PUBLISHER: DelveInsight | PRODUCT CODE: 1376844
PUBLISHER: DelveInsight | PRODUCT CODE: 1376844
DelveInsight's "Niemann-Pick Disease Type C (NPC) - Market Insights, Epidemiology, and Market Forecast - 2032" report delivers an in-depth understanding of the Niemann-Pick Disease Type C, historical and forecasted epidemiology as well as the Niemann-Pick Disease Type C market trends in the United States, EU4 (Germany, Spain, Italy, and France) and the United Kingdom, and Japan.
The Niemann-Pick Disease Type C market report provides current treatment practices, emerging drugs, market size, market share of the individual therapies, and current and forecasted 7MM from 2019 to 2032. The report also covers current Niemann-Pick Disease Type C (NPC) treatment practices/algorithms and unmet medical needs to curate the best of the opportunities and assess the underlying potential of the market.
Study Period: 2019-2032
Niemann-Pick Disease Type C (NPC) is a progressive, irreversible, pan-ethnic, and chronically debilitating neurovisceral lysosomal lipid storage disease characterized by visceral, neurological, and psychiatric manifestations. It involves the unique abnormalities of intracellular transport of endocytosed cholesterol with sequestration of unesterified cholesterol in lysosomes and late endosomes. It occurs due to the alterations in the trafficking of endocytosed cholesterol. It ultimately results in the accumulation of cholesterol and glycosphingolipids in various neurovisceral tissues.
At the cellular level, Niemann-Pick Type C can be caused by two different genetic mutations. A mutation in the NPC1 gene causes type C1 and type C2 is caused by a mutation in the NPC2 gene. NPC1 is found in the majority of cases as compared to NPC2. Although the exact function of NPC1 and NPC2 is still elusive, these proteins function coordinatedly and are involved in the cellular post-lysosomal/late endosomal transport of cholesterol and other molecules. NPC causes a secondary reduction of ASM activity, leading to all three forms of Niemann-Pick Disease
NPC diagnosis includes blood tests, neuroimaging tests, genetic tests, and skin biopsy. A progressive vertical supranuclear gaze palsy, gelastic cataplexy, ataxia, dystonia, and dementia strongly suggest the diagnosis.
Although no cure yet exists, the treatment of NPC disease has made significant strides in the past decade, from the earliest treatments with statins to the latest with sugars, such as miglustat and cyclodextrin. The management of NPC is based mainly on supportive care. Treatment focuses on managing symptoms with medication for seizures, sedatives for sleep disturbances, physical therapy to maintain mobility, and speech therapy to preserve communication as long as possible. Chest physiotherapy and antibiotics may help prevent regular lung infections. Individuals with the condition need a gastronomy tube for feeding when they can no longer swallow well enough to avoid choking or malnutrition.
Miglustat is the first and only specific drug approved for this disease in Europe in 2009 and Japan in 2012; its objective is to alleviate disease symptoms while attenuating neurodegeneration. In the US, the FDA declined to approve this drug in 2010 and called for more data. However, since the drug is already approved for treating Gaucher's disease in the US, it is being prescribed to NPC patients as an off-label therapy.
The rarity of the disease and lack of expertise translate into misdiagnosis, delayed diagnosis, and barriers to adequate care. Niemann-Pick disease is characterized by a highly heterogeneous presentation, making diagnosis difficult and often delayed.
As the market is derived using a patient-based model, the Niemann-Pick Disease Type C (NPC) epidemiology chapter in the report provides historical as well as forecasted epidemiology segmented by Total Diagnosed Prevalent cases of Niemann-Pick Disease Type C, Gender-specific Diagnosed Prevalent cases of Niemann-Pick Disease Type C, and Distribution of Diagnosed Prevalent Cases of Niemann-Pick disease Type C by type 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 drug chapter segment of the Niemann-Pick Disease Type C (NPC) report encloses a detailed analysis of Niemann-Pick Disease Type C late-stage, mid-stage, and mid-early stage (Phase III, Phase II/III, Phase II) pipeline drugs. It also helps understand the Niemann-Pick Disease Type C 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.
Presently four emerging therapies are focused on the treatment of Niemann Pick Disease Type C - Arimoclomol (Zevra Therapeutics), AZ-3102 (Azafaros A.G.), Trappsol(R) Cyclo or Hydroxypropyl-beta-cyclodextrin (Cyclo Therapeutics, Inc.) and IB1001 (N-acetyl-L-leucine) (IntraBio). These emerging therapies will provide much-needed relief for the patients and can significantly change the market dynamics in the 7MM countries during the forecast period (2023-2032) due to the absence of marketed therapies.
Until some years ago, Niemann-Pick disease treatment was based on anti-epileptics, anticholinergic, or antidepressants to alleviate symptoms, i.e., tremors, dystonia, or seizures. Niemann-Pick disease has no cure, and potential therapies should be addressed. The main goal is to develop treatments to minimize general symptoms and neurodegeneration.
Supportive therapy by multidisciplinary specialists treats different individual manifestations shown by Niemann-Pick type C patients. For instance, if a person is showing neurological concerns like spasticity, cataplexy, movement disorders, sleep disturbance, and seizures, then the treatment options are physical therapy, modafinil, trihexyphenidyl, melatonin, and antiseizure medicines are used respectively. If a person has difficulty with speech, speech therapy is usually recommended. Genetic counseling and general supportive care are also crucial for people suffering from Niemann-Pick Disease Type C.
Unfortunately, no treatment has yet proven able to change the actual course of NPC. Meanwhile, MIGLUSTAT is the first and only specific drug approved for this disease in Europe (2009) and Japan (2012); its objective is alleviating disease symptoms while attenuating neurodegeneration. In the US, the FDA declined to approve this drug in 2010 and called for more data. However, since the drug is already approved for treating Gaucher's disease in the US, it is being prescribed to NPC patients as an off-label therapy.
This section focuses on the uptake rate of the potential drug expected to be launched in the market during the study period 2019-2032. MIGLUSTAT is the first and only specific drug approved for this disease in Europe (2009) and Japan (2012).
The report provides insights into therapeutic candidates in Phase III, II, and I. It also analyzes key players involved in developing targeted therapeutics.
The report covers detailed information on designations, collaborations, mergers and acquisitions, licensing, and patent details for Niemann-Pick Disease Type C (NPC) emerging therapies.
To keep up with the 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 Niemann-Pick Disease Type C evolving treatment landscape, patient reliance on conventional therapies, patient therapy switching acceptability, drug uptake along with challenges related to accessibility, include Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, US, Professor of Pediatrics, Professor of Medicine, Rutgers New Jersey Medical School, US, and Department of Pediatrics, Jichi Medical University, Tochigi, Japan.
DelveInsight's analysts connected with 50+ KOLs to gather insights; however, interviews were conducted with 15+ KOLs in the 7MM. Centers such as the Willink Biochemical Genetics Unit, Royal Manchester Children's Hospital, UK, Neurology Service, Sant Joan de Deu Hospital, Spain, Boston Children's Hospital, US, etc., were contacted. Their opinion helps understand and validate current and emerging therapies and treatment patterns or Niemann-Pick Disease Type C 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. 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.
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.