clinical trial · NCT01733082
The Mycophenolate Pregnancy Registry
Genentech, Inc.·—·recruiting·n = 500
Heart Transplantation, Kidney Transplantation, Liver Transplantation, Autoimmune Diseases
brief 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.
started
Nov 20, 2012
primary completion
Dec 31, 2040
completion
Dec 31, 2040
last updated
Apr 15, 2026
sourced from ClinicalTrials.gov · pharmadog mirrors structured fields, not the full protocol