Genecombio Ltd.

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
GCB-002 in Treatment of Patients With Rett Syndrome	RETT Syndrome With Proven MECP2 Mutation	Enrolling by invitation	Not applicable	2026-09-15		NCT06739434
GCB-001 in Treatment of Patients With Type II (SMA) Spinal Muscular Atrophy	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Muscular Atrophy, Spinal, Type II, Spinal Muscular Atrophies of Childhood, central nervous system disorder, hereditary disease, inherited neurodegenerative disorder, motor neuron disorder, nervous system disorder, neurodegenerative disease, neuromuscular disease, spinal cord disorder, spinal muscular atrophy	Enrolling by invitation	Not applicable	2026-09-11		NCT06772402

Clinical trials