Diagnostics for chlamydia infection are crucial in identifying and diagnosing a sexually transmitted infection caused by Chlamydia trachomatis because they assist in preventing complications and controlling the spread of the infection. NAATs, culture tests, and serology tests, among others, enable rapid treatment initiation by establishing the presence of Chlamydia trachomatis DNA or antibodies.
The market is expanding rapidly, attributable to the rising testing frequency and growing demand for quick and reliable testing. The change from old conventional methods to molecular diagnostics has propelled the market forward, with over 1.6 million cases of chlamydia reported in the United States alone in 2021, emphasizing the critical need for accurate diagnostics for early detection, adequate treatment, and prevention of complications. Diagnostic technology advancements, such as quick and point-of-care testing options, are meeting rising demand and improving patient care.
Government initiatives, such as the National Chlamydia Screening Program (NCSP) in the UK, further drive the market's growth. These initiatives target high-risk individuals, focusing on rapid treatment and expanded testing in community settings. However, privacy concerns and societal stigma surrounding STD testing limit market growth, as individuals may be hesitant to undergo testing due to these factors. Despite these challenges, the high prevalence, growing awareness of early detection and treatment, and advancements in diagnostic technologies continue to drive the expansion of the market.
The introduction of novel technologies for diagnosing the disease will further offer lucrative opportunities in the review period. For instance, the Nucleic Acid Amplification Test (NAAT) is a recommended method for diagnosing chlamydia. It detects trachomatis DNA or RNA in biological samples with high sensitivity and specificity. The NAAT eliminates the need for pelvic exams in women and can be performed using vaginal swabs or urine samples, making it a convenient option.
North America holds a leading position in the market, driven by the high prevalence of chlamydia and new product developments by key players. The United States alone reported nearly 1.6 million cases in 2021, highlighting the significant burden of the infection. Product approvals contribute to market growth, such as Visby Medical's fast PCR diagnostic test and Abbott's Alinity m STI assay, both cleared by the FDA for detecting chlamydia. These advancements enhance diagnostic capabilities and provide convenient testing options for healthcare settings in the region.
Attribute |
Details |
Test Type |
Culture Test, Nucleic Acid Amplification Test (NAAT), Direct Fluorescent Antibody Test, Serology Test and Other |
By Type of Infections |
Genital Chlamydia Infection, Rectal Chlamydia Infection, Ocular Chlamydia Infection |
End User |
Diagnostics (Hospitals, Specialty Clinics, Diagnostics Centre), Therapeutics (Hospital Pharmacies, Drugstores, Retail Pharmacies, Online Pharmacies) |
Major companies operating in the market include Abbott, BD, Bio-Rad Laboratories, Inc, Quidel Corporation, DiaSorin SpA, AstraZeneca, and Teva Pharmaceutical Industries Limited. These players focus on geographical expansion and product launches to maintain their presence in the market. For instance, in May 2022, BD launched the BD COR MX instrument, an automated high-throughput molecular diagnostics platform in the US, featuring the BD CTGCTV2 assay that detects Chlamydia trachomatis, Neisseria gonorrhoeae, and Trichomonas vaginalis, addressing prevalent non-viral sexually transmitted infectious diseases with convenience and accuracy.
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