Substituted indazole derivatives of formula (I) or formula 2.(I) and pharmaceutically acceptable salts thereof, as defined in the specification, process for their preparation and pharmaceutical compositions comprising them are disclosed; the compounds of the invention may be useful in therapy in the treatment of diseases associated with a deregulated protein kinase activity, like cancer.本發明揭示如本說明書中所定義的式(I)或式2.(I)之經取代吲唑衍生物及其醫藥學上可接受之鹽,其等製備方法及包含其等之醫藥組合物;本發明化合物可適用於治療與蛋白激酶活性失調有關之疾病,如癌症。