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Alkaptonuria
An inborn error of amino acid metabolism resulting from a defect in the enzyme HOMOGENTISATE 1,2-DIOXYGENASE, an enzyme involved in the breakdown of PHENYLALANINE and TYROSINE. It is characterized by accumulation of HOMOGENTISIC ACID in the urine, OCHRONOSIS in various tissues, and ARTHRITIS.
Drugs by status
Phase 3 trials (1)
Organizations
Organization Involved with Phase 3 Indications (3)
Organization Involved with Phase 2 Indications (1)