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

Trial Details

NCT ID
NCT06378138
Phase
PHASE2 / PHASE3
Sponsor
Beijing InnoCare Pharma Tech Co., Ltd.
Status
RECRUITING
Cancer Type
Lymphoma
Interventions
  • ICP-248
  • Orelabrutinib
Locations (sample)
  • Bengbu, Anhui, China|32.94083,117.36083
  • Beijing, Beijing Municipality, China|39.9075,116.39723
  • Chongqing, Chongqing Municipality, China|29.56026,106.55771
  • Fuzhou, Fujian, China|26.06139,119.30611
  • Lanzhou, Gansu, China|36.05701,103.83987

Key Eligibility 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 lymp…
  • Having an indication for treatment that meets the criteria for iwCLL 2018
  • Subjects must have measurable lesion according to the Lugano 2014 Assessment Criteria.

For full eligibility, visit ClinicalTrials.gov.

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