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Crigler-Najjar Syndrome
A familial form of congenital hyperbilirubinemia transmitted as an autosomal recessive trait. It is characterized by icterus and brain damage caused by a glucuronyl transferase deficiency in the liver and faulty bilirubin conjugation.
Drugs by status
Phase 2 trials (5)
Other trials (1)
Organizations
Organization Involved with Phase 4 Indications (1)
Organization Involved with Phase 2 Indications (3)
Organization Involved with Other Experimental Indications (3)