UAE CDKL5 deficiency disorder (CDD) market Report 2023 to 2030

UAE CDKL5 deficiency disorder (CDD) market Analysis

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UAE CDKL5 deficiency disorder Market is projected to grow from $xx Mn in 2023 to $xx Mn by 2030, registering a CAGR of xx% during the forecast period of 2023 - 2030. The market for CDKL5 deficiency disorder is expanding as a result of increase in global prevalence of CDKL5 deficiency disorder and increase in awareness about neurological diseases. In addition, high expenditure on healthcare and genetic testing, growing demand for targeted therapies, increase in R&D spending for the discovery of novel pharmaceuticals are other reasons . This demand is fueling the development of better pharmaceuticals and other treatment methods for the accurate treatment of CDKL5 deficiency disorder. Some of the key players in the global CDKL5 deficiency disorder market include Marinus pharmaceuticals, REGENXBIO, Zogenix, PTC therapeutics and Ovid therapeutics/ Takeda

ID: IN10AERD076 CATEGORY: Rare Diseases GEOGRAPHY: UAE AUTHOR: Gaurav Bhongale

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UAE CDKL5 deficiency disorder (CDD) Market Analysis Summary

UAE CDKL5 deficiency disorder (CDD) Market is valued at around $1.76 Mn in 2022 and is projected to reach $3.05 Mn by 2030, exhibiting a CAGR of 7.1% during the forecast period 2023-2030.

The CDKL5 (cyclin-dependent kinase-like 5) deficiency disorder market refers to the pharmaceuticals and other methods used to treat CDKL5 (cyclin-dependent kinase-like 5) deficiency disorder. CDKL5 deficiency disorder (CDD) is a rare neurodevelopmental condition caused by pathogenic variants in the CDKL5 gene. A protein required for typical brain growth, nerve cell development and operation is produced by the CDKL5 gene. The amount of functional CDKL5 protein is decreased or its activity in neurons is altered by pathogenic variations in the CDKL5 gene. Early-onset, difficult-to-control seizures and neurodevelopmental impairment that affects speech, language, motor, and cognitive function are the most typical symptoms. Evidently, seizures are a significant issue in CDKL5. Most of the children who are affected begin to experience them within the first few weeks or months of life. With time, their pattern frequently develops and changes. Undoubtedly one of the most prevalent types of genetic epilepsy is CDKL5 deficient condition. The CDKL5 gene is located on the X chromosome, according to The Orphan Disease Centre. Females make up the majority of CDKL5 patients (>80%), although boys with CDKL5 deficiencies typically exhibit more severe symptoms.

The goals of treatment are to minimise symptoms, assist children suffering from disease and counsel their families to develop each child's potential. Children with CDKL5 meet with an interdisciplinary team of professionals at a unique CDKL5 clinic, where they receive a personalised treatment plan that is to be followed by the child's neighbourhood medical, therapeutic, and educational teams.

There are no approved treatments for CDD at the moment now. Antiepileptic medications, anticonvulsants, physiotherapy, occupational therapy, neurological speech therapy, and dietetics are all part of the multidisciplinary care used to treat CDD.

The most efficient way to provide necessary therapies is focused on maximising the individual's talents and encouraging any skills that may be developing is through a multidisciplinary team approach. Early intervention therapies include speech and augmentative communication therapy, occupational therapy, and physical therapy to be prioritised. The creation of an appropriate education plan, psychosocial support for the family, and an evaluation of the community resources available are all crucial components of management.

Patients with CDD frequently experience severe seizures that are challenging to manage with medication. There isn't a single anti-seizure drug that consistently works to treat CDD. From a few weeks to a few years, seizure-free periods may be possible with a combination of anti-seizure drugs. First-line treatments include administering antiepileptic and anticonvulsant drugs to each patient individually. If seizures recur, second-line treatments are chosen.

Market Dynamics

Market Drivers

Growing Incidence and Prevalence of CDKL5 deficiency disorder (CDD) Disease- As the incidence and prevalence of disease this acts as a market driving factor.

Unmet Medical Need- There are few effective treatments for CDKL5 deficiency disease. Due to the absence of effective treatments, there is an unmet medical need that may motivate research and development efforts to discover novel medicines or treatments to reduce symptoms and enhance the quality of life for those who are affected.

Increase in advocacy and awareness about neurological diseases - Greater public and scholarly attention may result from increased awareness, which may draw additional resources and financial support for R&D.

Incentives by Regulatory bodies -Regulatory bodies, such as the European Medicines Agency (EMA) and the U.S. Food and Drug Administration (FDA), offer incentives and support for the development of medications for rare diseases. These incentives can be in the form of orphan drug designation, expedited approval processes, and longer market exclusivity periods.

Technological Advancements- An increase in knowledge of genetics and technological developments like innovations in gene therapy, genome editing, and precision medicine methods is also a factor driving the market.

Market Restraints

Economic factors- High developmental costs of drugs and huge investments in Research and development can act as a restraint.

Cultural differences in collaborative research – This can also act as a restraint when research is carried out in collaboration between many countries.

Key players

Ultragenyx Pharmaceutical Orchard Therapeutics uniQure Astellas Pharma PTC Therapeutics Pfizer BioMarin Pharmaceutical Stealth Biotherapeutics Sarepta Therapeutics Bluebird bio

1. Executive Summary
1.1 Disease Overview
1.2 Global Scenario
1.3 Country Overview
1.4 Healthcare Scenario in Country
1.5 Patient Journey
1.6 Health Insurance Coverage in Country
1.7 Active Pharmaceutical Ingredient (API)
1.8 Recent Developments in the Country

2. Market Size and Forecasting
2.1 Epidemiology of Disease
2.2 Market Size (With Excel & Methodology)
2.3 Market Segmentation (Check all Segments in Segmentation Section)

3. Market Dynamics
3.1 Market Drivers
3.2 Market Restraints

4. Competitive Landscape
4.1 Major Market Share

4.2 Key Company Profile (Check all Companies in the Summary Section)

4.2.1 Company
4.2.1.1 Overview
4.2.1.2 Product Applications and Services
4.2.1.3 Recent Developments
4.2.1.4 Partnerships Ecosystem
4.2.1.5 Financials (Based on Availability)

5. Reimbursement Scenario
5.1 Reimbursement Regulation
5.2 Reimbursement Process for Diagnosis
5.3 Reimbursement Process for Treatment

6. Methodology and Scope

Market Segmentations For UAE CDKL5 deficiency disorder (CDD) Market

By Medication:

Traditional drugs
Emerging drugs

By End Users:

Hospital
Clinic
Others

Methodology for Database Creation

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How Do We Get It?

Our database is created and maintained through a combination of secondary and primary research methodologies.

1. Secondary Research

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Analyzing historical proprietary data collected from multiple projects.
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Ensuring data consistency and accuracy through rigorous validation processes.

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Searching through academic conferences, published research, citations, and social media platforms
Collecting and compiling diverse data to build a comprehensive and detailed database
Continuously updating our database with new information to ensure its relevance and accuracy

2. Primary Research

To complement and validate our secondary data, we engage in primary research through local tie-ups and partnerships. This process involves:

Collaborating with local healthcare providers, hospitals, and clinics to gather real-time data.
Conducting surveys, interviews, and field studies to collect fresh data directly from the source.
Continuously refreshing our database to ensure that the information remains current and reliable.
Validating secondary data through cross-referencing with primary data to ensure accuracy and relevance.

Combining Secondary and Primary Research

By integrating both secondary and primary research methodologies, we ensure that our database is comprehensive, accurate, and up-to-date. The combined process involves:

Merging historical data from secondary research with real-time data from primary research.
Conducting thorough data validation and cleansing to remove inconsistencies and errors.
Organizing data into a structured format that is easily accessible and usable for various applications.
Continuously monitoring and updating the database to reflect the latest developments and trends in the healthcare field.

Through this meticulous process, we create a final database tailored to each region and domain within the healthcare industry. This approach ensures that our clients receive reliable and relevant data, empowering them to make informed decisions and drive innovation in their respective fields.