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NCT Number: NCT06378138

ICP-248 in Combination With Orelabrutinib in Treatment-naïve Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma (APEX-03)

Evaluate the safety, tolerability and pharmacokinetics of ICP-248 in Combination with Orelabrutinib in Patients with Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma

Recruiting

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2 / Phase 3

Primary location

The First Affiliated Hospital of Bengbu Medical College, Bengbu, 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

  • Age ≥ 18 and ≤ 80 years.
  • CLL/SLL is diagnosed by histopathology and/or flow cytometry according to the 2016 World Health Organization (WHO) classification criteria for lymphohematopoietic neoplasms or meeting the criteria of 2018 International Workshop on Chronic Lymphocytic Leukemia (iwCLL 2018):
  • Having an indication for treatment that meets the criteria for iwCLL 2018
  • Subjects must have measurable lesion according to the Lugano 2014 Assessment Criteria.
  • Patients with an Eastern Cooperative Oncology Group (ECOG) performance status (PS) score of ≤ 2 and a life expectancy of ≥ 6 months.
  • Adequate hematologic function
  • Patients with basically normal coagulation function
  • Patients with adequate hepatic, renal, pulmonary and cardiac functions
  • Subjects are able to communicate with the investigator well and to complete the study as specified in the study.
  • Before the trial, the subjects shall understand the nature, significance, possible benefits, inconveniences and potential risks, as well as the study procedures of the trial in detail and voluntarily sign the written Informed Consent Form (ICF).

Exclusion criteria

  • Central nervous system involvement.
  • Concomitant Richter transformation.
  • Prior systemic treatment, excluding emergency pretreatment to reduce white blood cells and relieve leukostasis.
  • Requireing continuous glucocorticoid support or glucocorticoid therapy within 5 days.
  • History of allogeneic stem cell transplantation.
  • Major organ surgery (excluding aspiration biopsy) or significant trauma within 28 days prior to the first dose of the investigational drug or require elective surgery during the trial.
  • Presence of active infection that requires intravenous anti-infective therapy.
  • Hepatitis B or C virus infection.
  • History of immunodeficiency disease or Significant cardiovascular disease
  • Central nervous system disorders or Severe bleeding disorder
  • Alcohol or drug dependence.
  • Mental disorders or poor compliance.

Treatment and study plan

ICP-248

Drug

Eligible patients will receive ICP-248 orally as per the protocol,once daily for every 28 days as one treatment cycle

Orelabrutinib

Drug

Eligible patients will receive Orelabrutinib orally as per the protocol,once daily for every 28 days as one treatment cycle

Primary outcomes

  1. Adverse events (AEs) and serious adverse events (SAEs) evaluation according to CTCAE V5.0 or iwCLL 2018 criteria

    Time frame: Up to 6 years

  2. Changes from baseline in pulse.

    Time frame: Up to 6 years

  3. Changes from baseline in blood pressure.

    Time frame: Up to 6 years

  4. Changes from baseline in ECG QRS interval.

    Time frame: Up to 6 years

  5. Changes from baseline in ECG QT interval.

    Time frame: Up to 6 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 Phase II/III Study of ICP-248 in Combination With Orelabrutinib in Patients With Treatment-naïve Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma

Important dates

Study start
2024
Primary completion
2030
Study completion
2031
First posted
Apr 22, 2024
Registry last updated
Nov 21, 2025

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.

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