PUBLISHER: DelveInsight | PRODUCT CODE: 1553387
PUBLISHER: DelveInsight | PRODUCT CODE: 1553387
DelveInsight's "Molybdenum Cofactor Deficiency Type A (MoCoD-A) - Market Insights, Epidemiology, and Market Forecast - 2034" report delivers an in-depth understanding of the MOCOD-A, historical and forecasted epidemiology and the MOCOD-A market trends in the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan.
The Molybdenum Cofactor Deficiency Type A (MoCoD-A) market report provides current treatment practices, emerging drugs, market share of individual therapies, and current and forecasted 7MM MOCOD-A market size from 2020 to 2034. The report also covers current MOCOD-A treatment practices/algorithms and unmet medical needs to curate the best of the opportunities and assesses the underlying potential of the market.
Study Period: 2020-2034
Molybdenum Cofactor Deficiency Type A (MoCoD-A) Overview
Molybdenum cofactor (MoCo) deficiency (MoCoD) is a rare metabolic disorder characterized by severe progressive neurologic damage, disordered autonomic function, exaggerated startle reactions, dysmorphic facial features, alterations in muscle tone, progressive cerebral palsy, microcephaly, seizures, and early death, and caused by the functional loss of sulfite oxidase, one of four molybdenum-dependent enzymes in humans. MoCoD-A is characterized by intractable seizures, feeding difficulties, and severe neurological impairment, leading to death in early childhood. The epidemiology of MoCoD-A is challenging due to its rarity which prevents a challenge in the disease understanding.
Molybdenum Cofactor Deficiency Type A (MoCoD-A) Diagnosis
The diagnosis of MoCoD is established by identifying of biallelic pathogenic variants in GPHN, MOCS1, MOCS2, or MOCS3, or when unavailable, of significantly reduced activity of the enzyme sulfite oxidase in cultured fibroblasts. However, due to the low expression of sulfite oxidase in fibroblasts, differentiation between total and partial loss of enzyme activity is difficult to discern. Because of its high sensitivity, molecular genetic testing typically obviates the need for enzymatic testing and thus is the preferred diagnostic test for MoCoD.
The diagnosis of MoCoD-A is challenging due to its rarity, non-specific symptoms, and the need for genetic testing for confirmation. Confirming the diagnosis requires identifying biallelic mutations in the MOCS1 gene and detecting specific metabolites in blood or urine tests, which necessitates specialized genetic testing and biochemical analyses.
Further details related to diagnosis are provided in the report...
Molybdenum Cofactor Deficiency Type A (MoCoD-A) Treatment
The treatment of Molybdenum Cofactor Deficiency Type A (MoCoD-A) is challenging due to its rarity and the need for specialized care. The primary goal of treatment is to manage symptoms and prevent complications. MoCoD-A with severe neonatal symptoms has very few therapeutic options and overall the outcome is usually poor. Many infants require intubation for supportive ventilation due to seizure activity and/or poor mental status. For the most part, the approach is to inform parents and caregivers of the extremely poor prognosis and offer options of abstaining from aggressive resuscitative medical interventions and/or withdrawing life supportive measures.
Further details related to treatment are provided in the report...
As the market is derived using the patient-based model, the Molybdenum Cofactor Deficiency Type A (MoCoD-A) epidemiology chapter in the report provides historical as well as forecasted epidemiology segmented by Prevalent cases of MoCoD, Diagnosed Prevalent Cases of MoCoD, and Type-specific Diagnosed Prevalent Cases of MoCoD in the 7MM covering the United States, EU4 countries (Germany, France, Italy, and Spain) and the United Kingdom, and Japan, from 2020 to 2034.
The drug chapter segment of the MOCOD-A report encloses a detailed analysis of MOCOD-A marketed drugs and late-stage (Phase III and Phase II) pipeline drugs. It also understands MOCOD-A 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.
Marketed Drugs
Nulibry (Fosdenopterin): BridgeBio Pharma
Nulibry (fosdenopterin) is cyclic pyranopterin monophosphate (cPMP), a substrate replacement therapy that provides an exogenous source of cPMP, which is converted to molybdopterin. It is the first-in-class approved cPMP substrate replacement therapy to reduce the risk of mortality in patients with molybdenum cofactor deficiency (MoCoD) Type-A. It is the first and only FDA-approved therapy for MoCoD Type A. The mechanism of action of fosdenopterin is to provide an exogenous source of cPMP. Patients with MoCoD Type-A have mutations in the MOCS1 gene leading to deficient MOCS1A/B dependent synthesis of the intermediate substrate, cPMP.
MOCOD-A has a diverse treatment classification associated with the disease landscape. The management of MOCOD-A primarily revolves around the utilization of Standard of care as needed.
This section focuses on the uptake rate of potential drugs expected to launch in the market during 2020-2034.
Further detailed analysis of emerging therapies drug uptake in the report...
Molybdenum Cofactor Deficiency Type A (MoCoD-A) Pipeline Development Activities
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.
Pipeline Development Activities
The report covers information on collaborations, acquisitions and mergers, licensing, and patent details for MOCOD-A emerging therapies.
KOL Views
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 the secondary research. Industry Experts were contacted for insights on MOCOD-A evolving treatment landscape, patient reliance on conventional therapies, patient therapy switching acceptability, and drug uptake along with challenges related to accessibility, including KOL from Children's Hospital Colorado, University of Colorado Denver, United States, University of Cologne, Germany, Department of Pediatrics, Seirei-Mikatahara General Hospital, Japan, and others.
Delveinsight's analysts connected with 25+ KOLs to gather insights; however, interviews were conducted with 10+ KOLs in the 7MM. Their opinion helps understand and validate current and emerging therapies, treatment patterns, or MOCOD-A market trends. This will support the clients in potential upcoming novel treatments by identifying the overall scenario of the market and the unmet needs.
Qualitative Analysis
We perform Qualitative and market Intelligence analysis using various approaches, such as SWOT 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 analyzes 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.
Market Access and Reimbursement
The high cost of therapies for the treatment is a major factor restraining the growth of the global drug market. Because of the high cost, the economic burden is increasing, leading the patient to escape from proper treatment.
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.
Market Insights
Epidemiology Insights
Current Treatment Scenario, Marketed Drugs, and Emerging Therapies
The Molybdenum Cofactor Deficiency Type A (MoCoD-A) Epidemiology and Market Insight report for the 7MM covers the forecast period from 2024 to 2034, providing a projection of market dynamics and trends during this timeframe.
The Molybdenum Cofactor Deficiency Type A (MoCoD-A) market is limited. The major players are BridgeBio Pharma, and others which are currently developing drugs for the treatment of Molybdenum Cofactor Deficiency Type A (MoCoD-A).
The market size is estimated through data analysis, statistical modeling, and expert opinions. It may consider factors such as incident cases, treatment costs, revenue generated, and market trends.
The increase in diagnosed prevalent cases of Molybdenum Cofactor Deficiency Type A (MoCoD-A) and the launch of emerging therapies are attributed to be the key drivers for increasing Molybdenum Cofactor Deficiency Type A (MoCoD-A) market.
Introducing new therapies, advancements in diagnostic techniques, and innovations in treatment approaches can significantly impact the Molybdenum Cofactor Deficiency Type A (MoCoD-A) treatment market. Market forecast reports may provide analysis and predictions regarding the potential impact of these developments.
The market forecast report may include information on the competitive landscape, profiling key market players, their product offerings, partnerships, and strategies, and helping stakeholders understand the competitive dynamics of the Molybdenum Cofactor Deficiency Type A (MoCoD-A) market.
7.10.. Diagnosis
List to be continued in the report...