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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06351527
Other study ID # ICP-CL-01202
Secondary ID
Status Not yet recruiting
Phase Phase 1
First received
Last updated
Start date April 25, 2024
Est. completion date October 25, 2027

Study information

Verified date April 2024
Source InnoCare Pharma Inc.
Contact Alexia Lu
Phone 010-66609745
Email CO_HGRAC@innocarepharma.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Evaluate the Safety, Tolerability, Pharmacokinetics and Preliminary Efficacy of ICP-248 in Mature B-cell Malignancies


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 40
Est. completion date October 25, 2027
Est. primary completion date June 25, 2027
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: 1. Age = 18 and = 80 years. 2. Subjects with histopathologically and/or flow cytometry-confirmed diseases according to the 2016 World Health Organization (WHO) classification criteria for lymphohematopoietic neoplasms or meeting the International Workshop on Chronic Lymphocytic Leukemia (iwCLL) criteria 3. Relapsed disease 4. For subjects with R/R MCL: Patients must have measurable disease 5. Patients with an Eastern Cooperative Oncology Group (ECOG) performance status (PS) score of = 1 and a life expectancy of = 6 months. 6. Adequate hematologic function 7. Patients with basically normal coagulation function 8. Patients with adequate hepatic, renal, pulmonary and cardiac functions 9. Subjects are able to communicate with the investigator well and to complete the study as specified in the study. Exclusion Criteria: 1. Known central nervous system involvement by lymphoma/leukemia. 2. Known or suspected history of Richter's transformation. 3. Prior autologous stem cell transplant (unless = 3 months since transplant); or prior chimeric cell therapy (unless = 3 months since cell infusion). 4. A history of allogeneic stem cell transplantation. 5. An interval of less than 5 half-lives from the last dose of a strong CYP3A or CYP2C8 inhibitor or inducer (chemical agent, herbal medicine and dietary supplement) to the first dose of the investigational product, or a plan to use concurrently medications, dietary supplements or food (e.g., grapefruit or grapefruit juice) with strong CYP3A or CYP2C8 inhibitory or inductive effect during study participation 6. Presence of active infection that currently requires intravenous systemic antiinfective therapy. 7. History of immunodeficiency, including a positive human immunodeficiency virus (HIV) antibody test. 8. History of significant cardiovascular disease 9. Patients with previous or concomitant central nervous system disorders 10. Known alcohol or drug dependence 11. Female patients who are pregnant or lactating. 12. Unable to swallow tablets or presence of disease significantly affecting gastrointestinal function such as malabsorption syndrome, resection of the stomach or small bowel, bariatric surgery procedures, symptomatic inflammatory bowel disease, or partial or complete bowel obstruction.

Study Design


Related Conditions & MeSH terms


Intervention

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

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
InnoCare Pharma Inc.

Outcome

Type Measure Description Time frame Safety issue
Primary Maximum tolerated dose and/or recommended Phase 2 dose To evaluate the safety and tolerability of ICP-248 monotherapy in the selected B-cell malignancies and to determine the maximum tolerated dose (MTD) and recommended Phase 2 dose (RP2D) of ICP-248 monotherapy. 5 years
Primary To investigate the incidence, nature and severity of adverse events (AE) according to NCI-CTCAE V5.0 evaluation criteria. 5 years
See also
  Status Clinical Trial Phase
Recruiting NCT04277637 - Study of Bcl-2 Inhibitor BGB-11417 in Participants With Mature B-Cell Malignancies Phase 1
Active, not recruiting NCT04883957 - Study of BGB-11417 in Adult Participants With Mature B-cell Malignancies Phase 1
Active, not recruiting NCT04172246 - Study of Zanubrutinib in Japanese Participants With B-Cell Malignancies Phase 1/Phase 2