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

Trial statusRecruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age18-70
SponsorGuangzhou Lupeng Pharmaceutical Company LTD.

About this trial

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 \[Diffuse Large B-cell Lymphoma (DLBCL), Marginal Zone Lymphoma (MZL) or Mantle Cell Lymphoma (MCL)\].

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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.

Disqualifiers

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.

Trial design

Design model

Single group

Treatments tested in this trial

  • Rocbrutinib

    Drug

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

  • Rituximab

    Biological/Vaccine

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

  • Cyclophosphamide

    Drug

    750 mg/m2 administered intravenously once on Day 1 or 2 in a 21-day cycle for six cycles.

  • doxorubicin

    Drug

    50 mg/m2 administered intravenously once on Day 1 or 2 in a 21-day cycle for six cycles.

  • Vincristin

    Drug

    1.4 mg/m2 administered intravenously once on Day 1 or 2 in a 21-day cycle for six cycles.

  • Prednisone

    Drug

    100 mg orally once on Day 1 to Day 5 in a 21-day cycle for six cycles.

Treatment groups

112 Participants
are divided into 4 treatment groups
Group A: Dose EscalationExperimental treatment 6 interventions
Group B: Dose Expansion [non-GCB DLBCL]Experimental treatment 6 interventions
Group C: Dose Expansion [MCL]Experimental treatment 6 interventions
Group D: Dose Expansion [MZL]Experimental treatment 6 interventions

Trial outcomes

Primary outcomes

1

MTD

Standard phase I 3+3 design.

Time frame
Up to 21 days after the initial dose
2

Recommended Dose

Recommended Dose will be determined using available safety and pharmacokinetics data upon completion of the dose escalation phase.

Time frame
Up to 1.5 years
3

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

Time frame
From first dose of study drug to 28 days after the last dose of study drugs
4

Incidence of clinically significant laboratory abnormalities

Clinically significant abnormalities in hematology, chemistry, coagulation and urinalysis.

Time frame
From first dose of study drug to 28 days after last dose of study drug

Secondary outcomes

1

Objective Response Rate (ORR)

Assessment using the Lugano Response Criteria for Malignant Lymphoma.

Time frame
Evey 2 cycles for 8 cycles, and followed every 3cyles for 24 months
2

Complete remission (CR)

Assessment using the Lugano Response Criteria for Malignant Lymphoma.

Time frame
Evey 2 cycles for 8 cycles, and followed every 3cyles for 24 months
3

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.

Time frame
Measured from the date of the first remission to the date of earliest disease progression or death, and assessed up to 5 years.
4

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.

Time frame
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.

Other outcomes

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