A Phase 2/3 interventional study of ICP-248 and Orelabrutinib in Hematologic Malignancies, sponsored by Beijing InnoCare Pharma Tech Co., Ltd.. Recruiting at 53 sites in China. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2025-11-21.
Sponsored by Beijing InnoCare Pharma Tech Co., Ltd. · Phase 2/3, Interventional, and Treatment
Evaluate the safety, tolerability and pharmacokinetics of ICP-248 in Combination with Orelabrutinib in Patients with Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
1,464 studies on the registry are indexed under Hematologic Neoplasms; 433 are open to participants now.
This study's planned enrollment of 226 is above the median of 45 across 1,068 interventional studies indexed under Hematologic Neoplasms.
Browse Hematologic Neoplasms studies →Beijing InnoCare Pharma Tech Co., Ltd. is the lead sponsor of 57 studies on the registry; 34 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
Drug: ICP-248 · Drug: Orelabrutinib
Eligible patients will receive ICP-248 orally as per the protocol,once daily for every 28 days as one treatment cycle
Eligible patients will receive Orelabrutinib orally as per the protocol,once daily for every 28 days as one treatment cycle
Adverse events (AEs) and serious adverse events (SAEs) evaluation according to CTCAE V5.0 or iwCLL 2018 criteria
Time frame: Up to 6 years
Changes from baseline in pulse.
Time frame: Up to 6 years
Changes from baseline in blood pressure.
Time frame: Up to 6 years
Changes from baseline in ECG QRS interval.
Time frame: Up to 6 years
Changes from baseline in ECG QT interval.
Time frame: Up to 6 years
Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.
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Beijing InnoCare Pharma Tech Co., Ltd.