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Recently, promising results of the antitumor effects were observed in patients with metastatic castration-resistant prostate cancer treated with 177 Lu-labeled PSMA-ligands. Radionuclide therapy efficacy may even be improved by using the alpha emitter Ac-225. Higher efficacy is claimed due to high linear energy transfer specifically towards PSMA positive cells, causing more double-strand breaks. This study aims to manufacture [ 225 Ac]Ac-PSMA-I&amp;T according to good manufacturing practice guidelines for the translation of [ 225 Ac]Ac-PSMA-I&amp;T into a clinical phase 1 dose escalation study. Quencher addition during labeling was investigated. Quality control of [ 225 Ac]Ac-PSMA-I&amp;T was based on measurement of Fr-221 (218 keV), in equilibrium with Ac-225 in approximately six half-lives of Fr-221 (T½ = 4.8 min). Radio-(i)TLC methods were utilized for identification of the different radiochemical forms, gamma counter for concentration determination, and HPGe-detector for the detection of the radiochemical yield. Radiochemical purity was determined by HPLC. The final patient dose was prepared and diluted with an optimized concentration of quenchers as during labeling, with an activity of 8-12 MBq (±5%), pH &gt; 5.5, 100 ± 20 μg/dose, PSMA-I&amp;T, radiochemical yield &gt;95%, radiochemical purity &gt;90% (up to 3 h), endotoxin levels of &lt;5 EU/mL, osmolarity of 2100 mOsmol, and is produced according to current guidelines. The start of the phase I dose escalation study is planned in the near future.

Development of [225Ac]Ac-PSMA-I&T for Targeted Alpha Therapy According to GMP Guidelines for Treatment of mCRPC