- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT05860595
Bewertung der Sicherheit und Wirksamkeit der KL003-Zellinjektion bei der Behandlung transfusionsabhängiger β-Thalassämie.
This is a non-randomized, open-label, single-dose study. The aim of this study is to evaluate the safety and efficacy of the treatment with lentiviral vector encoding βA-T87Q-globin gene transduced autologous hematopoietic stem cells in subjects with transfusion-dependent β-thalassemia.
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
Subject participation for this study will be 24 months. Subjects who enroll in this study will be asked to participate in a subsequent 13-year follow-up for gene therapy products.
Studientyp
Einschreibung (Geschätzt)
Phase
- Unzutreffend
Kontakte und Standorte
Studienorte
-
-
Tianjin Municipality
-
Tianjin, Tianjin Municipality, China
- Regenerative Medicine Center
-
-
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
Inclusion Criteria:
- Male or female age between 3-35 years
- Diagnosis of transfusion-dependent β-thalassemia and a history of at least 100 mL/kg/year of pRBCs or ≥8 transfusions of pRBCs per year for the prior 2 years
- Documented baseline, or pretransfusion, Hb level≤7 g/dL
- Karnofsky performance status ≥70 for subjects≥16 years of age; Lansky performance status of ≥70 for subjects<16 years of age
- Eligible to undergo auto-HSCT
- Willing and able to follow the research procedures and conditions, with good compliance
- Willing to receive at least the 2 years follow-up and maintain detailed medical records, including transfusion history
- Subject and/or legal guardians voluntarily participated in this clinical trial and signed the informed consent form, and can complete all follow-up in accordance with the protocol requirements
Exclusion Criteria:
-
Subjects positive with the following etiological tests: human immunodeficiency virus(HIV-1-2), human cytomegalovirus (HCMV-DNA), EB virus (EBV-DNA), HBV (HBsAg/HBV-DNA positive), HCV antibody (HCV-Ab), Treponema pallidum antibody (TP-Ab)
-
Clinically significant and active bacterial, viral, fungal, or parasitic infection as determined by the clinical investigator
-
Contraindication to bone marrow collection
-
Any prior or current malignancy or myeloproliferative or significant immunodeficiency disorder
-
A white blood cell (WBC) count <3×10^9/L, and/or platelet count <100×10^9/L not related to hypersplenism
-
Diagnosis of composite α thalassemia
-
Participants with severe iron overload at the time of screening: severe iron overload of the liver showed by MRI, serum ferritin ≥ 5000 ng/mL, or moderate to severe iron overload of the heart
-
Presence of unusual antibody of red blood cell antigens or tested positive for platelet antibody
-
Meet the criteria for allo-HSCT and with an identified willing donor with a full HLA match
-
Prior receipt of gene therapy or allo-HSCT
-
Immediate family member (i.e. parent or siblings) with a known Familial Cancer Syndrome (including but not limited to hereditary breast and ovarian cancer syndrome, hereditary non-polyposis colorectal cancer syndrome and familial adenomatous polyposis)
-
Diagnosis of a significant psychiatric disorder of the subject that could seriously impede the ability to participate in the study
-
History of major organ damage including:
- Liver function test suggest AST or ALT levels >3× upper limit of normal (ULN);
- Total serum bilirubin value >2.5×ULN;if combined with Gilbert syndrome, total bilirubin >3×ULN and direct bilirubin value >2.5×ULN;
- History of bridging fibrosis, cirrhosis;
- Left ventricular ejection fraction <45%;
- New York Heart Association (NYHA) class III or IV congestive heart failure;
- Severe arrhythmia requiring medical treatment;
- Uncontrolled hypertension or unstable angina pectoris;
- Myocardial infarction or bypass or stent surgery within 12 months before drug administration;
- Valvular disease with clinical significance;
- Baseline calculated eGFR<60mL/min/1.73m2;
- Pulmonary function: FEV1/FVC<60% and/or diffusion capacity of carbon monoxide (DLco) <60% of prediction;
- Evidence of clinically significant pulmonary hypertension requiring medical intervention.
-
Uncorrectable coagulation dysfunction or history of severe bleeding disorder
-
Any other condition that would render the subject ineligible for HSCT, as determined by the attending transplant physician
-
Known allergy to clinical trial drug (plerixafor or G-CSF or busulfan) or ingredient(DMSO etc.)
-
Participation in another clinical study with an investigational drug within 30 days of Screening or participating in another clinical study with an investigational drug
-
Inoculated live vaccine within 6 weeks prior to screening
-
Pregnancy or breastfeeding women; Subjects or their sexual partners were unable to take medically recognized effective contraceptive measures during the 27-month study period
-
The subjects or their parents would not comply with the study procedures outlined in the protocol
-
Receipt of hydroxyurea therapy within 3 months before HSCT harvest
-
Patients considered to be ineligible for the study by the investigator for reasons other than the above
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: N / A
- Interventionsmodell: Einzelgruppenzuweisung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Experimental: KL003 cell injection Drug Product
Each recruited subject will accept KL003 Transplantation. |
Transplant of auto-HSC transduced with lentiviral vector encoding βA-T87Q-globin gene. |
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Transplantationsbedingte Mortalität innerhalb von 100 Tagen und innerhalb eines Jahres nach Reinfusion des Arzneimittels KL003
Zeitfenster: Bis zu 1 Jahr nach der Transplantation
|
Bis zu 1 Jahr nach der Transplantation
|
|
|
Percentage of participants with successful lentiviral vector transduced CD34+ stem cell engraftment
Zeitfenster: Up to 42 days post transplant
|
Successful engraftment was defined as neutrophil count [ANC] ≥0.5×10^9/L for 3 consecutive days |
Up to 42 days post transplant
|
|
Engraftment time of neutrophil
Zeitfenster: Up to 42 days post transplant
|
The first day when neutrophils ≥ 0.5×10^9/L for 3 consecutive days |
Up to 42 days post transplant
|
|
Engraftment time of platelet
Zeitfenster: Up to 42 days post transplant
|
The first day of platelet count ≥ 20.0×10^9/L for 7 consecutive days after platelet transfusion independence |
Up to 42 days post transplant
|
|
The number, frequency and severity of adverse events (AE) within 1 year after reinfusion of KL003 drug products
Zeitfenster: Up to 24 months post transplant
|
Frequency and severity of AEs & SAEs identified according to NCI CTCAE 5.0 |
Up to 24 months post transplant
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Die Dauer der Transfusionsunabhängigkeit
Zeitfenster: Bis zu 24 Monate nach der Transplantation
|
Bis zu 24 Monate nach der Transplantation
|
|
|
Veränderungen in der Häufigkeit und dem Volumen von Bluttransfusionen
Zeitfenster: Bis zu 24 Monate nach der Transplantation
|
Bis zu 24 Monate nach der Transplantation
|
|
|
The proportion of participants who meet the definition of transfusion independence (TI) for at least 6 months
Zeitfenster: Up to 24 months post transplant
|
TI is defined as Hb ≥ 90.0 g/L after reinfusion and without disease-related routine blood transfusion for 6 months |
Up to 24 months post transplant
|
Mitarbeiter und Ermittler
Mitarbeiter
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Primärer Abschluss (Geschätzt)
Studienabschluss (Geschätzt)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- IIT2023021
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .