WTX212A Monotherapy and in Combination With PD -1/PD-L1 Monoclonal Antibody

Trial Title: WTX212A Monotherapy and in Combination With PD -1/PD-L1 Monoclonal Antibody

NCT ID: NCT06106152

Condition: Advanced Lung Cancer

Conditions: Official terms:
Lung Neoplasms
Immune Checkpoint Inhibitors
Antibodies
Immunoglobulins
Antibodies, Monoclonal

Study type: Interventional

Study phase: Early Phase 1

Overall status: Recruiting

Study design:

Allocation: Non-Randomized

Intervention model: Parallel Assignment

Intervention model description: Single-center, open-label, exploratory study to evaluate the efficacy, safety, pharmacokinetics, and pharmacodynamics of WTX212A injection combined with PD -1/PD-L1 monoclonal antibody in patients with advanced lung cancer

Primary purpose: Treatment

Masking: None (Open Label)

Intervention:

Intervention type: Drug
Intervention name: WTX212A injection
Description: The WTX212A infusion is given every 21 days
Arm group label: Combined Study in patients with advanced lung cancer
Arm group label: Fixed-dose in patients with advanced lung cancer

Other name: autologous red blood cell PD-1 inhibitor conjugate

Intervention type: Drug
Intervention name: PD -1/PD-L1 monoclonal antibody
Description: The PD -1/PD-L1 monoclonal antibody is given every 21 days
Arm group label: Combined Study in patients with advanced lung cancer

Other name: PD -1/PD-L1antibody

Summary: This trial is a single-center, open-label designed investigator-initiated clinical study (IIT) to evaluate the efficacy, safety, pharmacokinetics, and pharmacodynamics of WTX212A injection WTX212A injection combined with PD -1/PD-L1 monoclonal antibody in patients with advanced lung cancer

Detailed description: The trial consist of Screening Period (30 days), Treatment Period (21*n days), Safety Follow-up Period (90 days) and Survival follow-up. About 20 subjects are planned to be enrolled in the study.

Criteria for eligibility:
Criteria:
Inclusion Criteria: - The subject signs an informed consent form, understands this study, is willing to follow and has the ability to complete all experimental procedures; - Regardless of gender, aged 18 to 75 years old (including threshold); - Histologically or cytologically confirmed locally advanced (stage IIB/IIC) or metastatic (stage IV) non-small cell lung cancer (NSCLC) with disease progression or intolerance after treatment or extensive stage small cell Lung cancer (SCLC) - Patients with lung cancer who have been treated with at least 1 line system therapy or cannot currently receive standard therapy, and who have been treated with PD-1 or PD-L1 inhibitor antibody in the terminal line therapy regimen for ≥ 2 cycles; - ECOG ≤1 - Expected life ≥ 3 months； - Male participants, their spouses, and female participants of childbearing age should agree to use a medically recognized effective contraceptive method from the signing of the informed consent form until 3 months after the last administration; Exclusion Criteria: - People with other serious medical diseases, including but not limited to: uncontrolled diabetes, active peptic ulcer, active bleeding, etc., and people with uncontrollable or serious cardiovascular diseases, - Patients with clinical symptoms and the need for repeated drainage of pleural and ascitic fluids; - Previous or recent history of pulmonary fibrosis, severe lung function damage caused by pneumoconiosis, radiation pneumonia, and drug-related pneumonia; - There have been adverse events related to the use of IO drugs that require permanent cessation of IO treatment; - Known to have other malignant tumors, currently progressing or completing treatment at least once in the past 3 years. Exceptions include early tumors that have received radical treatment (carcinoma in situ or grade 1 tumor, non ulcerative primary melanoma with a depth of less than 1mm and no lymph nodes involved), skin basal cell carcinoma, skin squamous cell carcinoma, cervical carcinoma in situ, or breast carcinoma in situ that has received potential radical treatment; - Subjects with symptomatic central nervous system (CNS) metastasis confirmed by imaging or pathological examination and clinically unstable for at least 14 days prior to enrollment who require steroid treatment; - Having hereditary bleeding tendencies or coagulation disorders, or a history of thrombosis, hemolysis, or hemorrhagic diseases; - Received significant surgical treatment or obvious traumatic injury within 28 days prior to the start of research treatment;

Gender: All

Minimum age: 18 Years

Maximum age: 75 Years

Healthy volunteers: No

Locations:

Facility:
Name: 2nd Affiliated Hospital, School of Medicine, Zhejiang University

Address:
City: Hangzhou
Zip: 310000
Country: China

Status: Recruiting

Contact:
Last name: Pingli Wang, M.D

Phone: +86 135 1680 8409
Email: pingliwang@zju.edu.cn

Start date: December 5, 2023

Completion date: December 31, 2025

Lead sponsor:
Agency: Second Affiliated Hospital, School of Medicine, Zhejiang University
Agency class: Other

Collaborator:
Agency: Westlake Therapeutics
Agency class: Industry

Source: Second Affiliated Hospital, School of Medicine, Zhejiang University

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT06106152