Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 12:57 AM
Ignite Modification Date:
2025-12-25 @ 12:57 AM
NCT ID:
NCT00224393
Eligibility Criteria:
Inclusion Criteria:
* \>=18 years of age.
* Laboratory values obtained \<=14 days prior to registration.
* No limitation on the cardiac ejection fraction
* Bilirubin \<3 mg/dL
* Absolute neutrophil count \>=500/microliters
* Histochemical diagnosis of amyloidosis as based on detection by polarizing microscopy of green bi-refringent material in Congo red-stained tissue specimens or characteristic electron microscopy appearance.
* Demonstrable M-protein in the serum/urine or clonal population of plasma cells in the bone marrow or immunohistochemical stain with anti-light chain anti-sera of amyloid fibrils.
* ECOG performance status 0, 1, 2, or 3.
* Symptomatic organ involvement with amyloid to justify therapy. This could include liver involvement, cardiac involvement, renal involvement, peripheral neuropathy, or soft tissue involvement. Must have more than purpura or carpal tunnel syndrome.
* Previously treated or untreated. No limit to prior therapy provided there is adequate residual organ function.
* Ability to provide informed consent.
* Ability to self-inject medication or have a caregiver who can administer the drug.
Exclusion Criteria:
* Amyloid-specific syndrome, such as, carpal tunnel syndrome or skin purpura as only evidence of disease. The finding of vascular amyloid only in a bone marrow biopsy specimen or in a plasmacytoma is not indicative of systemic amyloidosis.
* Presence of non-AL amyloidosis.
* Melphalan or other alkylating agents, high-dose dexamethasone or alpha interferon \<=4 weeks prior to registration.
* Concurrent use of corticosteroids, but patients may be on chronic steroids if they are being given for disorders other than amyloid, i.e., adrenal insufficiency, rheumatoid arthritis, etc.
* Any of the following:
* Pregnant women
* Nursing women
* Men or women of childbearing potential who are unwilling to employ adequate contraception (condoms, diaphragm, birth control pills, injections, intrauterine device \[IUD\], surgical sterilization, abstinence, etc.)
* Uncontrolled infection.
* Clinically overt multiple myeloma (monoclonal BMPC \>30%), and at least one of the following:
* Bone lesions
* Hypercalcemia
* Active malignancy with the exception of adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer, adequately treated Stage I or II cancer from which the patient is currently in complete remission, or any other cancer from which the patient has been disease-free for 5 years.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT00224393
Study Brief:
Protocol Section:
NCT00224393