MLD presenting at World Orphan Congress Europe

Shawn Ritchie, CEO and CSO, and Tara Smith, VP Therapeutics, will be in Barcelona to present updates on the MLD’s clinical development program for Rhizomelic Chondrodysplasia Punctata (RCDP). For more information on RCDP and the trial click here. More information on the conference is here.

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MLD and Laval University collaborators publish key Parkinson's disease plasmalogen paper

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MLD's Plasmalogen Drug PPI-1040 for RCDP receives FDA Orphan Drug Designation (ODD)