Xigris® (drotrecogin alfa [activated])

Consistent with the company's policy of public data disclosure, this clinical trial results section includes result summaries of completed Lilly-sponsored clinical studies conducted on Lilly marketed products since July 1, 2004. The results of all Phase I, II, and III trials conducted in support of a product’s initial registration will be disclosed regardless of outcome, no later than when the first indication is approved and the drug is commercially available for patient use anywhere in the world. The results of all subsequent Phase II, III, and IV trials conducted after initial approval will be similarly disclosed within one year of trial completion. A trial’s results, irrespective of study phase, will be disclosed as soon as possible if there are significant safety findings.

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The registry is also populated with the results of core efficacy and safety registration trials for products first approved after July 1, 1994.

Included are trial result summaries that are completed to date. The company will continue to disclose additional summaries and publication citations as they become available.

Summaries of clinical study results are intended to report the results of the study that were known at the time of each study's completion. The information contained in these summaries is not intended to promote or otherwise commercialize (directly or indirectly) any off-label or unapproved uses of Lilly medicines, nor is it intended to provide a comprehensive analysis of all data currently available regarding a particular drug. In some cases, more current information regarding a drug, including post-hoc analyses and meta-analyses, may be available as part of the general body of scientific knowledge in forms such as manuscripts, abstracts, or posters.

Clinical studies on Lilly products may also be sponsored and reported by parties other than Lilly in other clinical trial registries.

Trial Results

The following trial has been conducted for Xigris.

Disease Trial ID Trial Title Trial
Phase
Severe Sepsis
1678
A Phase 3 Study to Determine the Efficacy and Safety for Recombinant Human Activated Protein C in Severe Sepsis
3
Severe Sepsis
6716
Investigation of the Efficacy and Safety of Drotrecogin Alfa (Activated) in Pediatric Severe Sepsis
3
Severe Sepsis
5771
Long-Term Follow-Up of Survivors from the PROWESS Trial (An Observational Study)
3b
Severe Sepsis
6001
A Phase IIIb Study to Determine Efficacy and Safety of Extended Drotrecogin Alfa (Activated) Therapy in Patients with Persistent Requirement for Vasopressor Support After 96-Hour Infusion with Commercial Drotrecogin Alfa (Activated)
3b
Severe Sepsis
6416
A Safety Evaluation Of Xigris [Drotrecogin Alfa (Activated)] In Hematoapoietic Stem Cell Transplant Patients With Severe Sepsis
3b
Severe Sepsis
6669
Efficacy and Safety of Drotrecogin Alfa (activated) in Adult Patients with Early Stage Severe Sepsis
3b
Severe Sepsis
7252
Efficacy and Safety of Drotrecogin Alfa (Activated) in Adult Patients with Early Stage Severe Sepsis
3b
Severe Sepsis
5502
An Open Label Study Of Drotrecogin Alfa (Activated) (LY203638) in Severe Sepsis
3 / 4
Severe Sepsis
7159
An Open Label Study Of Drotrecogin Alfa (Activated) In Adult Patients With Severe Sepsis And Multiple Organ Dysfunctions: A Phase IV Protocol
4
Severe Sepsis
6009
The Pharmacokinetics of Xigris® [Drotrecogin Alfa (Activated)] in Patients =160 kg with Severe Sepsis
4
Severe Sepsis
6743
A Randomized, Double-Blind, Placebo-Controlled Trial of Prophylactic Heparin in Patients with Severe Sepsis and Higher Disease Severity Who Are Undergoing Treatment with Drotrecogin Alfa (Activated)
4