Skip to main content
OpenTrials
Active, Not Recruiting

NCT Number: NCT05043922

A Study to Evaluate the Efficacy and Safety of CYH33 in Patients With Recurrent/Persistent Ovary Clear Cell Carcinoma

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.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Notify Me

Key information

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Main Inclusion Criteria:

  • Female patients ≥ 18 years of age
  • Provide informed consent voluntarily.
  • Patients must have histologically or cytologically confirmed recurrent or persistent ovarian, fallopian tube, or peritoneum clear cell carcinoma.
  • Patients with recurrent/persistent ovary, fallopian tube or primary peritoneal clear cell carcinoma, who have identified PIK3CA status.
  • Patients must have failed standard chemotherapy.
  • ECOG-PS ≤ 1.
  • Patient must have adequate organ and bone marrow function measured within 28 days of screening.

Main Exclusion Criteria:

Patients are ineligible for this study if they meet any of the following criteria:

  • Patient has received any anticancer therapy
  • Patients who had prior treatment with any PI3K, mTOR or AKT inhibitor.
  • Radical radiation therapy within 4 weeks prior to the first dose of the investigational product or received local palliative radiation therapy for bone metastases within 2 weeks.
  • Any toxicities from prior treatment that have not recovered to baseline.
  • Patients who have been treated with any hematopoietic colony-stimulating growth factors ≤ 2 weeks prior to starting study drug.
  • Patients who have symptomatic CNS metastasis.
  • Major surgery or had significant traumatic injury within 28 days prior to the first dose of the investigational product or has not recovered from major side effects.
  • Known HIV infection with a history of acquired immunodeficiency syndrome (AIDS)-defining opportunity infection within the past 12 months; active hepatitis B and hepatitis C.
  • History of acute pancreatitis within 1 year of screening or past medical history of chronic pancreatitis.
  • Patients with clinically significant cardiovascular disease

Treatment and study plan

CYH33

Drug

a Selective PI3Kα Inhibitor

Primary outcomes

  1. Tumor ORR in patients with PIK3CA hotspot mutations.

    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.

Secondary outcomes

  1. PFS

    Time frame: through study completion, an average of 1 year

    PFS by BIRC using RECIST v1.1

  2. OS

    Time frame: through study completion, an average of 2 year

    OS in each of the PIK3CA mutation status cohort

  3. genetic and protein biomarker alterations

    Time frame: through study completion, an average of 1 year

    genetic and protein biomarker alterations that can impact PI3K signaling pathway

Other outcomes

  1. Safety and tolerability

    Time frame: through study completion, an average of 1 year

    type, incidence, duration, severity and seriousness of adverse events (AEs)

  2. DLT (Dose Limiting Toxicity) in Japanese patients

    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.

  3. Peak Plasma Concentration (Cmax)

    Time frame: 4weeks

    Pharmacokinetics parameters

  4. Area under the plasma concentration versus time curve (AUC)

    Time frame: 4weeks

    Pharmacokinetics parameters

Sponsors and collaborators

Lead sponsor

Haihe Biopharma Co., Ltd.

Industry

Registry information

Official study title

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

Important dates

Study start
2021
Primary completion
2024
Study completion
2026
First posted
Sep 14, 2021
Registry last updated
Jan 30, 2026

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.

Published trials that share one or more normalized conditions with this study.