| CPC G01N 33/6887 (2013.01) [A61K 38/1825 (2013.01); A61P 19/04 (2018.01); G01N 2333/78 (2013.01); G01N 2800/105 (2013.01); G01N 2800/52 (2013.01)] | 12 Claims |
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1. A method for treating a subject having a cartilage disorder characterized by articular cartilage injury or loss of articular cartilage, with an FGF-18 compound, comprising the following steps:
a) determining, from a sample from said subject, the quantity of at least one biomarker selected from the group consisting of CTX-II (C-terminal telopeptide of type II collagen) and ProC2 (neo-epitope of Collagen type II), and
b) administering intraarticularly the FGF-18 compound in an amount that is about 30-100 μg to the subject having lower than 350±2SD ng/mmol of CTX-II, and/or lower than 4.2±2SD ng/ml of ProC2, and
wherein the FGF-18 compound comprises amino acid residues 28-196 of SEQ ID NO: 1, optionally fused to a heterologous protein or chemical compound.
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