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- Sperimentazione clinica NCT07882173
Epcoritamab as Consolidative Therapy for Waldenstr(SqrRoot)(Delta)m Macroglobulinemia (WM) Treated With a Bruton Tyrosine Kinase Inhibitor (BTKi)
Epcoritamab as Consolidative Therapy for Waldenstrom Macroglobulinemia (WM) Treated With a Bruton Tyrosine Kinase Inhibitor (BTKi)
Background:
Waldenstrom macroglobulinemia (WM) is a type of blood cancer. It causes the blood to get thicker, which slows circulation and makes it harder to carry oxygen and other substances around the body. WM is treated with drugs called Bruton tyrosine kinase inhibitors (BTKi). But WM never goes away completely, and sometimes it gets worse despite treatment.
Objective:
To test a new drug (epcoritamab) in people with WM.
Eligibility:
People aged 18 years or older who have WM. They must have been taking a BTKi for a year or more.
Design:
Participants will be screened. They will have blood and urine tests. They will have imaging scans and a test of their heart function. They may have a bone marrow biopsy: A large needle will be used to remove a sample of the soft tissue and fluids from inside the hip bone.
Epcoritamab is injected under the skin, normally on the lower belly or thigh. Participants will be treated in 28-day cycles. They will have 12 treatment cycles. During the first cycle, they will come to the clinic to get an injection once a week for 4 weeks. After that, they will get 1 injection on the first day of each cycle.
Blood tests and imaging scans will be repeated at study visits. A saliva sample will be taken for genetic testing. Participants will also continue their normal treatment with BTKi.
After their last treatment with the study drug, participants will have 5 follow-up visits in 6 months. Tests, including a bone marrow biopsy, may be repeated. Follow-up visits will continue every 6 months for 3 (Omega) years or more.
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
Study Description:
This is a phase 2 study of adding epcoritamab as consolidative therapy for subjects with Waldenstrom macroglobulinemia (WM) receiving treatment with a Bruton tyrosine kinase inhibitor (BTKi), zanubrutinib or ibrutinib. Subjects will be treated with epcoritamab for twelve 28-day cycles. For cycle 1, patients will receive epcoritamab subcutaneously (SC) with step-up dosing (SUD; 0.16 mg on C1D1, 0.8 mg on C1D8, 3 mg on C1D15, 48 mg on C1D22). The first 3 subjects will start treatment with epcoritamab >=4 weeks apart and be hospitalized for 24 hours after the first full dose of 48 mg for observation. In the absence of grade >=3 cytokine release syndrome (CRS), subsequent subjects will be treated on an outpatient basis. Epcoritamab 48 mg SC will be administered every 4 weeks from cycles 2 to 12.
Subjects achieving complete remission (CR) or very good partial remission (VGPR) by serum IgM after 12 cycles of epcoritamab will be evaluated by bone marrow biopsy and aspirate 2 months after the last dose of epcoritamab, and elect to discontinue BTKi therapy if CR/VGPR is confirmed. For subjects who do not attain CR/VGPR, BTKi will continue as per standard of care.
Objectives:
Primary objective:
-Evaluate the efficacy of epcoritamab as consolidative therapy in WM treated with a BTKi
Secondary objectives:
- Evaluate the safety of epcoritamab as consolidative therapy in WM treated with a BTKi
- Evaluate other parameters of efficacy of epcoritamab as consolidative therapy in WM treated with a BTKi
Endpoints:
Primary Endpoint:
-Rate of CR/VGPR after 12 cycles of epcoritamab in WM treated with a BTKi
Secondary Endpoint:
- Rate of cytokine release syndrome (CRS), immune effector cell-associated neurotoxicity syndrome (ICANS), and IgM flare
- Incidence and severity of treatment-emergent adverse events (TEAEs)
- Progression-free survival (PFS)
- Duration of response after BTKi discontinuation
- Overall survival (OS)
Tipo di studio
Iscrizione (Stimato)
Fase
- Fase 2
Contatti e Sedi
Contatto studio
- Nome: Laura S Samples, M.D.
- Numero di telefono: (301) 827-1203
- Email: laura.samples@nih.gov
Backup dei contatti dello studio
- Nome: Lymphoid Malignancies Team Study Coordin
- Numero di telefono: (301) 827-1203
- Email: nhlbidi-rocdlmtrn@nih.gov
Luoghi di studio
-
-
Maryland
-
Bethesda, Maryland, Stati Uniti, 20892
- National Institutes of Health Clinical Center
-
Contatto:
- NIH Clinical Center Office of Patient Recruitment (OPR)
- Numero di telefono: TTY dial 711 800-411-1222
- Email: ccopr@nih.gov
-
-
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
- INCLUSION CRITERIA:
Patients must meet the following entry criteria to be eligible to participate in the study:
-
Age >=18 years
-
Ability to comprehend the investigational nature of the study and provide informed consent
-
Diagnosis of WM according to 11th International Workshop on WM (IWWM-11) (19)
- Presence of an IgM monoclonal protein
- Bone marrow involvement by lymphoplasmacytic lymphoma
-
Presence of MYD88 L265P mutation
-
Currently receiving a BTKi, zanubrutinib or ibrutinib, for >=12 months
-
Able to obtain a commercial supply of BTKi
-
Achieved partial response, minor response, or stable disease on a BTKi per IWWM-11 response criteria (19)
-
A female participant is eligible to participate if not pregnant or breastfeeding, and >=1 of the following conditions applies:
Is not a woman of childbearing potential (WOCBP)
OR
Is a WOCBP and
- Uses a contraceptive method
- Has a negative highly sensitive serum pregnancy test within 7 days before the first dose of study intervention.
-
Have an Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2 within 7 days prior to the first dose of study intervention.
-
The ability to swallow and retain oral medication.
-
Participants who are HBsAg positive are eligible if they have received HBV antiviral therapy for >=4 weeks and have undetectable HBV viral load prior to study entry.
Note: Participants should remain on anti-viral therapy throughout study intervention and for at least 12 months following discontinuation of epcoritamab. Hepatitis B screening tests should include HBsAg and anti-HBV.
-
Participants who received treatment for HCV that was intended to eradicate the virus are eligible if hepatitis C RNA levels are undetectable.
-
COVID 19 eligibility criteria:
Subject has no known active severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. If a subject has signs/symptoms suggestive of SARS-CoV-2 infection or have had recent known exposure to someone with SARS-CoV-2 infection, the subject must have a negative molecular (e.g., PCR) test, or 2 negative antigen test results at least 24 hours apart, to rule out SARS-CoV-2 infection.
Subjects who do not meet SARS-CoV-2 infection eligibility criteria must be screen failed and may only rescreen after they meet the following SARS-CoV-2 infection viral clearance criteria:
- No signs/symptoms suggestive of active SARS-CoV-2 infection
- Negative molecular (e.g., PCR) result or 2 negative antigen test results at least 24 hours apart
-
Adequate organ function as defined below.
**Adequate Organ Function Laboratory Values**
System
Laboratory Value
Hematological
Absolute neutrophil count (ANC)
>=1000/microL (a)
Platelets
>=75000/microL or >=50000/microLin the presence of bone marrow involvement or splenomegaly (a)
Hemoglobin
>=8 g/dL (a)
Renal
Creatinine
<=1.5 x ULN or eGFR >=30 mL/min
Hepatic
Total bilirubin
<=1.5 x ULN unless due to Gilbert's syndrome or controlled autoimmune hemolytic anemia (not requiring immunosuppressive other than <=20 mg of prednisolone daily)
AST and ALT
<=3 ULN
Coagulation
PT
aPTT
<=1.5 x ULN unless participant is receiving anticoagulant therapy
eGFR=estimated glomerular filtration rate; ALT =alanine aminotransferase; AST =aspartate aminotransferase; ULN=upper limit of normal; INR=international normalized ratio; PT=prothrombin time; aPTT=activated partial thromboplastin time
-
Growth factor and/or transfusion support is allowed to meet this requirement at Screening only if directly attributable to WM infiltration of the bone marrow, proven by bone marrow biopsy
EXCLUSION CRITERIA:
An individual who meets any of the following criteria will be excluded from participation in this study:
-
Active CNS involvement, including Bing-Neel syndrome
-
Active HBV/HCV infection.
-
Infection with HIV-1 or HIV-2. Exception: patients with well-controlled HIV (e.g., CD4 >350/mm^3 and undetectable viral load) are eligible.
-
Gastrointestinal dysfunction that may affect drug absorption (e.g., gastric bypass surgery, gastrectomy).
-
Ongoing active bacterial, viral, fungal, mycobacterial, parasitic, or other infection requiring systemic treatment (excluding prophylactic treatment) at the time of enrollment or within the previous 2 weeks prior to the first dose of epcoritamab, including COVID-19 infection. Note that a past COVID-19 infection may be a risk factor, but if resolved and the subject is vaccinated, it may be allowable to enroll the Subject.
-
Stroke or intracranial hemorrhage within 6 months of screening
-
Hypertensive urgency or emergency
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Active, clinically significant cardiovascular disease including:
-
Uncontrolled or symptomatic arrhythmias
-
Class 3 or 4 congestive heart failure as defined by New York Heart Association Functional Classification
- Association and/or known decreased ejection fraction <45%
-
Myocardial infarction, unstable angina or acute coronary syndrome within 6 months of screening.
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History of Mobitz II second-degree or third-degree heart block without a permanent pacemaker in place.
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QTcF >450 msecs based on Fridericia's formula
Note: QTcF value may be calculated as the numerical average of up to 3 separate readings for eligibility).
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Known allergy/sensitivity to epcoritamab
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History of severe bleeding disorder defined as an ongoing congenital or acquired condition that leads to an increased likelihood of bleeding (i.e., von Willebrand's disease or hemophilia).
-
History of a second malignancy, unless potentially curative treatment has been completed with no evidence of malignancy for 2 years.
Note: The time requirement does not apply to participants who underwent successful definitive resection of basal cell carcinoma of the skin, squamous cell carcinoma of the skin, or carcinoma in situ, excluding carcinoma in situ of the bladder.
-
Currently being treated with the following drugs:
- CYP3A strong inducers
- CYP3A strong inhibitors
Note: A washout period of at least 5 times the half-life after the last dose of any of the above treatments is required for a participant to be eligible for study enrollment.
-
Has received prior systemic anti-WM therapy besides a BTKi within 3 half-lives or 4 weeks (if prior therapy was a monoclonal antibody) of start of epcoritamab.
-
Has received prior radiotherapy within 2 weeks of start of epcoritamab or radiation-related toxicities requiring corticosteroids.
Note: Two weeks or fewer of palliative radiotherapy for non-CNS disease, with a 1-week washout, is permitted.
-
Has received a live vaccine or live-attenuated vaccine within 28 days before the first dose of epcoritamab. Administration of killed vaccines are allowed.
-
Patients requiring ongoing treatment with warfarin within 7 days of start of epcoritamab
-
Patients who have received > 140 mg of prednisone for 14 days prior to first dose of epcoritamab or those requiring > 10 mg prednisone (or equivalent) daily, unless needed for disease control.
-
Confirmed history or current autoimmune disease or other diseases resulting in permanent immunosuppression or requiring permanent immunosuppressive therapy. Low-dose (<=10 mg/day) prednisolone (or equivalent) for rheumatoid arthritis or similar conditions is allowed.
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Enrolled on another therapeutic clinical trial for WM at the start of epcoritamab. Concurrent enrollment on another therapeutic clinical trial or any trial designed to impact the efficacy of anti-cancer therapy is prohibited.
-
Has not adequately recovered after 4 weeks from major surgery or has ongoing surgical complications.
Note: Biopsy and placement of central venous access devices are not considered major surgery.
-
Has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial.
-
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: N / A
- Modello interventistico: Assegnazione di gruppo singolo
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Sperimentale: Epcoritamab
Epcoritamab will be administered as consolidative therapy in adults who have been receiving zanubrutinib or ibrutinib. |
Step-up epcoritamab dosing during cycle 1, followed by 48 mg every 4 weeks for cycles 2-12 |
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Rate of complete remission (CR) or very good partial remission (VGPR)
Lasso di tempo: 12 cycles (approximately 12 months after treatment begins)
|
CR: No detectable monoclonal IgM, normal bone marrow morphology with no lymphoplasmacytic lymphoma involvement, and resolution of any baseline extramedullary disease.VGPR: At least a 90% reduction in serum IgM from baseline or a serum IgM level within the normal range. |
12 cycles (approximately 12 months after treatment begins)
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Overall survival (OS)
Lasso di tempo: From the first dose of epcoritamab until death or up to 5 years after the first dose.
|
Time from treatment initiation to death from any cause. |
From the first dose of epcoritamab until death or up to 5 years after the first dose.
|
|
Duration of response (DOR) after BTKi discontinuation
Lasso di tempo: After BTKi discontinuation until loss of response, progression, death, or initiation of subsequent therapy.
|
The length of time that a confirmed CR or VGPR is maintained after BTKi therapy is discontinued. |
After BTKi discontinuation until loss of response, progression, death, or initiation of subsequent therapy.
|
|
Progression-free survival (PFS)
Lasso di tempo: From the first dose of epcoritamab until progression or death.
|
Time from treatment initiation to disease progression or death from any cause. |
From the first dose of epcoritamab until progression or death.
|
|
Treatment-emergent adverse events (TEAEs)
Lasso di tempo: From the first dose of epcoritamab through 60 days after the last dose, or until new systemic anticancer therapy.
|
Any new or worsened unfavorable medical occurrence after study treatment begins, regardless of whether it is considered treatment-related. |
From the first dose of epcoritamab through 60 days after the last dose, or until new systemic anticancer therapy.
|
|
IgM flare
Lasso di tempo: Baseline, during treatment, after treatment, and following BTKi discontinuation.
|
Measured through serial serum IgM. |
Baseline, during treatment, after treatment, and following BTKi discontinuation.
|
|
Immune effector cell associated neurotoxicity syndrome (ICANS)
Lasso di tempo: From the first epcoritamab dose through treatment and safety follow-up, approximately 60 days after the last dose.
|
ICANs will be assessed using the 10-point ICE tool. |
From the first epcoritamab dose through treatment and safety follow-up, approximately 60 days after the last dose.
|
|
Cytokine release syndrome (CRS)
Lasso di tempo: From the first epcoritamab dose through treatment and safety follow-up, approximately 60 days after the last dose.
|
CRS will be graded using the ASTCT CRS criteria. |
From the first epcoritamab dose through treatment and safety follow-up, approximately 60 days after the last dose.
|
Collaboratori e investigatori
Investigatori
- Investigatore principale: Laura S Samples, M.D., National Heart, Lung, and Blood Institute (NHLBI)
Pubblicazioni e link utili
Collegamenti utili
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Inizio studio (Stimato)
Completamento primario (Stimato)
Completamento dello studio (Stimato)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
- Malattie vascolari
- Malattia cardiovascolare
- Neoplasie
- Malattie del sistema immunitario
- Neoplasie per tipo istologico
- Malattie ematologiche
- Malattie linfatiche
- Malattie linfoproliferative
- Disturbi immunoproliferativi
- Neoplasie, plasmacellule
- Disturbi emostatici
- Paraproteinemie
- Disturbi delle proteine del sangue
- Disturbi emorragici
- Malattie emiche e linfatiche
- Macroglobulinemia di Waldenstrom
Altri numeri di identificazione dello studio
- 10002492
- 002492-H
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Informazioni su farmaci e dispositivi, documenti di studio
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