Drugs / Zenapax

Regulatory milestones approvals, filings & regulatory actions · 2 recorded

MilestoneJurisdictionBrandIndicationDateSentence it was read from
Withdrawn EU (EMA) Zenapax — 2009-01-01 europa.eu ↗
Approved EU (EMA) Zenapax — 1999-02-26 europa.eu ↗

Trials 4

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PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 22 trials
Phase 2 NCT00198146 Jul 2000 → Feb 2007 — Indiana University Completed No outcome recorded
Phase 2 NCT00001934 Sep 1999 → Aug 2005 multiple sclerosis National Institute of Neurological Disorders and Stroke (NINDS) Completed No outcome recorded
Phase 31 trial
Phase 3 NCT00048152 Dec 2000 → Mar 2006 — Hoffmann-La Roche Completed No outcome recorded
Phase 41 trial
Phase 4 NCT00138970 Jan 2002 → Feb 2005 disease related to solid organ transplantation University of Oslo School of Pharmacy Completed No outcome recorded

Evidence & citations 6 cited values

Every value below carries the sentence it was read from. 4 sources stand behind the page.

FieldValueCited text
Known as Zenapax ClinicalTrials.gov intervention name — accepted as the source's own label NCT00138970 ↗
3

NCT00048152 ↗

NCT00001934 ↗

NCT00198146 ↗

Known as Daclizumab “A Study to Assess Use of Zenapax (Daclizumab) and CellCept (Mycophenolate Mofetil) to Improve Kidney Function in Kidney Transplant Patients” NCT00048152 ↗
Action Inhibit “a humanized antibody against the IL-2Ra subunit (Zenapax(Registered Trademark)) will be used to inhibit T cell activation in MS patients” NCT00001934 ↗
Modality Monoclonal antibody “Effect of the Humanized Monoclonal Antibody Against the Interleukin-2 Receptor Alpha Subunit (IL-2R-Alpha; Zenapax(Registered Trademark)) on Inflammatory Activity in the CNS in...” NCT00001934 ↗
Route Intravenous “During treatment, patients will receive seven intravenous (I.V.) infusions of Zenapax in the clinic.” NCT00001934 ↗
Target IL2RA “a humanized antibody against the IL-2Ra subunit (Zenapax(Registered Trademark))” NCT00001934 ↗