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Clinical Study of JS007 in Patients With Advanced Solid Tumors

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ClinicalTrials.gov Identifier: NCT05049265
Recruitment Status : Not yet recruiting
First Posted : September 20, 2021
Last Update Posted : September 20, 2021
Sponsor:
Information provided by (Responsible Party):
Shanghai Junshi Bioscience Co., Ltd.

Brief Summary:
This is an open label, phase Ia clinical study to evaluate the safety, tolerability, pharmacokinetic (PK) profile, pharmacodynamic (PD) profile, immunogenicity and preliminary efficacy of JS007 in the patients with advanced solid tumors who have progressed after standard of care, or lack of effective standard therapeutic regimen. This study is divided into two periods: dose escalation period, dose expansion period.

Condition or disease Intervention/treatment Phase
Patients With Advanced Solid Tumors Biological: JS007 Phase 1

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 42 participants
Allocation: N/A
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Phase Ia Study to Evaluate The Safety, Tolerability, Pharmacokinetics And Pharmacodynamics Of Single-dose and Multiple-dose Of JS007 Injection In Patients With Advanced Solid Tumors
Estimated Study Start Date : September 20, 2021
Estimated Primary Completion Date : September 20, 2022
Estimated Study Completion Date : September 20, 2022

Arm Intervention/treatment
Experimental: JS007 Biological: JS007
JS007 only




Primary Outcome Measures :
  1. MTD [ Time Frame: Up to 12 approximately months ]
    The maximum tolerated dose (MTD) is defined as the highest dose at which DLT (Dose-Limiting Toxicity)occurs in <1/3 subjects

  2. DLT [ Time Frame: 21 days after first infusion of study drug ]
    DLT is defined as any of the specified toxicities evaluated as at least possibly related with the study drug within 21 days after the first dose (NCI-CTCAE v5.0)

  3. Adverse Events [ Time Frame: Up to 12 approximately months ]
    AE is assessed according to NCI-CTCAE 5.0

  4. Serious Adverse Events [ Time Frame: Up to 12 approximately months ]
    SAE(Serious adverse event) is assessed according to NCI-CTCAE 5.0

  5. Incidence of immune-related adverse events (irAE) [ Time Frame: Up to 12 approximately months ]
    IrAE is assessed according to NCI-CTCAE 5.0

  6. severity of immune-related adverse events (irAE) [ Time Frame: Up to 12 approximately months ]
    IrAE is assessed according to NCI-CTCAE 5.0


Secondary Outcome Measures :
  1. peak concentration (Cmax) [ Time Frame: Up to 12 approximately months ]
    Pharmacokinetic (PK) profile: drug concentration in individual subject at different time points after administration; pharmacokinetic parameters peak concentration (Cmax);

  2. trough concentration (Ctrough) [ Time Frame: Up to 12 approximately months ]
    Pharmacokinetic (PK) profile: drug concentration in individual subject at different time points after administration; pharmacokinetic parameters trough concentration (Ctrough)

  3. time to peak (Tmax) [ Time Frame: Up to 18 approximately months ]
    Pharmacokinetic (PK) profile: drug concentration in individual subject at different time points after administration; pharmacokinetic parameters time to peak (Tmax);

  4. area under the plasma drug concentration-time curve (AUC0-t ) [ Time Frame: Up to 12 approximately months ]
    Pharmacokinetic (PK) profile: drug concentration in individual subject at different time points after administration; pharmacokinetic parameters area under the plasma drug concentration-time curve (AUC0-t )

  5. area under the plasma drug concentration-time curve (AUC0-inf) [ Time Frame: Up to 12 approximately months ]
    Pharmacokinetic (PK) profile: drug concentration in individual subject at different time points after administration; pharmacokinetic parameters area under the plasma drug concentration-time curve (AUC0-inf);

  6. elimination half-life (t1/2) [ Time Frame: Up to 12 approximately months ]
    Pharmacokinetic (PK) profile: drug concentration in individual subject at different time points after administration; pharmacokinetic parameters elimination half-life (t1/2)

  7. clearance rate (CL) [ Time Frame: Up to 12 approximately months ]
    Pharmacokinetic (PK) profile: drug concentration in individual subject at different time points after administration; pharmacokinetic parameters clearance rate (CL);

  8. apparent volume of distribution(Vd) [ Time Frame: Up to 12 approximately months ]
    Pharmacokinetic (PK) profile: drug concentration in individual subject at different time points after administration; apparent volume of distribution(Vd)

  9. volume of distribution (Vss) [ Time Frame: Up to 12 approximately months ]
    Pharmacokinetic (PK) profile: drug concentration in individual subject at different time points after administration; pharmacokinetic parameters volume of distribution (Vss)

  10. mean retention time (MRT) [ Time Frame: Up to 12 approximately months ]
    Pharmacokinetic (PK) profile: drug concentration in individual subject at different time points after administration; pharmacokinetic parameters mean retention time (MRT)

  11. The number of lymphocyte in peripheral blood before and after administration [ Time Frame: Up to 12 approximately months ]
    The number of lymphocyte in peripheral blood before and after administration

  12. The proportion of lymphocyte in peripheral blood before and after administration [ Time Frame: Up to 12 approximately months ]
    The proportion of lymphocyte in peripheral blood before and after administration

  13. anti-drug body (ADA) [ Time Frame: Up to 12 approximately months ]
    incidence of anti-drug body (ADA)

  14. neutralizing antibody (Nab) [ Time Frame: Up to 12 approximately months ]
    incidence of neutralizing antibody (Nab)

  15. neutralizing antibody (Nab) [ Time Frame: Up to 12 approximately months ]
    concentration of neutralizing antibody (Nab)


Other Outcome Measures:
  1. ORR [ Time Frame: Up to 12 approximately months ]
    The efficacy evaluated by the investigator in accordance with RECIST 1.1 criteria (solid tumors), including objective response rate (ORR).

  2. DOR [ Time Frame: Up to 12 approximately months ]
    The efficacy evaluated by the investigator in accordance with RECIST 1.1 criteria (solid tumors) , including duration of response (DOR);

  3. DCR [ Time Frame: Up to 12 approximately months ]
    The efficacy evaluated by the investigator in accordance with RECIST 1.1 criteria (solid tumors) , including disease control rate (DCR);

  4. PFS [ Time Frame: Up to 12 approximately months ]
    The efficacy evaluated by the investigator in accordance with RECIST 1.1 criteria (solid tumors) , including progression-free survival (PFS)

  5. OS [ Time Frame: Up to 12 approximately months ]
    The efficacy evaluated by the investigator in accordance with RECIST 1.1 criteria (solid tumors) , including overall survival (OS);

  6. CTLA-4(cytotoxic T lymphocyte-associated antigen-4) [ Time Frame: Up to 12 approximately months ]
    Expression of CTLA-4 in tumor tissues before administration

  7. FoxP3(transcription factor Forkhead box P3) [ Time Frame: Up to 12 approximately months ]
    Expression of FoxP3 in tumor tissues before administration

  8. IDO((indoleamine 2,3-dioxy- genase) [ Time Frame: Up to 12 approximately months ]
    Expression of IDO in tumor tissues before administration

  9. mutation of immune related genes in tumor tissues before administration [ Time Frame: Up to 12 approximately months ]
    mutation of immune related genes in tumor tissues before administration

  10. expression of immune related genes in tumor tissues before administration [ Time Frame: Up to 12 approximately months ]
    expression of immune related genes in tumor tissues before administration



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


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Ages Eligible for Study:   18 Years to 75 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion criteria:

  1. Male or female patients with age of 18~75 years;
  2. Signed informed consent form;
  3. Confirmed histological or cytological diagnosis of advanced or recurrent solid tumor with previous standard therapy failure, no available standard therapy or refusal of standard therapy;
  4. Consent to provide tumor tissue (FFPE archival sample within 2 years, or newly obtained tissue blocks, or unstained slides from FFPE);
  5. Having at least one measurable lesion in accordance with the response evaluation criteria in solid tumors (RECIST V1.1).
  6. Life expectancy ≥ 3 months;
  7. Eastern Cooperative Oncology Group (ECOG) Performance Status score 0 or 1 (Appendix 1);
  8. Functional indicators of organs must fulfill the following criteria:

    i. White blood cell ≥ 2.5 × 109/L ii. Neutrophils ≥ 1.5 × 109/L iii. Platelets ≥ 85 × 109/L iv. Hemoglobin ≥ 90 g/L v. Blood creatinine ≤ 1.5 × ULN, or creatinine clearance > 40 ml/min (calculated according to Cockcroft-Gault formula, see Appendix) vi. Aspartate aminotransferase (AST), alanine aminotransferase (ALT) ≤ 2.5 × ULN (for known liver metastases: AST and ALT ≤ 5×ULN) vii. Total bilirubin ≤ 1.5 × ULN (For subjects with Gilbert's Syndrome or known liver metastases, ≤ 2×ULN is acceptable)

Exclusion criteria:

  1. The patient with metastasis to the central nervous system (CNS);
  2. The patient requires systemic steroids or anti-convulsant drugs, or patients with risk of intracerebral hemorrhage judged by the investigator;
  3. Patients with primary CNS tumor or meningeal metastasis;
  4. Having used systemic anticancer therapy, including radiotherapy, chemotherapy, hormone therapy, surgery, or molecular targeted therapy, within 4 weeks prior to the first dose, or all adverse events except hair loss have not recovered to CTCAE Grade 1 or below;
  5. Having other not curable cancers in the past 5 years, excluding the cured or treatable ones, such as basal skin carcinoma, squamous cell skin carcinoma, superficial bladder carcinoma, prostate carcinoma in situ, cervical carcinoma in situ, breast carcinoma in situ, etc;
  6. Active autoimmune diseases required systemic treatment in the past 2 years, excluding vitiligo, type I diabetes, and autoimmune thyroiditis indued hypothyroidism that is curable by thyroid hormone replacement therapy;
  7. Active tuberculosis (TB);
  8. Confirmed infection of human immunodeficiency virus (HIV) or acquired immunodeficiency syndrome (AIDS);
  9. Active infection with hepatitis B virus (HBV) or hepatitis C virus (HCV):

    1. HBsAg positive and HBV DNA ≥ 1000 IU/mL;
    2. Positive test results of HCV RNA.
  10. Women who are pregnant or breastfeeding;
  11. Patients who are unavailable for venipuncture and/or intolerable for intravenous catheterization;
  12. Interstitial lung disease;
  13. History or basis of any clinically significant cardiovascular diseases as follows: abnormal electrocardiogram indicating additional risk for patients at the discretion of investigator; history of congestive heart failure (CHF) of grade III or above as documented by New York Heart Association (NYHA) criteria; history of cerebral infarction or myocardial infarction within 3 months prior to first dose; uncontrolled hypertension (systolic blood pressure > 160 mmHg or diastolic blood pressure > 100 mmHg); unstable angina; serious uncontrolled arrhythmia; baseline left ventricular ejection fraction (LVEF) < 50% or cardiac wall motion abnormalities identified by echocardiogram (ECHO).
  14. Patients accepting other study drugs or anti-infective vaccine (e.g., influenza vaccine, and varicella vaccine) within 28 days prior to the first dose, and COVID-19 (Corona Virus Disease 2019)vaccine is permitted
  15. Patients with anti-tumor vaccine therapy within 3 months prior to the first dose, and prophylactic HPV(human papilloma virus) vaccine is permitted;
  16. Previous treatment with anti-CTLA-4 drugs;
  17. Patients accepting systemic corticosteroids treatment at the doses of immunosuppressive effects (prednisone > 10 mg/day or equivalent level) within 2 weeks before the first dose; patients accepting immunosuppressive agents or glucocorticoids (at doses equivalent to prednisone > 10 mg/day) within 2 weeks before the first dose. Note: Epinephrine replacement therapy (equivalent to prednisone ≤ 10 mg/day) is allowed for patients without active immune disorder . Topical, intraocular, intra-articular, intranasal, and inhaled corticosteroids, which lead to (low systemic absorption, are allowed; short-term corticosteroids treatment is allowed for prophylactic therapy (e.g., be allergic to contrast media) or non-autoimmune diseases (e.g., delayed hypersensitivity reactions after exposure to allergens).
  18. Patient accepting any antitumor traditional Chinese patent medicine within 2 weeks prior to the first dose (any antitumor traditional Chinese patent medicine is prohibited during this study).
  19. Active infection requiring systematic treatment/antibiotics. Patient accepting intravenous anti-infective therapy with one week prior to the first dose or undergoing systematic anti-infective agents ≥ 7 days;
  20. Received live attenuated vaccines within 4 weeks prior to the first dose, or plan to receive live attenuated vaccines during the study;
  21. Allergic to any component of JS007;
  22. Patients are not ineligible if meet at least one of the following conditions prior to the first dose :

    i. Major surgery requiring general anesthesia within 4 weeks prior to the first dose; ii. Surgery requiring local/epidural anesthesia within 72 hours prior to the first dose; iii. Skin biopsy requiring local anesthesia within 1 hour prior to the first dose.

  23. Patients who are not appropriate for this trial due to other reasons at the discretion of the investigator.

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 ClinicalTrials.gov identifier (NCT number): NCT05049265


Contacts
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Contact: Pan He, Postgraduate 8615172333540 pan_he@junshipharma.com

Locations
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China
Ruijin Hospital Affiliated to Shanghai Jiaotong University School of Medical
Shanghai, China, 200025
Contact: Yan Shi, PhD       shibaiwan12@vip.sina.com   
Sponsors and Collaborators
Shanghai Junshi Bioscience Co., Ltd.
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Responsible Party: Shanghai Junshi Bioscience Co., Ltd.
ClinicalTrials.gov Identifier: NCT05049265    
Other Study ID Numbers: JS007-001-I
First Posted: September 20, 2021    Key Record Dates
Last Update Posted: September 20, 2021
Last Verified: August 2021

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Neoplasms