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A Study to Evaluate SHR-1210 in Patients With Advanced or Metastatic NSCLC

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT03085069
Recruitment Status : Unknown
Verified September 2018 by Jiangsu HengRui Medicine Co., Ltd..
Recruitment status was:  Recruiting
First Posted : March 21, 2017
Last Update Posted : September 11, 2018
Information provided by (Responsible Party):
Jiangsu HengRui Medicine Co., Ltd.

Brief Summary:

This is an open-label, single-arm, multi-center, phase 2 Study to evaluate SHR-1210(anti-PD-1 antibody) in in adult Chinese patients with advanced or metastatic non-small cell lung cancer who failed or progressed to prior first-line systemic treatment.

Enrolled subjects will be assigned to 4 cohorts on the basis of PD-L1 expression in tumor cells(<1%, ≥1%-25%, ≥25%-50%, ≥50%) all will be treated with the standard SHR-1210 dose (200mg) , Q2W, until documented progressive disease (PD) occurs. Subjects will return to the clinic once every two weeks. Radiographic disease assessments will be performed every 6 weeks.

The primary study hypothesis is that treatment with SHR-1210 improves Objective Response Rate when compare with standard second-line therapy, no matter how much PD-L1 expression in tumor.

Condition or disease Intervention/treatment Phase
Lung Neoplasms Carcinoma, Non-Small-Cell Lung Respiratory Tract Neoplasms Nec Lung Disease Respiratory Tract Disease Neoplasm, Bronchial Carcinoma, Bronchogenic Biological: SHR-1210 Phase 2

Detailed Description:

In similar clinical trials, anti-PD-1 and anti-PD-L1 antibodies produce durable responses in approximately 20% of unselected patients with advanced non-small-cell lung cancer. Developing reliable, validated biomarkers that identify patients with an increased probability of response to these antibodies remains a challenge.

Because the PD-1 pathway may be a key mechanism of immune escape in a subgroup of patients with non-small-cell lung cancer, PD-L1 expression in tumor or inflammatory cells is a candidate biomarker. However, PD-L1 expression has not been formally validated as a biomarker in contemporaneously collected tumor tissue.

Additionally the purpose of the study is to assess the correlation between the expression of PD-L1 in the tumor and the response to treatment with SHR-1210 in non-small cell lung cancer.

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 120 participants
Allocation: Non-Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: An Open-label, Single-arm, Multi-center, Phase 2 Study to Evaluate SHR-1210(Anti-PD-1 Antibody) in Patients With Advanced or Metastatic Non-Small Cell Lung Cancer
Actual Study Start Date : June 9, 2017
Estimated Primary Completion Date : September 2018
Estimated Study Completion Date : June 2019

Resource links provided by the National Library of Medicine

Arm Intervention/treatment
Experimental: PD-L1 expression in tumor ≥ 50%
Subjects receive SHR-1210 intravenous at the dose 200mg on Day 1 every 2 weeks
Biological: SHR-1210
SHR-1210 is a humanized anti-PD1 IgG4 monoclonal antibody

Experimental: PD-L1 expression in tumor ≥25-50%
Subjects receive SHR-1210 intravenous at the dose 200mg on Day 1 every 2 weeks
Biological: SHR-1210
SHR-1210 is a humanized anti-PD1 IgG4 monoclonal antibody

Experimental: PD-L1 expression in tumor ≥ 1-25%
Subjects receive SHR-1210 intravenous at the dose 200mg on Day 1 every 2 weeks
Biological: SHR-1210
SHR-1210 is a humanized anti-PD1 IgG4 monoclonal antibody

Experimental: PD-L1 expression in tumor < 1%
Subjects receive SHR-1210 intravenous at the dose 200mg on Day 1 every 2 weeks
Biological: SHR-1210
SHR-1210 is a humanized anti-PD1 IgG4 monoclonal antibody

Primary Outcome Measures :
  1. Objective response rate [ Time Frame: Determined using RECIST v1.1 criteria, up to approximately 1 year ]
    Objective response is defined as best overall response (CR or PR) across all assessment time points during the period from enrolment to termination of trial treatment.

Secondary Outcome Measures :
  1. Duration of Response Rate [ Time Frame: Determined using RECIST v1.1 criteria, up to approximately 1 year ]
  2. Overall Survival Rate at 12-month [ Time Frame: up to approximately 1 year ]
  3. Progression-Free Survival [ Time Frame: Determined using RECIST v1.1 criteria, up to approximately 1 year ]
  4. Number of participants with treatment-related adverse events (AEs) [ Time Frame: up to approximately 1 year ]
    assessed by NCI-CTCAE v4.03

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 80 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  1. Subjects with histologically- or cytologically- documented NSCLC who present with Stage IIIB-IV disease (according to version 7 of the International Association for the Study of Lung Cancer Staging Manual in Thoracic Oncology), or disease recurrence or progression following multi-modal therapy (radiation therapy, surgical resection or radical chemo-radiotherapy in locally advanced disease).
  2. Fresh cutting specimens or hollow needle aspiration specimens must be provided. A formalin fixed, paraffin-embedded (FFPE) tumor tissue block or unstained slides of tumor sample (must be recent) must be available for biomarker evaluation. In the case of unstained slides, a minimum of 8 slides are necessary to conduct the planned biomarker analyses. Specimens must be received by the central lab prior to randomization. Biopsy should be excisional, incisional or core needle.
  3. Subjects must have experienced disease recurrence or progression during or after one prior platinum-containing doublet chemotherapy regimen for advanced or metastatic disease:

    1. Subjects who received maintenance therapy (non-progressors with platinum-based doublet chemotherapy) and progressed are eligible.
    2. Subjects who received adjuvant or neoadjuvant platinum-doublet chemotherapy (after surgery and/or radiation therapy) and developed recurrent or metastatic disease within 6 months of completing therapy are eligible.
    3. Subjects with recurrent disease > 6 months after adjuvant or neoadjuvant platinum based chemotherapy, who also subsequently progressed during or after a platinum-doublet regimen given to treat the recurrence, are eligible.
  4. Subjects with sensitizing EGFR mutation positive or ALK rearrangement positive, must have experienced disease recurrence or progression during or after one prior tyrosine kinase inhibitor regimen, who also have PD-L1 expression in tumor ≥ 50%, are eligible.
  5. Subjects must have measurable disease by CT or MRI per RECIST 1.1 criteria; Radiographic Tumor Assessment performed within 28 days of randomization.
  6. Eastern Cooperative Oncology Arm (ECOG) performance status of ≤ 1.
  7. All baseline laboratory requirements will be assessed and should be obtained within -14 days of randomization. Screening laboratory values must meet the following criteria.

    1. Absolute neutrophil count ≥ 1.5 × 109/L (1500/mm3)
    2. Platelets ≥ 80× 109/L (100,000/mm3)
    3. Hemoglobin ≥ 9.0 g/dL (90 g/L)
    4. Total bilirubin (TBIL) ≤ 1.5 × upper limit of normal (ULN)
    5. Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 2.5 × upper limit of normal(ULN); for subjects with liver metastases, ALT and AST ≤ 5 × ULN
    6. Serum creatinine ≤1.5 × ULN or creatinine clearance > 45 mL/minute (using Cockcroft/Gault formula)
  8. Female participants of childbearing potential must have a negative serum pregnancy test within -7 days of randomization and must be willing to use very efficient barrier methods of contraception or a barrier method plus a hormonal method starting with the screening visit through 60 days (about 5 drug half-life + menstrual cycle) after the last dose of SHR-1210. Male participants with a female partner(s) of child-bearing potential must be willing to use very efficient barriermethods of contraception from screening through 120 days (about 5 drug half-life + sperm depletion cycle) after the last dose of SHR-1210.
  9. Subjects must be willing and able to comply with scheduled visits, treatment schedule, laboratory tests including completion of patient reported outcomes questionnaires and other requirements of the study. Subjects must have signed and dated an IRB/IEC approved written informed consent form in accordance with regulatory and institutional guidelines. This must be obtained before the performance of any protocol related procedures that are not part of normal subject care.

Exclusion Criteria:

  1. Target Disease Exceptions

    1. Subjects with active CNS metastases are excluded. Subjects are eligible if CNS metastases are adequately treated and subjects are neurologically returned to baseline (except for residual signs or symptoms related to the CNS treatment) for at least 2 weeks prior to enrollment. In addition, subjects must be either off corticosteroids, or on a stable or decreasing dose of ≤ 10 mg daily prednisone (or equivalent).
    2. Subjects with carcinomatous meningitis.
  2. Medical History and Concurrent Diseases

    1. Subjects with active, known or suspected autoimmune disease. Subjects in conditions not expected to recur in the absence of an external trigger are permitted to enroll.
    2. Subjects with a condition requiring systemic treatment with either corticosteroids (>10 mg daily prednisone equivalent) or other immunosuppressive medications within 14 days of first administration of study treatment. Inhaled or topical steroids, and adrenal replacement steroid doses > 10 mg daily prednisone equivalent, are permitted in the absence of active autoimmune disease.
    3. Prior therapy with immunostimulatory medications or tumor vaccines within 6 months.
    4. Prior therapy with anti-PD-1, anti-PD-L1, anti-PD-L2, or anti-CTLA-4 antibody (including any other antibody or drug specifically targeting T-cell co-stimulation or checkpoint pathways).
    5. Treatment with any investigational agent within 5 half-life of the agent, before the first administration of study treatment.
    6. Subjects with a history of interstitial lung disease.
    7. Subjects received lung radiation therapy within 6 months.
    8. Other active malignancy requiring concurrent intervention.
    9. Subjects with previous malignancies (except non-melanoma skin cancers, and the following in situ cancers: bladder, endometrial, cervical/dysplasia) are excluded unless a complete remission was achieved at least 5 years prior to study entry.
    10. Subjects have had prior chemotherapy within 3 weeks prior to study, or have had prior targeted small molecule therapy within 1 weeks prior to study, or have had prior radiation therapy or surgical operation within 4 weeks prior to study, or have had prior anti-tumor biotherapy within 3 weeks prior to study. All toxicities attributed to prior anti-cancer therapy other than alopecia and fatigue must have resolved to grade 1 (NCI CTCAE version 4) or baseline before administration of study drug.
    11. Subjects must have recovered from the effects of major surgery or significant traumatic injury at least 14 days before the first dose of study treatment
    12. Subjects with active pulmonary tuberculosis.
    13. Subjects with hemoptysis or hemorrhagic quantity per day is 2.5 ml or above within 4 weeks prior to study.
  3. Physical and Laboratory Test Findings

    1. Known history of testing positive for human immunodeficiency virus (HIV) or known acquired immunodeficiency syndrome (AIDS).
    2. Positive test for hepatitis B virus surface antigen (HBV sAg) or hepatitis C virus ribonucleic acid (HCV RNA) indicating acute or chronic infection. (HBV: HBsAg positive and HBV DNA ≥ 500 IU/mL ; HVC: HCV RNA positive and abnormal liver function).
  4. Allergies and Adverse Drug Reaction

    1. History of severe hypersensitivity reactions to other monoclonal antibodies.
    2. History of severe hypersensitivity reaction to intravenous infusion.
  5. Other Exclusion Criteria Any other serious or uncontrolled medical disorder, active infection, physical exam finding, laboratory finding, altered mental status, or psychiatric condition that, in the opinion of the investigator, would limit a subject's ability to comply with the study requirements, substantially increase risk to the subject, or impact the interpretability of study results.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT03085069

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Contact: Xiaoyan Kang, MD 021-60453139
Contact: Ying Liang, MD 021-60453192

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China, Guangdong
Guangdong Lung Cancer Institute (GLCI),Guangdong General Hospital (GGH) Recruiting
Guangzhou, Guangdong, China, 510080
Contact: Yilong Wu, Professor    86-20-83827812      
Principal Investigator: Yilong Wu, Professor         
Sponsors and Collaborators
Jiangsu HengRui Medicine Co., Ltd.
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Study Director: Xiaoyan Kang, MD Jiangsu Hengrui Pharmaceutical Co., Ltd.
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Responsible Party: Jiangsu HengRui Medicine Co., Ltd. Identifier: NCT03085069    
Other Study ID Numbers: SHR-1210-II-201-NSCLC
First Posted: March 21, 2017    Key Record Dates
Last Update Posted: September 11, 2018
Last Verified: September 2018
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Undecided

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Jiangsu HengRui Medicine Co., Ltd.:
Additional relevant MeSH terms:
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Carcinoma, Non-Small-Cell Lung
Lung Neoplasms
Respiratory Tract Neoplasms
Carcinoma, Bronchogenic
Bronchial Neoplasms
Lung Diseases
Respiratory Tract Diseases
Neoplasms, Glandular and Epithelial
Neoplasms by Histologic Type
Thoracic Neoplasms
Neoplasms by Site
Bronchial Diseases