopenia will be critical for maintaining independence and reducing the burden of age-related disability.
"Sarcopenia- Pipeline Insight, 2025" report outlays comprehensive insights of present scenario and growth prospects across the indication. A detailed picture of the Sarcopenia pipeline landscape is provided which includes the disease overview and Sarcopenia treatment guidelines. The assessment part of the report embraces, in depth Sarcopenia commercial assessment and clinical assessment of the pipeline products under development. In the report, detailed description of the drug is given which includes mechanism of action of the drug, clinical studies, NDA approvals (if any), and product development activities comprising the technology, Sarcopenia collaborations, licensing, mergers and acquisition, funding, designations and other product related details.
In humans and rodents, 15-PGDH gene expression is elevated in muscle coincident with the onset of age-induced muscle weakness. PGE2, a lipid signaling molecule with multiple beneficial effects on the motor unit, including enhanced muscle quality and improved function of the neuromuscular junction, is reduced in skeletal muscle of aged mice due to increased activity of 15-PGDH. Inhibiting 15-PGDH in aged muscle may be a strategy to increase physiologic levels of PGE2 to improve muscle quality and function. Currently, the drug is in the Phase I stage of its development for the treatment of Sacropenia.
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Geography Covered
- Global coverage
Sarcopenia: Understanding
Sarcopenia: Overview
Sarcopenia is a progressive, age-related condition characterized by the loss of skeletal muscle mass, strength, and function. It primarily affects older adults and is associated with an increased risk of falls, frailty, reduced mobility, and overall decline in quality of life. While aging is the primary driver, other contributing factors include chronic diseases, inflammation, hormonal changes, poor nutrition, and physical inactivity. Sarcopenia is now recognized as a distinct disease by the World Health Organization (WHO) and is increasingly gaining attention in clinical research due to its significant impact on aging populations.The pathophysiology of sarcopenia involves a combination of muscle protein imbalance, mitochondrial dysfunction, neuromuscular degradation, and increased inflammatory cytokines. A decline in anabolic hormones, such as testosterone and growth hormone, coupled with an increase in catabolic processes, accelerates muscle degradation. Additionally, insulin resistance and chronic low-grade inflammation contribute to muscle atrophy and impaired regeneration. The loss of type II muscle fibers, which are responsible for quick and powerful movements, further exacerbates functional impairment.
Diagnosis of sarcopenia typically relies on criteria that assess muscle mass, strength, and physical performance. Common diagnostic tools include dual-energy X-ray absorptiometry (DXA) or bioelectrical impedance analysis (BIA) for muscle mass evaluation, handgrip strength tests for muscle strength, and gait speed measurements for functional assessment. The European Working Group on Sarcopenia in Older People (EWGSOP) and other international bodies have developed guidelines to standardize diagnosis and classification, which helps in identifying individuals at risk and guiding clinical management.
Treatment and prevention strategies for sarcopenia focus on resistance exercise, adequate protein intake, and potential pharmacological interventions. Strength training remains the most effective intervention for improving muscle mass and function, while ensuring sufficient dietary protein - especially leucine-rich sources - supports muscle synthesis. Emerging therapeutic approaches include myostatin inhibitors, selective androgen receptor modulators (SARMs), and anti-inflammatory agents, though none have yet been widely approved for clinical use. As the global population ages, addressing sarcopenia will be critical for maintaining independence and reducing the burden of age-related disability.
"Sarcopenia- Pipeline Insight, 2025" report outlays comprehensive insights of present scenario and growth prospects across the indication. A detailed picture of the Sarcopenia pipeline landscape is provided which includes the disease overview and Sarcopenia treatment guidelines. The assessment part of the report embraces, in depth Sarcopenia commercial assessment and clinical assessment of the pipeline products under development. In the report, detailed description of the drug is given which includes mechanism of action of the drug, clinical studies, NDA approvals (if any), and product development activities comprising the technology, Sarcopenia collaborations, licensing, mergers and acquisition, funding, designations and other product related details.
Report Highlights
The companies and academics are working to assess challenges and seek opportunities that could influence Sarcopenia R&D. The therapies under development are focused on novel approaches to treat/improve Sarcopenia.Sarcopenia Emerging Drugs Chapters
This segment of the Sarcopenia report encloses its detailed analysis of various drugs in different stages of clinical development, including phase II, I, preclinical and Discovery. It also helps to understand clinical trial details, expressive pharmacological action, agreements and collaborations, and the latest news and press releases.Sarcopenia Emerging Drugs
- BIO101: Biophytis
- MF-300: Epirium Bio
In humans and rodents, 15-PGDH gene expression is elevated in muscle coincident with the onset of age-induced muscle weakness. PGE2, a lipid signaling molecule with multiple beneficial effects on the motor unit, including enhanced muscle quality and improved function of the neuromuscular junction, is reduced in skeletal muscle of aged mice due to increased activity of 15-PGDH. Inhibiting 15-PGDH in aged muscle may be a strategy to increase physiologic levels of PGE2 to improve muscle quality and function. Currently, the drug is in the Phase I stage of its development for the treatment of Sacropenia.
- TRN005: Turn Biotechnologies
Sarcopenia: Therapeutic Assessment
This segment of the report provides insights about the different Sarcopenia drugs segregated based on following parameters that define the scope of the report, such as:Major Players in Sarcopenia
- There are approx. 18+ key companies which are developing the therapies for Sarcopenia. The companies which have their Sarcopenia drug candidates in the most advanced stage, i.e. phase II include, Biophytis.
Phases
The report covers around 20+ products under different phases of clinical development like
- Late stage products (Phase III)
- Mid-stage products (Phase II)
- Early-stage product (Phase I) along with the details of
- Pre-clinical and Discovery stage candidates
- Discontinued & Inactive candidates
Route of Administration
Sarcopenia pipeline report provides the therapeutic assessment of the pipeline drugs by the Route of Administration. Products have been categorized under various ROAs such as- Oral
- Intravenous
- Subcutaneous
- Parenteral
- Topical
Molecule Type
Products have been categorized under various Molecule types such as
- Recombinant fusion proteins
- Small molecule
- Monoclonal antibody
- Peptide
- Polymer
- Gene therapy
Product Type
Drugs have been categorized under various product types like Mono, Combination and Mono/Combination.Sarcopenia: Pipeline Development Activities
The report provides insights into different therapeutic candidates in phase II, I, preclinical and discovery stage. It also analyses Sarcopenia therapeutic drugs key players involved in developing key drugs.Pipeline Development Activities
The report covers the detailed information of collaborations, acquisition and merger, licensing along with a thorough therapeutic assessment of emerging Sarcopenia drugs.Sarcopenia Report Insights
- Sarcopenia Pipeline Analysis
- Therapeutic Assessment
- Unmet Needs
- Impact of Drugs
Sarcopenia Report Assessment
- Pipeline Product Profiles
- Therapeutic Assessment
- Pipeline Assessment
- Inactive drugs assessment
- Unmet Needs
Key Questions
Current Treatment Scenario and Emerging Therapies:
- How many companies are developing Sarcopenia drugs?
- How many Sarcopenia drugs are developed by each company?
- How many emerging drugs are in mid-stage, and late-stage of development for the treatment of Sarcopenia?
- What are the key collaborations (Industry-Industry, Industry-Academia), Mergers and acquisitions, licensing activities related to the Sarcopenia therapeutics?
- What are the recent trends, drug types and novel technologies developed to overcome the limitation of existing therapies?
- What are the clinical studies going on for Sarcopenia and their status?
- What are the key designations that have been granted to the emerging drugs?
Key Players
- Biophytis
- Epirium Bio
- Turn Biotechnologies
- Immunis
- Oncocross
- BPGbio, Inc.
Key Products
- BIO101
- MF-300
- TRN005
- IMM01-STEM
- OC514
- BPM31510
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Table of Contents
IntroductionExecutive SummarySarcopenia - Analytical PerspectiveSarcopenia Key CompaniesSarcopenia Key ProductsSarcopenia - Unmet NeedsSarcopenia - Market Drivers and BarriersSarcopenia - Future Perspectives and ConclusionSarcopenia Analyst ViewsSarcopenia Key CompaniesAppendix
Sarcopenia: Overview
Pipeline Therapeutics
Therapeutic Assessment
Mid Stage Products (Phase II)
BIO101: Biophytis
Early Stage Products (Phase I)
MF-300: Epirium Bio
Preclinical Stage Products
TRN005: Turn Biotechnologies
Discovery Stage Products
Drug name: Company name
Inactive Products
List of Tables
List of Figures
Companies Mentioned (Partial List)
A selection of companies mentioned in this report includes, but is not limited to:
- Biophytis
- Epirium Bio
- Turn Biotechnologies
- Immunis
- Oncocross
- BPGbio, Inc.