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A Study of SHR-1210 in Combination With BP102 in Subjects With Non-squamous NSCLC

Sponsor
Jiangsu HengRui Medicine Co., Ltd. (Industry)
Overall Status
Terminated
CT.gov ID
NCT03666728
Collaborator
(none)
5
Enrollment
1
Location
1
Arm
15.3
Actual Duration (Months)
0.3
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

SHR-1210 is a humanized anti-PD1 IgG4 monoclonal antibody. This is a Phase II, multicenter, open-label study designed to evaluate the safety and efficacy of SHR-1210 with BP102 in subjects who are chemotherapy naive and have Stage IIIB~IV non-squamous NSCLC. The primary end points are ORR and PFS.

In this study, subjects will receive SHR-1210 combined with BP102 until progression or unacceptable toxicity (SHR-1210 or BP102 for a maximum of 2 years).

Condition or Disease Intervention/Treatment Phase
Phase 2

Study Design

Study Type:
Interventional
Actual Enrollment :
5 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
An Open-label, Single-arm, Multi-center, Phase 2 Study to Evaluate SHR-1210 Combination With BP102 in Patients With Advanced or Metastatic Non-Small Cell Lung Cancer Whose PD-L1 Positive and EGFR/ALK Wild Type.
Actual Study Start Date :
Nov 30, 2018
Actual Primary Completion Date :
Mar 11, 2020
Actual Study Completion Date :
Mar 11, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: SHR-1210+BP102

Subjects receive SHR-1210 200 mg and BP102 15 mg/kg in day 1 intravenously every 3 weeks, until disease progression or unacceptable toxicity.

Drug: SHR-1210
SHR-1210 was administered 200 mg iv every 3 weeks

Drug: BP102
BP102 was administered 15 mg/kg iv every 3 weeks

Outcome Measures

Primary Outcome Measures

  1. Objective response rate (ORR) [up to approximately 1 year]

    ORR, determined using RECIST v1.1, defined as best overall response (CR or PR) across all assessment time points during the period from enrolment to termination of trial treatment.

  2. Progression-Free Survival (PFS) [up to approximately 1 year]

    PFS, defined as the time from randomization to the first occurrence of disease progression as determined by the investigator with use of RECIST v1.1 or death from any cause, whichever occurs first. Patients who have not experienced disease progression or death at the time of analysis will be censored at the time of last tumor assessment.

Secondary Outcome Measures

  1. Time to Response (TTR) [up to approximately 1 year]

    Determined using RECIST v1.1 criteria

  2. Duration of Response Rate (DoR) [up to approximately 1 year]

    Determined using RECIST v1.1 criteria

  3. Disease Control Rate (DCR) [up to approximately 1 year]

    Determined using RECIST v1.1 criteria

  4. Overall Survival Rate at 12-month (OSR) [up to 1 year]

  5. Number of participants with treatment-related adverse events (AEs) [up to approximately 1 year]

    Incidence, nature, and severity of adverse events graded according to the NCI CTCAE v4.03.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:

  • Eastern Cooperative Oncology Group (ECOG) performance status of ≤ 1;

  • Subjects who are chemotherapy naive and have Stage IIIB-IV non-squamous NSCLC;

  • Gene diagnostic tests must show that subjects are with wild type of EGFR, ALK and ROS1;

  • Known PD-L1 status as determined by immunohistochemistry assay performed on previously obtained archival tumor tissue or tissue obtained from a biopsy at screening;

  • No prior systemic treatment;

  • Adequate hematologic and end organ function;

  • 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 6 months after the last dose Male participants with a female partner(s) of child-bearing potential must be willing to use very efficient barrier methods of contraception from screening through 6 months after the last dose.

Exclusion Criteria:

  • Significant cardiovascular disease;

  • Prior treatment with immune checkpoint blockade therapies, anti-programmed death-1, and anti-PD-L1 therapeutic antibodies;

  • History of autoimmune disease;

  • Malignancies other than NSCLC within 5 years prior to randomization, with the exception of those with a negligible risk of metastasis or death treated with expected curative outcome;

  • Severe infection within 4 weeks prior to randomization;

  • Administration of a live, attenuated vaccine within 4 weeks before randomization or anticipation that such a live attenuated vaccine will be required during the study;

  • Major surgical procedure within 4 weeks prior to randomization;

  • History of hemoptysis within 12 weeks prior to randomization;

  • Inadequately controlled hypertension;

  • Evidence of bleeding diathesis or coagulopathy;

  • Prior allogeneic bone marrow transplantation or solid organ transplant;

  • Positive test for HIV, and patients with active hepatitis B or hepatitis C.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Zhejiang Cancer Hospital Hangzhou Zhejiang China 310022

Sponsors and Collaborators

  • Jiangsu HengRui Medicine Co., Ltd.

Investigators

  • Study Director: Jiangsu HengRui Medicine Co., Ltd., Jiangsu HengRui Medicine Co., Ltd.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Jiangsu HengRui Medicine Co., Ltd.
ClinicalTrials.gov Identifier:
NCT03666728
Other Study ID Numbers:
  • SHR-1210-II-211
First Posted:
Sep 12, 2018
Last Update Posted:
Mar 17, 2021
Last Verified:
Mar 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:
Lung Neoplasms

Study Results

No Results Posted as of Mar 17, 2021