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Clinical Trial Summary

The Mycophenolate Pregnancy Registry is designed as a prospective, observational registry collecting data regarding mycophenolate exposure during pregnancy, and pregnancy outcomes, fetal and infant outcomes after exposure. Early and later term pregnancy outcomes will be solicited at selected gestational time points. Structural and functional birth defects identified in the perinatal period through one year of life will be collected and classified. This is a non-proprietary registry and is a component of a comprehensive pregnancy Risk Evaluation and Mitigation Strategy (REMS) plan required by the FDA for all mycophenolate-formulations, including CellCept, Myfortic and any generic formulations.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Autoimmune Diseases
  • Heart Transplantation, Kidney Transplantation, Liver Transplantation, Autoimmune Diseases

NCT number NCT01733082
Study type Observational
Source Genentech, Inc.
Contact Reference Study ID Number: ML22679 https://forpatients.roche.com
Phone 888-662-6728 (U.S. and Canada)
Email global.rochegenentechtrials@roche.com
Status Recruiting
Phase
Start date November 30, 2012
Completion date May 30, 2025