Is NCT06977711 recruiting in San Antonio, TX?

Yes, NCT06977711 is currently recruiting participants at its San Antonio, TX location. This diffuse large b-cell lymphoma clinical trial is actively enrolling qualified participants.

How do I join the diffuse large b-cell lymphoma clinical trial in San Antonio?

To join this clinical trial in San Antonio, 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 San Antonio 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.

Diffuse Large B-cell Lymphoma Clinical Trial in San Antonio, TX

About This Diffuse Large B-cell Lymphoma Study in San Antonio

This study is developed by the investigator and is a, phase I, single arm, clinical trial that will enroll subjects with untreated diffuse large B-cell lymphoma (DLCBL) at high risk for poor outcome. The types of treatments given will be shared with participants. The aims are: 1. To assess the safety and how well the participants tolerate the treatment 2. Assess the response of the tumor to treatment to estimate complete response 3. Assess the response of the tumor to treatment to estimate progression-free survival

Sponsor: The University of Texas Health Science Center at San Antonio

Who Can Participate

Inclusion Criteria

Men and women 18 years of age or older.

Pathologically proven diffuse large B-cell lymphoma (DLBCL) not otherwise specified (NOS). \- Patients with Diffuse large B-cell lymphoma/ high grade B-cell lymphoma with MYC (myelocytomatosis oncogene) and BCL2 (B-cell lymphoma 2) rearrangements are allowed.

No prior systemic therapy for lymphoma.

Subject has provided informed consent.

Subject is willing and able to comply with clinic visits and procedure outlined in the study protocol.

Eastern Cooperative Oncology Group (ECOG) performance status of 0-2.

Life expectancy of ≥3 months.

Ann Arbor stage II-IV

National Comprehensive Cancer Network - International Prognostic Index (NCCN-IPI) risk score of ≥ 2

Measurable disease, meaning at least 1 lymph node or other lymphomatous lesion with a long axis of ≥1.5 cm by CT imaging, and at least one FDG-avid lesion by FDG-PET scan.

Left ventricular ejection fraction of at least 45% by either echocardiography or radionucleotide angiography.

Ability to swallow oral tablets without difficulty.

All subjects with preserved reproductive potential must agree to practice abstinence or employ contraceptive measures for the duration of treatment and for 10 months (if female) or 7 months (if male) following final dosing. All male subjects are considered to have reproductive potential. Female subjects of reproductive potential are those who: i) are not at least 50 years old and have no menses for 24 consecutive months; or ii) have not been rendered surgically sterile (having undergone hysterectomy and/or bilateral salpingo-oophorectomy). Female subjects of reproductive potential must have a negative serum pregnancy test (minimum sensitivity 25 IU/L or equivalent units of human chorionic gonadotropin (hCG) within 7 days of first day of drug dosing.

Meet the following clinical laboratory requirements:

Creatinine clearance ≥30 ml/min by Cockcroft-Gault formula;

Total bilirubin ≤ 1.5 × upper limit of normal (ULN) (unless indirect bilirubin is elevated due to Gilbert's syndrome or hemolysis);

Aspartate aminotransferase (AST) and alanine aminotransferase (ALT)≤ 3 × ULN;

Platelet count ≥ 50,000/µL, with or without transfusion support;

Absolute Neutrophil Count (ANC) ≥ 1000/µL, with or without chronic granulocyte growth factor support;

Hemoglobin ≥8 g/dL, with or without transfusion support.

Exclusion Criteria

Allergy or intolerance to roflumilast.

Allergy or intolerance to loncastuximab

Any active malignancy other than DLBCL

Current participation in another interventional clinical study

Prior allogeneic bone marrow transplant within 12 months of screening date.

Prior autologous stem cell transplant within 6 months of screening date.

Immunotherapy, chemotherapy, radiotherapy, or investigational therapy within 6 months prior to drug dosing.

Active central nervous system (CNS) involvement by lymphoma, including untreated symptomatic epidural disease.

Active uncontrolled infection.

Poorly controlled depressive symptoms and/ or currently under management for depression that is poorly controlled.

Significant disease or medical conditions, as assessed by the Investigator and Sponsor, that would substantially increase the risk benefit ratio of participating in the study. This includes, but is not limited to, acute myocardial infarction within the last 6 months, unstable angina, uncontrolled diabetes mellitus, significant active infections, and congestive heart failure New York Heart Association Class III-IV.

Second malignancy, except treated basal cell or localized squamous skin carcinomas, localized prostate cancer, or other malignancies for which subjects are not on active anti-cancer therapies and have had no evidence of active malignancy for at least 1 year.

History of major surgery within 3 weeks or minor surgery within 1 week of roflumilast administration. Major surgery includes, for example, any open or laparoscopic entry into a body cavity, or operative repair of fracture; minor surgery includes, for example, open surgical biopsy of palpable/superficial lymph node, or placement of vascular access device.

Other medical or psychiatric illnesses or organ dysfunction, which in the opinion of the investigator, would either compromise the subject's safety or interfere with the evaluation of the safety of the study agent.

Corrected QT interval (QTc) prolongation (defined as a QTc \>450 ms for males and \>470 ms for females -Fridericia's correction-) or other clinically significant ECG abnormalities as assessed by the investigator.

Baseline serum troponin above the upper limit of normal.

Baseline serum brain natriuretic peptide (BNP )above the age-adjusted upper limit of normal.

Baseline amylase above the upper limit of normal.

Subjects known to be HIV-positive must not have multi-drug resistant HIV infection, cluster of differentiation 4 (CD4) counts \< 150/µl or other concurrent AIDS-defining conditions. Serologic screening for HIV is required within the 6 months prior to study enrollment.

Subjects positive for Hepatitis B surface antigen (HBsAg) or Hepatitis C-virus ribonucleic acid (HCV RNA), unless both AST and ALT≤1.25 x ULN and there is no known history of chronic active hepatitis. Serologic screening for hepatitis B and C testing is required within the 6 months prior to study enrollment.

Subjects with moderate or severe liver impairment, as defined by a Child-Pugh class of B or C.

Women who are pregnant or breastfeeding.

Current use of any of the following medications: boceprevir, carbamazepine, ciprofloxacin, cobicistat, conivaptan, enzalutamide, fluvoxamine, itraconazole, ketoconazole, mitotane, phenytoin, posaconazole, rifampin, ritonavir, St. John's Wort, telaprevir, voriconazole, or zafirlukast.

Current use of non-nucleoside reverse transcriptase inhibitors (NNRTI) including efavirenz, rilpivirine, etravirine, delavirdine, nevirapine, and lersivirine.

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 San Antonio?

Yes, this clinical trial (NCT06977711) has an active research site in San Antonio, TX 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.

Diffuse Large B-cell Lymphoma Treatment Options in San Antonio, TX

If you're searching for diffuse large b-cell lymphoma treatment options in San Antonio, TX, this clinical trial (NCT06977711) 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 San Antonio research site is actively enrolling participants for this clinical trial. You'll receive care from experienced diffuse large b-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 diffuse large b-cell lymphoma clinical trials near you to find additional studies recruiting in your area.

Diffuse Large B-cell Lymphoma Clinical Trial in San Antonio, TX

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