Second Clinical Site for STAR-LLD Ph 1b Trial in Multiple Myeloma opened
Pedro Lichtinger, CEO of Starton, conveyed a positive outlook, expressing confidence by stating, “We are very pleased with the acceleration of our Phase 1b clinical study and with efficacy and tolerability patient outcomes to date. Results like these keep our team laser focused on achieving our important mission to have patients live longer while improving their quality of life, all while driving value for our stakeholders.” Mr. Lichtinger underscored the absence of significant hematologic toxicity and drug-related adverse events, aligning with the findings from preclinical studies conducted during the Investigational New Drug (IND) enabling phase.
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“FDA clearance of the IND for ORM-1153 is an important milestone for Orum, bringing another first-in-class DAC into the clinic and extending our approach into CD123-expressing hematologic malignancies,” said Olaf Christensen, M.D., Chief Medical Officer of Orum Therapeutics. “By combining cell-selective delivery with targeted protein degradation in a single molecule,
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