The preparation of a polyazamacrocyclic-nitrotriazole conjugate for radiolabeling with the therapeutic radioisotope viz. ¹⁷⁷Lu is described. The nitroimidazole used for the present study is [N-2′(carboxyethyl)-2-(3′-nitro-1′-triazolyl)acetamide], the carboxylic acid derivative of sanazole, which possesses an optimal combination of desired properties such as, selective toxicity for hypoxic cells, lowered lipophilicity resulting in lowered neurotoxicity. The bifunctional chelating agent is a DOTA derivative viz. 1,4,7,10-tetraaza-1-(4′-aminobenzylacetamido)-cyclododecane-4,7,10- triacetic acid (p-amino-DOTA-anilide). ¹⁷⁷Lu was produced in adequate specific activity (110TBq/g) and high radionuclidic purity (~100%) by irradiating enriched (60.6% ¹⁷⁶Lu) Lu₂O₃ target and used for radiolabeling of the sanazole–BFCA conjugate. ~98% Complexation yield was achieved under optimized conditions. The complex has been characterized by paper chromatography and HPLC studies. Bioevaluation studies in Swiss mice bearing fibrosarcoma tumors revealed moderate tumor uptake (0.88%/g at 1h post-injection) with favorable tumor to blood (4.00 at 1h post-injection) and tumor to muscle (4.63 at 1h post-injection) ratios.