CX-5461 (Pidnarulex) for aggressive B‑cell lymphomas with MYC gene changes
Phase 1b/2 Trial of Pidnarulex in MYC Aberrant Lymphoma
This trial tests whether the IV drug CX-5461 (Pidnarulex) is safe and can shrink or control aggressive B‑cell lymphomas that have MYC gene changes in adults who have already had other treatments.
Quick facts
| Phase | Phase1; Phase2 |
|---|---|
| Study type | Interventional |
| Enrollment | 50 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | National Cancer Institute (NCI) NIH |
| Drugs / interventions | chimeric antigen receptor, immunotherapy |
| Locations | 4 sites (Irvine, California and 3 other locations) |
| Trial ID | NCT07069699 on ClinicalTrials.gov |
What this trial studies
This is a phase 1 dose‑escalation followed by a phase 2 trial using IV CX-5461 given on days 1 and 8 of 21‑day cycles to define safety, the recommended phase 2 dose, and early anti‑tumor activity in MYC‑aberrant aggressive B‑cell lymphomas. Phase 1 focuses on dose‑limiting toxicities, pharmacokinetics, and effects on gene expression, while phase 2 measures objective response rate. Patients undergo serial tumor biopsies, PET/CT imaging, blood sampling including ctDNA, and lumbar punctures to study CSF distribution and mechanisms of response or resistance. Treatment continues until disease progression or unacceptable toxicity with follow‑up visits for up to five years.
Who should consider this trial
Good fit: Ideal candidates are adults with Burkitt lymphoma, double‑expressor lymphoma, or high‑grade B‑cell lymphoma with MYC and BCL2 and/or BCL6 rearrangements who have received prior therapies and for whom standard curative or palliative options are no longer effective.
Not a fit: Patients with other lymphoma subtypes, children under 18, those with inadequate blood counts or organ function, or those who still have effective standard treatment options are unlikely to benefit from this trial.
Why it matters
Potential benefit: If successful, CX-5461 could provide a new targeted option that controls or shrinks high‑risk MYC‑driven B‑cell lymphomas that have limited effective treatments.
How similar studies have performed: Pol I inhibition with agents like CX-5461 is a relatively novel strategy with promising preclinical results and limited early‑phase clinical data, so definitive proof of benefit in MYC‑driven lymphomas has not yet been established.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients must have one of the following subtypes of aggressive B-cell non-Hodgkin lymphomas: double-expressor lymphoma (DEL), high-grade B-cell lymphoma (HGBL) with MYC and BCL2 and/or BCL6 rearrangement, or Burkitt lymphoma (BL). Eligible patients must have received at least two prior lines of treatment for diffuse large B-cell lymphoma (DLBCL) or at least one prior line of therapy for Burkitt Lymphoma and must have disease for which no standard curative or palliative treatment options exist or remain effective (Quin et al., 2016) * Age ≥ 18 years. Because no dosing or adverse event (AE) data are currently available on the use of CX-5461 (Pidnarulex) in patients \< 18 years of age, children are excluded from this study * Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2 (Karnofsky ≥ 60%). ECOG 3 is allowed if directly related to lymphoma per treating provider * Absolute neutrophil count ≥ 1,000/mcL * Platelets ≥ 50,000/mcL * Total bilirubin ≤ 1.5 institutional upper limit of normal (ULN) * Patients with documented Gilbert's syndrome may be included if total bilirubin is ≤ 3 × ULN and direct bilirubin is within normal limits * Aspartate aminotransferase (AST)(serum glutamic oxaloacetic transaminase \[SGOT\])/ alanine aminotransferase (ALT) (serum glutamic pyruvic transaminase \[SGPT\]) ≤ 3 × institutional upper limit of normal (ULN) * Glomerular filtration rate (GFR) ≥ 60 mL/min/, calculated by multiplying the estimated (e)GFR (mL/min/1.73 m\^2) by the individual's body surface area (BSA, calculated using an accepted formula) and dividing by 1.73 m\^2 * Human immunodeficiency virus (HIV)-infected patients on effective anti-retroviral therapy with undetectable viral load within 6 months are eligible for this trial * For patients with evidence of chronic hepatitis B virus (HBV) infection, the HBV viral load must be undetectable on suppressive therapy, if indicated * Patients with a history of hepatitis C virus (HCV) infection must have been treated and cured. For patients with HCV infection who are currently on treatment, they are eligible if they have an undetectable HCV viral load * Patients with a prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy assessment of the investigational regimen are eligible for this trial * Patients with known history or current symptoms of cardiac disease, or history of treatment with cardiotoxic agents, should have a clinical risk assessment of cardiac function using the New York Heart Association Functional Classification. To be eligible for this trial, patients should be class II or better * Patients with cytopenia related to abnormal bone marrow function in the setting of bone marrow involvement with lymphoma or post chimeric antigen receptor (CAR) T-cell are allowed to enroll if deemed safe by treating provider * Patients without clinical evidence of central nervous system (CNS) lymphoma * The effects of CX-5461 (Pidnarulex) on the developing human fetus are unknown. For this reason, women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control or abstinence) 14 days prior to study entry and for the duration of study participation and for at least 6 months after the last dose of study drug. Should a woman become pregnant or suspect she is pregnant while she or her partner is participating in this study, she should inform her treating physician immediately. Women should not breastfeed while taking CX-5461 (Pidnarulex) and for 6 months after cessation of treatment. Men treated or enrolled on this protocol must also agree to use adequate contraception 14 days prior to the study, for the duration of study participation, and 6 months after completion of CX-5461 (Pidnarulex) administration. Women of childbearing age should not donate egg(s) and men should not donate sperm for the duration of study participation and 6 months after completion of the last dose CX-5461 (Pidnarulex) * Willingness to provide blood and biopsy samples for research purposes * Ability to understand and the willingness to sign a written informed consent document Exclusion Criteria: * Patients must have recovered from clinically significant adverse events (AEs) of their most recent cancer immunotherapy to grade 1 or less (with the exception for alopecia or lymphopenia) * Eligibility of subjects receiving any medications or substances known to affect or with the potential to affect the activity of CX-5461 (Pidnarulex) will be determined based on their potential to interact with the CYP3A4 isozyme. Specifically, subjects taking strong CYP3A4 inhibitors or strong CYP3A4 inducers will be excluded from participation in the trial. For medications or substances not listed, or in cases of uncertainty, the Principal Investigator may consult with a medical expert or a pharmacologist to make an informed decision regarding eligibility * Patients with a baseline corrected QT (QTc) interval \> 480 msec * Patients who are receiving any other investigational agents * History of allergic reactions attributed to compounds of similar chemical or biologic composition to CX-5461 (Pidnarulex) * Patients with uncontrolled intercurrent illness or any other significant condition(s) that would make participation in this protocol unreasonably hazardous * Pregnant women are excluded from this study because CX-5461 (Pidnarulex) is an agent with the potential for teratogenic or abortifacient effects. Because there is an unknown but potential risk for AEs in nursing infants secondary to treatment of the mother with CX-5461 (Pidnarulex), breastfeeding should be discontinued if the mother is treated with CX-5461 (Pidnarulex)
Where this trial is running
Irvine, California and 3 other locations
- UCI Health - Chao Family Comprehensive Cancer Center and Ambulatory Care — Irvine, California, United States (Recruiting)
- UC Irvine Health/Chao Family Comprehensive Cancer Center — Orange, California, United States (Recruiting)
- University of Oklahoma Health Sciences Center — Oklahoma City, Oklahoma, United States (Recruiting)
- University of Pittsburgh Cancer Institute (UPCI) — Pittsburgh, Pennsylvania, United States (Recruiting)
Study contacts
- Principal investigator: Sami Ibrahimi — Yale University Cancer Center LAO
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.