U.S. clinical testing of Theseus Imaging's Hynic-Annexin V molecular imaging agent appears set to resume. The firm is planning phase II studies in the U.S. to assess the predictive value of the radiopharmaceutical at various times following a single course of chemotherapy, according to Theseus parent North American Scientific of Chatsworth, CA.
The clinical study is designed to provide information about product safety, biodistribution, and imaging technique after chemotherapy in non-small cell lung cancer patients, NAS said. The firm's investigational new drug (IND) application was opened May 9 after Theseus had responded to comments from the Food and Drug Administration. Theseus had pulled its initial IND application in January.
By AuntMinnie.com staff writersJune 13, 2003
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