ICP-248
DrugEligible patients will receive ICP-248 orally as per the protocol,once daily for every 28 days as one treatment cycle
NCT Number: NCT06378138
Evaluate the safety, tolerability and pharmacokinetics of ICP-248 in Combination with Orelabrutinib in Patients with Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
Interested in participating?
Request Info18 year–80 year
All sexes
Interventional
Phase 2 / Phase 3
The First Affiliated Hospital of Bengbu Medical College, Bengbu, Anhui, China
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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
Time frame: Up to 6 years
Time frame: Up to 6 years
Time frame: Up to 6 years
Time frame: Up to 6 years
Time frame: Up to 6 years
Contact information is provided by the study sponsor or research team.
Beijing InnoCare Pharma Tech Co., Ltd.
Industry
A Phase II/III Study of ICP-248 in Combination With Orelabrutinib in Patients With Treatment-naïve Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
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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