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Rabbit Antithymocyte Globulin (Thymoglobuline) With Ciclosporin for Patients With Acquired Aplastic Anaemia (RATGAA07)
This study is currently recruiting participants.
Verified by European Group for Blood and Marrow Transplantation, October 2008
First Received: May 9, 2007   Last Updated: October 8, 2008   History of Changes
Sponsors and Collaborators: European Group for Blood and Marrow Transplantation
Genzyme
Information provided by: European Group for Blood and Marrow Transplantation
ClinicalTrials.gov Identifier: NCT00471848
  Purpose

To assess the tolerability and effectiveness of rabbit antithymocyte globulin (ATG, Thymoglobuline) with ciclosporin in the first line treatment of patients with acquired severe aplastic anaemia, and patients with non-severe aplastic anaemia and who are transfusion dependent.


Condition Intervention Phase
Aplastic Anemia
Drug: rabbit antithymocyte globulin
Phase II

MedlinePlus related topics: Anemia
Drug Information available for: Cyclosporine Cyclosporin
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Non-Randomized, Open Label, Historical Control, Single Group Assignment, Efficacy Study
Official Title: Prospective Phase II Study of Rabbit Antithymocyte Globulin (ATG, Thymoglobuline®, Genzyme) With Ciclosporin for Patients With Acquired Aplastic Anaemia and Comparison With Matched Historical Patients Treated With Horse ATG and Ciclosporin

Further study details as provided by European Group for Blood and Marrow Transplantation:

Primary Outcome Measures:
  • Response [ Time Frame: at 6months ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Failure free and overall survival [ Time Frame: at 2 years ] [ Designated as safety issue: No ]

Estimated Enrollment: 35
Study Start Date: August 2008
Estimated Study Completion Date: December 2010
Estimated Primary Completion Date: January 2010 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Treatment Arm: Experimental
Antithymocyte globuline with cyclosporin in first line treatment of patients with acquired severe aplastic anaemia and patients with non-severe aplastic anaemia who are transfusion dependent
Drug: rabbit antithymocyte globulin
1.5 vials/10kg daily for 5 days

Detailed Description:

Traditionally horse antithymocyte globulin (ATG) has been the preferred animal source of ATG as first line treatment for acquired aplastic anaemia (AA) patients who are ineligible for bone marrow transplantation (BMT). For severe AA (SAA) the combination of ATG and Ciclosporin (CSA) results in response in 60-75% of patients and the response is superior to using either agent alone. The addition of granulocyte colony stimulating factor (G-CSF) to the combination of ATG and CSA has so far shown no significant benefit in terms of response and survival, but an EBMT prospective study is currently evaluating this further in a larger number of patients. For patients with NSAA who are transfusion dependent, the combination of ATG and CSA was shown to be superior to CSA alone in an EBMT prospective randomised study, with a higher response rate, superior blood counts and improved disease free survival using the combination of ATG with CSA.

There have been no phase II studies of rabbit ATG (Thymoglobuline®) in the treatment of AA as first line therapy. Preliminary results from a small single centre study compared horse ATG (ATGAM) with rabbit ATG (Fresenius) in children and showed response rates of 93% and 47%, respectively, but it is likely that different preparations of rabbit ATG will vary in their efficacy. Rabbit ATG is more commonly used for a second course following relapse or lack of response to a first course of horse ATG. Rabbit ATG in combination with CSA and G-CSF was used in patients with SAA who had failed to respond to a course of horse ATG with CSA and G-CSF. Overall response (transfusion independence) was seen in 23/30 (77%) of patients after a median of 95 days and complete response (neutrophils > 2.0, haemoglobin > 11, and platelets > 100) in 9/30 (30%). Rabbit ATG was well tolerated; no anaphylaxis or severe side effects were reported. Another study of 43 patients treated with rabbit ATG and CSA following non-response or relapse after horse ATG and CSA, showed 30% response rate among non-responding patients and 65% response rate for relapsing patients.

Studies comparing the antibody specificities between Thymoglobuline® and Lymphoglobuline® are in broad agreement, but (a) Lymphoglobuline® has fewer studies and those reported are older, because the product is older and has been less extensively developed (b) antibodies against certain epitopes are inconsistently present (c) not all antibody specificities have been examined in some studies and (d) different methods of testing have been used. There is a view that it is the immunogen and not the animal species which is most important in creating differences between different ATGs.

  Eligibility

Ages Eligible for Study:   16 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. Must fulfil definition of aplastic anaemia:

    There must be at least two of the following:

    • haemoglobin < 10g/dl
    • platelet count < 50 x 109/l
    • neutrophil count < 1.5 x 109/l, and a hypocellular bone marrow on bone marrow biopsy

    SAA as defined by a hypocellular bone marrow of <25% cellularity and two of the following:

    • neutrophil count < 0.5 x 109/l
    • platelets < 20 x 109/l
    • reticulocytes < 20 x 109/l

    NSAA as defined by a hypocellular bone marrow and cytopenia in at least two cell lines and neutrophil count > 0.5 x 109/l, and red cell and/or platelet transfusion dependence

  2. Have acquired aplastic anaemia
  3. Time from diagnosis to study registration maximum 6 months
  4. No prior treatment except for haemopoietic growth factors given for no more than four weeks, and androgens
  5. Age minimum 16 years with no upper age limit

Exclusion Criteria:

  1. Eligibility for an HLA-matched sibling donor transplant for SAA patients
  2. Prior therapy with ATG or CSA
  3. Haematopoeitic growth factors more than 4 weeks before study enrolment
  4. Diagnosis of Fanconi anaemia, dyskeratosis congenita or congenital bone marrow failure syndrome
  5. Evidence of myelodysplastic disease
  6. Paroxysmal nocturnal haemoglobinuria with evidence of significant haemolysis, history of PNH associated thrombosis or a PNH clone >50% by flow cytometry
  7. Diagnosis or previous history of carcinoma (except local cervical, basal cell, squamous cells, or melanoma)
  8. Subject is pregnant (e.g. positive HCG test) or is breast feeding
  9. Severe uncontrolled infection or unexplained fever >38oC
  10. Subjects who have hepatic, renal cardiac, metabolic or other concurrent diseases of such severity that life expectancy is less than 3 months
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00471848

Contacts
Contact: Judith Marsh 0044 208 725 3545 judith.marsh@kch.nhs.uk
Contact: Alain Barrois 0031 71 526 9722 ebmtcto@LUMC.NL

Locations
France
Hopital St. Louis Not yet recruiting
Paris, France, 75475
Contact: Gérard Socié     0033 1 42 499824     gerard.socie@paris7.jussieu.fr    
Principal Investigator: Gérard Socié            
Germany
Universitätsklinikum - Institut für klinische Transfusionsmedizin Not yet recruiting
Ulm, Germany, 89081
Contact: Hubert Schrezenmeier     0049 731 150 550     h.schrezenmeier@blutspende.de    
Principal Investigator: Hubert Schrezenmeier            
Italy
Ospedale San Martino Not yet recruiting
Genova, Italy, 16132
Contact: Andrea Bacigalupo     0039 010 355 469     andrea.bacigalupo@hsanmartino.liguria.it    
Principal Investigator: Andrea Bacigalupo            
Switzerland
University Hospital Not yet recruiting
Basel, Switzerland, 4031
Contact: André Tichelli     0041 61 265 4254     tichelli@datacomm.ch    
Principal Investigator: André Tichelli            
United Kingdom
St George's Hospital/ St George's University of London Recruiting
London, United Kingdom, Sw17 0RE
Contact: Judith Marsh     0044 208 725 3545     jmarsh@sgul.ac.uk    
Principal Investigator: Judith Marsh            
Sponsors and Collaborators
European Group for Blood and Marrow Transplantation
Genzyme
Investigators
Principal Investigator: Judith Marsh St George's Hospital/ St George's University of London
  More Information

Additional Information:
No publications provided

Responsible Party: ( European Group for Blood and Marrow Transplantation )
Study ID Numbers: EudraCT: 2007-000902-55, RATGAA07
Study First Received: May 9, 2007
Last Updated: October 8, 2008
ClinicalTrials.gov Identifier: NCT00471848     History of Changes
Health Authority: United Kingdom: Medicines and Healthcare Products Regulatory Agency;   France: Afssaps - French Health Products Safety Agency;   Switzerland: Swissmedic;   Germany: Paul-Ehrlich-Institut;   Italy: Ethics Committee

Keywords provided by European Group for Blood and Marrow Transplantation:
Thymoglobuline
Rabbit ATG
Ciclosporin
Aplastic Anemia

Study placed in the following topic categories:
Cyclosporine
Immunologic Factors
Hematologic Diseases
Aplastic Anemia
Clotrimazole
Miconazole
Tioconazole
Anemia
Cyclosporins
Immunosuppressive Agents
Antilymphocyte Serum
Antifungal Agents
Anemia, Aplastic
Antirheumatic Agents
Bone Marrow Diseases

Additional relevant MeSH terms:
Anti-Infective Agents
Cyclosporine
Immunologic Factors
Molecular Mechanisms of Pharmacological Action
Hematologic Diseases
Physiological Effects of Drugs
Anemia
Enzyme Inhibitors
Cyclosporins
Immunosuppressive Agents
Pharmacologic Actions
Antilymphocyte Serum
Therapeutic Uses
Antifungal Agents
Anemia, Aplastic
Antirheumatic Agents
Bone Marrow Diseases
Dermatologic Agents

ClinicalTrials.gov processed this record on May 07, 2009