Image Source : GOV.UK
The UK’s Medicines and Healthcare products Regulatory Agency (MHRA) has granted marketing authorisation to the Serum Institute of India for its novel tuberculosis skin test, SIILTIBCY. The test offers improved accuracy in TB detection, regardless of BCG vaccination status, and will soon be available across the UK.
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The Serum Institute of India has received a significant regulatory milestone with the UK’s MHRA granting marketing authorisation for its innovative tuberculosis diagnostic, SIILTIBCY. This approval follows a similar endorsement by the European Commission earlier this year, positioning SIILTIBCY as a next-generation TB skin test with enhanced sensitivity and specificity.
SIILTIBCY is designed to detect TB infection irrespective of prior BCG vaccination, addressing a long-standing limitation in traditional TB diagnostics. The test uses recombinant antigens rdESAT-6 and rCFP-10, which were classified as new active substances by the Committee for Medicinal Products for Human Use (CHMP).
Key highlights from the announcement include:
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SIILTIBCY will be launched across the UK and other EU/EEA countries starting Q1 2025, subject to local logistics.
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The test is expected to improve early TB detection and support public health efforts in high-burden regions.
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It is part of Serum Institute’s broader strategy to expand its global footprint in infectious disease diagnostics.
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The approval reinforces the institute’s reputation for delivering high-quality, affordable healthcare solutions worldwide.
Sources: Serum Institute of India Press Release, MHRA Product Database, SIILTIBCY.com.
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