- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT07585071
IASO206 in Patients With Relapsed/Refractory Autoimmune Hemolytic Anemia
6 maj 2026 uppdaterad av: Jun Shi, Institute of Hematology & Blood Diseases Hospital, China
Phase I Clinical Study on the Safety and Tolerability of IASO206 Injection in Patients With Relapsed/Refractory Autoimmune Hemolytic Anemia
This study is an open-label, single-arm early exploratory clinical study, aiming to evaluate the safety, tolerability and preliminary efficacy of IASO206 Injection (In Vivo CAR-T) in Patients with Relapsed/Refractory Autoimmune Hemolytic Anemia
Studieöversikt
Status
Har inte rekryterat ännu
Betingelser
Intervention / Behandling
Studietyp
Interventionell
Inskrivning (Beräknad)
18
Fas
- Fas 1
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studiekontakt
- Namn: Lele Zhang, PhD
- Telefonnummer: 15811139278
- E-post: zhanglele@ihcams.ac.cn
Studera Kontakt Backup
- Namn: Jun Shi, PhD
- Telefonnummer: 13752253515
- E-post: shijun@ihcams.ac.cn
Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
- Vuxen
- Äldre vuxen
Tar emot friska volontärer
Nej
Beskrivning
Inclusion Criteria:
- Age 18 to 75 years, gender unrestricted.
- Diagnosis of AIHA (including warm antibody type, warm-cold antibody type, cold agglutinin disease) or Evans syndrome, consistent with Chinese Expert Consensus on Diagnosis and Treatment of Autoimmune Hemolytic Anemia (2023), 2019 International Consensus for Diagnosis and Management of Autoimmune Hemolytic Anemia (Blood Rev, 2020), or Chinese Expert Consensus on Diagnosis and Treatment of Evans Syndrome (2024 Edition).
- Patients with relapsed/refractory disease after multiple lines of therapy must meet all of the following criteria: hemoglobin < 10 g/dL with clinical manifestations of hemolytic anemia; prior treatment with at least 2 immunosuppressive drugs (must include CD20 monoclonal antibody); glucocorticoid therapy for at least 3 months (excluded are patients with contraindications to glucocorticoids, severe infection, severe osteoporosis, previous fracture, or inability to tolerate glucocorticoids); cumulative dose of CD20 monoclonal antibody at least 375 mg/m² × 4, or total dose 2.0 g, or at least 6 administrations (at least 1 week apart each time).
- ECOG score ≤ 2.
- Expected survival time ≥ 12 weeks.
- Adequate organ function confirmed by laboratory tests: serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 1.5 × upper limit of normal (ULN); minimum pulmonary reserve defined as grade ≤ 1 dyspnea and oxygen saturation ≥ 93% without oxygen supplementation; creatinine clearance (estimated by Cockcroft-Gault) ≥ 45 mL/min; cardiac ejection fraction ≥ 50%, no pericardial effusion on echocardiogram (ECHO), and no clinically significant abnormal electrocardiogram (ECG).
- Subjects and their partners agree to use effective barrier or medical contraceptive measures (excluding rhythm method) from signing informed consent until 1 year after administration.
- Subjects must provide written informed consent approved by the Ethics Committee prior to initiation of screening procedures
Exclusion Criteria:
- Subject with confirmed lymphoproliferative neoplasms.
- Subject with secondary AIHA induced by drugs or infection.
- Subject with congenital immunodeficiency diseases, other hereditary or acquired hemolytic diseases.
- Subject with a history of organ or stem cell transplantation.
- Subject with a history of organ infarction within the past 6 months.
- Subject who have received prior BCMA-targeted therapy.
- Subject who received plasma cell-targeted cell therapy within 3 months before screening, or in whom prior cell therapy products are still detectable in peripheral blood.
Subject who received any of the following treatments within the specified periods prior to study enrollment:
- Anti-CD20 monoclonal antibody < 12 weeks;
- Sutimlimab or other marketed biological products < 5 half-lives;
- Plasma exchange < 4 weeks;
- Splenectomy < 12 weeks.
Subject with any of the following cardiovascular diseases:
- Left ventricular ejection fraction (LVEF) ≤ 45%;
- Active heart disease or congestive heart failure (New York Heart Association [NYHA] Class III or IV);
- Severe arrhythmia requiring treatment (excluding atrial fibrillation, paroxysmal supraventricular tachycardia);
- QTcB interval ≥ 450 ms for males, ≥ 470 ms for females;
- Myocardial infarction, bypass surgery, or stent implantation within 6 months before study;
- Other cardiac diseases judged by the investigator to be unsuitable for enrollment.
- Unstable systemic diseases judged by the investigator, including but not limited to severe hepatic or renal diseases requiring medical treatment.
Subject with a history of other primary malignancies within 5 years before screening, except:
- Resected and cured non-melanoma skin cancer (e.g., basal cell carcinoma);
- Cured carcinoma in situ (e.g., cervical, bladder, or breast cancer);
- Other primary cancers with no evidence of recurrence for more than 5 years after treatment.
- Subject who underwent major surgery within 4 weeks before screening and are judged unsuitable for enrollment by the investigator.
- Subject with uncontrolled active fungal, viral, bacterial, mycobacterial, or other infections (persistent infection-related signs/symptoms without improvement after appropriate anti-infective therapy) or infections requiring intravenous anti-infective therapy.
- Positive hepatitis B surface antigen (HBs-Ag) or hepatitis B e antigen (HBe-Ag); positive hepatitis B e antibody (HBe-Ab) or hepatitis B core antibody (HBc-Ab) with HBV-DNA copy number above the lower limit of quantification; positive hepatitis C (HCV) antibody; positive human immunodeficiency virus (HIV) antibody; active syphilis infection (excluding those with only positive syphilis-specific antibody).
- Subject who received live viral vaccines within 4 weeks before enrollment.
- Subject who are participating in other interventional clinical studies during IASO206 Injection treatment with a drug half-life < 5; subject receiving active investigational drugs during the entire study period, or who intend to participate in another clinical trial, or receive treatments outside the protocol.
- Pregnant or lactating females.
- Subject with psychiatric disorders, disturbance of consciousness, or central nervous system diseases, including but not limited to epilepsy and Parkinson's disease.
- Subject with hypersensitivity to components of IASO206 Injection or supportive medications required for the management of CAR-T therapy-related toxicities (e.g., tocilizumab).
- Other conditions judged by the investigator to be unsuitable for enrollment.10. Other Information
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
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: IASO206
Subjects will receive a single infusion of IASO206 injection in a 3+3 dose-escalation design.
Three ascending dose cohorts are planned: 1E8 TU, 3E8 TU, and 5E8 TU.
In each dose cohort, the first subject will be observed for at least 3 weeks after infusion before subsequent subjects in the same cohort receive IASO206 injection.
|
The third-generation self-inactivating lentiviral vector that carries a BCMA-targeted CAR.
Administered in one infusion.
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Incidence and severity of adverse events
Tidsram: Up to 3 months after IASO206 infusion
|
Assessed by CTCAE Version 5.0.
|
Up to 3 months after IASO206 infusion
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Proportion of patients achieving response
Tidsram: At Weeks 4, 8, and 12, and Months 4, 5, and 6 after IASO206 infusion
|
Response assessment is primarily assessed based on hemoglobin, and should be performed after discontinuation of glucocorticoids or other immunosuppressive therapies for at least 2 weeks.
|
At Weeks 4, 8, and 12, and Months 4, 5, and 6 after IASO206 infusion
|
Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart (Beräknad)
15 juni 2026
Primärt slutförande (Beräknad)
31 december 2026
Avslutad studie (Beräknad)
31 december 2028
Studieregistreringsdatum
Först inskickad
6 maj 2026
Först inskickad som uppfyllde QC-kriterierna
6 maj 2026
Första postat (Faktisk)
13 maj 2026
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
13 maj 2026
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
6 maj 2026
Senast verifierad
1 maj 2026
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- IASO206CI003
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
NEJ
Läkemedels- och apparatinformation, studiedokument
Studerar en amerikansk FDA-reglerad läkemedelsprodukt
Nej
Studerar en amerikansk FDA-reglerad produktprodukt
Nej
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