Safety and Efficacy Study of NGGT003 in Hemophilia A Patients

Prior treatment

• Plan major surgery within 52 weeks;
• Previous gene therapy treatment;
• Participation in any other clinical trial before the screening and have taken medication within four weeks or five half-lives of the study drug;

Other illness

• Positive for hepatitis B surface antigen, hepatitis C, human immunodeficiency virus (HIV)，syphilis test;
• History of being positive for FVIII inhibitors;
• Have other bleeding factors except hemophilia;
• Have contraindications to glucocorticoid, including but not limited to allergy to glucocorticoids, epilepsy, new unhealed fractures, in trauma repair period, uncontrolled infection, severe osteoporosis, etc, which assessed and determined by the investigators;
• Have serious diseases or active infections in cardiovascular, respiratory, digestive tract, endocrine, renal, blood, nervous, mental and other systems before screening;
• With hepatitis, cirrhosis, liver cancer or other major liver diseases;
• History of malignant tumors;
• Any other condition that may not be appropriate for the study in the opinion of the investigator.

Lab values

• Clinically significant abnormalities in liver function test: alanine aminotransferase (ALT) \>1.5 × upper limit of normal (ULN) and/or aspartate aminotransferase (AST) \>1.5× ULN;TBil）\>1.5×ULN；Serum creatinine (Scr) \>1.5×ULN; hemoglobin \<110g/L, platelets \<10e9/L;
• History of allergy to human albumin;
• Abnormal and clinical significant vital signs, physical examination, laboratory examination or other related examination results during the screen, which are not suitable for trial according to the investigator;

• Voluntarily sign the informed consent form;
• Male, age ≥18 years old;
• Diagnosed with hemophilia A according to the "Guidelines for Diagnosis and Treatment of Hemophilia A (2022 Edition)", and the endogenous FVIII activity level was \<1 IU/dL (\<1%);
• The exposure days (EDs) of treatment with any recombinant or plasma-derived FVIII product were ≥150 days;
• Anti-AAV neutralizing antibody titer ≤1:5, binding antibody titer ≤1:100;
• Bleeding events and/or FVIII product injections have occurred within 12 weeks before screening;
• No history of allergy to FVIII products;
• FVIII inhibitor titer﹤0.6BU/mL;
• Commitment to use other drugs during the study requires the consent of the investigator;
• Willing and able to comply with study procedures and requirements;
• Willing to use effective contraceptive methods within 52 weeks after administration.