Phase I Study of Sintilimab in Healthy Chinese Male Subjects

NCT05337267 | Completed Phase 1

• 1 other identifier: CIBI308K102
• Study Type: interventional
• Target: 117
• Locations: 1 country
• Sites: 1

Brief Summary

The purpose of this study is to evaluate the pharmacokinetic similarity of sintilimab with different manufacturing process in healthy male subjects. Another purpose is to determine safety, and immunogenicity of sintilimab with different manufacturing process，also to determine Pharmacodynamics of sintilimab with different manufacturing process in 12 healthy male subjects.

Conditions

Healthy Male Subjects

Outcome Measures

Primary Outcomes (4)

• Pre-experiment: Treatment-emergent Adverse Events (TEAEs) graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events Version 5.0 (NCI-CTCAE v5.0) incidence.

  Day 43

• Pre-experiment: Serious Adverse Events (SAEs) graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events Version 5.0 (NCI-CTCAE v5.0) incidence.

  Day 43

• Formal test: Bioequivalence results using the area under the plasma concentration-time curve (AUC0-inf) as the judging indicators.

  Day 57

• Bioequivalence results using the peak serum drug concentration (Cmax) as the judging indicators.

  Day 57

Secondary Outcomes (7)

• Other PK parameters: Area under the plasma concentration-time curve (AUClast)

  Day 57

• Other PK parameters: Volume of distribution (V)

  Day 57

• Other PK parameters: Clearance (CL) .

  Day 57

• Other PK parameters: Half-life (t1/2). Other PK parameters, including but not limited to elimination half-life (t1/2).

  Day 57

• The occurrence of Neutralizing antibodies Antibody(NAb)

  Day 57

Study Arms (2)

sintilimab (after the change)

EXPERIMENTAL

Drug: sintilimab (before the change)

sintilimab (before the change)

ACTIVE COMPARATOR

Drug: sintilimab (after the change)

Interventions

sintilimab (after the change) DRUG

0.3mg/kg，I.V.，single dose

sintilimab (before the change)

sintilimab (before the change) DRUG

0.3mg/kg，I.V.，single dose

sintilimab (after the change)

Eligibility Criteria

• Age: 18 Years - 45 Years
• Gender Eligibility Details: Age≥18 years and ≤45 years, healthy male subjects
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Males aged 18 to 45 (including both ends);
• Body Mass Index (BMI) is 19.0\~28.0 kg/m2 (including both ends), and body weight is 62.0\~73.0kg (including both ends);
• The investigator is assessed as a healthy male subject based on a complete medical history, including physical examination, vital signs, 12-lead electrocardiogram and laboratory tests;
• Subjects agree to use reliable contraceptive measures (such as abstinence, sterilization, contraceptives, injectable contraceptive medroxyprogesterone or subcutaneous implant contraception, etc.) during the study period and within 6 months after the study drug infusion. );
• Fully understand the purpose of the trial, understand the pharmacological effects of the study drug and possible adverse reactions; and abide by the trial process and voluntarily sign the informed consent.

You may not qualify if:

• Those with a history of chronic liver, kidney, cardiovascular, neurological/mental, digestive tract, respiratory, urinary, endocrine and other systemic diseases;
• Those with a history of autoimmune diseases (see Annex 1);
• Regular drinkers within 6 months prior to screening (regular drinkers are defined as drinking more than 2 units per day on average, or drinking more than 14 units per week on average: 1 unit = 360ml of beer or 45ml of alcohol for 40 % above spirits or 150ml wine);
• Subjects who have had opportunistic infections within 6 months before screening (such as: herpes zoster, active cytomegalovirus, Pneumocystis carinii, histoplasma, aspergillus, mycobacteria, etc. );
• Known history of recurrent or chronic infection, history of chronic or recurrent infection, including but not limited to: chronic kidney infection, chronic chest infection (such as bronchiectasis), sinusitis, recurrent urinary tract infection, Open, draining or infected skin wounds;
• Those with a history of acute infection within 2 weeks before screening;
• A history of malignant tumor, unless it is a skin squamous cell carcinoma or basal cell carcinoma that has been successfully resected and has no evidence of metastasis;
• Those who are suspected or confirmed to be allergic or have had severe drug or food allergy reactions in the past, have a clear history of allergies and/or are allergic to the study drug or its components after inquiries;
• Have used any drugs (including traditional Chinese medicines and vitamins) within 2 weeks before screening, or the last medication is less than 5 half-lives of the drug from the test administration day, whichever is longer;
• Those who have used anti-PD-1/PD-L1 drugs in the past;
• Those who have participated in other interventional clinical trials within 3 months before screening;
• Those who lost blood, donated blood or received any blood product transfusion of ≥400 ml within 3 months before screening;
• Those who received major surgery or hospitalization due to illness within 3 months before screening;
• Those who have been vaccinated with live vaccines within 6 months before screening, or who are expected to receive live vaccines during the study period;
• Those with a history of drug abuse or positive drug screening results within 12 months before screening;

Sponsors & Collaborators

• Innovent Biologics (Suzhou) Co. Ltd.: lead

Study Sites (1)

Hunan Cancer Hospital

Changsha, Hunan, 410006, China

Location

MeSH Terms

Interventions

sintilimab

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: QUADRUPLE
• Who Masked: PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
• Purpose: OTHER
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: March 22, 2022
• First Posted: April 20, 2022
• Study Start: April 13, 2022
• Primary Completion: May 24, 2023
• Study Completion: July 24, 2023
• Last Updated: August 21, 2023

Record last verified: 2022-12

Data Sharing

• IPD Sharing: Will not share

Locations

CN (1)