Los diagnósticos complementarios son pruebas in vitro que brindan información sobre las respuestas terapéuticas de los pacientes a un tratamiento específico. Se trata de un dispositivo médico in vitro que brinda información necesaria para el manejo seguro y eficaz de un medicamento o producto biológico correspondiente. Esta prueba diagnóstica ayuda al médico a determinar si un producto terapéutico específico es beneficioso para los pacientes y puede compensar cualquier posible efecto secundario o riesgo grave.
El aumento de los distintos tipos de cáncer entre las personas es el principal factor que impulsa el crecimiento del mercado. A medida que aumenta el número de ensayos clínicos y la demanda de secuenciación de última generación , también lo hará el mercado de diagnóstico complementario. Otro factor que impulsa dicho crecimiento es la importancia de los productos de este mercado en la producción de diversos tipos de medicamentos.
Se espera que el mercado de diagnósticos complementarios crezca significativamente durante el período de pronóstico, debido a un aumento en la I+D de terapias dirigidas, un aumento en la demanda de medicina de precisión con creciente atención en las economías emergentes, el descubrimiento de nuevos biomarcadores para diversas afecciones y un mayor número de necesidades insatisfechas para el tratamiento del cáncer.
Con los avances en la secuenciación hereditaria y la genómica, ahora se acepta ampliamente que los medicamentos pueden generar resultados variables en diferentes personas. Una mejor comprensión de las características hereditarias o los biomarcadores de un individuo puede hacer avanzar el acto de supervisar "la medicación correcta, en el momento perfecto, en la dosis correcta, para el individuo perfecto". Las compañías farmacéuticas y biofarmacéuticas trabajan constantemente para implementar sistemas analíticos de elección del paciente en las primeras etapas del desarrollo de medicamentos con el fin de proporcionar tratamientos específicos al competidor adecuado. Esto contribuye al crecimiento del mercado de diagnósticos complementarios.
| ATRIBUTO | DETALLES |
| Periodo de estudio | 2020-2029 |
| Año base | 2022 |
| Año estimado | 2022 |
| Año pronosticado | 2022-2029 |
| Periodo histórico | 2018-2020 |
| Unidad | Valor (miles de millones de USD) |
| Segmentación | Por oferta, por tecnología, por indicación, por usuario final, por región |
| Por tecnología de resina |
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| Por tecnología |
|
| Por indicación |
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| Por el usuario final |
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| Por región |
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La introducción de la COVID-19 ha obstaculizado el consumo de diagnósticos complementarios. Además, los principales actores del mercado sufrieron una caída significativa de los ingresos como resultado de la pandemia de COVID-19, debido a una reducción en el volumen de pruebas y otros factores. En lo que respecta a los ingresos, el mercado creció un 15,1% en 2020, en comparación con el 19,8% en 2019.
Los ingresos generados por los principales actores disminuyeron significativamente en 2020. Por ejemplo, Myriad Genetics, Inc. informó una disminución del 34,5 % en los ingresos por diagnóstico molecular en 2020 en comparación con 2019. Además, Abbott Laboratories informó una disminución del 4,0 % en los ingresos por diagnósticos de laboratorio básicos en 2020 en comparación con 2019.
Sin embargo, el levantamiento de las restricciones de confinamiento, las órdenes de quedarse en casa en muchos países, la introducción de nuevas pruebas de diagnóstico y el restablecimiento de la red de la cadena de suministro fueron factores clave en la recuperación de las pruebas en 2021. Como resultado, la reanudación de las pruebas de diagnóstico del cáncer y la introducción de nuevas pruebas de diagnóstico impulsaron la demanda en 2021.
The companion diagnostics market size had crossed USD 3.5 Billion in 2020 and will observe a CAGR of more than 13.34% up to 2029.
Major factors driving the companion diagnostics market growth include the significant growth of companion diagnostics in drug development and rising incidence of cancer and growing adoption of targeted therapies.
Qiagen, Agilent Technologies, Roche, Abbott Laboratories, Inc., BioMerieux, Ventana Medical Systems, Myriad Genetics, Inc., Resonance Health Ltd, Leica Microsystems, Life Technologies, F. Hoffmann-L Roche Ltd., Illumina, Inc., Guardant Health, Thermo Fisher Scientific Inc., Danaher Corporation are the major companion diagnostics market players.
The region's largest share is in North America. Products manufactured in nations like US and Canada that perform similarly and are inexpensively accessible to the general public have led to the increasing appeal.
The companion diagnostics market is segmented based on products, technology, indication, end user, and region, global trends and forecast.
On the basis of products, the market is segmented into assays, kits & reagents, software & services. Due to increase in demand for kits and reagents, the assays, kits and reagents segment is estimated to lead.
On the basis of technology, the market is segmented into polymerase chain reaction, next-generation sequencing, in situ hybridization, immunohistochemistry.
Based on technology, the pcr segment currently dominates the global market and is expected to do so throughout the forecast period. Cost effectiveness, high sensitivity, and specificity, which can be used for simple automated platforms, are some key factors driving market growth. Furthermore, the pcr, which is another key driver of this segment, can determine the sequencing of unknown etiologies of many diseases. However, the next generation sequencing segment is expected to grow rapidly during the forecast period due to key advantages such as higher sensitivity to detect low-frequency variants, shorter turnaround time for large sample volumes, the ability to sequence hundreds to thousands of genes or gene regions simultaneously, and so on.
On the basis of indication, the market is segmented into cancer, neurological diseases, infectious diseases, cardiovascular diseases.
The cancer segment is currently the largest revenue generator and is expected to grow significantly during the forecast period. Some key factors driving the growth of the cancer segment include increased cancer prevalence, increased r&d activities for cancer, increased unmet needs for cancer treatment, increased number of fda approved companion diagnostics, and increased patient awareness of personalized medicine.
Cancer research has discovered significant differences in gene sequence and expression patterns that can serve as the foundation for targeted therapy. Furthermore, many biomarkers for various cancers have been identified, for which companion diagnostics have been developed. Companion diagnostics are widely used in various types of cancer, including lung cancer, colorectal cancer, breast cancer, and blood cancer, which are the leading causes of death.
On the basis of end user, the market is segmented into pharmaceutical & biopharmaceutical companies, contract research organizations, laboratories.
There is no denying that contract research organizations (cros) are becoming more important in the development of companion diagnostics. As the demand for personalized medicine grows, cros are uniquely positioned to assist pharmaceutical and biotechnology companies in developing customized treatments based on a patient's unique genetic makeup.
Companion diagnostics are diagnostic tests used to identify patients who are likely to benefit from a specific treatment. They can also be used to track a patient's response to therapy and make necessary adjustments. Cancer, cardiovascular disease, and infectious diseases are just a few of the conditions that can be treated with companion diagnostics.
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The Companion Diagnostics Market by region includes North America, Asia-Pacific (APAC), Europe, South America, and Middle East & Africa (MEA).
North America is expected to lead the global companion diagnostics market. This could explain the high incidence rate of cancer and other chronic diseases, as well as the rising cost of healthcare in the area. Furthermore, market development is expected to drive an increase in the number of healthcare organisations working on generated genomic databases to better understand the human genome, as well as increased research activities in this area using companion diagnostic kits.
The European market for companion diagnostics is expected to be the second-largest during the review period. The expansion of the regional industry is expected to fuel the participation of a large number of companies as well as increased research and development activities aimed at improving personalised drug treatment for cancer patients. Furthermore, rising per capita income increases the preference for personalised treatment, fueling further consumer growth.
Because of the rapidly increasing number of cancer, cardiovascular, and neurological patients, Asia-Pacific is expected to be the fastest growing region. Furthermore, the rising prevalence of infectious diseases has a positive impact on business development. The high prevalence of cancer, increasing proteomics and genomics research, rising research funding, increasing investments by pharmaceutical and biotechnology firms, and rising awareness of personalised therapeutics in many APAC countries are expected to drive the growth of the APAC companion diagnostics market.
The Middle East and Africa market is expected to grow steadily due to an increase in cancer cases and a growing preference for customised drugs. The Middle East and Africa market is expected to grow steadily due to an increase in the number of hospitals and research labs, increased investment by healthcare firms, an increase in cancer cases, and increased drug discovery.
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