| CPC G01N 33/6887 (2013.01) [A61K 38/1825 (2013.01); A61P 19/04 (2018.01); G01N 2800/10 (2013.01); G01N 2800/52 (2013.01)] | 13 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, the quantity of at least one biomarker selected from the group consisting of CIM (Collagen type I degraded by metalloproteinase), C3M (Collagen type 3 degraded by metalloproteinase) and CRPM (C-reactive protein degraded by metalloproteinase), and
b) administering intraarticularly the FGF-18 compound in an amount that is about 30-100 μg to the subject having lower than 30.0±2SD ng/mL of CIM (Collagen type I degraded by metalloproteinase) and/or lower than 12.0±2SD ng/mL of C3M (Collagen type 3 degraded by metalloproteinase) and/or lower than 10.0±2SD ng/mL of CRPM (C-reactive protein degraded by metalloproteinase),
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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