Phase Ib Study of Rocbrutinib in Combination With R-CHOP in Patients With Newly Diagnosed B-cell Non-Hodgkin Lymphoma

B-cell Non-Hodgkin Lymphoma Clinical Trial

Official title:

A Phase Ib Study to Assess Safety and Preliminary Efficacy of Rocbrutinib in Combination With R-CHOP in Patients With Newly Diagnosed B-NHL

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06251180
• Other study ID #: LP-168-CN301
• Status: Recruiting
• Phase: Phase 1
• Start date: April 10, 2024
• Est. completion date: December 31, 2029

Study information

• Verified date: April 2024
• Source: Guangzhou Lupeng Pharmaceutical Company LTD.
• Contact: Yue Shen, Ph D
• Phone: 86-020-31605119
• Email: yshen[@]lupengbio.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is an open-label, multicentre Phase Ib study to evaluate the safety and preliminary efficacy of new generation Bruton Tyrosine Kinase inhibitor Rocbrutinib in combination to R-CHOP (Rituximab, Cyclophosphamide, Doxorubicin, Vincristin, Prednison) in adult patients with newly diagnosed, previously untreated B-cell Non-Hodgkin Lymphoma [Diffuse Large B-cell Lymphoma (DLBCL), Marginal Zone Lymphoma (MZL) or Mantle Cell Lymphoma (MCL)].

Description:

OUTLINE:

Dose escalation portion(Part A): In the dose escalation portion of the study, the escalating doses of Rocbrutinib combined with R-CHOP may be explored, using the 3+3 principle for dose determination. If dose escalation is acceptable, and subsequently will determine the recommended Phase 2 dose.

Dose expansion portion(Part B): This will be conducted as a multicenter, open-label study, including three cohorts(Cohort 1: non-GCB DLBCL; Cohort 2: MZL; Cohort 3: MCL). Eligible subjects will receive Rocbrutinib combined with R-CHOP for 6 cycles, then Rocbrutinib plus Rituximab for 2 cycles, and followed by Rocbrutinib maintenance for 2 years.

After completion of study treatment, patients are followed up every 12 weeks for 1 year, then every 24 weeks for 4 year.

PRIMARY OBJECTIVES:

I. To evaluate the safety of Rocbrutinib in combination to R-CHOP in B-cell Non-Hodgkin Lymphoma, including the maximum tolerated dose (MTD), dose limiting toxicities(DLT), adverse events (AEs), clinically significant laboratory abnormalities.

2. To determine the recommended dose. 3. To determine the pharmacokinetic characteristics of Rocbrutinib in combination to R-CHOP.

SECONDARY OBJECTIVES:

I. To determine the overall response rate, the complete response rate, duration of remission, survival outcomes (progression free survival, event free survival, overall survival) in DLBCL/ Non-germinal Center(non-GCB) DLBCL.

2. To determine the overall response rate, the complete response rate, duration of remission, survival outcomes (progression free survival, event free survival, overall survival) in MZL.

3. To determine the overall response rate, the complete response rate, duration of remission, survival outcomes (progression free survival, event free survival, overall survival) in MCL.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 112
• Est. completion date: December 31, 2029
• Est. primary completion date: December 31, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

• Participants was histopathologically diagnosed with any of the following diseases:

DLBCL, MZL or MCL (if enrolled in the dose expansion phase, histological confirmation of non-GCB subtype), and have not previously received anti-tumor systemic therapy or local radiation therapy for the above diseases.

• Participants must have at least one measurable lesion.

• ECOG physical status score 0-2.

• Life expectancy =6 months.

• International Prognostic Index (IPI) score = 2 (only participants with DLBCL in dose expansion portion).

• Adequate coagulation, liver, kidney, and hematopoietic functions:PT and APTT <1.5x ULN; serum bilirubin <1.5x ULN except in participants with Gilbert's syndrome who must have a serum bilirubin of <3x ULN, AST and ALT = 3x ULN or < 5x ULN if hepatic involvement are present; serum creatinine (Scr) =1.5 x ULN, or calculated creatinine clearance = 30ml/min by Cockcroft-Gault formula.; ANC=1500/mm3, hemoglobin=8.0 g/dL, and platelets >100,000/mm3 unless deemed related to lymphoma involvement in the bone marrow and felt potentially reversible by the treating physician.

• Women of childbearing potential must have a negative serum or urine (beta-human chorionic gonadotropin [beta-hCG]) at screening.

• Women of childbearing potential and men who are sexually active with a woman of childbearing potential must be practicing a highly effective contraceptive measures of during and after the study (90 days after the last dose of ROCBRUTINIB and 12 months after the last dose of Rituximab). Men must agree to not donate sperm during and for up to 90 days after he last dose of ROCBRUTINIB.

• Participants voluntarily enrolled and signed the informed consent form, and followed the trial treatment and visits.

Exclusion Criteria:

• Participants are allergic to Rocbrutinib or any of its excipients; Participants who are assessed by the investigator as being unable to tolerate the R-CHOP regimen.

• Participants with known central nervous system involvement with lymphoma. or diagnosis of primary central nervous system lymphoma (PCNSL) or primary mediastinal large B-cell lymphoma (PMBL).

• Participants with DLBCL had a history of indolent lymphoma such as FL or CLL (Richter's transformation), or was histopathologically comfirmed with FL (regardless of grade) coexistentially.

• Prior treatment with solid organ transplantation or hematopoietic stem cell transplantation(HSCT) ; expected HSCT during the study.

• Major surgery within 4 weeks of study entry or expected major surgery during the study.

• Prior another non-antitumor or medical instruments clinical trials within 4 weeks.

• Known bleeding diseases (such as von Willebrand's disease or hemophilia A, hemophilia B, etc.), or have bleeding tendency.

• Prior treatment with warfarin or equivalent vitamin K antagonists within 14 days; requires anticoagulation with warfarin or equivalent vitamin K antagonists.

• Prior treatment with strong/moderate CYP3A4 inhibitors within 5 days or prior foods with inhibitory effects on CYP3A4 within 3 days at screening; requires chronic treatment with moderate/strong CYP3A inhibitors or inducers, or OATP1B1/OATP1B3 sensitive substrates during the study.

• Participants with other malignancies other than the target indications of this study within the past three years.

• Prior treatment with the cumulative dose of doxorubicin =150 mg/m2 (or other anthracyclines at doses converted based on cumulative cardiac toxicity)

• Any serious medical condition including but not limited to uncontrolled hypertension, uncontrolled congestive heart failure or =Class 2 cardiac disease as defined by the New York Heart Association Functional Classification or LVEF less than 40%, uncontrolled or symptomatic arrhythmias with corrected QT interval (QTc) > 480 msec, uncontrolled diabetes mellitus, active/symptomatic coronary artery disease, COPD, renal failure, severe hepatic disease, uncontrolled active infection, active hemorrhage.

• Known HIV infection, or syphilis infection, or hepatitis B DNA or hepatitis C RNA positive.

• Known diseases that affect drug swallowing or absorption.

• Unfit to participate in this study in the investigator's opinion.

Related Conditions & MeSH terms

• B-cell Non-Hodgkin Lymphoma
• Lymphoma
• Lymphoma, B-Cell
• Lymphoma, Non-Hodgkin

Intervention

Drug:
• Rocbrutinib
orally once daily in a 21-day cycle for eight cycles, and as maintenance for 2 years.

Biological:
• Rituximab
375 mg/m2 administered intravenously once on Day 1 in a 21-day cycle for eight cycles.

Drug:
• Cyclophosphamide
750 mg/m2 administered intravenously once on Day 1 or 2 in a 21-day cycle for six cycles.
• doxorubicin
50 mg/m2 administered intravenously once on Day 1 or 2 in a 21-day cycle for six cycles.
• Vincristin
1.4 mg/m2 administered intravenously once on Day 1 or 2 in a 21-day cycle for six cycles.
• Prednisone
100 mg orally once on Day 1 to Day 5 in a 21-day cycle for six cycles.

Locations

Country	Name	City	State
China	Sun Yat-sen University Cancer Center	Guangzhou	Guangdong

Sponsors (1)

Lead Sponsor	Collaborator
Guangzhou Lupeng Pharmaceutical Company LTD.

Country where clinical trial is conducted

China, 

References & Publications (2)

Younes A, Sehn LH, Johnson P, Zinzani PL, Hong X, Zhu J, Patti C, Belada D, Samoilova O, Suh C, Leppa S, Rai S, Turgut M, Jurczak W, Cheung MC, Gurion R, Yeh SP, Lopez-Hernandez A, Duhrsen U, Thieblemont C, Chiattone CS, Balasubramanian S, Carey J, Liu G, — View Citation

Younes A, Thieblemont C, Morschhauser F, Flinn I, Friedberg JW, Amorim S, Hivert B, Westin J, Vermeulen J, Bandyopadhyay N, de Vries R, Balasubramanian S, Hellemans P, Smit JW, Fourneau N, Oki Y. Combination of ibrutinib with rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) for treatment-naive patients with CD20-positive B-cell non-Hodgkin lymphoma: a non-randomised, phase 1b study. Lancet Oncol. 2014 Aug;15(9):1019-26. doi: 10.1016/S1470-2045(14)70311-0. Epub 2014 Jul 17. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	MTD	Standard phase I 3+3 design.	Up to 21 days after the initial dose
Primary	Recommended Dose	Recommended Dose will be determined using available safety and pharmacokinetics data upon completion of the dose escalation phase.	Up to 1.5 years
Primary	Incidence of AEs	Type, frequency and severity of AEs, relationship of AEs to study treatment Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version 5.0 Type, frequency and severity of AEs, relationship of AEs to study treatment Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version 5.0	From first dose of study drug to 28 days after the last dose of study drugs
Primary	Incidence of clinically significant laboratory abnormalities	Clinically significant abnormalities in hematology, chemistry, coagulation and urinalysis.	From first dose of study drug to 28 days after last dose of study drug
Primary	Cmax of Rocbrutinib	Maximum plasma concentration (Cmax) of Rocbrutinib.	Up to 24 hours post dose
Primary	Tmax of Rocbrutinib	Time to maximum plasma concentration (Tmax) of Rocbrutinib.	Up to 24 hours post dose
Primary	T1/2 of Rocbrutinib	The terminal elimination half-life (t1/2).	Up to 24 hours post dose
Primary	AUC0-t of Rocbrutinib	Area under the plasma concentration-time curve (AUC) from 0 to the time of the last measurable concentration of Rocbrutinib.	Up to 24 hours post dose
Primary	CL/F of Rocbrutinib	Apparent clearance (CL/F) of Rocbrutinib.	Up to 24 hours post dose
Secondary	Objective Response Rate (ORR)	Assessment using the Lugano Response Criteria for Malignant Lymphoma.	Evey 2 cycles for 8 cycles, and followed every 3cyles for 24 months
Secondary	Complete remission (CR)	Assessment using the Lugano Response Criteria for Malignant Lymphoma.	Evey 2 cycles for 8 cycles, and followed every 3cyles for 24 months
Secondary	Duration of Response(DOR)	DOR is defined as the number of days from the date of the first remission to the date of earliest disease progression or death.	Measured from the date of the first remission to the date of earliest disease progression or death, and assessed up to 5 years.
Secondary	Progression-Free Survival(PFS)	PFS is defined as the number of days from the date of the first dose of study drug to the date of earliest disease progression or death.	Measured from the date of first dose of study drug to the date of earliest disease progression or death or last visit, and assessed up to 5 years.
Secondary	Event-free Survival (EFS)	EFS is defined as the number of days from the date of first dose to the date of earliest evidence of disease progression/relapse, or initiation of new non-protocol-specified antitumor therapy without documented progression, or death.	Measured from the date of first dose to the date of earliest evidence of disease progression, initiation of new non-protocol-specified antitumor therapy without documented progression, death, and for up to 5 years after the last subject is enrolled.
Secondary	Overall survival (OS)	OS is defined as the number of days from the date of first dose to the date of death.	Measured from the date of date of first dose to the date of death or last visit, and for up to 5 years after the last subject is enrolled.