{
"info": {
"nct_id": "NCT01750762",
"official_title": "Phase I Study of Lenalidomide to Augment Anti-Tumor Immunity Following Allogeneic Transplantation",
"inclusion_criteria": "* Histologically confirmed multiple myeloma or lymphoma and evidence of disease at least 100 days after an allogeneic stem cell or bone marrow transplantation\n* Lymphoma patients must have measurable disease\n* No previous cancer therapy within 4 weeks\n* Life expectancy of at least 3 months\n* Free of prior malignancies for at least 5 years with the exception of currently treated basal cell, squamous cell carcinoma of the skin or carcinoma in situ of the cervix or breast\n* Must be registered into RevAssist program and willing and able to comply with RevAssist requirements\n* Willing to commit to abstinence or use one highly effective method of birth control and another effective method of birth control at the same time\nHealthy volunteers allowed\nMust have minimum age of 18 Years",
"exclusion_criteria": "* Pregnant or breastfeeding\n* Any other serious medical condition\n* Any condition that places the subject at unacceptable risk if he/she were to participate in the study\n* Use of experimental drug or therapy within 28 days of baseline\n* Known significant hypersensitivity to thalidomide or lenalidomide\n* Development of erythema nodosum if characterized by desquamating rash while taking thalidomide or similar drugs\n* Chemotherapy or radiotherapy within 4 weeks\n* Known seropositive for acute HIV, hepatitis B or C\n* Significant concurrent infections\n* Non-hematological acute GvHD and/or hematological toxicity of Grade 3 or higher\n* Moderate or severe chronic GVHD",
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},
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