CRANBURY, N.J. , Dec. 14, 2017 (GLOBE NEWSWIRE) -- Amicus Therapeutics (Nasdaq:FOLD) submitted a new drug application (NDA) to the U.S. Food and Drug Administration (FDA) to request approval of the oral precision medicine migalastat HCl ("migalastat") for the treatment of patients 16 years and
260+ Fabry Patients on Reimbursed Galafold™ (Migalastat) and On Target to Reach 300 Patients by Year-End 2017 U.S. NDA Submission for Migalastat Planned in 4Q17 Pompe Retrospective and Prospective Data Collection Studies Initiated Additional Pompe Clinical Data to be Presented at WORLD Symposium™
CRANBURY, N.J. , Oct. 25, 2017 (GLOBE NEWSWIRE) -- Amicus Therapeutics (Nasdaq:FOLD) today announced a conference call and live audio webcast on Wednesday, November 8, 2017 at 8:30 a.m. ET to discuss financial results for the third quarter ended September 30, 2017 .
Mean Six-Minute Walk Distance Improved in ERT-Naive Patients (+42 Meters at 6 Months, +75 Meters at 9 Months) and ERT-Switch Patients (+35 Meters at 6 Months, +37 Meters at 9 Months) Persistent & Durable Reductions in Key Disease Biomarkers Pulmonary Function Generally Improved or Remained
CRANBURY, N.J. , Sept. 20, 2017 (GLOBE NEWSWIRE) -- Amicus Therapeutics (Nasdaq:FOLD) announced that John F. Crowley , Chairman and Chief Executive Officer, will participate in a corporate overview and fireside chat at the LEERINK Partners Roundtable Series: Rare Disease & Immuno-Oncology in New
Study Did Not Meet Primary Endpoints Conference Call and Webcast Today at 8:30am ET CRANBURY, N.J. , Sept. 13, 2017 (GLOBE NEWSWIRE) -- Amicus Therapeutics , Inc. (Nasdaq:FOLD) reported that top-line data from the randomized, double-blind, placebo-controlled Phase 3 clinical study (ESSENCE, SD-005)