LONDON--(BUSINESS WIRE)--Technavio has announced their latest pipeline analysis report on the spinal muscular atrophy market. The report includes a detailed analysis of the pipeline molecules under investigation within the defined data collection period to treat spinal muscular atrophy.
This report by Technavio presents a detailed analysis of the market, including regulatory framework, drug development strategies, recruitment strategies, and key companies that are expected to play an essential role in the growth of the market in the future.
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Spinal muscular atrophy: Market overview
Spinal Muscular Atrophy (SMA) is a genetic disorder that results in the weakening of the muscles and affects muscle movement. It is common in infants, and it progresses with time. Infants with SMA have a breakdown of nerve cells in the brain and the spinal cord, due to which the brain stops sending control signals that control the muscle movement to the spinal cord. The muscles shrink and become weak, making it tough for the patients to control the head movement, sit without any external support and walk. People with a family history of SMA are at higher risks of developing the disease than the ones with no family history of SMA.
According to a senior market research analyst at Technavio, “As per the data represented by SMA Foundation, the incidence of SMA across all genders, races, and ethnic backgrounds is estimated to be 1 in every 10,000 children born. On the gender front, the probability of an infant developing SMA is almost equal in males and females. With the rising incidences of the disease, the drug development for spinal muscular atrophy is expected to rise during the next few years.”
Spinal muscular atrophy: Segmentation analysis
This pipeline analysis report segments the spinal muscular atrophy market based on therapies employed (monotherapy), RoA (oral, intravenous, and intrathecal), therapeutic modality (small molecule, gene, biological, oligonucleotide and cell), targets (SMN2, SMN1, acetylcholine receptor, 4-aminobutyrate transaminase, myostatin, SMN, and troponin-tropomyosin complex), MoA (SMN2 protein modulator, gene therapy, acetylcholine receptor modulator, cell replacement, 4-aminobutyrate transaminase inhibitor, myostatin activation inhibitor, SMN protein stabilizer, and troponin-tropomyosin complex stimulant ), geographical segmentation (Italy, France, Germany, Japan, US and Belgium) and recruitment status (active, not recruiting, not yet recruiting, and recruiting). It provides an in-depth analysis of the prominent factors influencing the market, including drivers, opportunities, trends, and industry-specific challenges.
Based on therapeutic modality, more than 45% of the molecules that are being investigated for the treatment of spinal muscular atrophy are small molecule.
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Some of the key topics covered in the report include:
Scope of the Report
Drug Development Landscape
- Drugs under development
- Indications coverage
Drug Development Strategies
- Therapies employed
- Therapeutic modality
- Geographical coverage
- Recruitment status
- Type of players
- Company overview
Discontinued or Dormant Molecules
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