A Study to Evaluate the Pharmacokinetics，Safety and Tolerability of PEG Recombinant Human Coagulation Factor VIII-Fc Fusion Protein for Injection

Severe Hemophilia A Clinical Trial

Official title:

An Open-Label, Multicenter Evaluation of the Pharmacokinetics，Safety and Tolerability of PEG Recombinant Human Coagulation Factor VIII-Fc Fusion Protein for Injection (FRSW117) in Patients With Severe Hemophilia A.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04864743
• Other study ID #: CTR20210830
• Status: Completed
• Phase: Phase 1
• Start date: June 22, 2021
• Est. completion date: October 17, 2021

Study information

• Verified date: May 2023
• Source: Jiangsu Gensciences lnc.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The primary objectives of the study are to evaluate the Pharmacokinetics，Safety and tolerability of PEG Recombinant Human Coagulation Factor VIII-Fc Fusion Protein for Injection (FRSW117) in patients with severe hemophilia A. The secondary objectives are to monitor anti-durg antibodies and anti-PEG antibodies levels in patients with severe hemophilia A

Recruitment information / eligibility

• Status: Completed
• Enrollment: 13
• Est. completion date: October 17, 2021
• Est. primary completion date: October 17, 2021
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 12 Years to 65 Years

Eligibility

Inclusion Criteria:

• Patients with clinically confirmed hemophilia A (coagulation factor VIII <1%) and previous medical records confirming exposure to coagulation factor VIII for =150 days (EDs =150).
• Non-immunodeficient, with some immunity (CD4 > 200/µL).
• Platelet count >100×10^9/L.
• Normal prothrombin time (PT) or international normalized ratio (INR) <1.3.
• Negative lupus anticoagulant.
• Fully understand, informed about this study and sign the informed consent form, voluntarily participate in the clinical study and have the ability to complete all study procedures

Exclusion Criteria:

• Hypersensitivity to the test substance or its excipients (including rodent or hamster protein).
• Pre-existing hypersensitivity or allergic reactions to FVIII or IgG2 injection therapy.
• Positive FVIII inhibitor at screening (=0.6 BU/mL), or previous history of FVIII inhibitor Positive history, or family history of inhibitors.
• Patients with other coagulation disorders in addition to hemophilia A.
• The results of vWF antigen examination lower than normal.
• Severe anemia and need blood transfusion (hemoglobin < 60g/L).
• Patients who have received any standard half-lives FVIII formulations (e.g., Kogenate, Kovaltry, Advate, Xyntha, etc.) or received any other half-life-extending FVIII formulations within 4 days or 5 half-lives (whichever is longer) before administration.
• Patients who had used emecizumab within 6 months prior to administration.
• Patients with fever, upper respiratory tract infection or allergy symptoms within the previous 2 weeks before screening.
• Suffer from other diseases that may increase the risk of bleeding or the risk of thrombosis.
• Severe cardiovascular and cerebrovascular diseases: such as cerebral hemorrhage, stroke, myocardial infarction, unstable angina pectoris, congestive heart failure(the current New York Heart Association cardiac function grade III, Hypertension that cannot be controlled with drug treatment: systolic blood pressure> 160 mmHg or diastolic blood pressure> 95 mmHg.
• Clinically significant of other systematic diseases: alcoholism, drug abuse, mental disorders and mental retardation.
• Significant hepatic or renal impairment (ALT and AST > 2×ULN; serum bilirubin level > 3 × upper limit of normal (ULN)).
• Abnormal kidney function: BUN > 2×ULN, Cr > 2.0mg/dL.
• One or more clinically significant tests for Hepatitis B Virus Surface Antigen, Human Immunodeficiency Virus (HIV), Antisyphilitic spirulina (TPHA) and Hepatitis C Virus (HCV) Antibody.
• Patients who received any anticoagulant or antiplatelet therapy within a week prior screening or need to receive an anticoagulant or antiplatelet therapy during the period of clinical trials.
• Systemic immunomodulators (e.g., corticosteroids [equivalent dose of 10 mg/ day prednisone], A-interferon, immunoglobulin, cyclophosphamide, cyclosporine, etc.) were used within 14 days prior to administration or during the study period.
• Patients having major surgery or receiving blood or blood components transfusion within 4 weeks prior screening or having planned major surgery schedule during the study.
• Patients who previously participated in the other clinical trials within a month prior screening.
• Any life-threatening disease or condition which, according to the investigator's judgment, could not benefit from the trial participation.
• Patient who is considered by the other investigators not suitable for clinical study.

Related Conditions & MeSH terms

• Hemophilia A
• Severe Hemophilia A

Intervention

Drug:
• ADVATE
a single dose.
• FRSW117
a single dose.

Locations

Country	Name	City	State
China	Nanfang Hospital of Southern Medical University	Guangzhou	Guangzhou
China	Jinan central hospital	Jinan	Shandong
China	Institute of Hematology & Blood Diseases Hospital Chinese Academy of Medical Sciences & Peking Union Medical College.	Tianjin	Tianjin
China	People's Hospital of Zhengzhou	Zhengzhou	Henan

Sponsors (1)

Lead Sponsor	Collaborator
Jiangsu Gensciences lnc.

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Cmax from time 0 to the last data point for FRSW117 Measured by One-Stage Clotting Assay.	Maximum plasma activity during a dosing interval for participants.	Pre-dose to 216 hours after the end of the infusion for Arm1; Pre-dose to 288 hours after the end of the infusion for Arm2
Primary	Arm1 - T½ from time 0 to the last data point for FRSW117 Measured by One-Stage Clotting Assay.	Time required for the activity of the drug to reach half of its original value for participants.	Pre-dose to 216 hours after the end of the infusion for Arm1; Pre-dose to 288 hours after the end of the infusion for Arm2
Primary	Arm1 - CL from time 0 to the last data point for FRSW117 Measured by One-Stage Clotting Assay.	Rate at which the body removes the drug, measured as the volume of the plasma cleared of drug per unit time per unit weight for participants.	Pre-dose to 216 hours after the end of the infusion for Arm1; Pre-dose to 288 hours after the end of the infusion for Arm2
Primary	Arm1 - MRT from time 0 to the last data point for FRSW117 Measured by One-Stage Clotting Assay.	The average time that a drug molecule is present in the systemic circulation for participants.	Pre-dose to 216 hours after the end of the infusion for Arm1; Pre-dose to 288 hours after the end of the infusion for Arm2
Primary	Arm1 - Incremental recovery from time 0 to the last data point for FRSW117 Measured by One-Stage Clotting Assay.	The rise in FVIII activity in IU/dL per unit dose administered in IU/kg for participants.	Pre-dose to 216 hours after the end of the infusion forArm1; Pre-dose to 288 hours after the end of the infusion for Arm2
Primary	Arm1 - Cmax from time 0 to the last data point for ADVATE Measured by One-Stage Clotting Assay.	Maximum plasma activity during a dosing interval for participants.	Pre-dose to 72 hours after the end of the infusion for Arm1; Pre-dose to120 hours after the end of the infusion for Arm2
Primary	Arm1 - T½ from time 0 to the last data point for ADVATE Measured by One-Stage Clotting Assay.	Time required for the activity of the drug to reach half of its original value for participants.	Pre-dose to 72 hours after the end of the infusion for Arm1; Pre-dose to120 hours after the end of the infusion for Arm2
Primary	Arm1 - CL from time 0 to the last data point for ADVATE Measured by One-Stage Clotting Assay.	Rate at which the body removes the drug, measured as the volume of the plasma cleared of drug per unit time per unit weight for participants.	Pre-dose to 72 hours after the end of the infusion for Arm1; Pre-dose to120 hours after the end of the infusion for Arm2
Primary	Arm1 - MRT from time 0 to the last data point for ADVATE Measured by One-Stage Clotting Assay.	The average time that a drug molecule is present in the systemic circulation for participants.	Pre-dose to 72 hours after the end of the infusion for Arm1; Pre-dose to120 hours after the end of the infusion for Arm2
Primary	Arm1 - Incremental recovery from time 0 to the last data point for ADVATE Measured by One-Stage Clotting Assay.	The rise in FVIII activity in IU/dL per unit dose administered in IU/kg for participants.	Pre-dose to 72 hours after the end of the infusion for Arm1; Pre-dose to120 hours after the end of the infusion for Arm2
Primary	Number of participants with treatment-emergent adverse events (TEAEs).	Adverse events in the study were classified and evaluated according to the National Cancer Institute's Common Terminology for Adverse Events (NCI CTCAE V5.0).	assessed up to four weeks after FRSW117 administration.
Secondary	Evaluation of the level of anti-PEG-rF?Fc antibody production in participants		assessed up to four weeks after FRSW117 administration.
Secondary	Evaluation of the level of anti-PEG antibody production in participants		assessed up to four weeks after FRSW117 administration.
Secondary	Number of participants with inhibitor development.	Number of participants who developed a positive FVIII inhibitor level (=0.6 Bethesda unit [BU]) during the study was summarized and classified as participants developing low titer inhibitor (i.e. = 5.0 BU) and participants developing high titer inhibitor (i.e. > 5.0 BU).	assessed up to four weeks after FRSW117 administration.