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Myrcludex B has shown promising efficacy in Phase 2a trials. Phase 2b clinical trials for Myrcludex B in combination with tenofovir for HBV/HDV co-infected patients have completed patient recruitment with 120 patients across 15 clinical centers in Russia and Germany. The drug has received PRIME eligibility from the European Medicines Agency (EMA), recognizing its potential to address an unmet medical need.
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