Therapy of Chronic Cold Agglutinin Disease With Eculizumab (DECADE)
The recruitment status of this study is unknown because the information has not been verified recently.
Verified February 2011 by University Hospital, Essen.
Recruitment status was Recruiting
Recruitment status was Recruiting
Sponsor:
University Hospital, Essen
Collaborator:
Alexion Pharmaceuticals
Information provided by:
University Hospital, Essen
ClinicalTrials.gov Identifier:
NCT01303952
First received: February 24, 2011
Last updated: NA
Last verified: February 2011
History: No changes posted
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Purpose
Evaluation of the efficacy and safety of eculizumab in symptomatic or transfusion-dependent patients with untreated or refractory hemolytic cold agglutinin disease(CAD)
| Condition | Intervention | Phase |
|---|---|---|
|
Cold Agglutinin Disease |
Drug: Eculizumab |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Endpoint Classification: Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Therapy for Chronic Cold Agglutinin Disease: A Prospective, Non-Randomized Multi-Center Study Demonstrating the Efficacy of Terminal Complement Inhibition in Patients With Cold Agglutinin Disease Using Eculizumab |
Resource links provided by NLM:
Further study details as provided by University Hospital, Essen:
Primary Outcome Measures:
- LDH [ Time Frame: From baseline to 26 weeks ] [ Designated as safety issue: No ]Primary endpoint for this study is: lactate dehydrogenase (LDH) in U/l change from baseline to 26 weeks
Secondary Outcome Measures:
- Transfusion avoidance [ Time Frame: From baseline to 26 weeks ] [ Designated as safety issue: No ]
- PRBC units transfused [ Time Frame: From baseline to 26 weeks ] [ Designated as safety issue: No ]
- Change in hemoglobin levels [ Time Frame: From baseline to 26 weeks ] [ Designated as safety issue: No ]
- Haptoglobin [ Time Frame: From baseline to 26 weeks ] [ Designated as safety issue: No ]
- Hemopexin [ Time Frame: From baseline to 26 weeks ] [ Designated as safety issue: No ]
- Free hemoglobin [ Time Frame: From baseline to 26 weeks ] [ Designated as safety issue: No ]
- Reticulocytes [ Time Frame: From baseline to 26 weeks ] [ Designated as safety issue: No ]
- SF-36v2 QLQ [ Time Frame: From baseline to 26 weeks ] [ Designated as safety issue: No ]
- FACIT-F SCALE version 4 [ Time Frame: From baseline to 26 weeks ] [ Designated as safety issue: No ]
- Six-Minute Walk Test [ Time Frame: From baseline to 26 weeks ] [ Designated as safety issue: No ]
- Circulatory symptoms [ Time Frame: From baseline to 26 weeks ] [ Designated as safety issue: No ]
- Thrombosis record [ Time Frame: From baseline to 26 weeks ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 15 |
| Study Start Date: | February 2011 |
| Estimated Study Completion Date: | December 2012 |
| Estimated Primary Completion Date: | August 2012 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| Experimental: Eculizumab |
Drug: Eculizumab
Weekly treatment with eculizumab (600 mg) via IV infusion for 4 doses followed the next week by eculizumab (900 mg) IV infusion and maintenance treatment with Eculizumab (900 mg) via IV infusion every other week for 21 weeks
|
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Individuals at least 18 years of age
- Diagnosis of CAD defined by the combination of chronic hemolysis, cold agglutinin titer (IgM or IgA) >64 at 4°C, positive direct antiglobulin test (DAT) when performed with polyspecific antiserum, negative (or only weakly positive) anti-IgG, and strongly positive with anti-C3d
- LDH level > 2 x upper limit of normal (ULN)
- Clinical symptoms requiring treatment, such as anemia, anemia-related symptoms or hemolysis-related symptoms
- Sufficient supplementation of iron, folic acid and vitamin B12 prior to treatment phase
- Patient must be willing and able to give written informed consent;
- Patients must be vaccinated against N. meningitidis at least 14 days prior treatment
- Patient must avoid conception during the trial using a method that is most appropriate for their physical state and culture
Exclusion Criteria:
- Active aggressive lymphoma requiring therapy or an active non-lymphatic malignant disease other than basal cell carcinoma or CIS of the cervix
- Liver disease with elevated LDH
- Absolute neutrophil count < 500/µL
- Presence or suspicion of active bacterial or viral infection, in the opinion of the Investigator, at treatment start or severe recurrent bacterial infections
- Participation in any other investigational drug trial or exposure to other investigational agent, device, or procedure within 30 days prior to screening period
- Pregnant, breast-feeding, or intending to conceive during the course of the study, including the Post-treatment Phase
- History of bone marrow/stem cell transplantation
- Inability to cooperate or any condition that, in the opinion of the investigator, could increase the patient's risk by participating in the study or confound the outcome of the study
- Hypersensitivity to eculizumab, to murine proteins or to one of the excipients
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01303952
Contacts
| Contact: Alexander Roeth, MD | +49 201 723 ext 84219 | alexander.roeth@uk-essen.de |
Locations
| Germany | |
| Department of Hematology, University Hospital Essen | Recruiting |
| Essen, Germany, 45122 | |
| Contact: Alexander Roeth, MD +49 201 723 ext 84219 alexander.roeth@uk-essen.de | |
| Contact: Andreas Huettmann, PD MD +49 201 723 ext 1861 andreas.huettmann@uk-essen.de | |
Sponsors and Collaborators
University Hospital, Essen
Alexion Pharmaceuticals
Investigators
| Principal Investigator: | Alexander Roeth, MD | Department of Hematology, University Hospital Essen |
More Information
Additional Information:
DECADE Trial Flyer 
Publications:
| Responsible Party: | Alexander Roeth, MD, University Hospital Essen |
| ClinicalTrials.gov Identifier: | NCT01303952 History of Changes |
| Other Study ID Numbers: | CAD01, 2009-016966-97 |
| Study First Received: | February 24, 2011 |
| Last Updated: | February 24, 2011 |
| Health Authority: | Germany: Paul-Ehrlich-Institut |
Keywords provided by University Hospital, Essen:
|
cold agglutinin disease hemolysis eculizumab terminal complement inhibition |
Additional relevant MeSH terms:
|
Anemia, Hemolytic, Autoimmune Anemia, Hemolytic Anemia Hematologic Diseases Autoimmune Diseases Immune System Diseases |
Agglutinins Cold agglutinins Immunologic Factors Physiological Effects of Drugs Pharmacologic Actions Hemagglutinins |
ClinicalTrials.gov processed this record on June 17, 2013