Drugs / Oprelvekin

Trials 5 · a red edge is where a trial was stopped

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PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 1/21 trial
Phase 1/2 NCT00012298 Apr 2001 → Apr 2010 MALT lymphoma, Waldenstrom macroglobulinemia, chronic lymphocytic leukemia/small lymphocytic lymphoma, nodal marginal zone B-cell lymphoma +1 National Cancer Institute (NCI) Terminated No outcome recorded
Phase 24 trials
Phase 2 NCT00994929 Jan 2010 → Apr 2012 hemophilia A, von Willebrand disease (hereditary or acquired) University of Pittsburgh Completed No outcome recorded
Phase 2 NCT00886743 Sep 2009 → Dec 2015 thrombocytopenia Pfizer Terminated No outcome recorded
Phase 2 NCT00524225 Feb 2008 → Jun 2012 von Willebrand disease 1 Margaret Ragni Terminated No outcome recorded
Phase 2 NCT00524342 Jan 2008 → Dec 2010 von Willebrand disease 1 Margaret Ragni Completed No outcome recorded

Evidence & citations 9 cited values

Every value below carries the sentence it was read from. 6 sources stand behind the page.

FieldValueCited text
Known as oprelvekin ClinicalTrials.gov intervention name — accepted as the source's own label NCT00886743
3

NCT00524342

NCT00012298

NCT00524225

Known as IL-11 “Neumega (Oprelvekin, Interleukin 11, IL-11) 25 mcg/kg subcutaneously, given for 4 days preoperatively, and on day 5 preoperatively, and for up to 2 days postoperatively” NCT00524225
1

“Oprelvekin, Interleukin 11, IL-11NCT00524342

Known as Interleukin 11 “Neumega (Oprelvekin, Interleukin 11, IL-11) 25 mcg/kg subcutaneously, given for 4 days preoperatively, and on day 5 preoperatively, and for up to 2 days postoperatively” NCT00524225
1

“Oprelvekin, Interleukin 11, IL-11” NCT00524342

Known as Neumega Neumega (Oprelvekin, Interleukin 11, IL-11) 25 mcg/kg subcutaneously, given for 4 days preoperatively, and on day 5 preoperatively, and for up to 2 days postoperatively” NCT00524225
1

NCT00994929

Known as Neumega (Oprelvekin, Interleukin 11, IL-11) Neumega (Oprelvekin, Interleukin 11, IL-11)NCT00524342
Known as Recombinant Interleukin-11 “Phase II Clinical Efficacy Trial of Recombinant Interleukin-11 (rhIL-11, Neumega) in Subjects With Type 1 Von Willebrand Disease Undergoing Surgery” NCT00524225
Known as rhIL-11 “We, therefore, conducted a single-center Phase II clinical trial to determine safety and biologic efficacy of recombinant interleukin-11 (rhIL-11, Neumega®) in patients with...” PMID 23238591 Dec 2012
1

“Phase II Clinical Efficacy Trial of Recombinant Interleukin-11 (rhIL-11, Neumega) in Subjects With Type 1 Von Willebrand Disease Undergoing Surgery” NCT00524225

Modality Protein / enzyme biologic “Recombinant Interleukin-11” NCT00524225
Route Subcutaneous “by subcutaneous injection” NCT00524225