Clinical Trial of YH32364 in Patients With Locally Advanced or Metastatic EGFR Overexpressing Solid Tumors

Yuhan

Status and phase: Enrolling; Phase 2; Phase 1

Conditions: EGFR Overexpression; Locally Advanced Solid Tumor; Metastatic Solid Tumor

Treatments: Drug: YH32364

Study type: Interventional

Funder types: Industry

Identifiers

NCT06975410

YH32364-101

Details and patient eligibility

About

This is a study for people with locally advanced or metastatic cancer for whom previous treatment was not successful. Adults aged 18 and over with advanced cancer with Epidermal Growth Factor Receptor (EGFR) overexpressing can join the study. The purpose of this study is to find out whether a medicine called YH32364 helps people with locally advanced or metastatic cancers with EGFR overexpression.

Full description

YH32364 is a new type of immunotherapy called a bispecific antibody that targets both Epidermal Growth Factor Receptor (EGFR) and 4-1BB. EGFR is a gene involved in cancer growth, and many cancer treatments aim to target it. 4-1BB, an immune-modulating protein, plays an important role in boosting T cell activity to combat cancer.

YH32364 is a treatment designed to activate 4-1BB specifically in tumors, aiming to avoid the liver-related side effects seen with previous 4-1BB treatments. It also helps block EGFR signals, assumed to make EGFR-targeted therapies more effective by overcoming resistance.

This study is consists of two parts. In Part 1, participants will be assigned sequentially to one of six dose levels, ranging from the lowest to the highest dose as determined by the sponsor, in order to identify an appropriate dosage.

In Part 2, participants will be randomly assigned to one of the two optimal dose levels identified in Part 1 to confirm the recommended dose.

The YH32364 will be administered via intravenous (IV) infusion once every two weeks. Participants will be required to visit the study site regularly for treatment and assessments. During all the visits, the doctors check participants' health and take note of any unwanted effects.

Enrollment: 80 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Must sign an informed consent form (ICF) prior to any study specific procedures
• ECOG performance status 0 or 1
• Estimated life expectancy of at least 3 months
• A woman must not be breastfeeding
• Have at least one measurable lesion, not previously irradiated and not chosen for biopsy during the study screening period, that can be accurately measured at baseline ≥10 mm in the longest diameter (except lymph nodes which must have a short axis of ≥15 mm) with computerized tomography (CT) or magnetic resonance imaging (MRI), are suitable for accurate repeated measurements.

[Dose Escalation Only] Locally advanced or metastatic EGFR overexpressing solid tumor* that is refractory or intolerable on all available standard therapy and that is considered uncurable by local therapy

* One of the following pathologically confirmed EGFR overexpressing (IHC3+ or IHC2+) tumors.

• Head and neck squamous cell carcinoma (HNSCC)
• Non-small cell lung cancer (NSCLC): squamous cell carcinoma (SqCC)
• Esophageal squamous cell carcinoma (ESCC)
• Biliary tract cancer (BTC)
• Uterine cervical cancer
• Vulvar cancer
• Urothelial cancer
• Squamous cell carcinoma of other origin of tumor (e.g., skin squamous cell tumor)

[Dose Expansion Only] Cohort 1: Pathologically confirmed EGFR overexpressing (IHC3+ or IHC2+), locally advanced or metastatic HNSCC other than nasopharyngeal carcinoma (NPC)* that is refractory or intolerable on all available standard therapy and that is considered uncurable by local therapy.

Exclusion criteria

• Known uncontrolled central nervous system (CNS) metastases, spinal cord compression, and/or carcinomatous meningitis

• Have history of a second primary cancer with the exception of

  • curatively treated non-melanomatous skin cancer
  • curatively treated cervical or breast carcinoma in situ, or
  • other malignancy with no known active disease present and no treatment administered during the last 2 years

• Have history of or current Class II, III or IV heart failure as defined by the New York Heart Association (NYHA)

• Have history of acute coronary syndromes, including myocardial infarction, coronary artery bypass graft, unstable angina, coronary angioplasty or stenting within past 24 weeks

• Have history of (non-infectious) interstitial lung disease (ILD) or pneumonitis that required steroids, or any evidence of current ILD or pneumonitis

• Have autoimmune disease that has required systemic treatment

• Infection with human immunodeficiency virus (HIV)

• Active chronic hepatitis B or chronic hepatitis C

[Prior/Concomitant Therapy]

• Have received systemic steroid therapy
• Previous treatment with a 4-1BB/CD137-modulating agent
• Have used a live vaccine within 4 weeks
• Have received treatment with immunotherapy, biological therapies, targeted small molecules, or hormonal therapies
• Have received radiation therapy
• Have received cytotoxic chemotherapy

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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80 participants in 1 patient group

YH32364

Experimental group

Description:

Dose Escalation Part: Dose Escalation part is designed to assess the safety and tolerability of YH32364 and to identify the Maximum Tolerated dose (MTD) and/or two dose levels for recommended dose (RD) selection. Dose Expansion Part: Dose Expansion part will consist of multiple cohorts by cancer types. Cohort 1 will be initiated to determine the RD after completion of Part 1. The RD will be determined among two dose levels investigated in Cohort 1 based on the totality of available data including PK, biomarkers, dose-response, safety, and efficacy.

Treatment:

Drug: YH32364