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New treatment option for Chronic Lymphocytic Leukemia
Official title Phase II Study of Combined Pirtobrutinib, Venetoclax and Obinutuzumab (PVO) Time-limited Treatment for Patients With Recurrent Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma (CLL/SLL).
ClinicalTrials.gov ID: NCT06967610
What this study is testing
What is Pirtobrutinib?
Pirtobrutinib is an investigational medicine, given as an once-daily, being studied as a potential treatment for chronic lymphocytic leukemia.
Plain-language explanation of the investigational treatment - it is being studied and is not an approved or proven therapy. The study team can confirm the details.
- What it's testing
- To learn if the drug combination pirtobrutinib, venetoclax, and obinutuzumab can help to control relapsed CLL/SLL.
- Phase 2: a mid-size study of how well it works
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older
You may be able to join if
- Eligibility Criteria:
- Age 18 years or older.
- Diagnosis of CLL/SLL per 2018 iwCLL criteria (See Appendix 1).
- Participants with previously treated CLL requiring therapy based on 2018 iwCLL criteria.
- The participant is able to take oral medications.
You likely can't join if
- Participants who experienced progression of disease according to 2018 iwCLL criteria while on venetoclax will be excluded.
- Patient with prior history of Richter's syndrome or current Richter's Syndrome.
- Participants with known hypersensitivity to any of the excipients of pirtobrutinib, venetoclax,obinutuzumab or to any intended study medications.
- Known or suspected history of central nervous system (CNS) involvement by CLL/SLL.
- History of bleeding diathesis.
- Participants who experienced a major bleeding event on a prior BTK inhibitor. NOTE: Major bleeding is defined as bleeding having one or more of the...
See the full eligibility criteria
Who can join
- Eligibility Criteria:
- Age 18 years or older.
- Diagnosis of CLL/SLL per 2018 iwCLL criteria (See Appendix 1).
- Participants with previously treated CLL requiring therapy based on 2018 iwCLL criteria.
- The participant is able to take oral medications.
- Willing and capable of giving signed informed consent which includes compliance with the requirements and restrictions listed in the informed consent form (ICF) and in the protocol.
- Prior or ongoing therapy with covalent BTKi is allowed, but not required.
- Prior or ongoing therapy (at least for six months) with BCL2i is allowed, but not required. Prior therapy with combined BTKi and BCL2i or triplet BTKi, BCL2 and anti-CD20 mAb is allowed, but Participants need to be at...
- Participants are required to have the following washout periods prior to planned Cycle 1 Day1 (C1D1).
- Targeted agents, investigational agents, therapeutic monoclonal antibodies or cytotoxic chemotherapy: 5 half-lives or 2 weeks, whichever is shorter
- immunoconjugated antibody treatment within 10 weeks
- broad field radiation (≥ 30% of the bone marrow or whole brain radiotherapy) must be completed 14 days prior to enrollment
- palliative limited field radiation must be completed 7 days prior to enrollment
- Prior treatment-related AEs must have recovered to Grade ≤ 1 with the exception of alopecia and Grade 2 peripheral neuropathy.
- Eastern Cooperative Oncology Group (ECOG) Performance Status ≤2.
- Participants must have adequate renal and hepatic function:
- Serum bilirubin ≤1.5 x upper limit of normal (ULN) or ≤3 x ULN for Participants with Gilbert's disease or disease involvement by CLL/SLL.
- Serum creatinine clearance of ≥30ml/min (calculated or measured).
- ALT and AST ≤3.0 x ULN, unless clearly due to documented disease involvement, in which case ALT and AST ≤5.0 x ULN
- Adequate bone marrow function:
- Platelet count of ≥50,000/μl, with no platelet transfusion in prior 2 weeks.
- ANC ≥750/μl in the absence of growth factor support within 7 days of screening assessment.
- Hemoglobin ≥8g/dL, independent of transfusions within 7 days of screening assessment. Please refer to Appendix 4 for details of adjustments of toxicities in participants with abnormal baseline values)
- Adequate coagulation, defined as activated partial thromboplastin time (aPTT) or partial thromboplastin time and prothrombin time (PT) or international normalized ratio (INR) not greater than 1.5 x ULN.
- Women of childbearing potential must have a negative serum beta human chorionic gonadotropin (β-hCG) pregnancy test result at the time of screening and serum or urine β-hCG pregnancy test within 7 days prior to the...
What rules you out
- Participants who experienced progression of disease according to 2018 iwCLL criteria while on venetoclax will be excluded.
- Patient with prior history of Richter's syndrome or current Richter's Syndrome.
- Participants with known hypersensitivity to any of the excipients of pirtobrutinib, venetoclax,obinutuzumab or to any intended study medications.
- Known or suspected history of central nervous system (CNS) involvement by CLL/SLL.
- History of bleeding diathesis.
- Participants who experienced a major bleeding event on a prior BTK inhibitor. NOTE: Major bleeding is defined as bleeding having one or more of the following features: life-threatening bleeding with signs or symptoms of...
- History of stroke or intracranial hemorrhage within 6 months of enrollment.
- Participants requiring therapeutic anticoagulation with warfarin or another vitamin K antagonists.
- Major surgery within 4 weeks of planned start of study therapy.
- A significant history of renal, neurologic, psychiatric, endocrine, metabolic or immunologic disorder, that, in the opinion of the Investigator, would adversely affect the participant's participation in this study or...
- History of allogeneic or autologous stem cell transplant (SCT) or chimeric antigen receptor-modified Tcell (CAR-T) therapy within 60 days of enrollment or presence of any of the following, regardless of prior SCT and/or...
- active graft versus host disease (GVHD);
- cytopenia from incomplete blood cell count recovery post-transplant;
- need for anti-cytokine therapy for toxicity from CAR-T therapy; residual symptoms of neurotoxicity \> Grade 1 from CAR-T therapy;
- ongoing immunosuppressive therapy (\> 20 mg prednisone or equivalent daily).
- Active uncontrolled auto-immune cytopenia (e.g., autoimmune hemolytic anemia [AIHA], idiopathic thrombocytopenic purpura [ITP]) for which new therapy was introduced or existing therapy was escalated within the 4 weeks...
- Participants who experienced grade \>3 arrhythmia on prior treatment with BTK inhibitor.
- Significant cardiovascular disease, defined as any of the following:
- Unstable angina or acute coronary syndrome within the past 2 months.
- History of myocardial infarction within 6 months prior to planned start of study treatment.
- Documented left ventricular ejection fraction (LVEF) by any method of ≤ 45% in the 12 months prior to planned start of study treatment.
- ≥ Grade 3 New York Heart Association (NYHA) functional classification system of heart failure.
- uncontrolled or symptomatic arrhythmias
- Prolongation of the QT interval corrected (QTc - see Appendix 3) for heart rate using Fredericia's Formula (QTcF) \> 470 msec on an EKG during screening.
- QTcF is calculated using Fredericia's Formula (QTcF = QT/(RR\^0.33)
- Correction of suspected drug-induced QTcF prolongation or prolongation due to electrolyte abnormalities can be attempted at the Investigator's discretion, and only if clinically safe to do so with either discontinuation...
- Correction of QTc for underlying bundle branch block (BBB) permissible. Participants with pacemakers are eligible if they have no history of fainting or clinically relevant arrhythmias while using the pacemaker
- Hepatitis B or hepatitis C testing indicating active/ongoing infection based on screening laboratory tests as defined as:
- Hepatitis B virus (HBV): Participants with positive hepatitis B surface antigen (HBsAg) are excluded. Participants with positive hepatitis B core antibody (anti-HBc) and negative HBsAg require hepatitis B polymerase...
- Hepatitis C virus (HCV): positive hepatitis C antibody. If positive hepatitis C antibody result, participant will need to have a negative result for hepatitis C ribonucleic acid (RNA) . Participants who are hepatitis C...
- Evidence of other clinically significant uncontrolled condition(s) including, but not limited to, uncontrolled systemic infection (viral, bacterial, parasitic or fungal) or other clinically significant active disease...
- Known Human Immunodeficiency Virus (HIV) infection, regardless of CD4 count. For participants with unknown HIV status, HIV testing will be performed at screening and result must be negative for enrollment.
- Known active CMV infection. Participants with unknown or negative status are eligible.
- Vaccination with live vaccine within 28 days prior to enrollment
- Clinically significant active malabsorption syndrome or other condition likely to affect gastrointestinal (GI) absorption of the oral administered study treatments.
- Active other malignancy unless in remission and with life expectancy \> 2 years. with exception of participants diagnosed with basal cell or squamous cell carcinoma of the skin or carcinoma "in situ" of the cervix or...
- Current treatment with strong cytochrome P450 3A4 (CYP3A4) inhibitors or inducers. A washout period of at least 5 half-lives of these agents following discontinuation before study entry is required (treatment with...
- Current treatment with the following P-gp inhibitors: amiodarone, clarithromycin, cyclosporine, erythromycin, ketoconazole, and verapamil. A washout period of at least 5 half-lives of the inhibitor before study entry is...
- Participants that are pregnant or plan to become pregnant during the study or within 1 month of the last dose of study treatment. 25) Participants that are lactating or plan to breastfeed during the study or within 1...
The study team makes the final eligibility decision.
Where it's taking place
- Houston, Texas, United States
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Houston, Texas, United States. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.