Autoimmune Disease, Inflammation, Polyarthritis, Rheumatism, Rheumatoid Arthritis
Conditions
Keywords
monoclonal antibody, diagnostics, RA, Immunoglobulins, molecular target, Tc99m-pertechnetate, Fab-fragment of Anti-human CD4, Radiopharmaceutical, chronic inflammatory diseases, active Rheumatoid Arthritis
Brief summary
Rheumatoid arthritis (RA) is a disease with a large economic impact due to the long lasting disabling nature of the disease. Furthermore, diagnosis of the disease is difficult and only a scheme with different symptoms is used to diagnose rheumatoid arthritis, often only by probability. Due to the fact that effective disease modifying pharmacological treatment is available and should be started early in established cases of RA, in combination with the adverse effect potential of these substances (e.g. methotrexate), a fast reliable diagnostic tool to diagnose rheumatoid arthritis would be highly appreciated by the medical community and the patients. Furthermore, for invasive treatments (surgery, puncture), an imaging method to display the activity pattern in different joints would be a major advantage. For the evaluation of the effectiveness of pharmacological therapy in rheumatoid arthritis, up to now, radiological measurements of the destruction process of the joints are used. This method has the disadvantage that it is time consuming insofar as changes in the radiological images must occur. It allows only an evaluation if the joints are destructed (which should be excluded by the new therapy regimen). Again, a quantifiable method for the determination of the effects of new therapeutic approaches would be highly appreciated.
Detailed description
The substance will be used as iv injection due to the protein nature of the antibody and, to ensure a fast distribution within the body. The study will be performed as an open clinical trial due to the fact that the applied radiation has to be documented; the use of placebo radiation would be unethical. It is expected, that the new antibody fragment with its radioactive linkage will display an image of the activity distribution of the disease. Due to the fact that only patients with active disease have to be imaged and, to allow for comparison of the activity and the clinical distribution of the disease, this proof of concept study (phase I study) will be performed in patients with active disease. Healthy volunteers could not display an activity pattern of the disease. Furthermore, it seems to be unethical to use volunteers for studies with radioactivity with such a risk/benefit ratio (radiation risks vs. missing chance of display of tissue distribution) in a proof of concept study.
Interventions
RADIATIONFab-fragment of Anti-human CD4
Sterile lyophilized Powder for Preparation of a Solution and sterile labelling Buffer labelling with Tc99m-Pertechnetat Intravenous injection
Sponsors
Technische Universität Dresden
University of Leipzig
Biotectid GmbH
Study design
Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
50 Years to 80 Years
Healthy volunteers
No
Inclusion criteria
* Male and female subjects above 50 years of age * Suffering from joint pain which is due to active rheumatoid arthritis * Obvious signs of inflammation in at least one joint (e.g. swelling, erythema, or local elevated temperature) * Otherwise healthy * Informed consent
Exclusion criteria
* Patients 80 years and older * Clinically significant disease of the cardiovascular system, respiratory system, hepato-biliary system or central nervous system (CNS) * Excretory hepatic or renal insufficiency * Regular intake of any drug, except for hormone replacement therapy in females * Previous administration of xenogenous proteins * History of anaphylactic reaction to any drug administered by a parenteral pathway * Previous participation in a radiopharmaceutical drug trial (unless the effective dose acquired by participation in the current trial will remain below 10 mSv) * Participation in any clinical drug trial within 3 months prior to enrolment * Women of child-bearing potential (child-bearing potential to be ruled out by one of the following: at least 2 years past menopause, hysterectomy, bilateral oophorectomy, or bilateral tubal ligation) * Long term medication with strong antiphlogistic agents/pain killers such as methotrexate, corticoids, or immunosuppressants prior to enrolment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| safety and tolerability of this diagnostic agent | duration of study |
Secondary
| Measure | Time frame |
|---|---|
| endpoint for the proof of concept will be the number of patients needed to obtain a series of equal results | duration of study |
Countries
Germany
Outcome results
None listed