- ICH GCP
- Registr klinických studií v USA
- Klinická studie 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
Přehled studie
Postavení
Detailní popis
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.
Typ studie
Zápis (Odhadovaný)
Fáze
- Fáze 2
- Fáze 1
Kontakty a umístění
Studijní místa
-
-
California
-
Duarte, California, Spojené státy, 91010
- City of Hope Medical Center
-
Vrchní vyšetřovatel:
- Tycel J. Phillips
-
Kontakt:
- Tycel J. Phillips
- Telefonní číslo: 82405 626-256-4673
- E-mail: tphillips@coh.org
-
-
Kritéria účasti
Kritéria způsobilosti
Věk způsobilý ke studiu
- Dospělý
- Starší dospělý
Přijímá zdravé dobrovolníky
Popis
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)
Studijní plán
Jak je studie koncipována?
Detaily designu
- Primární účel: Léčba
- Přidělení: Nerandomizované
- Intervenční model: Sekvenční přiřazení
- Maskování: Žádné (otevřený štítek)
Zbraně a zásahy
Skupina účastníků / Arm |
Intervence / Léčba |
|---|---|
|
Experimentální: 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.
|
Podstoupit odběr vzorku krve
Ostatní jména:
Podstoupit PET/CT
Ostatní jména:
Podstoupit PET/CT
Ostatní jména:
Podstoupit biopsii kostní dřeně
Ostatní jména:
Vzhledem k PO
Ostatní jména:
Podléhat tkáňové biopsii
Ostatní jména:
|
|
Experimentální: 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.
|
Podstoupit odběr vzorku krve
Ostatní jména:
Vzhledem k tomu, IV
Ostatní jména:
Podstoupit PET/CT
Ostatní jména:
Podstoupit PET/CT
Ostatní jména:
Podstoupit biopsii kostní dřeně
Ostatní jména:
Vzhledem k PO
Ostatní jména:
Podléhat tkáňové biopsii
Ostatní jména:
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Co je měření studie?
Primární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
Incidence of dose limiting toxicities (DLT)
Časové okno: During cycle 1 (Cycle length = 28 days)
|
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.
|
During cycle 1 (Cycle length = 28 days)
|
|
Maximum tolerated dose (MTD) of golcadomide
Časové okno: Up to 3 years
|
If single agent is tolerable, we will subsequently explore golcadomide in combination with rituximab.
|
Up to 3 years
|
|
MTD of golcadomide in combination with rituximab
Časové okno: Up to 3 years
|
Patients would remain on therapy until unacceptable toxicity, treating physician discretion or PD.
|
Up to 3 years
|
|
Overall response rate (ORR)
Časové okno: Up to 3 years
|
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.
|
Up to 3 years
|
|
Progression free survival (PFS)
Časové okno: 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
|
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.
|
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
|
Sekundární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
Incidence of adverse events
Časové okno: Up to 3 years
|
Will be graded by NCI CTCAE v 5.0.
Toxicity will be summarized by type, severity, and attribution.
|
Up to 3 years
|
|
Duration of response (DOR) of the combination of golcadomide and rituximab
Časové okno: From the first achievement of PMR or CMR to time of progressive disease (PD) or death, whichever earlier, assessed up to 3 years
|
DOR will be estimated using the product-limit method of Kaplan and Meier.
|
From the first achievement of PMR or CMR to time of progressive disease (PD) or death, whichever earlier, assessed up to 3 years
|
|
Duration of complete response (DOCR) of the combination of golcadomide and rituximab
Časové okno: Time from the first achievement of CMR to time of PD or death, whichever earlier, assessed up to 3 years
|
DOCR will be estimated using the product-limit method of Kaplan and Meier.
|
Time from the first achievement of CMR to time of PD or death, whichever earlier, assessed up to 3 years
|
|
Complete response (CR) of the combination of golcadomide and rituximab
Časové okno: Up to 3 years
|
CR rate will be estimated by binary proportions, along with the 95% exact binomial confidence intervals.
|
Up to 3 years
|
Spolupracovníci a vyšetřovatelé
Sponzor
Spolupracovníci
Vyšetřovatelé
- Vrchní vyšetřovatel: Tycel J Phillips, City of Hope Medical Center
Termíny studijních záznamů
Hlavní termíny studia
Začátek studia (Odhadovaný)
Primární dokončení (Odhadovaný)
Dokončení studie (Odhadovaný)
Termíny zápisu do studia
První předloženo
První předloženo, které splnilo kritéria kontroly kvality
První zveřejněno (Aktuální)
Aktualizace studijních záznamů
Poslední zveřejněná aktualizace (Aktuální)
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
Naposledy ověřeno
Více informací
Termíny související s touto studií
Další relevantní podmínky MeSH
- Novotvary
- Onemocnění imunitního systému
- Novotvary podle histologického typu
- Lymfatická onemocnění
- Lymfoproliferativní poruchy
- Imunoproliferativní poruchy
- Lymfom, Non-Hodgkin
- Lymfom
- Hemická a lymfatická onemocnění
- Lymfom, plášťová buňka
- Aminokyseliny, peptidy a proteiny
- Proteiny
- Vyšetřovací techniky
- Klinické laboratorní techniky
- Diagnostické techniky a postupy
- Diagnóza
- Chirurgické postupy, operativní
- Cytologické techniky
- Cytodiagnosis
- Protilátky, monoklonální
- Protilátky
- Imunoglobuliny
- Imunoproteiny
- Krevní proteiny
- Sérové globuliny
- Globuliny
- Diagnostické techniky, chirurgické
- Techniky chemie, analytické
- Analýza spektra
- Protilátky, monoklonální, omyl odvozený
- Rituximab
- Biopsie
- Manipulace se vzorkem
- Magnetická rezonanční spektroskopie
- CT-P10
Další identifikační čísla studie
- 25448 (Jiný identifikátor: City of Hope Medical Center)
- P30CA033572 (Grant/smlouva NIH USA)
- NCI-2026-02921 (Identifikátor registru: CTRP (Clinical Trial Reporting Program))
Informace o lécích a zařízeních, studijní dokumenty
Studuje lékový produkt regulovaný americkým FDA
Studuje produkt zařízení regulovaný americkým úřadem FDA
produkt vyrobený a vyvážený z USA
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