Poniard, a US biopharmaceutical company focused on oncology, has reached its enrollment target of 400 patients in the pivotal Phase III SPEAR trial of picoplatin in patients with recurrent small cell lung cancer who have failed prior platinum-containing, first-line chemotherapy or who have progressed within six months of first-line therapy.
The multicenter, randomized, controlled trial compares picoplatin plus best supportive care, to best supportive care alone, to evaluate the efficacy and safety of picoplatin after relapse. Results will be reported later this year.
"The data from this trial is event-driven and we expect that the overall survival data from the SPEAR trial will show a significant survival advantage compared to patients who receive best supportive care alone," said chief medical officer Robert De Jager. "We believe this is the first important step to provide a new treatment option for the many SCLC patients who do not achieve clinical benefit from current first-line therapies. This would be a significant accomplishment for this aggressive tumor type that has very few Food and Drug Administration-approved drugs," he added.
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