Ornithine Transcarbamylase Deficiency Treatment Market |
The ornithine transcarbamylase deficiency treatment market is estimated to be valued at US$ 810.4 Mn in 2023 and is expected to exhibit a CAGR of 4.2% over the forecast period 2023 to 2030, as highlighted in a new report published by Coherent Market Insights.
Market Overview:
Ornithine transcarbamylase (OTC) deficiency is an inherited disorder that
causes a buildup of ammonia in the blood due to the body's inability to flush
out excess nitrogen. Symptoms range from harmful neurodevelopmental issues to
life-threatening hyperammonemia. Treatment strategies involve dietary
restrictions, oral supplementation, and drug therapies that help bypass or
support compromised metabolic pathways. Key products available include
carbamoylase phosphate synthetase-1, glyceryl triacetyl esters of long-chain
fatty acids, and ornithine ketoacid supplements.
Market Dynamics:
The ornithine transcarbamylase deficiency treatment market is expected to
experience high growth over the forecast period, driven by two major factors.
Firstly, increased diagnosis rates especially among newborns through metabolic
screening programs are expanding the patient pool needing long-term management.
Various developed countries have made newborn screening for urea cycle
disorders including OTC deficiency mandatory under national healthcare schemes.
Secondly, advancements in therapeutic options beyond emergency interventions
like hemodialysis are providing optimized treatment outcomes. Promising pipeline
drugs targeting harmful metabolites and gene therapies are further improving
care pathways.
SWOT Analysis
Strength: Ornithine transcarbamylase deficiency treatment market has three
approved drugs which are effective in managing the disorder symptoms. The
increasing awareness programmes about rare diseases is positively impacting the
market growth. Availability of medical reimbursement in developed regions
benefit the patients access to treatment.
Weakness: High cost of drugs limits their uptake in low and middle-income
countries. Lack of patient support programs in underdeveloped regions pose
challenges.
Opportunity: Advancements in gene therapy and new drug delivery mechanisms
provide lucrative opportunities. Growing investments by biopharma companies for
developing novel treatment augers well for the market.
Threats: Stringent regulatory environment for approval of new drugs can hamper
timely access to treatment. Threat from alternative treatment therapies affects
market revenues.
Key Takeaways
The global Ornithine
Transcarbamylase Deficiency Treatment Market Share is expected to
witness high growth, exhibiting CAGR of
4.2% over the forecast period, due to increasing launch of new therapies
and drugs. North America region currently dominates the market due to growing
research activities and availability of reimbursement in the region.
Regional analysis
North America is expected to dominate the ornithine transcarbamylase deficiency
treatment market during the forecast period. This is attributed to growing
research on therapeutic options and availability of treatment and diagnosis in
the region. Europe also captures significant market share due to rising
healthcare infrastructure and supportive regulations. Asia Pacific demonstrates
fastest growth due to rising healthcare spending, growing incidence of rare
genetic disorders, and increasing awareness.
Key players
Key players operating in the ornithine transcarbamylase deficiency treatment
market are Horizon Therapeutics Plc, Bausch Health Companies Inc.,  Danone, Â
Nestlé,  Ultragenyx Pharmaceutical., Arcturus Therapeutics, Inc. ,  Abbott.,
 Swedish Orphan Biovitrum AB,  Acer Therapeutics Inc.,  Assertio Holdings,
Inc., iECURE, Â and Translate Bio, Inc. These players are entering into
collaborations to develop advanced treatment and expand market presence.
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