From WisPolitics.com/WisBusiness.com …
— Cellectar Biosciences, a drug development firm that spun off from UW-Madison, is touting “compelling” new data on the effectiveness of its cancer therapy.
The company yesterday showcased the results in a presentation at the American Society of Clinical Oncology Annual Meeting in Chicago. The data came from its Phase 2 clinical trial for iopofosine 131, which is used to deliver a targeted radioisotope to treat specific cancers.
The results “demonstrated significant efficacy” for the 24-person study group, which included patients treated with Cellectar’s drug following a different treatment with post-Bruton Tyrosine Kinase inhibitor, or BTKi therapy.
Jarrod Longcor, chief operating officer for the company, says these patients “represent a distinct clinical population” within those with Waldenström macroglobulinemia, a rare form of blood cancer. They face limited treatment response and “rapid disease progression” following the end of BTKi therapy, according to Longcor.
“We are highly encouraged by these results … which demonstrate compelling efficacy and durable responses,” he said, noting they were seen even in this “particularly challenging patient population” that has progressed following earlier therapy.
Yesterday’s presentation highlighted the trial’s 100% clinical benefit rate and 87.5% overall response rate, as well as the 79.2% major response rate, indicating a partial response or better.
President and CEO James Caruso says the company plans to pursue accelerated approval in the United States and start a Phase 3 study later this year to confirm its findings.
“We remain committed to bringing iopofosine to the thousands of patients who may benefit from this therapy,” he said in a statement.
See the release below.
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