Skip to main content
OpenTrials
Recruiting

NCT Number: NCT07082686

A Study to Evaluate the Efficacy and Safety of ICP-248 in Subjects With Relapsed or Refractory Mantle Cell Lymphoma (APEX-06)

This is a single-arm, multi-center, open-label, phase 2 study to evaluate the efficacy and safety of ICP-248 in subjects with relapsed or refractory mantle cell lymphoma.

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • ≥ 18 years old.
  • Histopathologically confirmed MCL expressing Cyclin D1 and/or t (11;14) chromosomal translocation.Formalin-fixed paraffin-embedded (FFPE) tissues or sections for diagnosis must be provided. It is for the approval of pathological diagnosis by the central pathology laboratory.
  • The patient was diagnosed with relapsed or refractory mantle cell lymphoma, and the previous treatment needs to meet the following requirements:
  • Failure of at least one adequate prior line of anti-CD20-containing therapy;
  • Failure of at least one adequate prior line of BTK inhibitor (BTKi)-containing therapy.
  • Failure of the last line of therapy.
  • At least one measurable lesion according to the Lugano 2014 criteria,.
  • ECOG performance status of 0-2 .

Exclusion criteria

  • Current or prior history of central nervous system (CNS) lymphoma.
  • Prior use of BCL-2 inhibitors (e.g., venetoclax/ABT-199, etc.).
  • Autologous stem cell transplantation or cellular therapy within 3 months prior to the first dose of ICP-248.
  • Prior allogeneic hematopoietic stem cell transplantation.

Treatment and study plan

ICP-248

Drug

Eligible patients will receive ICP-248 orally as per the protocol

Primary outcomes

  1. Overall response rate (ORR) according to Lugano 2014 assessed by the independent review committee (IRC)

    Time frame: 3 years

Secondary outcomes

  1. According to Lugano 2014: IRC and investigator assessed complete response rate (CRR)

    Time frame: 3 years

  2. Investigator-assessed ORR

    Time frame: 3 years

  3. According to Lugano 2014: IRC and investigator assessed disease control rate (DCR).

    Time frame: 3 years

  4. According to Lugano 2014: IRC and investigator assessed duration of response (DOR).

    Time frame: 3 years

  5. According to Lugano 2014: IRC and investigator assessed time to initial response (TTR).

    Time frame: 3 years

  6. According to Lugano 2014: IRC and investigator assessed progression-free survival (PFS) .

    Time frame: 3 years

  7. Overall survival (OS)

    Time frame: 3 years

  8. Adverse event (AE) assessed according to CTCAE v5.0 criteria

    Time frame: 3 years

  9. Functional Assessment Of Cancer Therapy-Lymphoma (Fact-Lym) and European Quality Of Life Five Dimension Five Level Scale Questionnaire (Eq-5D-5L).

    Time frame: 3 years

  10. Area under the plasma concentration versus time curve (AUC)

    Time frame: 3 years

  11. minimal residual disease (MRD) status

    Time frame: 3 years

  12. Peak Plasma Concentration (Cmax)

    Time frame: 3 years

  13. Time of maximum observed plasma(Tmax)

    Time frame: 3 years

  14. Trough concentration(Ctrough)

    Time frame: 3 years

  15. Apparent clearance (CL/F)

    Time frame: 3 years

Study contacts

Contact information is provided by the study sponsor or research team.

Alexia Lu

CONTACT

[email protected]

010-66609745

Sponsors and collaborators

Lead sponsor

Beijing InnoCare Pharma Tech Co., Ltd.

Industry

Registry information

Official study title

A Single-arm, Multi-center, Open-label, Phase 2 Study to Evaluate the Efficacy and Safety of ICP-248 in Subjects With Relapsed or Refractory Mantle Cell Lymphoma

Important dates

Study start
2025
Primary completion
2027
Study completion
2028
First posted
Jul 24, 2025
Registry last updated
Jul 23, 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.

Published trials that share one or more normalized conditions with this study.