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OpenTrials
Completed

NCT Number: NCT05051891

A Randomized, Open-label, Multi-center, Phase III Study of Orelabrutinib in Combination With Rituximab, Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone (R-CHOP) vs. R-CHOP Alone in Patients With Treatment-naїve Mantle Cell Lymphoma

To evaluate the efficacy of orelabrutinib combined with R-CHOP vs. R-CHOP alone in the treatment of treatment-naїve mantle cell lymphoma.

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Key information

Age range

60 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Anhui Province Cancer Hospital, Hefei, Anhui, China

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 65 < age <80, or 60 ≤ age ≤65 and is ineligible for autologous stem cell transplantation as assessed by the investigator
  • Histopathological confirmed MCL and either expression of cyclin D1 or t (11;14) chromosomal translocation (in association with CD20). The verification will be based on central review of the local pathology report.
  • No previous systemic treatment for MCL.
  • ECOG physical strength score is 0-2.
  • Expected survival time >6 months.
  • Voluntary written informed consent prior to screening.

Exclusion criteria

  • Uncontrolled or significant cardiovascular diseases
  • History of stroke or intracranial hemorrhage within 6 months before first administration of study treatment.
  • Any mental or cognitive impairments which may limit the subject 's understanding and execution of informed consent as well as study compliance;
  • Pregnant or breastfeeding women and those who do not agree to take contraceptive measures.
  • Conditions in which a potentially life-threatening illness or severe organ dysfunction is not considered appropriate by the investigator.

Note: Other protocol defined Inclusion/Exclusion criteria may apply.

Treatment and study plan

Orelabrutinib and R-CHOP

Drug

Orelabrutinib in Combinaion with Rituximab, Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone (R-CHOP)

R-CHOP

Drug

Rituximab, Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone (R-CHOP)

Primary outcomes

  1. PFS

    Time frame: Up to 6 years

    To evaluate the Progression-free Survival (PFS) by the Independent Review Committee (IRC) according to the 2014 International Working Group Criteria for Non-Hodgkin Lymphoma (iwNHL).

Secondary outcomes

  1. ORR

    Time frame: Up to 6 years

    Objective Response Rate

  2. CRR

    Time frame: Up to 6 years

    Complete Response Rate

  3. OS

    Time frame: Up to 6 years

    Overall Survival

Sponsors and collaborators

Lead sponsor

Beijing InnoCare Pharma Tech Co., Ltd.

Industry

Registry information

Important dates

Study start
2021
Primary completion
2025
Study completion
2025
First posted
Sep 21, 2021
Registry last updated
Mar 31, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.