Clinical Study of LY-M001 Injection in the Treatment of Adolescents With Type I Gaucher Disease

Launched by SHANGHAI JIAO TONG UNIVERSITY SCHOOL OF MEDICINE · Jul 25, 2024

Keywords

ClinConnect Summary

This clinical trial is studying a new treatment called LY-M001 injection for adolescents aged 12 to 18 with Type I Gaucher Disease, a genetic disorder that affects how the body breaks down certain fats. The main goals of the study are to check how safe the treatment is, how well it works, and whether it causes any immune reactions in these young patients. The trial is currently looking for participants and includes a main study phase followed by long-term follow-up to monitor effects.

To be eligible, participants must have a confirmed diagnosis of Type I Gaucher Disease, which includes specific genetic mutations and symptoms. They should be newly diagnosed or have previously received treatment, with a gap before starting this study. Participants will need to agree to follow all study procedures and attend follow-up appointments. It's important to note that certain medical conditions or recent treatments may exclude someone from joining the study. This trial offers an opportunity to potentially benefit from a new treatment while contributing to important research in Gaucher Disease.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • 1. The subject and/or parent, caregiver, or legal representative must be willing and able to provide written informed consent/consent for the study in accordance with applicable regulations and guidelines and comply with all study access and procedures, including the use of any data collection devices that can be used to directly record participant data;
• • 2. Gender is not limited, 12 years old ≤ 18 years old;
• • 3. Patients with double allele mutation of glucocerebrosidase gene (GBA1) and decreased glucocerebrosidase activity were confirmed by laboratory tests and met the clinical manifestations of type I Gaucher disease;
• • 4. Subjects were newly treated or treated patients with type I Gaucher disease; For patients treated with enzyme replacement therapy (ERT) or substrate clearance therapy (SRT) before screening, 5 drug half-lives are required before administration;
• • 5. The subject is willing to participate in all study follow-up and comply with all study procedures and evaluations;
• • 6. The subject must be willing to refrain from donating blood, organs, tissues, or cells at any time after receiving treatment;
• • 7. Pregnant Women (WOCBP) subjects tested negative for pregnancy. Note: WOCBP is defined as a female subject who has not achieved postmenopausal status (continuous amenorrhea for at least 12 months with no clear cause other than menopause) after menstruating, and who has no surgical (i.e., bilateral ovariectomy, fallopian tube removal, and/or hysterectomy) or other investigator identified cause of permanent infertility (e.g., mallear tube agenesis).
• Exclusion Criteria:
• • 1. Positive AAV8 neutralizing antibody (antibody titer \> 1:10).
• • 2. Patients with type II or III Gaucher disease (GD2 or GD3), or with suspected Gaucher disease as assessed by the investigator (e.g., subjects with Gaucher disease-related central nervous system manifestations or abnormal electroencephalogram \[EEG\] examination).
• • 3. Active and progressive bone diseases that are expected to require surgical treatment within the next 6 months.
• • 4. The subjects were judged by the investigator to have idiopathic thrombocytopenic purpura (ITP), thrombotic thrombocytopenic purpura (TTP), thrombocytopenia, anemia, hepatomeglia, splenomeglia, and/or osteoporosis unrelated to GD (bone mineral density z-score ±2).
• • 5. Treatment with an investigational drug in another clinical study within 28 days prior to screening or 5 half-lives, whichever is older.
• 6. Evidence of a history of clinically significant liver disease or hepatotoxin exposure that meets, but is not limited to, any of the following at the time of screening:
• • ① Progressive hepatomegaly larger than 3 times the normal volume
• • ② History of stage 2 or above hepatic fibrosis
• • ③AST, ALT, or TBIL were 1.5 times higher than the upper limit of normal (ULN)
• • ④ Immune hepatitis Hepatitis B surface antigen (HBsAg) positive, and hepatitis B virus deoxyribonucleic acid (HBV-DNA) positive (HBV-DNA\>103 copy number /mL); Or take hepatitis B drugs (such as interferon, lamivudine, adefovir and entecavir); Or hepatitis C virus (HCV) antibody positive.
• 7. The subject's blood indicators have any of the following:
• • ① The hemoglobin value was \<8.0 g/dL
• • ② Platelet count \<40 × 109/L
• • 8. Refractory epilepsy.
• • 9. Human immunodeficiency virus (HIV) antibody positive or treponema syphilis antibody positive.
• • 10. Subjects had significant clinical comorbidities (such as malignant tumors, primary biliary cirrhosis, or autoimmune liver disease) that the investigators believed might affect the study data or confounding the findings.
• • 11. Subjects have received or plan to receive bone marrow transplantation, hematopoietic stem cell transplantation, and/or major organ transplantation, including but not limited to liver transplantation, kidney transplantation, etc.
• • 12. 3 months before screening, subjects received treatment with erythropoietin, whole blood transfusion, or red blood cell transfusion; Or received platelet transfusion 1 month before screening.
• • 13. Allergic to any component of LY-M001 injection.
• • 14. Previous treatment with any type of gene therapy or cell therapy.
• • 15. Use of systemic immunosuppressant or steroid therapy within 3 months prior to administration (other than immunosuppressive therapy prescribed for prophylactic administration).
• • 16. Any condition in which the subject is unable to undergo magnetic resonance imaging (MRI) studies (including hypersensitivity to anesthetics or contrast agents).
• • 17. Have received live attenuated vaccine within 4 months prior to screening or plan to receive live attenuated vaccine during clinical trials.
• • 18. Other situations in which the investigator considers the subject inappropriate for study participation.