Centro Hospitalar e Universitário de Coimbra

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
A Study of PBFT02 in Participants With FTD and Mutations in the Granulin Precursor (GRN) or C9ORF72 Genes	Frontotemporal Lobar Degeneration, Nutritional and Metabolic Diseases, Pick disease, TDP-43 proteinopathy, brain disorder, central nervous system disorder, cognitive disorder, dementia, frontotemporal dementia, frontotemporal dementia with motor neuron disease, metabolic disease, nervous system disorder, neurodegenerative disease, proteostasis deficiencies, psychiatric disorder	Active, not recruiting	Phase 1 / Phase 2	2026-05-15		NCT04747431
Study of the Role of Genetic Modifiers in Hemoglobinopathies	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Hemic and Lymphatic Diseases, alpha thalassemia spectrum, anemia, beta thalassemia, familial hemolytic anemia, hematologic disorder, hemolytic anemia, hereditary disease, inherited hemoglobinopathy, sickle cell disease, thalassemia	Recruiting	Not stated	2024-03-20		NCT05799118

Clinical trials