BERLIN, Sept. 30, 2026 /PRNewswire/ -- Roche (SIX: RO, ROP; OTCQX: RHHBY) announced today that TIB MOLBIOL, a subsidiary of Roche Diagnostics, has launched the LightMix® Newborn TREC/SMN1/HBB kit, an in vitro diagnostic test for newborn screening in countries accepting the CE mark. The test simultaneously screens for Spinal Muscular Atrophy (SMA), Severe Combined Immunodeficiency Disease (SCID), and Sickle Cell Disease (SCD). This launch provides a crucial, ready-to-use solution for private and academic hospital labs, enabling the early detection of devastating conditions to drastically improve patient outcomes.
"When a baby is born with a condition like SMA or SCID, every single day counts," said Marcus Droege, CEO of TIB MOLBIOL. "Catching these diseases before symptoms appear isn't just about early diagnosis; it's the difference between a child thriving or facing severe, lifelong disability. By expanding our compliant newborn screening tools across Europe, we are helping laboratories transition to high-precision solutions that ensure no critical diagnosis is delayed."
Early diagnosis empowers clinicians with clear, actionable information, providing answers for patients and their families and enabling them to access the appropriate treatments sooner. This screening test exemplifies Roche's integrated approach to healthcare by acting as a first-tier trigger for immediate follow-up testing and therapeutic intervention.
For example, after identifying SMA, a rare disorder causing progressive muscle weakness and nerve degeneration, at birth, clinicians can immediately initiate treatment with targeted therapies. Catching SMA early may halt severe nerve damage, prevent permanent disability, and allow for normal growth milestones1.
Similarly, early detection of SCD allows for timely interventions, including preventive penicillin and specialised immunisations, which can drastically lower infant mortality2. In conditions like SCID, historically known as "bubble boy disease", infants lack a functioning immune system and are highly susceptible to severe infections. Early detection allows for lifesaving treatments such as bone marrow transplants before dangerous infections occur3.
The LightMix® Newborn TREC/SMN1/HBB kit runs on established LightCycler systems.
About the diseases
Spinal Muscular Atrophy (SMA) is a genetic neuromuscular disorder causing progressive degeneration of nerve cells in the spinal cord, leading to muscle weakness. It is caused by homozygous deletions of survival motor neuron 1 (SMN1) exon 7. Early detection allows treatment to start before symptoms appear, leading to better muscle function.
Severe Combined Immunodeficiency (SCID) is a group of rare, life-threatening genetic disorders characterised by a lack of functioning T cells, leaving infants with virtually no immune system. Without prompt medical intervention, it is fatal within the first year or two of life.
Sickle Cell Disease (SCD) is an inherited red blood cell disorder caused by a genetic mutation in the HBB gene. Red blood cells become rigid and sickle-shaped, breaking down prematurely and blocking blood vessels. Timely care lowers the risk of severe infections, sudden spleen failure, and early childhood death.4
About TIB MOLBIOL
TIB MOLBIOL, a subsidiary of Roche Diagnostics, has supplied the global market with reagents for research and medical diagnostics since 1990. Started as a manufacturer of custom oligonucleotides, the company has built a broad portfolio of molecular PCR assays used in medical diagnostics, research, and industrial manufacturing worldwide. TIB MOLBIOL's portfolio of assays are available for LightCycler systems, cobas 5800/6800/8800 omni utility channels and digital LightCycler systems, particularly for infectious and genetic diseases. The assays are offered as ready-to-use kits for established syndromic panels, as well as modular kits that enable customers to create customized panels by combining individual assays. TIB MOLBIOL is headquartered in Berlin (Germany). For more information about the PCR assays and systems, please visit www.diagnostics.roche.com or www.tib-molbiol.com.
About Roche
Roche (SIX: RO, ROP; OTCQX: RHHBY) is a healthcare company uniquely placed to prevent, stop and cure diseases by uniting leading science and technology across diagnostics, medicines and digital solutions.
Roche was founded in Basel, Switzerland in 1896 and today is a leading provider of transformative medicines and diagnostics for millions of people in over 150 countries around the world. It is dedicated to tackling healthcare challenges that place the greatest strain on patients, families, communities and healthcare systems. Across its Diagnostics and Pharmaceutical divisions, Roche focuses on areas including oncology, neurology, cardiovascular and metabolic diseases, ophthalmology, infectious diseases and immunology with the aim of providing real and positive change for patients, the people they love and the professionals who care for them.
Genentech in the United States is a fully owned subsidiary in the Roche Group. Roche is the majority shareholder in Chugai Pharmaceutical, a major innovator in the Japanese therapeutic antibody market.
For more information, please visit www.roche.com.
All trademarks used or mentioned in this release are protected by law.
References
[1] Phan HC, Taylor JL, Hannon H, Howell R. Newborn screening for spinal muscular atrophy: Anticipating an imminent need. Semin Perinatol. 2015 Apr;39(3):217-29. doi: 10.1053/j.semperi.2015.03.006. PMID: 25979781.
[2] Elendu C, Amaechi DC, Alakwe-Ojimba CE, Elendu TC, Elendu RC, Ayabazu CP, Aina TO, Aborisade O, Adenikinju JS. Understanding Sickle cell disease: Causes, symptoms, and treatment options. Medicine (Baltimore). 2023 Sep 22;102(38):e35237. doi: 10.1097/MD.0000000000035237. PMID: 37746969; PMCID: PMC10519513.
[3] Biggs CM, Haddad E, Issekutz TB, Roifman CM, Turvey SE. Newborn screening for severe combined immunodeficiency: a primer for clinicians. CMAJ. 2017 Dec 18;189(50):E1551-E1557. doi: 10.1503/cmaj.170561. PMID: 29255099; PMCID: PMC5738248.
[4] Ochocinski D, Dalal M, Black LV, Carr S, Lew J, Sullivan K, Kissoon N. Life-Threatening Infectious Complications in Sickle Cell Disease: A Concise Narrative Review. Front Pediatr. 2020 Feb 20;8:38. doi: 10.3389/fped.2020.00038. PMID: 32154192; PMCID: PMC7044152.
For further information please contact
Yvette Petillon, Group Media Relations
Phone: +41 79 961 92 50
e-Mail: yvette.petillon@roche.com
Kathryn Ager, Senior Communications Business Partner Roche Diagnostics
Phone: +44 7745 115046
e-Mail: kathryn.ager@roche.com
Brien Mahoney, Head of Communications Molecular Labs
Phone: +1 925-699-8512
e-Mail: brien.mahoney@roche.com
View original content to download multimedia:https://www.prnewswire.co.uk/news-releases/roche-launches-newborn-screening-test-for-three-severe-genetic-conditions-302893267.html
Eine anonyme E-Mail an die US-Botschaft in Bern hat kurz vor dem Auftritt von US-Präsident Donald Trump beim Weltwirtschaftsforum in Davos ein Ermittlungsverfahren der Schweizer Bundesanwaltschaft ausgelöst – und zur Festnahme einer WEF-Mitarbeiterin geführt. Inzwischen ist klar: Die gegen die IT-Expertin erhobenen Vorwürfe eines geplanten Attentats waren nicht zu belegen. Die Bundesanwaltschaft teilte mit, die in der Sache eröffneten Ermittlungen wegen strafbarer Vorbereitungshandlungen zu einem Mord seien eingestellt worden.
Die Warnmail war laut Medienberichten der Tamedia-Gruppe wenige Stunden vor Trumps Rede eingegangen. Der anonyme Absender schilderte in fehlerhaftem Englisch eine angeblich „dringliche Bedrohung“ für das Leben des US-Präsidenten in Davos und bezeichnete die später festgenommene Frau iranischer Herkunft als Agentin, die eine entsprechende Operation koordiniert habe. Die US-Botschaft leitete den Hinweis an die Schweizer Behörden weiter; diese erklärten, sie hätten die Warnung „sehr ernst“ genommen und seien „sofort aktiv“ geworden.
Tatsächlich arbeitete die Beschuldigte nicht am Tagungsort in Davos, sondern in der WEF-Zentrale im Genfer Vorort Cologny. Dort wurde sie nach Angaben der Bundesanwaltschaft festgenommen, mehrere Stunden lang bis tief in die Nacht vernommen und ihre Telefone sowie ihr Computer wurden beschlagnahmt und ausgewertet. Im Zuge dieser Maßnahmen habe sich jedoch gezeigt, dass sich keiner der in der anonymen E-Mail erhobenen Punkte erhärten ließ. Für alle Aspekte der Anschuldigungen seien keine Beweise gefunden worden, hieß es zur Begründung für die Einstellung des Verfahrens.
Die betroffene Mitarbeiterin, eine gebürtige Iranerin, war nach den Medienberichten kurz nach dem Vorfall beim WEF nicht mehr beschäftigt. Zu den Gründen äußerte sich die Organisation nicht; auf entsprechende Anfragen gab es zunächst keine Stellungnahme. Damit bleiben nach dem spektakulären Fehlalarm vorerst Fragen offen – etwa zur Herkunft und Glaubwürdigkeit des anonymen Hinweises –, während die Schweizer Strafverfolger den Fall strafrechtlich abgeschlossen haben.