Life science and clinical research company Thermo Fisher Scientific Inc (NYSE:TMO) on Wednesday announced the launch of the CorEvitas Adolescent Alopecia Areata (AA) Registry to address the need for real-world, adolescent-specific data on this autoimmune condition.
The international registry will support research on disease burden, treatment effectiveness, and safety.
Now active in Europe and the United States., the registry recently enrolled its first patients in both regions. It is the 12th independent CorEvitas registry, complementing an existing adult AA registry launched in 2023. The initiative operates under the guidance of dermatology experts from Yale School of Medicine, Harvard Medical School, and Dermatology Physicians of Connecticut.
Designed to collect data on safety events, medication patterns, and treatment outcomes, the registry will track adolescent AA patients over time. AA affects approximately 2% of the global population, with many cases emerging in childhood or adolescence. The condition is associated with psychosocial challenges and a higher prevalence of other autoimmune diseases.
CorEvitas, part of Thermo Fisher Scientific's PPD clinical research business, provides regulatory-grade patient data across multiple disease areas. Its independent registry model has been recognized by regulators for long-term post-authorization safety studies.
WuXi Biologics honoured for water security by CDP
Johnson & Johnson reports breakthrough overall survival data for EGFR-mutated lung cancer treatment
Niagen Bioscience secures US patent for nicotinamide riboside salt forms
Sobi forms research collaboration for development of Gamifant in sepsis
Black Diamond Therapeutics and Servier agree global licensing deal for BDTX-4933
Health Canada approves KEYTRUDA for advanced or recurrent endometrial carcinoma
Medivir secures European patent for fostrox and lenvatinib combination in liver cancer treatment
SIFI enters scientific collaboration with UCSF on Acanthamoeba Keratitis
Johnson & Johnson's nipocalimab granted FTD for treatment of Sjogren's disease
Vascarta launches phase I VAS101 clinical study in osteoarthritis
GRIN Therapeutics' Radiprodil receives Orphan Drug designation
Evommune enrols first patient in EVO301 Phase 2 trial
BioArctic receives US FDA orphan drug designation OOPD for exidavnemab
Physiomics secures GBP102,000 contract with UK biotech for ADC therapy development