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Safety and Dose Finding Study of Xigris in Hemodialysis Patients (Xigris1003)

Primary Purpose

End Stage Renal Disease

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Drotrecogin alfa activated (Xigris)
Sponsored by
George Washington University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for End Stage Renal Disease focused on measuring Hemodialysis, Anticoagulation, Xigris, PTT

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. >18
  2. Usually used heparin with HD

Exclusion Criteria:

  1. Plt <100
  2. Pregnancy
  3. H/o bleeding diathesis
  4. H/o CVA
  5. Pt on Ticlid/plavix/warfarin
  6. SBP >200
  7. BASELINE PTT>50
  8. INR>1.6

Sites / Locations

  • The George Washington University Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Xigris

Arm Description

Drotrecogin alfa activated (Xigris) used as anticoagulant in patients treated with hemodialysis.

Outcomes

Primary Outcome Measures

Mean Partial Thromboplastin Time (PTT) at 15 Minutes
PTT level during a hemodialysis treatment will be used to assess the effectiveness of Xigris as an anticoagulant.
Mean Partial Thromboplastin Time (PTT) at 30 Minutes
PTT level during a hemodialysis treatment will be used to assess the effectiveness of Xigris as an anticoagulant.
Mean Partial Thromboplastin Time (PTT) at 60 Minutes
PTT level during a hemodialysis treatment will be used to assess the effectiveness of Xigris as an anticoagulant.
Mean Partial Thromboplastin Time (PTT) at 120 Minutes
PTT level during a hemodialysis treatment will be used to assess the effectiveness of Xigris as an anticoagulant.
Mean Partial Thromboplastin Time (PTT) at 180 Minutes
PTT level during a hemodialysis treatment will be used to assess the effectiveness of Xigris as an anticoagulant.

Secondary Outcome Measures

Full Information

First Posted
July 14, 2010
Last Updated
January 6, 2022
Sponsor
George Washington University
Collaborators
Eli Lilly and Company
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1. Study Identification

Unique Protocol Identification Number
NCT01227187
Brief Title
Safety and Dose Finding Study of Xigris in Hemodialysis Patients
Acronym
Xigris1003
Official Title
Safety and Dose Finding Study of Xigris (Drotrecogin Alfa Activated) as an Anti-coagulant in End Stage Renal Disease (ESRD) Patients Treated With Hemodialysis (HD)
Study Type
Interventional

2. Study Status

Record Verification Date
November 2020
Overall Recruitment Status
Completed
Study Start Date
October 2008 (undefined)
Primary Completion Date
November 2010 (Actual)
Study Completion Date
December 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
George Washington University
Collaborators
Eli Lilly and Company

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of the study is to assess the safety of Xigris (Drotrecogin alfa) as an anticoagulant at different dose levels during dialysis treatment in patients with End Stage Renal Disease (ESRD).
Detailed Description
In United States, there are over 300,000 patients with ESRD who require hemodialysis. Clinical hemodialysis takes place three times a week and is dependent on adequate anticoagulation throughout the three to four hour procedure. Infection is one of the most common causes of death for patients with ESRD treated with hemodialysis (25%). Xigris (drotrecogin alfa activated) is a recombinant form of human activated protein C and is successfully used for treatment of adult patients with severe sepsis. In addition to its fibrinolytic properties, drotrecogin alpha has both an anti-inflammatory effect, and an anti-coagulant effect. However, there are few safety and no efficacy data on the effect of Xigris in ESRD patients as an anticoagulant.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
End Stage Renal Disease
Keywords
Hemodialysis, Anticoagulation, Xigris, PTT

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
12 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Xigris
Arm Type
Experimental
Arm Description
Drotrecogin alfa activated (Xigris) used as anticoagulant in patients treated with hemodialysis.
Intervention Type
Drug
Intervention Name(s)
Drotrecogin alfa activated (Xigris)
Other Intervention Name(s)
Drotrecogin alfa (activated)
Intervention Description
We will test different dose regimens of Drotrecogin alfa activated (Xigris) to determine the optimal dose to achieve PTT between 65 and 100 secs. The initial patients will receive Xigris dosed at an infusion rate of 12 mcg/kg/h via pre-filter arterial drip chamber via a standard IV pump. The PTT will be assessed at baseline,15,30,60,120 and 180 mins. Xigris dose will be adjusted in the following patients if the afferent PTT rises above 100 secs (normal range 25-40 secs) or if PTT remains <65 secs. If PTT remains less than 65 secs, the dose will be increased to the second dose regiment of 18 mcg/kg/hr. The dose escalation will continue in increments of 6 mcg/kg/h to a maximum dose of 36 mcg/kg/h. Each patient will receive Xigris only once.
Primary Outcome Measure Information:
Title
Mean Partial Thromboplastin Time (PTT) at 15 Minutes
Description
PTT level during a hemodialysis treatment will be used to assess the effectiveness of Xigris as an anticoagulant.
Time Frame
PTT level at 15 minutes after start up of Xigris during the hemodialysis treatment.
Title
Mean Partial Thromboplastin Time (PTT) at 30 Minutes
Description
PTT level during a hemodialysis treatment will be used to assess the effectiveness of Xigris as an anticoagulant.
Time Frame
PTT level at 30 minutes after start up of Xigris during the hemodialysis treatment.
Title
Mean Partial Thromboplastin Time (PTT) at 60 Minutes
Description
PTT level during a hemodialysis treatment will be used to assess the effectiveness of Xigris as an anticoagulant.
Time Frame
PTT level at 60 minutes after start up of Xigris during the hemodialysis treatment.
Title
Mean Partial Thromboplastin Time (PTT) at 120 Minutes
Description
PTT level during a hemodialysis treatment will be used to assess the effectiveness of Xigris as an anticoagulant.
Time Frame
PTT level at 120 minutes after start up of Xigris during the hemodialysis treatment.
Title
Mean Partial Thromboplastin Time (PTT) at 180 Minutes
Description
PTT level during a hemodialysis treatment will be used to assess the effectiveness of Xigris as an anticoagulant.
Time Frame
PTT level at 180 minutes after start up of Xigris during the hemodialysis treatment.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: >18 Usually used heparin with HD Exclusion Criteria: Plt <100 Pregnancy H/o bleeding diathesis H/o CVA Pt on Ticlid/plavix/warfarin SBP >200 BASELINE PTT>50 INR>1.6
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lakhmir S Chawla, MD
Organizational Affiliation
George Washington University
Official's Role
Principal Investigator
Facility Information:
Facility Name
The George Washington University Hospital
City
Washington
State/Province
District of Columbia
ZIP/Postal Code
20037
Country
United States

12. IPD Sharing Statement

Citations:
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8840287
Citation
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8840285
Citation
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Safety and Dose Finding Study of Xigris in Hemodialysis Patients

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