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Study to Evaluate the Bioavailability of Tislelizumab Via Subcutaneous Injection in First-Line Treatment of Participants With Advanced or Metastatic Non-Small Cell Lung Cancer

Phase 1
Active, not recruiting
Conditions
Non-small Cell Lung Cancer
Interventions
Drug: Histology-Based Chemotherapy Doublet
Registration Number
NCT06091943
Lead Sponsor
BeiGene
Brief Summary

This is an open-label, multicenter, Phase 1 clinical study to evaluate the bioavailability of tislelizumab subcutaneous (SC) injection in the first-line treatment of participants with advanced or metastatic non-small cell lung cancer (NSCLC). This clinical study will be divided into 2 parts: dose/injection site exploration (Part 1) and dose expansion (Part 2).

Detailed Description

Not available

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
62
Inclusion Criteria
  • Able to sign a written consent form, understand, and agree to comply with requirements of the study.
  • Documented locally advanced or recurrent NSCLC that is not eligible for curative surgery and/or definitive radiotherapy, with or without chemotherapy, or metastatic non-squamous or squamous NSCLC.
  • No prior systemic treatment for advanced or metastatic NSCLC, including but not limited to chemotherapy or targeted therapy.
  • At least one measurable lesion as assessed by RECIST v1.1.
  • Eastern Cooperative Oncology Group (ECOG) PS ≤ 1.
  • Adequate organ function as indicated by laboratory tests.
Exclusion Criteria
  • Participants diagnosed with NSCLC that harbor a driver mutation (eg, EGFR-sensitizing mutation, ALK fusion oncogene, and BRAF V600E mutation or ROS1 mutation).
  • Participant has received any Chinese herbal medicine or Chinese patent medicines used to control cancer within 14 days before first dose of study drug.
  • Active leptomeningeal disease or uncontrolled, untreated brain metastasis.
  • Active autoimmune diseases or history of autoimmune diseases that may relapse.
  • Any cancer ≤ 5 years before first dose of study drug except for the specific cancer under investigation in this study and any locally recurring cancer that has been treated curatively (eg, resected basal or squamous cell skin cancer, superficial bladder cancer, localized prostate cancer, carcinoma in situ of the cervix or breast).
  • Any condition that required systemic treatment with either corticosteroids (> 10 mg daily of prednisone or equivalent) or other immunosuppressive medication ≤ 14 days before first dose of study drug.

Note: Other protocol defined Inclusion/Exclusion criteria may apply.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SEQUENTIAL
Arm && Interventions
GroupInterventionDescription
Part 1: Dose/Injection Site ExplorationTislelizumab IVDifferent injection sites will be evaluated; participants will receive tislelizumab in predefined administration sequences plus histology-based chemotherapy consisting of either cisplatin/carboplatin and pemetrexed or carboplatin and paclitaxel/nab-paclitaxel depending on the cancer subtype.
Part 1: Dose/Injection Site ExplorationTislelizumab SCDifferent injection sites will be evaluated; participants will receive tislelizumab in predefined administration sequences plus histology-based chemotherapy consisting of either cisplatin/carboplatin and pemetrexed or carboplatin and paclitaxel/nab-paclitaxel depending on the cancer subtype.
Part 1: Dose/Injection Site ExplorationHistology-Based Chemotherapy DoubletDifferent injection sites will be evaluated; participants will receive tislelizumab in predefined administration sequences plus histology-based chemotherapy consisting of either cisplatin/carboplatin and pemetrexed or carboplatin and paclitaxel/nab-paclitaxel depending on the cancer subtype.
Part 2: Dose ExpansionTislelizumab SCThe recommended dose of tislelizumab SC determined from Part 1 plus histology-based chemotherapy consisting of either cisplatin/carboplatin and pemetrexed or carboplatin and paclitaxel/nab-paclitaxel depending on the cancer subtype will be evaluated.
Part 2: Dose ExpansionHistology-Based Chemotherapy DoubletThe recommended dose of tislelizumab SC determined from Part 1 plus histology-based chemotherapy consisting of either cisplatin/carboplatin and pemetrexed or carboplatin and paclitaxel/nab-paclitaxel depending on the cancer subtype will be evaluated.
Primary Outcome Measures
NameTimeMethod
Part 2: Number of Participants with Adverse Events (AEs) and Serious Adverse Events (SAEs)Up to approximately 27 months

Number of participants with AEs and SAEs and laboratory abnormalities, reported during the AE reporting period and characterized by type, frequency, severity (as graded by National Cancer Institute-Common Terminology Criteria for Adverse Events Version 5.0 \[NCI-CTCAE v5.0\]), timing, seriousness, and relationship to study therapy.

Part 1 and 2: Area under the concentration-time curve (AUC) of Tislelizumab SCUp to approximately 3.5 months
Part 1 and 2: Concentration at the end of dosing interval (Ctrough) of Tislelizumab SCUp to approximately 3.5 months
Part 1: Bioavailability of Tislelizumab SCUp to approximately 2 months
Part 2: Maximum observed plasma concentration (Cmax) of Tislelizumab SCUp to approximately 3.5 months
Part 2: Accumulation ratio (Rac) of Tislelizumab SCUp to approximately 3.5 months
Part 2: Elimination half-life (t1/2) of Tislelizumab SCUp to approximately 3.5 months
Secondary Outcome Measures
NameTimeMethod
Part 1: Maximum observed concentration (Cmax) of Tislelizumab SCUp to approximately 2 months
Part 1: Number of Participants with Adverse Events (AEs) and Serious Adverse Events (SAEs)Up to approximately 27 months

Number of participants with AEs and SAEs and laboratory abnormalities, reported during the AE reporting period and characterized by type, frequency, severity (as graded by NCI-CTCAE v5.0), timing, seriousness, and relationship to study therapy.

Part 1 and 2: Number of Participants with Anti-Tislelizumab AntibodiesUp to 25 months
Part 2: Overall Response Rate (ORR) of Tislelizumab SCUp to approximately 27 months

ORR is defined as the percentage of participants who had confirmed complete response (CR) or partial response (PR) as determined from tumor assessments by investigator per Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST v1.1).

Part 2: Duration of Response (DOR) of Tislelizumab SCUp to approximately 27 months

DOR is defined as the time from the first determination of an objective response per RECIST v1.1 until the first documentation of disease progression or death due to any cause, whichever occurs first as assessed by the investigator.

Part 2: Progression-Free Survival (PFS)Up to approximately 27 months

PFS is defined as the time from the date of the first dose of study drug(s) to the date of the first documentation of progressive disease assessed by the investigator using RECIST v1.1 or death due to any cause, whichever occurs first.

Trial Locations

Locations (15)

Jining No Peoples Hospital East Branch

🇨🇳

Jining, Shandong, China

Deyangs People Hospital

🇨🇳

Deyang, Sichuan, China

Cancer Hospital Chinese Academy of Medical Sciences

🇨🇳

Beijing, Beijing, China

Beijing Cancer Hospital

🇨🇳

Beijing, Beijing, China

Peking Union Medical College Hospital

🇨🇳

Beijing, Beijing, China

Fujian Cancer Hospital

🇨🇳

Fuzhou, Fujian, China

Mengchao Hepatobiliary Hospital of Fujian Medical University

🇨🇳

Fuzhou, Fujian, China

Henan Cancer Hospital

🇨🇳

Zhengzhou, Henan, China

The First Affiliated Hospital of Nanchang University Branch Donghu

🇨🇳

Nanchang, Jiangxi, China

Shandong Cancer Hospital

🇨🇳

Jinan, Shandong, China

Shanxi Provincial Cancer Hospital

🇨🇳

Taiyuan, Shanxi, China

Shanxi Bethune Hospital

🇨🇳

Taiyuan, Shanxi, China

Huzhou Central Hospital

🇨🇳

Huzhou, Zhejiang, China

Arensia Exploratory Medicine Llc

🇬🇪

Tbilisi, Georgia

The Institute of Oncology, Arensia Exploratory Medicine

🇲🇩

Chisinau, Moldova, Republic of

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