- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT07578077
Golcadomide in Combination With Rituximab for the Treatment of Patients With Relapsed or Refractory Mantle Cell Lymphoma
A Phase 1/2 Study of the CELMoD Agent Golcadomide in Combination With Rituximab in Patients With Relapsed or Refractory Mantle Cell Lymphoma
Panoramica dello studio
Stato
Descrizione dettagliata
PRIMARY OBJECTIVES:
I. To evaluate the safety and tolerance of golcadomide in mantle cell lymphoma (MCL) patients who were resistant or intolerant to covalent bruton's tyrosine kinase inhibitors (cBTKi).
II. To evaluate the safety and tolerance of golcadomide in combination with rituximab in MCL patients who were resistant or intolerant to cBTKi.
III. To estimate the efficacy of golcadomide and rituximab in MCL patients who were resistant or intolerant to cBTKi.
SECONDARY OBJECTIVES:
I. To evaluate the complete response rate (CR) of the combination of golcadomide and rituximab.
II. To evaluate the durability of response by the duration of response (DOR) and duration of complete response (DOCR).
EXPLORATORY OBJECTIVES:
I. Correlate clinical response with changes in baseline T cell characteristics and cytokine profiles.
II. To measure the rate of minimal residual disease undetectability in responding patients.
OUTLINE: This is a phase I, dose-escalation study of golcadomide followed by a phase II study. Patients are assigned to 1 of 2 phases.
PHASE I: Patients receive golcadomide orally (PO) once daily (QD) on days 1-14 of each cycle. Cycles repeat every 28 days for up to 24 cycles in the absence of disease progression or unacceptable toxicity. Patients also undergo blood sample collection and positron emission tomography (PET)/computed tomography (CT) throughout the trial. Patients undergo bone marrow biopsy and may undergo tissue biopsy on study.
PHASE II: Patients receive golcadomide PO QD on days 1-14 of each cycle. Patients also receive rituximab intravenously (IV) on days 1, 8, 15 and 22 of cycle 1 and then day 1 of even cycles. Cycles repeat every 28 days for up to 24 cycles in the absence of disease progression or unacceptable toxicity. Patients also undergo blood sample collection and PET/CT throughout the trial. Patients undergo bone marrow biopsy and may undergo tissue biopsy on study.
After completion of study treatment, patients are followed up at 30 days, and then up to 3 years.
Tipo di studio
Iscrizione (Stimato)
Fase
- Fase 2
- Fase 1
Contatti e Sedi
Luoghi di studio
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California
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Duarte, California, Stati Uniti, 91010
- City of Hope Medical Center
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Investigatore principale:
- Tycel J. Phillips
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Contatto:
- Tycel J. Phillips
- Numero di telefono: 82405 626-256-4673
- Email: tphillips@coh.org
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
- Adulto
- Adulto più anziano
Accetta volontari sani
Descrizione
Inclusion Criteria:
- Documented informed consent of the participant and/or legally authorized representative
Agreement to allow the use of archival tissue from diagnostic tumor biopsies
- If unavailable, exceptions may be granted with study principal investigator (PI) approval
- Ability to adhere to the study protocol
- Age: ≥ 18 years
- Eastern Clinical Oncology Group (ECOG) ≤ 2
Histologically confirmed diagnosis of MCL
- Immunohistochemistry of the biopsy
- Flow cytometry of the biopsy
- Relapsed/ refractory disease
- Relapsed/refractory (R/R) MCL after at least one line of therapy including resistant or intolerant to a cBTKi
- Fully recovered from the acute toxic effects (except alopecia) to ≤ grade 1 to prior anti-cancer therapy
- Ability to swallow pills
Without bone marrow involvement: Absolute neutrophil count (ANC) > 1.5 × 10^9/L (ANC > 1,500/mm^3)
- With bone marrow involvement: ANC > 1.0 × 10^9/L (ANC > 1000/mm^3)
- NOTE: Growth factor is not permitted within 14 days of ANC assessment unless cytopenia is secondary to disease involvement. For patients with significant marrow involvement, eligibility may be confirmed at the discretion of the treating investigator
Without bone marrow involvement: Platelets ≥ 75,000/mm^3
- With bone marrow involvement: Platelets ≥ 50,000/mm^3
- NOTE: Platelet transfusions are not permitted within 14 days of platelet assessment unless cytopenia is secondary to disease involvement
- Total bilirubin ≤ 1.5 × upper limit of normal (ULN) (≤ 1.5 × ULN if Gilbert's disease)
- Aspartate aminotransferase (AST) =< 2.5 × ULN
- Alanine aminotransferase (ALT) ≤ 2.5 × ULN unless elevation is attributable to underlying disease, in which case ALT ≤ 3.0 × ULN
- Creatinine clearance of ≥ 30 mL/min per 24 hour urine test or the Cockcroft-Gault formula
- If not receiving anticoagulants: International normalized ratio (INR) OR prothrombin (PT) ≤ 1.5 × ULN. If on anticoagulant therapy: PT must be within therapeutic range of intended use of anticoagulants
- If not receiving anticoagulants: Activated partial thromboplastin time (aPTT) ≤ 1.5 × ULN. If on anticoagulant therapy: aPTT must be within therapeutic range of intended use of anticoagulants
- Seronegative for HIV
- Seronegative for hepatitis C virus (HCV), hepatitis B virus (HBV) (surface antigen negative)
Meets other institutional and federal requirements for infectious disease titer requirements
- Note Infectious disease testing to be performed within 28 days prior to day 1 of protocol therapy
- Woman of childbearing potential must have a negative pregnancy test using a highly sensitive assay (minimum sensitivity 25 IU/L) performed within 10 to 14 days and again within 24 hours prior to receiving the first dose of golcadomide/BMS-986369
Agreement by females of childbearing potential to use two effective methods of contraception simultaneously without interruption, for at least 28 days before starting study treatment, throughout the entire duration of study treatment, during dose interruptions, and for at least 28 days after the last dose of golcadomide/BMS-986369. The two methods of contraception must include one highly effective method and one additional effective method. Compliance will be documented using the Clinical Trial Pregnancy Risk Awareness Checklist, which must be completed and provided to participants at screening and prior to dispensing of study drug. An individual of childbearing potential (IOCBP) is defined as:
- A person who has achieved menarche, has not undergone a documented hysterectomy or bilateral oophorectomy, and has not been naturally postmenopausal for at least 12 consecutive months. Amenorrhea resulting from medical interventions (such as cancer therapy), rather than natural menopause, does not exclude childbearing potential.
Criteria:
- Achievement of menarche (onset of menstruation).
No history of surgical sterilization:
- No documented hysterectomy
- No documented bilateral oophorectomy
Not naturally postmenopausal:
- Defined as absence of menses for ≥ 12 consecutive months due to natural causes (not due to medical interventions such as chemotherapy, hormonal therapy, or radiotherapy)
- Amenorrhea due to medical causes (e.g., cancer therapy, hormonal treatment) does not qualify as natural menopause and does not exclude childbearing potential
Exclusion Criteria:
- Chemotherapy, radiation therapy (except for palliative radiation therapy [XRT]), biological therapy, immunotherapy within 21 days or five half-lives (whichever is shorter for non-radiation therapy) prior to day 1 of protocol therapy
- Strong CYP3A4 inducers/ inhibitors within 14 days prior to day 1 of protocol therapy
- Herbal medications
- History of metastatic cancer
Unstable cardiac disease as defined by one of the following:
- Cardiac events such as myocardial infarction (MI) within the past 6 months
- New York Heart Association (NYHA) heart failure class III-IV
- Uncontrolled atrial fibrillation or hypertension
- History of allergic reactions attributed to compounds of similar chemical or biologic composition to study agents
- Clinically significant uncontrolled illness
- Known seropositive or active infection with HIV, HBV, or HCV
- Known active bacterial, viral, fungal, mycobacterial, parasitic, or other infection (excluding fungal infections of nail beds) at study enrollment or any major episode of infection (as evaluated by the investigator) within 4 weeks prior to the first study treatment
- Females only: Pregnant or breastfeeding
- Any other condition that would, in the investigator's judgment, contraindicate the patient's participation in the clinical study due to safety concerns with clinical study procedures
- Prospective participants who, in the opinion of the investigator, may not be able to comply with all study procedures (including compliance issues related to feasibility/logistics)
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Non randomizzato
- Modello interventistico: Assegnazione sequenziale
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Sperimentale: Phase I (Golcadomide)
Patients receive golcadomide PO QD on days 1-14 of each cycle.
Cycles repeat every 28 days for up to 24 cycles in the absence of disease progression or unacceptable toxicity.
Patients also undergo blood sample collection and PET/CT throughout the trial.
Patients undergo bone marrow biopsy and may undergo tissue biopsy on study.
|
Sottoponiti al prelievo di campioni di sangue
Altri nomi:
Sottoponiti a PET/TC
Altri nomi:
Sottoponiti a PET/TC
Altri nomi:
Sottoponiti a biopsia del midollo osseo
Altri nomi:
Dato PO
Altri nomi:
Sotto biopsia tissutale
Altri nomi:
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Sperimentale: Phase II (Golcadomide, rituximab)
Patients receive golcadomide PO QD on days 1-14 of each cycle.
Patients also receive rituximab IV on days 1, 8, 15 and 22 of cycle 1 and then day 1 of even cycles.
Cycles repeat every 28 days for up to 24 cycles in the absence of disease progression or unacceptable toxicity.
Patients also undergo blood sample collection and PET/CT throughout the trial.
Patients undergo bone marrow biopsy and may undergo tissue biopsy on study.
|
Sottoponiti al prelievo di campioni di sangue
Altri nomi:
Dato IV
Altri nomi:
Sottoponiti a PET/TC
Altri nomi:
Sottoponiti a PET/TC
Altri nomi:
Sottoponiti a biopsia del midollo osseo
Altri nomi:
Dato PO
Altri nomi:
Sotto biopsia tissutale
Altri nomi:
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Incidence of dose limiting toxicities (DLT)
Lasso di tempo: During cycle 1 (Cycle length = 28 days)
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The adverse events will be graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events, version 5.0 (NCI CTCAE v 5.0).
Toxicity will be summarized by type, severity, and attribution.
DLT will be individually described.
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During cycle 1 (Cycle length = 28 days)
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Maximum tolerated dose (MTD) of golcadomide
Lasso di tempo: Up to 3 years
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If single agent is tolerable, we will subsequently explore golcadomide in combination with rituximab.
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Up to 3 years
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MTD of golcadomide in combination with rituximab
Lasso di tempo: Up to 3 years
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Patients would remain on therapy until unacceptable toxicity, treating physician discretion or PD.
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Up to 3 years
|
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Overall response rate (ORR)
Lasso di tempo: Up to 3 years
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Defined as achieving a best response of either complete metabolic response (CMR) or partial metabolic response (PMR) in a response-evaluable participant after the start of protocol therapy and prior to disease progression and/or start of other anti-lymphoma therapy.
ORR will be estimated by binary proportions, along with the 95% exact binomial confidence intervals.
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Up to 3 years
|
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Progression free survival (PFS)
Lasso di tempo: From start of protocol treatment to time of disease relapse/progression or death due to any cause, whichever occurs earlier, assessed up to 3 years
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PFS will be estimated using the product-limit method of Kaplan and Meier along with the Greenwood estimator of standard error; 95% confidence interval will be constructed based on log-log transformation.
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From start of protocol treatment to time of disease relapse/progression or death due to any cause, whichever occurs earlier, assessed up to 3 years
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Incidence of adverse events
Lasso di tempo: Up to 3 years
|
Will be graded by NCI CTCAE v 5.0.
Toxicity will be summarized by type, severity, and attribution.
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Up to 3 years
|
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Duration of response (DOR) of the combination of golcadomide and rituximab
Lasso di tempo: From the first achievement of PMR or CMR to time of progressive disease (PD) or death, whichever earlier, assessed up to 3 years
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DOR will be estimated using the product-limit method of Kaplan and Meier.
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From the first achievement of PMR or CMR to time of progressive disease (PD) or death, whichever earlier, assessed up to 3 years
|
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Duration of complete response (DOCR) of the combination of golcadomide and rituximab
Lasso di tempo: Time from the first achievement of CMR to time of PD or death, whichever earlier, assessed up to 3 years
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DOCR will be estimated using the product-limit method of Kaplan and Meier.
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Time from the first achievement of CMR to time of PD or death, whichever earlier, assessed up to 3 years
|
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Complete response (CR) of the combination of golcadomide and rituximab
Lasso di tempo: Up to 3 years
|
CR rate will be estimated by binary proportions, along with the 95% exact binomial confidence intervals.
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Up to 3 years
|
Collaboratori e investigatori
Sponsor
Collaboratori
Investigatori
- Investigatore principale: Tycel J Phillips, City of Hope Medical Center
Studiare le date dei record
Studia le date principali
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
Termini MeSH pertinenti aggiuntivi
- Neoplasie
- Malattie del sistema immunitario
- Neoplasie per tipo istologico
- Malattie linfatiche
- Malattie linfoproliferative
- Disturbi immunoproliferativi
- Linfoma non Hodgkin
- Linfoma
- Malattie emiche e linfatiche
- Linfoma, cellule del mantello
- Aminoacidi, peptidi e proteine
- Proteine
- Tecniche investigative
- Tecniche di laboratorio clinico
- Tecniche e procedure diagnostiche
- Diagnosi
- Procedure chirurgiche, operative
- Tecniche citologiche
- Citodiagnosi
- Anticorpi, monoclonali
- Anticorpi
- Immunoglobuline
- Immunoproteine
- Proteine del sangue
- Globuline sieriche
- Globuline
- Tecniche diagnostiche, chirurgiche
- Tecniche di chimica, analitiche
- Analisi dello spettro
- Anticorpi, monoclonali, derivati da murina
- Rituximab
- Biopsia
- Gestione dei campioni
- Spettroscopia di risonanza magnetica
- CT-P10
Altri numeri di identificazione dello studio
- 25448 (Altro identificatore: City of Hope Medical Center)
- P30CA033572 (Sovvenzione/contratto NIH degli Stati Uniti)
- NCI-2026-02921 (Identificatore di registro: CTRP (Clinical Trial Reporting Program))
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
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prodotto fabbricato ed esportato dagli Stati Uniti
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