Amicus Therapeutics Inc. lost more than half its market value Friday after the drug maker said it has delayed plans to seek U.S. approval of its treatment for a rare genetic disorder because of questions from regulators.
The Cranbury, N.J., company was expected to submit a new drug application for its migalastat monotherapy, known as Galafold, by the end of the year to the U.S. Food and Drug Administration. However, Amicus said...
Read Full Story