Is NCT06534060 recruiting in Omaha, NE?

Yes, NCT06534060 is currently recruiting participants at its Omaha, NE location. This t-cell lymphoma clinical trial is actively enrolling qualified participants.

How do I join the t-cell lymphoma clinical trial in Omaha?

To join this clinical trial in Omaha, complete the eligibility form on this page. A study coordinator will contact you to discuss next steps and determine if you qualify.

Is participation in this Omaha clinical trial free?

Yes, all study-related care is provided at no cost to qualified participants. Many studies also offer compensation for time and travel expenses.

T-cell Lymphoma Clinical Trial in Omaha, NE

Who Can Participate

Inclusion Criteria

Male or female ≥ 18 years of age.

Patients with r/r TCL per WHO 2022 criteria.

r/r CTCL that has failed ≥ 2 prior lines of standard of care (SoC) therapy.

r/r PTCL that has failed ≥ 1 prior lines of SoC therapy. Note: patients with CD30+ disease should have received brentuximab vedotin.

Has available tumor tissue or is willing to undergo a biopsy procedure.

CD5 positivity confirmed by local laboratory using an approved diagnostic test or LDT. CD5 positivity is currently defined as having ≥ 50% CD5 expression. An exploratory cohort will enroll patients with CD5 expression below 50%.

Karnofsky performance score ≥ 70% or higher.

Prior CAR T-cell therapy must have occurred \> 60 days prior to study enrollment and must have no evidence of CAR persistence.

Measurable or detectable disease

PTCL per Lugano criteria

CTCL per Global (ISCL/EORTC/USCCL) criteria.

Prior autologous or allogenic hematopoietic stem cell transplant (HSCT) must have occurred more than 60 days prior to study enrollment.

Adequate bone marrow function defined as:

Absolute neutrophil count (ANC) ≥ 1500/μL (≥ 1000/μL for patients with prior HSCT or marrow involvement)

Absolute lymphocyte count ≥200 cells/μL

Hemoglobin ≥ 8 g/dL (transfusion permitted)

Platelet count ≥ 75 000/μL (≥50 000/μL for patients with marrow involvement).

Organ function as follows:

Cardiac: left ventricular ejection fraction (LVEF) ≥ 50% by Echo or radionuclide scan.

Pulmonary: oxygen saturation ≥ 92% (room air).

Renal: calculated creatinine clearance \> 30 mL/min.

Total bilirubin \< 1.5 x ULN (\< 2 × upper limit of normal (ULN)) if liver involvement).

If no liver involvement and total bilirubin ≥1.5 x ≤ ULN, direct bilirubin \< ULN (Gilbert syndrome)

Aspartate aminotransferase / alanine aminotransferase \< 3 × ULN (5 x ULN if liver involvement).

Albumin \> 2.5 g/dL.

For females of childbearing potential (defined as \< 24 months of amenorrhea or not surgically sterile \[absence of ovaries and/or uterus\]), a negative serum pregnancy test must be documented at screening, and prior to lymphodepletion (conditioning).

For females of childbearing potential and males, a highly effective method of contraception together with a barrier method must be used from the start of lymphodepletion (conditioning) and for at least 12 months after the last dose of study agent.

Exclusion Criteria

Sezary syndrome. For other tumor types, if there is a suspicion of significant circulating disease at time of leukapheresis, discuss eligibility with medical monitor prior to proceeding.

Contraindication to leukapheresis.

Prior treatment with any CD5-targeted therapy.

Any evidence of the following active viral infections:

HIV infection.

Chronic hepatitis B virus (cHBV) infection with detectable viral load. Patients with cHBV, who are receiving anti-viral prophylaxis, may be enrolled if they are asymptomatic for \>5 days prior to signing informed consent (ICF).

Hepatitis C (HCV) infection with detectable viral load. Patients cured of HCV may be enrolled.

Presence of any active, uncontrolled systemic bacterial, viral or fungal infection requiring intravenous (IV) anti-infectives, including clinically significant viral infection or uncontrolled viral reactivation of Epstein-Barr virus, Cytomegalovirus, Adenovirus, BK-virus, or Human herpesvirus 6. If treated with anti-infective agents, patients must be asymptomatic for \>5 days prior to enrollment.

History of any malignancy within 2 years with the exception of cured stage 1 cancers or CIS and potentially indolent cancers not requiring active treatment or controlled with hormone therapy. Discuss patients with indolent cancers with the medical monitor.

History of hypersensitivity reactions to products containing murine proteins.

Active CNS lymphoma.

Evidence of acute graft versus host disease (aGVHD) \> Grade 2 Mount Sinai Acute GVHD International Consortium (MAGIC) or chronic GVHD \> mild (NIH) requiring ongoing systemic steroids and/or multiagent therapy.

Patients who have received systemic immunosuppressive therapy for treatment of GVHD within 28 days of leukapheresis.

Currently requiring systemic corticosteroid therapy (10 mg/day or less of prednisone or equivalent doses of other systemic steroids are allowed for control of non-exclusionary pre-existing conditions). A 2-week washout is required prior to leukapheresis and prior to lymphodepletion for patients on \> 10 mg/day prednisone equivalent.

Patients who have received donor lymphocyte infusions within 28 days of MB-105 infusion.

Comorbidity that would impair the patient's ability to receive or tolerate MB-105 and/or affect participation in the study:

History of cardio- or cerebrovascular disease including myocardial infarction, unstable angina, or congestive heart failure (NYHA class III-IV) within 6 months or cerebrovascular accident (CVA; stroke) within 12 months prior to informed consent.

History of central nervous system (CNS) disorder(s) such as an uncontrolled seizure disorder, dementia, cerebellar disease, or any autoimmune disease with CNS involvement.

Any serious underlying medical or psychiatric condition deemed by the investigator and medical monitor to be exclusionary due to risk to the patient or to protocol compliance.

History of autoimmune disorders, including rheumatic diseases and thyroid disorders (though patients with a history of thyroid disease who have undergone successful therapy may be suitable). Exemptions for mild or limited disease may be granted after discussion between the Investigator and sponsor's medical monitor.

Participated in active treatment on other interventional research clinical trials \< 30 days before enrollment (participation in follow-up permitted). Contact the medical monitor to discuss prior experimental agents targeting the T cell lineage and the appropriate washout period.

Received bendamustine prior to enrollment (unless received an allo-HSCT in the interim).

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Omaha?

Yes, this clinical trial (NCT06534060) has an active research site in Omaha, NE that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

T-cell Lymphoma Treatment Options in Omaha, NE

If you're searching for t-cell lymphoma treatment options in Omaha, NE, this clinical trial (NCT06534060) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Omaha research site is actively enrolling participants for this phase 2 clinical trial. You'll receive care from experienced t-cell lymphoma specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all t-cell lymphoma clinical trials near you to find additional studies recruiting in your area.

T-cell Lymphoma Clinical Trial in Omaha, NE

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