CYH33
Druga Selective PI3Kα Inhibitor
NCT Number: NCT05043922
The purpose of this study is to determine the treatment efficacy of CYH33 monotherapy in patients with recurrent or persistent ovarian, fallopian tube or primary peritoneal clear cell carcinoma harboring PIK3CA hotspot mutation, who received prior systemic anti-tumor treatment.
This study is active but is not currently recruiting participants.
Notify Me18 year and older
Female
Interventional
Phase 2
Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing, China
The purpose of this study is to determine whether treatment with single agent CYH33 significantly improves ORR compared to historical efficacy data in patients with recurrent/persistent ovarian clear cell carcinoma (OCCC) harboring PIK3CA hotspot mutations who received prior systemic anti-tumor treatment.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Main Inclusion Criteria:
Main Exclusion Criteria:
Patients are ineligible for this study if they meet any of the following criteria:
a Selective PI3Kα Inhibitor
Time frame: through study completion, an average of 1 year
Tumor ORR per Response Evaluation Criteria in Solid Tumours (RECIST) v1.1 in patients with PIK3CA hotspot mutations.
Time frame: through study completion, an average of 1 year
PFS by BIRC using RECIST v1.1
Time frame: through study completion, an average of 2 year
OS in each of the PIK3CA mutation status cohort
Time frame: through study completion, an average of 1 year
genetic and protein biomarker alterations that can impact PI3K signaling pathway
Time frame: through study completion, an average of 1 year
type, incidence, duration, severity and seriousness of adverse events (AEs)
Time frame: 4 weeks
Number and proportion of patients who experienced DLT during the first 28-day of treatment in Japanese patients in safety run-in study.
Time frame: 4weeks
Pharmacokinetics parameters
Time frame: 4weeks
Pharmacokinetics parameters
Haihe Biopharma Co., Ltd.
Industry
A Phase II, Open-Label, Multicenter Study to Evaluate the Efficacy and Safety of CYH33, a Selective PI3Kα Inhibitor in Patients With Recurrent/Persistent Ovary, Fallopian Tube or Primary Peritoneal Clear Cell Carcinoma
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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