- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT07847411
Study of Velaglucerase Beta ERT in Children With Gaucher Disease
A Multi-center, Open-label Study to Evaluate the Safety and Efficacy of Velaglucerase Beta Enzyme Replacement Therapy in Children With Gaucher Disease
This is a Phase 3, multicenter, open-label, single-arm study to evaluate the safety, efficacy, PK, PD, and immunogenicity of velaglucerase beta in untreated children with GD1 or GD3 for 39 weeks.
Studieöversikt
Status
Intervention / Behandling
Studietyp
Inskrivning (Beräknad)
Fas
- Fas 3
Kontakter och platser
Studiekontakt
- Namn: Charlene Song
- Telefonnummer: +86 18817946880
- E-post: xiaoling.song@canbridgepharma.com
Studera Kontakt Backup
- Namn: Amelia Zhou
- Telefonnummer: +86 18016327369
- E-post: feng.zhou@canrbdigepharma.com
Studieorter
-
-
Shanghai Municipality
-
Shanghai, Shanghai Municipality, Kina
- Room 202, 2nd Floor, 780 Cailun Road, Pilot Free Trade Zone
-
Kontakt:
- Amelia Zhou
- Telefonnummer: +86 18016327369
- E-post: feng.zhou@canrbdigepharma.com
-
-
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
Tar emot friska volontärer
Kön som är behöriga för studier
Beskrivning
Inclusion Criteria:
-
Subject has a documented diagnosis of GD1 or GD3 according to the diagnostic criteria of the Expert Consensus on the Diagnosis and Treatment of Gaucher Disease in Chinese Children 2021;
-
Written informed consent provided by the subject's parent/legally authorized representative;
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Subject is less than 12 years of age;
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Subject has GD-related splenomegaly, defined as at least 2 to 3 cm below the left costal margin by palpation, and one or more of the following:
- GD-related anemia, with a decrease of ≥1 g/dL in hemoglobin concentration below the lower limit of normal for age of the central laboratory; or
- GD-related hepatomegaly by palpation; or
- GD-related thrombocytopenia, with a platelet count < 100 × 10^9/L;
-
Subject has not received ERT or SRT for at least 3 months prior to screening; Female subjects of childbearing age have a negative serum pregnancy test during screening.
Exclusion Criteria:
- Treatment with investigational drugs (including ambroxol) within 30 days or 5 half-lives, whichever is longer, prior to screening;
- Subjects have received erythropoietin, whole blood transfusion or transfusion of red blood cells, or long-term (continuous treatment for more than 3 months) systemic corticosteroids 3 months prior to screening; or received a platelet transfusion within 1 month prior to screening;
- Subject has non-Gaucher disease-related anemia (such as due to iron, folic acid, and/or vitamin B12 deficiency or infection/immune-mediated reasons);
- Subject has had a prior hepatectomy and/or splenectomy (including partial liver and/or splenectomy) or plans to have a hepatectomy and/or splenectomy (including partial liver and/or splenectomy) during the study;
- Subject has received organ transplantation, including hematopoietic stem cell transplantation;
- Subject has had a history of CTCAE Grade 3 or above infusion-related reaction or hypersensitivity reaction to imiglucerase or other ERTs (approved or experimental).
- Injection with a live vaccine within 30 days of the first study dose.
Studieplan
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: N/A
- Interventionsmodell: Enskild gruppuppgift
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Experimentell: velaglucerase beta 60 U/kg
This is a single-arm study. All subjects will receive velaglucerase beta 60 U/kg IV Q2W for 37 weeks. |
All subjects will receive velaglucerase beta 60 U/kg IV Q2W for 37 weeks with two weeks of follow-up through Week 39 (9 months). |
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Primary Endpoints
Tidsram: From Baseline to Week 39
|
Incidence and number of TEAE, characterized by type, severity, seriousness (SAE), and relatedness to velaglucerase |
From Baseline to Week 39
|
|
Mean percent change in MN spleen volume
Tidsram: From Baseline to Week 39
|
Normal spleen volume = 0.2% body weight. Multiples of normal (MN) spleen volume= actual MRI testing volume / normal spleen volume |
From Baseline to Week 39
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Mean change in hemoglobin concentration (g/dL)
Tidsram: From baseline to Week 39
|
From baseline to Week 39
|
|
|
Mean percent change in MN liver volume
Tidsram: From Baseline to Week 39
|
Normal liver volume = 2.5% body weight. Multiples of normal (MN) liver volume= actual MRI testing volume / normal liver volume |
From Baseline to Week 39
|
|
Mean percent change in platelet count ( 10^9/L)
Tidsram: From Baseline to Week 39
|
From Baseline to Week 39
|
|
|
Mean change in height Z-score
Tidsram: From Baseline to Week 39
|
From Baseline to Week 39
|
|
|
Mean change in weight Z-score
Tidsram: From Baseline to Week 39
|
From Baseline to Week 39
|
Samarbetspartners och utredare
Sponsor
Studieavstämningsdatum
Studera stora datum
Studiestart (Beräknad)
Primärt slutförande (Beräknad)
Avslutad studie (Beräknad)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Faktisk)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Nyckelord
Ytterligare relevanta MeSH-villkor
- Hjärnsjukdomar
- Sjukdomar i centrala nervsystemet
- Sjukdomar i nervsystemet
- Metabolism, medfödda fel
- Genetiska sjukdomar, medfödda
- Metaboliska sjukdomar
- Lipidmetabolismstörningar
- Lysosomala lagringssjukdomar
- Hjärnsjukdomar, metabola, medfödda
- Hjärnsjukdomar, metaboliska
- Lipidmetabolism, medfödda fel
- Lysosomala lagringssjukdomar, nervsystemet
- Sfingolipidoser
- Lipidoser
- Medfödda, ärftliga och neonatala sjukdomar och abnormiteter
- Närings- och metabola sjukdomar
- Gauchers sjukdom
Andra studie-ID-nummer
- CAN103-GD-301
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
IPD-planbeskrivning
only IPD used in the results publication
Tidsram för IPD-delning
Beginning 3 months and ending 3 years after the publication of results
Kriterier för IPD Sharing Access
The criteria that must be met the types of analyses that qualify for data sharing.
A proposal that describes planned analyses must be submitted.
IPD-delning som stöder informationstyp
- STUDY_PROTOCOL
- SAV
Läkemedels- och apparatinformation, studiedokument
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