PUBLISHER: DelveInsight | PRODUCT CODE: 1415481
PUBLISHER: DelveInsight | PRODUCT CODE: 1415481
DelveInsight's "Multiple System Atrophy- Market Insights, Epidemiology and Market Forecast- 2032" report delivers an in-depth understanding of the Multiple System Atrophy, historical and forecasted epidemiology as well as the Multiple System Atrophy market trends in the United States, EU4 (Germany, Spain, Italy, and France) and the United Kingdom, and Japan.
The Multiple System Atrophy market report provides current treatment practices, emerging drugs, market share of individual therapies, and current and forecasted 7MM MSA market size from 2019 to 2032. The report also covers current MSA treatment practices/algorithms and unmet medical needs to curate the best of the opportunities and assesses the underlying potential of the market.
Study Period: 2019-2032.
Multiple system atrophy is a rare, rapidly progressing, fatal neurodegenerative disorder of uncertain etiology that is clinically characterized by a variable combination of Parkinsonism, cerebellar impairment, and autonomic and motor dysfunctions. Depending on the predominant clinical phenotype, the disease is sub-classified into a parkinsonian variant (MSA-P) associated with SND, a cerebellar (MSA-C) variant with OPCA with predominant cerebellar features, and a combination of both forms, referred to as "mixed" MSA
The accurate clinical diagnosis of MSA is based on a careful medical history and meticulous neurological examination. Ancillary investigations are helpful to support the diagnosis, rule out potential mimics, and define therapeutic strategies. This review summarizes diagnostic investigations useful in diagnosing MSA.
Current consensus guidelines include neuroimaging criteria for the diagnosis of possible MSA. These include the presence of atrophy of the putamen, middle cerebellar peduncle, pons or cerebellum on brain magnetic resonance imaging (MRI), and putamen, brainstem or cerebellum hypo metabolism on brain fluorodeoxyglucose (FDG) positron emission tomography (PET), as well as dopaminergic denervation on PET or single photon emission computed tomography (SPECT).
Brain MRI is the gold standard imaging technique for the evaluation of parkinsonian and cerebellar syndromes, including MSA. A brain MRI including standard sequences and diffusion weighted imaging (DWI) should be included in the initial evaluation of every patient with suspected MSA. Several brain MR modalities are available.
Current therapeutic management is based on symptomatic treatment. To date, no curative treatment is available for MSA.
Tremor, rigidity, bradykinesia, and postural instability are core features of MSA-P and are observed irrespective of subtype in nearly 90% of cases. A poor or unstained response to levodopa is common and among the core diagnostic features of MSA, helping to differentiate MSA-P from PD. Nearly a third of MSA-P patients benefit from levodopa therapy, but temporarily with a mean duration of 3.5 years in one study. Levodopa remains the first-line therapy with trial up to 2 g total daily dose of levodopa (titrated from 100 mg to 300 mg 3-4 times daily) recommended for at least 3 months. Clinically significant improvement is a 30% decrease in the UMSARS. Levodopa may worsen OH or cause other more severe side effects less common among PD patients. Reports of deterioration with the medication withdrawal, even in the context of apparent nonresponse, are common and may justify the continuation of treatment.
As the market is derived using the patient-based model, the Multiple System Atrophy epidemiology chapter in the report provides historical as well as forecasted epidemiology segmented by, total diagnosed prevalent cases of Multiple System Atrophy, gender-specific diagnosed prevalent cases of Multiple System Atrophy, age-specific diagnosed prevalent cases of Multiple System Atrophy, type-specific diagnosed prevalent cases of Multiple System Atrophy, and nOH symptomatic cases of multiple system atroph in the 7MM covering the United States, EU4 countries (Germany, France, Italy, and Spain) and the United Kingdom, and Japan from 2019 to 2032. The total diagnosed prevalent cases of Multiple System Atrophy in the 7MM comprised approximately 51 thousand cases in 2022 and are projected to increase during the forecasted period.
The drug chapter segment of the Multiple System Atrophy report encloses a detailed analysis of Multiple System Atrophy marketed drugs and late-stage (Phase-III and Phase-II) pipeline drugs. It also helps to understand the MSA clinical trial details, expressive pharmacological action, agreements and collaborations, approval and patent details, advantages and disadvantages of each included drug, and the latest news and press releases.
TD-9855 is an investigational, once-daily Norepinephrine Reuptake Inhibitor (NRI) in development for treating patients with symptomatic neurogenic orthostatic hypotension (nOH). It has a high affinity for binding to norepinephrine transporters. By blocking the action of these transporters, ampreloxetine causes an increase in extracellular concentrations of norepinephrine.
Note: Detailed emerging therapies assessment will be provided in the final report.
The current therapeutic management of Multiple System Atrophy is based on symptomatic treatment and has witnessed little change since a decade. Considering the approved market segment, NORTHERA (droxidopa) is the world's first approved therapy for symptomatic nOH.
Moreover, the upcoming treatment landscape is poised to see further expansion after the emergence of new classes such as Ampreloxetine, is in Phase III for treating patients with symptomatic neurogenic orthostatic hypotension. Lu AF82422, a monoclonal antibody; AAV2-GDNF, a gene therapy is in early phase of clinical investigation for MSA. Such novel drugs are expected to change the dynamics of the current treatment regime.
Currently, no disease-modifying agent is approved. The drug used to treat PD (parkinsonism), most notably levodopa (SINEMET), is also prescribed for MSA individuals. However, the efficacy of such medications varies greatly among affected individuals. Apart from levodopa, other drugs used to treat PD may be used to treat MSA individuals. These include dopamine agonists such as ropinirole (Requip) and pramipexole (Mirapexin), which increase the activity of dopamine receptors in the brain. This helps the brain receive dopamine signals. Midodrine hydrochloride (ProAmatine) has been used to treat low blood pressure, sometimes associated with MSA. Adrenergic drugs such as ephedrine may be used to treat low blood pressure. L-threo-dihydroxyphenylserine (L-DOPS or L-threo-DOPS) can also treat low blood pressure.
The major challenge and unmet need in MSA treatment are that no drug is approved for the direct treatment of MSA. The key competitive factors that may affect the success of these products, and any other product candidates that are yet to reach the market, if approved, are likely to be efficacy, safety, convenience, cost, the availability of generic competition, and the reimbursement from government and/or other third-party payers.
Few new agents are being developed and tested as potential treatments for MSA; the emerging drugs include Ampreloxetine, Lu AF82422, AAV2-GDNF, and others.
This section focuses on the rate of uptake of the potential drugs expected to get launched in the market during the study period 2019-2032. For example, for Ampreloxetine, we expect the drug uptake to be medium with a probability-adjusted peak share of around 27%, and years to the peak is expected to be 6 years from the year of launch.
The report provides insights into different therapeutic candidates in Phase III, Phase II, and Phase I stage. It also analyzes key players involved in developing targeted therapeutics.
The report covers detailed information on collaborations, acquisitions and mergers, licensing, and patent details for Multiple System Atrophy emerging therapies.
To keep up with current market trends, we take KOLs and SMEs' opinions working in the domain through primary research to fill the data gaps and validate our secondary research. Industry Experts contacted for insights on MSA evolving treatment landscape, patient reliance on conventional therapies, patient's therapy switching acceptability, and drug uptake along with challenges related to accessibility, include Medical/scientific writers, Medical Professors, Director of Henry Mayo Newhall Memorial Hospital, and Others.
DelveInsight's analysts connected with 50+ KOLs to gather insights, however, interviews were conducted with 15+ KOLs in the 7MM. Centers such as Brain Research Institute, University of California, University of Utah, Johannes-Gutenberg-University etc. were contacted. Their opinion helps to understand and validate current and emerging therapies and treatment patterns or Multiple System Atrophy market trends. This will support the clients in potential upcoming novel treatments by identifying the overall scenario of the market and the unmet needs.
We perform Qualitative and market Intelligence analysis using various approaches, such as SWOT analysis, and Conjoint Analysis. In the SWOT analysis, strengths, weaknesses, opportunities, and threats in terms of disease diagnosis, patient awareness, patient burden, competitive landscape, cost-effectiveness, and geographical accessibility of therapies are provided. These pointers are based on the Analyst's discretion and assessment of the patient burden, cost analysis, and existing and evolving treatment landscape.
Conjoint Analysis is done to analyze multiple approved and emerging therapies based on relevant attributes such as safety, efficacy, frequency of administration, route of administration, and order of entry. Scoring is given based on these parameters to analyze the effectiveness of therapy.
Further, the therapies' safety is evaluated wherein the acceptability, tolerability, and adverse events are majorly observed, and it sets a clear understanding of the side effects posed by the drug in the trials. In addition, the scoring is also based on the route of administration, order of entry and designation, probability of success, and the addressable patient pool for each therapy. According to these parameters, the final weightage score and the ranking of the emerging therapies are decided.
Reimbursement is a crucial factor affecting the drug's market access. Often, the decision to reimburse comes down to the drug's price relative to the benefit it produces in treated patients. NORTHERA patient support provides support to the patients requiring NORTHERA prescription. According to this plan, the patient's health insurance plan will determine the financial coverage, the amount they will pay for prescriptions, and additional savings they may be eligible for.
The report further provides detailed insights on the country-wise accessibility and reimbursement scenarios, cost-effectiveness scenario of approved therapies, programs making accessibility easier and out-of-pocket costs more affordable, insights on patients insured under federal or state government prescription drug programs, etc.