A Clinical Study to Evaluate the Safety and Tolerability of JS107 in Advanced or Metastatic Solid Tumors

NCT ID: NCT05502393

Last Updated: 2022-08-16

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE1
• Total Enrollment: 118 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2022-07-26
• Study Completion Date: 2024-12-31

Brief Summary

The purpose of this phase I clinical study was to evaluate the safety and tolerability of JS107 monotherapy and combination with Toripalimab in patients with Advanced or Metastatic Solid Tumors.

Conditions

Advanced Solid Tumors

Study Design

• Allocation Method: NA
• Intervention Model: SEQUENTIAL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

JS107

Group Type: EXPERIMENTAL

JS107

Intervention Type: DRUG

JS107, i.v., q3w

JS107 combination with Toripalimab

Group Type: EXPERIMENTAL

JS107

Intervention Type: DRUG

JS107, i.v., q3w

Toripalimab

Intervention Type: DRUG

Toripalimab i.v., q3w

Interventions

JS107

JS107, i.v., q3w

Intervention Type: DRUG

Toripalimab

Toripalimab i.v., q3w

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. The subjects voluntarily participated in the study with full informed consent and signed written informed consent form;

2. Aged ≥18 years and ≤75 years when the subject signed the informed consent;

3. Locally advanced unresectable or metastatic malignant solid tumors diagnosed histologically ;

4. Provide past tumor samples or fresh tumor tissue biopsy samples;

5. The physical status score is 0 or 1 on the Eastern Oncology Collaboration (ECOG) scale;

6. The expected survival is ≥3 months;

7. There should be at least one measurable lesion according to RECIST V1.1 evaluation criteria;

9. Good organ function；

10. Within 7 days prior to the first dose, women of reproductive age must be confirmed as having a negative serum pregnancy test and consent to use effective contraception during the duration of study drug use and for 6 months after the last dose. Male patients with a female partner of reproductive age agreed to use effective contraception during the study drug use period and for 6 months after the last dose.

Exclusion Criteria

1. Prior treatment with drugs or other therapies targeting CLDN18.2;

2. A history of severe allergic reactions to other monoclonal antibodies or to any component of JS107, or to other drugs or excipients involved in the trial protocol ;

3. Received radiotherapy (except palliative radiotherapy for symptom control), chemotherapy, targeted therapy, endocrine therapy and other antitumor therapies, or other investigational drugs within 4 weeks before the administration of the first dose;

4. Received any monoclonal antibody or antibody conjugate within 4 weeks prior to administration of the first study drug or within 5 half-lives (depend on whichever is shorter);

5. Persons who have an immunodeficient disease or the other chronic immunosuppressive therapy, or who have received systemic immunomodulatory drugs (including, but not limited to, interferon or IL-2) within 14 days before first dose or within the 5 half-life of the drug (depend on whichever is longer), or received systemic glucocorticoid therapy (10mg daily of prednisone or equivalent glucocorticoids) or other systemic immunosuppressive therapy within 14 days before first dose;

6. Received any live vaccine (e.g. influenza vaccine against infectious diseases, chickenpox vaccine, etc.) within 14 days before first dose;

7. Serious infection (CTCAE> grade 2) occurred within 14 days before the first dose;

8. Patients with other malignant tumors except for the tumor treated in the study within 5 years prior to the administration of the first study drug (exceptions included: cured malignancies that had not recurred within 3 years prior to study enrollment; Completely resected basal and squamous cell skin cancers; Complete resection of any type of carcinoma in situ, etc.);

9. Major organ surgery was performed or significant trauma was present within 4 weeks before the first administration of the study drug;

10. Weight loss 10% within 2 months before drug administration, or other indicators of severe malnutrition, or body mass index (BMI)<17.5 at the time of signing the informed consent.

11. The following conditions were present within 6 months prior to the first study dose: myocardial infarction, severe/unstable angina, NYHA class 2 or higher cardiac insufficiency, clinically significant supraventricular or ventricular arrhythmia, and symptomatic congestive heart failure , hypertensive crisis, or hypertensive encephalopathy; patients with known hypertension, coronary artery disease, congestive heart failure not meeting the above criteria, or left ventricular ejection fraction <50% must be treated with optimal stabilization as determined by the treating physician medical plan;

12. Pericardial effusion, pleural effusion or abdominal effusion with clinical symptoms, signs or requiring symptomatic treatment;

13. Poorly controlled pain related;

14. The presence of uncontrolled or symptomatic active central nervous system (CNS) metastases, which can be manifested by the onset of clinical symptoms, cerebral edema, spinal cord compression, carcinomatous meningitis, leptomeningeal disease, and/or progressive growth;

15. Active infection, including tuberculosis (clinical diagnosis including clinical history, physical examination and imaging findings, as well as TB tests according to local medical routine), hepatitis B, hepatitis C or human immunodeficiency virus (HIV antibody positive);

16. History of autoimmune disease;

17. Idiopathic pulmonary fibrosis, drug-induced pneumonia, machine-induced pneumonia (bronchiolitis obliterans), radioactive pneumonia with clinical symptoms or requiring steroid treatment, active pneumonia, or other moderate to severe lung diseases that seriously affect lung function ;

18. Pregnant or lactating women;

19. History of allogeneic organ transplantation or allogeneic hematopoietic stem cell transplantation;

20. Have serious psychological or mental abnormality, which affects the compliance of the subject to participate in this clinical study;

21. Participated in any other clinical trial within 28 days prior to the first administration of study drug;

22. Other conditions deemed inappropriate for study participation by the investigator.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Shanghai Junshi Bioscience Co., Ltd.

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Ruihua Xu, M.D.

Role: PRINCIPAL_INVESTIGATOR

Sun Yat-sen University

Locations

Fujian Cancer Hospital

Fuzhou, Fujian, China

Site Status: NOT_YET_RECRUITING

Sun Yat-sen University Cancer Center

Guangzhou, Guangdong, China

Site Status: RECRUITING

The First Affiliated Hospital of Zhejiang University Medical College

Hangzhou, Zhejiang, China

Site Status: NOT_YET_RECRUITING

Countries

China

Central Contacts

Ruihua Xu, M.D

Role: CONTACT

xurh@sysucc.org.cn

86 020-87342479

Furong Liu, Medicie Postgraduate

Role: CONTACT

liufr@sysucc.org.cn

86 020-87342479

Facility Contacts

Rongbo Lin, M.D.

Role: primary

Rongbo_lin@163.com

86 0591-83660063

Ruihua Xu, M.D.

Role: primary

xurh@sysucc.org.cn

86 020-87342479

Jianzhen Shan, M.D.

Role: primary

jianzhenshan@163.com

86 0571-87236114

Other Identifiers

JS107-001-I

Identifier Type: -

Identifier Source: org_study_id