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:
2025-12-24 @ 9:26 PM
Ignite Modification Date:
2025-12-24 @ 9:26 PM
NCT ID:
NCT00978432
Eligibility Criteria:
Inclusion Criteria:
1. de novo or transformed Diffuse large B cell non-Hodgkin lymphoma (DLBCL). DLBCL-like lymphomas allowed:
* Epstei-Barr virus (EBV)+ DLBCL in elderly,
* DLBCL with chronic inflammation,
* Primary cutaneous DLBCL, leg type,
* B cell lymphoma unclassifiable - between DLBCL and Burkitt lymphoma,
* B cell lymphoma unclassifiable - between large B cell lymphoma and classical Hodgkin lymphoma,
* Anaplastic lymphoma kinase (ALK)+ large B cell lymphoma,
* T cell histiocyte rich large B cell lymphoma
* Primary mediastinal B cell lymphoma
* Follicular grade 3 B cell lymphoma
2. Refractory or relapsed disease to \>/= 1 prior treatment regimen: should include autologous stem cell transplant unless patient refused or ineligible.
3. Age \> 18 years old
4. Eastern Cooperative Oncology Group (ECOG) performance status \<2.
5. Measurable or evaluable disease by physical exam, radiographs or bone marrow involvement
6. Frozen tumor or paraffin-embedded sample available.
7. 3-4 core fresh/fresh-frozen biopsy specimens available. Leukapheresis may be done for patients with leukocytosis.
8. Laboratory Values per protocol.
Exclusion Criteria:
1. Laboratory Values
* Grade 3 hyperlipidemia (Serum cholesterol \>400mg/dl or serum triglycerides \>5 x ULN)
* Serum Glucose \> 250mg/dl on \>/= 2 checks on 2 separate days
* Diabetics accepted if sugars controlled
2. Unlimited prior chemotherapy regimens, however:
* No prior exposure to RAD001 or LBH589 or drugs that target mTOR (sirolimus, temsirolimus, etc) or HDAC (vorinostat)
* No valproic acid during study or 5 days preceding start of first drug
* No chemotherapy, biologics or immunotherapy \< 2 weeks before registration (6 weeks if last received bis-chloroethylnitrosourea (BCNU) or mitomycin C). Subjects must be recovered from therapy-related non-hematological toxicities to \< grade 1 or baseline if started with \> grade 1 toxicity.
* No time limit for radiation prior to registration.
* No radioimmunotherapy \< 2 months prior to registration. Subjects must be recovered from therapy-related toxicities to \< grade 1 or baseline if started with \> grade 1 toxicity.
* No prior allogeneic stem cell transplantation unless allogeneic engraftment is \<2%.
* Subjects receiving chronic, systemic treatment with corticosteroids = to \>20mg of prednisone per day.
* Subjects receiving replacement for adrenal insufficiency allowed.
* Topical or inhaled corticosteroids allowed.
3. History of other primary malignancy \< 3 years ago, except inactive basal, squamous cell carcinoma of the skin or superficial melanoma only requiring excision, prostate cancer with a prostate specific antigen (PSA) stable for \>/=3 months, carcinoma in situ of cervix.
4. Major surgery \< 4 weeks before or Minor surgery \< 2 weeks before registration. Subjects must be recovered from toxicities to \< grade 1 or baseline if started with \> grade 1 toxicity.
5. Investigational drugs \< 4 weeks prior to registration.
6. Impaired Cardiac Function per protocol.
7. Pregnant or breastfeeding females or adults of reproductive potential not using effective birth control
8. Diffusing capacity or transfer factor of the lung for carbon monoxide (DLCO) \< 40% if tested (per protocol).
9. Impaired lung function: O2 saturation 88% or less at rest on room air by Pulse Oximetry.
10. Immunization with live attenuated vaccines \< 1 week of study entry
11. Impaired GI function or GI disease that may alter absorption of RAD001 or LBH589
12. Concurrent severe \&/or uncontrolled medical conditions
13. Medications with risk of prolonging QT interval or inducing torsade de pointes or interacting with LBH589 and RAD001 may be used per the protocol.
14. Active bleeding tendency
15. Positive for HIV.
16. Positive for Hepatitis C virus (HCV).
17. History of non-compliance to medical regimens.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT00978432
Study Brief:
Protocol Section:
NCT00978432