End of Ph 2 Meeting with FDA for Annamycin in AML Completed
“The Moleculin team, along with our regulatory advisors and key opinion leaders, discussed with FDA the MB-106 safety and efficacy clinical findings and proposed next steps for our AML clinical development program,” commented Walter Klemp, Chairman and Chief Executive Officer of Moleculin. “We are grateful to the FDA for what we consider to be a very productive meeting and look forward to reporting its outcome before the end of August.”
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