A Clinical Study to Evaluate the Safety and Tolerability of JS001sc in Advanced Nasopharyngeal Carcinoma

A Randomised, Open-label, Phase I Dose Exploration Study to Compare Single, Multiple, and Long-term Dosing of Toripalimab Injection (Subcutaneous) With Toripalimab Injection (IV) in Patients With Advanced Nasopharyngeal Carcinoma

The purpose of this phase I clinical study was to evaluate the safety and tolerability of JS001sc monotherapy and combination with gemcitabine and cisplatin (GP) in patients with Advanced nasopharyngeal carcinoma.

Study Overview

• Status: Recruiting
• Conditions: Advanced Nasopharyngeal Carcinoma
• Intervention / Treatment: Biological: Toripalimab injection(subcutaneous)/JS001sc; Biological: Toripalimab injection(subcutaneous)/JS001sc; Biological: Toripalimab injection(subcutaneous)/JS001sc; Biological: Toripalimab /JS001

Detailed Description

This study is the first human study of Toripalimab injection(subcutaneous) .Patients with advanced nasopharyngeal carcinoma were planned to be enrolled.

Two cohorts were initially proposed, Toripalimab injection (subcutaneous) Q3W combination with gemcitabine and cisplatin (GP) regimen and JS001sc long-term dosing combined with GP regimen.

Cohort 1: JS001sc Q3W SC combined with GP regimen chemotherapy; Cohort 2: JS001sc long period SC combined with GP regimen chemotherapy; IV cohort (if applicable): the Safety Monitor Committe (SMC) will discuss whether to conduct an IV cohort and determine the dose/frequency of the IV cohort, based on the initial safety and clinical pharmacological data of triprilimab injection in combination with the GP regimen; Additional cohort (if applicable): the exploration of additional dosing/frequency will be discussed by the SMC based on prior safety and clinical pharmacological data.

Subjects with no disease progression (PD) after the combination chemotherapy period (JS001/JS001SC combined with GP regimen, in one therapeutic cycle of three weeks, for at most 6 cycles) will enter the monotherapy maintenance period.JS001/JS001sc monotherapy maintenance treatment of the same dose/frequency f the combination chemotherapy period.Based on the preliminary safety and clinical pharmacological data, SMC will discusses whether to change the dose/frequency.

• Study Type: Interventional
• Enrollment (Anticipated): 24
• Phase: Phase 1

Contacts and Locations

Study Locations

• China
  • Guangdong
    • Guangzhou, Guangdong, China, 510060
      • Recruiting
      • Sun Yat-sen University Cancer Center
      • Contact: Ruihua Xu, M.D.; Phone Number: 86 13922206676; Email: xurh@sysucc.org.cn

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 75 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

1. The subjects voluntarily participated in the study with full informed consent and signed written informed consent form;
2. Recurrent/metastatic nasopharyngeal carcinoma diagnosed histologically and/or cytologically,Patients with no loco-regional therapy or radical therapy of primary metastatic （UICC&AJCC 8th edition) or recurrent nasopharyngeal carcinoma after radical therapy.No previous systematic treatment for recurrent or metastatic disease.
3. Patients with recurrent nasopharyngeal carcinoma after radical therapy must be satisfied that the disease recurrence more than 6 months after the last radiotherapy or chemotherapy.
4. There should be at least one measurable lesion according to RECIST V1.1 evaluation criteria. The lesions that have previously received radiotherapy should not be considered as target lesions unless there is definite progression after radiotherapy.
5. Age of 18-75 years (inclusive), male or female;
6. The physical status score is 0 or 1 on the Eastern Oncology Collaboration (ECOG) scale;
7. The expected survival is ≥3 months;

8. Major organ functions meet the following requirements.No blood transfusion or blood products, hematopoietic stimulating factors or other drugs were used to correct blood cell counts within 14 days prior to the examination：

   Neutrophil absolute count ≥1.5 × 109/L;

   Platelet count ≥ 100 × 109/L;

   Hemoglobin ≥ 90 g/L;

   Serum albumin ≥ 30 g/L;

   Serum total bilirubin ≤ 1.5 × upper limit of normal (ULN) with biliary obstruction resolved prior to randomization;

   Alkaline phosphatase (ALP)≤ 3 × ULN, ALP≤ 5 × ULN (Patients may have liver or bone metastasis);

   Albumin ≥ 30 g/L;

   Serum creatinine (Cr) ≤ 1.5 × ULN, Cr clearance ≥ 60 mL/min (Cockcroft -Gault Formulas, refer to attachment 2);

   International Normalized Ratio (INR), prothrombin time (PT), and activated Partial thrombin Time (aPTT) ≤ 1.5× ULN (Patients should not have received anticoagulant therapy);If Patients receiving anticoagulant therapy that they should use a steady dose;

9. 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 150 days after the last dose. Women of childbearing age are defined as sexually mature women: 1) no hysterectomy or bilateral ovariectomy, 2) Natural menopause did not last for 24 consecutive months (Amenorrhea after cancer treatment does not rule out fertility);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. A history of severe allergic reactions to to any component of JS001;
2. A history of hypersensitivity to gemcitabine or cisplatin or any excipients;
3. Prior treatment with Anti-PD-1 antibody, anti-PD-L1 or anti-CTLA-4 antibody;
4. Received antitumor therapy ,Such as, chemotherapy, radiotherapy,immune therapy therapy, biological drugs therapy or other investigational drugs within 4 weeks or 5 half-lives period （Choose the shorter one）before the administration of the first dose;Receive traditional Chinese medicine or Chinese patent medicine preparations with anti-tumor indications within 2 weeks prior to initial administration;
5. Within 28 days prior to the first study drug administration, there are other major surgeries except for the diagnosis of nasopharynx carcinoma, or assessed by researchers and specialists that they did not have fully recovered from the complications of major surgery;
6. The toxic response of previous anti-tumor treatment has not been restored to CTCAE 0-1, except for hair loss and pigmentation.Irreversible toxicity reasonably expected not to be aggravated by the drug under study (e.g. hearing loss). They can be included after confirmation with the sponsor.
7. A subject with clinical symptoms of CNS and/or cancer meningitis (such as cerebral edema, hormone intervention, or brain metastases) No clear surgery and/or radiotherapy for spinal cord compression, or for spinal cord compression that previously diagnosed and treated, no evidence indicates that the first study of pre -dating diseases in clinical stability ≥2 weeks of clinical clinic; Received the treatment of brain or meningeral membrane, such as clinical stability has been maintained for at least 2 months, and has stopped systemic hormone therapy (dose> 10 mg/day dawnone or other curative hormones such as);
8. Poorly controlled the thoracic effusion, pericardial effusion, or ascites that need to be drained (thoracic ascites ≥1 times/month)

9. Poorly controlled tumor-related pain:

   For patients who need analgesic treatment, they must receive a stable dose treatment before participating in the study ; Before entering the group, a clinical indication lesions should be treated for local treatment (for example, bone metastases or metastasis of neurotransidal);

10. Featured pulmonary fibrosis, drug -induced pneumonia, mechanized pneumonia (that is, occlusion fine pineitis), radioactive pneumonia with clinical symptoms or steroids, active pneumonia or other medium -weight lungs that seriously affect lung function that seriously affect lung function disease;
11. The first 4 weeks before the medication found that there were necrotic lesions, and the researchers judged that there was a risk of hemorrhage;
12. Within the first 5 years of administration, there are other malignant tumors other than nasopharyngeal cancer (except for cured cervical in situ cancer, base or squamous cell skin cancer, limited prostate cancer or Ductal carcinoma in situ of breast);
13. The subject has any active autoimmune disease or a history of autoimmune diseases within two years. Except for the following situations: 1) patients with thyroid dysfunction, receiving stable dose thyroid hormone replacement treatment; 2) receiving stable insulin therapy schemes Later, patients with type I diabetes were obtained; 3) skin diseases that do not need to be treated with whole body, such as psoriasis, vitiligo, etc. (for more comprehensive list of autoimmune diseases, see Annex 4);
14. Severe infections (CTCAE> 2) within 28 days before the administration (CTCAE> 2), such as severe pneumonia, fungal ledis, infection complications, etc. that need to be hospitalized;
15. Availability with active lung tuberculosis (TB) is undergoing anti -tuberculosis treatment or screening within one year before receiving anti -tuberculosis treatment;
16. It suffers from corticosteroids that require long -term use of immunosuppressive drug treatment, or the use of immunosuppressive dose (dose> 10 mg/day or other curative hormones such as 10 mg/day);
17. Received any live vaccine within 4 weeks before the medication (for example, vaccines for infectious diseases, such as influenza vaccines, chickenpox vaccines, etc.);
18. Women of pregnancy or lactation;
19. Known human immune defect virus (HIV) positive patients;
20. Hepatitis B core antibodies (HBCAB) or hepatitis B surface antigen (HBSAG) positive detection of HBV DNA copy number ≥1000CPS/ml or reference value limit;
21. Hepatitis C (HCV) antibody positive at the same time detected HCV RNA copies of positive;
22. Patients who have been transplanted in the same kind of album bone marrow or previously performed physical organ transplantation;
23. There are severe nerve or mental illness, including dementia and seizures;
24. Due to NCI-CTCAE ≥ 2 peripheral neuropathy;
25. With major cardiovascular diseases, such as the New York Heart Diseases (NYHA) heart function grading II or above heart disease (see Annex 3), the myocardial infarction and control within 3 months before the first study; Unstable angina pectoris; Knitrines of patients with coronary arteries, congestive heart failure of the above standards, or left ventricular ejection scores <50%of patients must use the optimized stable medical plan determined by the doctor. If appropriate, you can consult the heart. Sick expert;
26. Investigators are judged that they are not suitable for other situations in this study, including but not limited to any disease or medical history that may confuse the results o study and interfere with patients.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Parallel Assignment
• Masking: None (Open Label)

Number of Arms

4

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: JS001sc Q3W	Biological: Toripalimab injection(subcutaneous)/JS001sc; JS001sc Q3W combination with gemcitabine and cisplatin.; Biological: Toripalimab injection(subcutaneous)/JS001sc; JS001sc long period combination with gemcitabine and cisplatin.; Biological: Toripalimab injection(subcutaneous)/JS001sc; Additional cohort (if applicable)
Experimental: JS001sc long period	Biological: Toripalimab injection(subcutaneous)/JS001sc; JS001sc Q3W combination with gemcitabine and cisplatin.; Biological: Toripalimab injection(subcutaneous)/JS001sc; JS001sc long period combination with gemcitabine and cisplatin.; Biological: Toripalimab injection(subcutaneous)/JS001sc; Additional cohort (if applicable)
Experimental: JS001 IV (if applicable); the Safety Monitor Committe (SMC) will discuss whether to conduct an IV cohort and determine the dose/frequency of the IV cohort, based on the initial safety and clinical pharmacological data of triprilimab injection in combination with the GP regimen;	Biological: Toripalimab /JS001; JS001 IV (if applicable) .
Experimental: Additional cohort (if applicable); The exploration of additional dosing/frequency will be discussed by the SMC based on prior safety and clinical pharmacological data	Biological: Toripalimab injection(subcutaneous)/JS001sc; JS001sc Q3W combination with gemcitabine and cisplatin.; Biological: Toripalimab injection(subcutaneous)/JS001sc; JS001sc long period combination with gemcitabine and cisplatin.; Biological: Toripalimab injection(subcutaneous)/JS001sc; Additional cohort (if applicable)

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Cmax	Maximum observed serum concentration	At designated time points (Approximately 2 years)
Tmax	Time of maximum observed serum concentration	At designated time points (Approximately 2 years)
AUC	Area Under the Concentration-Time Curve	At designated time points (Approximately 2 years)
CL	Clearance	At designated time points (Approximately 2 years)
Volume of Distribution	V	At designated time points (Approximately 2 years)
F	Bioavailability	At designated time points (Approximately 2 years)
Ctrough	Trough observed serum toripalimab concentration	At designated time points (Approximately 2 years)

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Immunogenicity	Incidence of anti-drug antibody (ADA) and/or neutralizing antibody (Nab), titer of ADA positive samples	Up to approximately 24 months from first patient in.
ORR	Objective response rate (ORR) was assessed based on RECIST V1.1 criteria	Up to approximately 24 months from first patient in.
adverse events (AE), immune-related adverse events (irAE) and serious adverse events (SAE)	To evaluate incidence, severity and outcome of adverse events (AE), immune-related adverse events (irAE) and serious adverse events (SAE)	Until 2 years after the last subject was enrolled

Collaborators and Investigators

• Sponsor: Shanghai Junshi Bioscience Co., Ltd.

Study record dates

Study Major Dates

• Study Start (Actual): October 21, 2022
• Primary Completion (Anticipated): December 30, 2023
• Study Completion (Anticipated): December 30, 2025

Study Registration Dates

• First Submitted: February 21, 2023
• First Submitted That Met QC Criteria: February 21, 2023
• First Posted (Actual): March 2, 2023

Study Record Updates

• Last Update Posted (Actual): March 2, 2023
• Last Update Submitted That Met QC Criteria: February 21, 2023
• Last Verified: February 1, 2023

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Neoplasms by Histologic Type; Neoplasms; Neoplasms by Site; Neoplasms, Glandular and Epithelial; Pharyngeal Neoplasms; Otorhinolaryngologic Neoplasms; Head and Neck Neoplasms; Nasopharyngeal Diseases; Pharyngeal Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases; Nasopharyngeal Neoplasms; Carcinoma; Nasopharyngeal Carcinoma
• Other Study ID Numbers: JS001sc-001-I

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No