Cancer Hospital Chinese Academy of Medical Sciences
Beijing, Beijing Municipality, 100000, China
NCT Number: NCT04539496
This study includes single agent/combination dose exploration study and the phase II study. The primary purpose of the dose exploration study is to determine the maximum tolerated dose(MTD)/recommended phase II dose(RP2D) of XZP-3287 and assess its safety and preliminary efficacy in solid tumor patients. The phase II study aims to explore the efficacy and safety profiles of XZP-3287 as a single- agent in hormone receptor(HR) positive, human epidermal growth factor receptor 2(HER2) negative advanced breast cancer.
This study is active but is not currently recruiting participants.
Notify Me18 year–70 year
All sexes
Interventional
Phase 1 / Phase 2
Beijing, Beijing Municipality, 100000, China
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Combination dose exploration study:Patients with locally advanced or metastatic breast cancer with hormone receptor positive (HR+) and her2-negative (HER2-) were not eligible for surgical resection or radiotherapy for the purpose of cure, and had no clinical indications for chemotherapy, and received endocrine therapy ≤1 line.
The phase II study: Locally advanced or metastatic breast cancer diagnosed histologically or cytologically not suitable for surgery or radical radiotherapy; HR+ and HER2- ; have locally advanced disease not amenable to curative treatment by surgery or metastatic disease; progress after previous endocrine therapy; at least 1 chemotherapy regimen in the previous adjuvant or metastasis contains paclitaxel; there should be at least 2 prior chemotherapy regimens;
Exclusion criteria
The phase II study:Have a history of any other cancer (except nonmelanoma skin cancer or carcinoma in-situ of the cervix), unless in complete remission with no therapy for a minimum of 3 years.
XZP-3287: 360 mg BID, oral; Letrozole: 2.5 mg QD, oral; Anastrozole: 1 mg QD, oral; Fulvestrant: 500 mg intramuscular injection on C1D1, C1D15, the first day of each subsequent cycle (28 days a cycle)
Time frame: Up to 30 days after the end of treatment
AEs as characterized by frequency and severity (as graded by National Cancer Institute Common Terminology Criteria for Adverse Events [NCI CTCAE] version 4.03 for single agent dose exploration study and CTCAE 5.0 for combination exploration study)
Time frame: From baseline to the date of first documentation of progression or death , whichever came first, assessed approximately up to 2 years after the last entered participant
ORR is the percentage of participants with a best overall response (BOR) of complete response (CR) or partial response (PR) as defined by RECIST v1.1.
Time frame: From baseline to the date of first documentation of progression or death, whichever came first, assessed approximately up to 2 years after the last entered participant
PFS is defined as the time from the date of the first treatment until first observation of objective progressive disease or death, whichever comes first.
Time frame: From baseline to the death from any cause, assessed approximately up to 2 years after the last entered participant
OS is defined from the date of the first treatment to the date of death from any cause.
Time frame: From baseline to the date of first documentation of progression or death, whichever came first, assessed approximately up to 2 years after the last entered participant
DoR is defined from the date of CR or PR to date of disease progression or death due to any cause.
Time frame: From baseline to the date of first documentation of progression or death, whichever came first, assessed approximately up to 2 years after the last entered participant
DCR is the percentage of participants with a best overall response of CR, PR or stable disease (SD) as defined by RECIST v1.1.
Time frame: From baseline to the date of first documentation of progression or death, whichever came first, assessed approximately up to 2 years after the last entered participant
Percentage of participants with best overall response of CR, PR, or SD with duration of SD for at least 6 Months.
Time frame: From baseline up to month 3
Mean steady state exposure of XZP-3287 and its metabolites.
Time frame: From baseline to the date of first documentation of progression or death, whichever came first, assessed approximately up to 2 years after the last entered participant
ORR is the percentage of participants with a best overall response (BOR) of complete response (CR) or partial response (PR) as defined by RECIST v1.1.
Time frame: Up to 30 days after the end of treatment
AEs as characterized by frequency and severity (as graded by CTCAE 5.0 )
This study is active but is not currently recruiting participants.
Notify MeSihuan Pharmaceutical Holdings Group Ltd.
Industry
A Multicenter, Open-label Phase I/II Study of XZP-3287 in Metastasis Solid Tumors in China
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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