A Phase 2 Study to Evaluate the Efficacy, Safety and Pharmacokinetics of YL202 in Patients With BC

Locally Advanced or Metastatic Breast Cancer Clinical Trial

Official title:

A Multicenter, Open-Label, Phase 2 Study to Evaluate the Efficacy, Safety and Pharmacokinetics of YL202 in Patients With Locally Advanced or Metastatic Breast Cancer With TNBC, HR-Positive, HER2-Zero-expression or HER2-Low-expression

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT06439771
• Other study ID #: YL202-CN-202-01
• Status: Active, not recruiting
• Phase: Phase 2
• Start date: April 23, 2024
• Est. completion date: July 29, 2028

Study information

• Verified date: June 2024
• Source: MediLink Therapeutics (Suzhou) Co., Ltd.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study is a multicenter, open-label, phase 2 clinical study to evaluate the efficacy, safety and pharmacokinetics of YL202 in patients with locally advanced or metastatic breast cancer with TNBC, HR-positive, HER2-zero-expression or HER2-low-expression

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 180
• Est. completion date: July 29, 2028
• Est. primary completion date: July 30, 2026
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

1. Have been informed of the study before the start of the study and voluntarily sign name and date on the informed consent form.

2. Patients with locally advanced or metastatic disease (according to the UICC and AJCC staging system [Version 8]) who are not candidates for curative surgery or radiotherapy.

3. Patients who are pathologically confirmed advanced/unresectable or metastatic breast cancer with HR-negative and HER2-negative,.

4. Patients who are confirmed HR positive and HER2-Zero-expression and HER2-Low-expression.

5. Breast cancer patients who have previously failed treatments of HER2-ADC or TROP2-ADC.

6. Have at least 1 extracranial measurable lesion as a target lesion per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1

7. Have Adequate organ and bone marrow function within 7 days prior to the first dose.

8. Female patients of childbearing potential must agree to use highly effective contraception from screening throughout the duration of the study and for at least 6 months after the last dose of study drug.

9. Have a expected survival = 3 months.

10. Have ability and willingness to comply with protocol-specified visits and procedures.

Exclusion Criteria:

1. Have prior treatment with an agent targeting HER3.

2. Have prior intolerance to treatment with topoisomerase I inhibitor or an ADC that consists of topoisomerase I inhibitor.

3. Have been enrolled in another clinical study concurrently unless it is an observational clinical study or in the follow-up phase of an interventional study.

4. Have insufficient washout period for prior anticancer therapy prior to first dose of the study drug.

5. Have major surgery (excluding diagnostic surgery) within 4 weeks prior to the first dose of study drug or anticipation of major surgery during the study.

6. Have prior allogeneic bone marrow transplant or prior solid organ transplant.

7. Have received treatment with systemic steroids.

8. Have received any live vaccine within 4 weeks prior to the first dose of study drug or intend to receive a live vaccine during the study.

9. Leptomeningeal metastases or carcinomatous meningitis, spinal cord compression.

10. Brain metastases with the exceptions.

11. Have uncontrolled or clinically significant cardiovascular and cerebrovascular disease.

12. Have clinically significant concomitant pulmonary diseases.

13. Have a diagnosis of Gilbert's syndrome.

14. Have pleural effusion, abdominal effusion.

15. Have a history of gastrointestinal perforation and or fistula within 6 months prior to the first dose.

16. Have serious infection.

17. Patients with human immunodeficiency virus (HIV) infection.

18. Have active hepatitis B virus (HBV) or hepatitis C virus (HCV) infection.

19. Have any other primary malignancy within 5 years prior to the first dose of study drug.

20. Have unresolved toxicities from prior anticancer therapy.

21. Have a history of severe hypersensitivity reactions to the drug substance, inactive ingredients in the drug product, or other monoclonal antibodies.

22. Lactating women, or women who are confirmed to be pregnant by pregnancy test within 3 days prior to the first dose.

Related Conditions & MeSH terms

• Breast Neoplasms
• Locally Advanced or Metastatic Breast Cancer

Intervention

Drug:
• YL202 should be intravenously infused
For each patient, YL202 should be intravenously infused over 60±10 min.

Locations

Country	Name	City	State
China	Fudan University Shanghai Cancer Center	Shanghai	Shanghai

Sponsors (1)

Lead Sponsor	Collaborator
MediLink Therapeutics (Suzhou) Co., Ltd.

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	ORR assessed according to RECIST v1.1	ORR: defined as the proportion of patients who achieved a best overall response of complete response (CR) or partial response (PR).	By the end of trial date, approximately within 36 months
Primary	Determination of the recommended dose of YL202 in the pivotal clinical study		By the end of trial date, approximately within 36 months
Secondary	Progression-free survival (PFS) assessed according to RECIST v1.1		By the end of trial date, approximately within 36 months
Secondary	Clinical benefit rate (CBR) assessed based on RECIST v1.1		By the end of trial date, approximately within 36 months
Secondary	Depth of response (DpR) assessed based on RECIST v1.1		By the end of trial date, approximately within 36 months
Secondary	Disease control rate (DCR) assessed based on RECIST v1.1		By the end of trial date, approximately within 36 months
Secondary	Duration of response (DOR) assessed based on RECIST v1.1		By the end of trial date, approximately within 36 months
Secondary	Time to response (TTR) assessed based on RECIST v1.1		By the end of trial date, approximately within 36 months
Secondary	Evaluate the overall survival (OS)		By the end of trial date, approximately within 36 months
Secondary	Adverse event (AE), described in terms of type, frequency, severity, time, and relationship with study treatment		Approximately within 36 months
Secondary	Characterize the PK parameter AUC	steady-state area under curve (AUC)	Approximately within 36 months
Secondary	Characterize the PK parameter Cmax	peak concentration (Cmax)	Approximately within 36 months
Secondary	Characterize the PK parameter Ctrough	trough concentration (Ctrough)	Approximately within 36 months
Secondary	Characterize the PK parameter CL	clearance (CL)	Approximately within 36 months
Secondary	Characterize the PK parameter Vd	volume of distribution (Vd)	Approximately within 36 months
Secondary	Characterize the PK parameter t1/2	half-life (t1/2)	Approximately within 36 months
Secondary	Incidence of anti-YL202 antibody		Approximately within 36 months
Secondary	Evaluate the corelaton between different levels of HER3 expression and the sum of CR rate, PR rate and SD rate		Approximately within 36 months