Deze pagina is automatisch vertaald en de nauwkeurigheid van de vertaling kan niet worden gegarandeerd. Raadpleeg de Engelse versie voor een brontekst.

Phase 1 Study of Allo-RevCAR01-T-CD123 in Patients With Selected CD123 Positive Hematologic Malignancies (1b Dose Expansion) (RevSTAR-123)

21 september 2026 bijgewerkt door: AvenCell Europe GmbH

Multicenter, open-label, fase 1-onderzoek van Allo-RevCAR01-T-CD123 bestaande uit genetisch gemodificeerde T-cellen die reverse chimere antigeenreceptoren dragen (Allo RevCAR01 T) in combinatie met CD123-doelmodule (R-TM123) voor de behandeling van patiënten met Geselecteerde hematologische maligniteiten Positief voor CD123

The Allo-RevCAR01-T-CD123 drug is a combination of a cellular component (Allo-RevCAR01-T) with a recombinant antibody derivative (R-TM123), which together form the active drug. The cellular component Allo-RevCAR01-T consists of an allogeneic human T-cell genetically multi-edited and expressing a reversed, universal chimeric antigen receptor (RevCAR) presenting an extracellular peptide epitope (RevCAR epitope). R-TM123 functions as a bridging module between Allo-RevCAR01-T and a CD123-expressing target cancer cell by selectively binding the RevCAR epitope and CD123.

Studie Overzicht

Toestand

Werving

Conditie

Interventie / Behandeling

Studietype

Ingrijpend

Inschrijving (Geschat)

37

Fase

  • Fase 1

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studiecontact

Studie Contact Back-up

Studie Locaties

  • Duitsland
      • Cologne, Duitsland, 50937
        • Voltooid
        • Universitätsklinikum Köln
      • Essen, Duitsland, 45147
      • Frankfurt, Duitsland, 60590
      • Hamburg, Duitsland, 20246
        • Nog niet aan het werven
        • Universitätsklinikum Hamburg-Eppendorf
        • Contact:
      • Hanover, Duitsland
      • Heidelberg, Duitsland, 69120
    • Baden-Wurttemberg
      • Ulm, Baden-Wurttemberg, Duitsland, 89081
    • Bavaria
      • Munich, Bavaria, Duitsland, 81377
      • Würzburg, Bavaria, Duitsland, 97080
        • Werving
        • Universitätsklinikum Würzburg
        • Contact:
    • Hesse
      • Marburg, Hesse, Duitsland, 35032
    • Saxony
      • Dresden, Saxony, Duitsland, 01307
    • State of Berlin
      • Berlin, State of Berlin, Duitsland, 13353
  • Nederland
    • Gelderland
      • Rotterdam, Gelderland, Nederland, 3015
    • HV
    • RB Groningen
      • Groningen, RB Groningen, Nederland, 9700
        • Voltooid
        • University Medical Center Groningen (UMCG)

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

18 jaar en ouder (Volwassen, Oudere volwassene)

Accepteert gezonde vrijwilligers

Nee

Geslachten die in aanmerking komen voor studie

Allemaal

Beschrijving

Inclusion Criteria (Dose Expansion):

1. Male or female participants, age ≥18 years. 2. HLA type of participant must match at HLA B and C loci 3. Participants with CD123+ AML with morphologically relapsed or refractory disease (>5% BM blasts). CD123 positivity is defined as ≥20% of leukemic cells expressing CD123 at any point in the course of disease.

  1. Up to third relapse for whom all standard or life-extending therapies have failed and for whom no potentially curative therapies are available or who are intolerant to such therapies.
  2. Without prior myeloproliferative neoplasm (MPN) or MDS/MPN (including leukemic transformation of MPN, "blast phase", and "accelerated phase" MPN), and without hyperproliferative disease requiring cytoreductive treatment within 4 weeks from the screening or with WBC above ULN at screening.
  3. Exceptions to minimum CD123 expression are not allowed. 4. Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1. 5. Life expectancy of at least 3 months in the judgment of the investigator. 6. Adequate renal and hepatic laboratory assessments. 7. Adequate cardiac function. 8. Long-term central venous access existing (e.g., tunneled CV catheter or port-system) or willing to have such a device inserted to ensure continuous R-TM123 administration.

9. Able to give written informed consent. 10. Weight is greater than the minimum weight required for a specific batch to ensure that the dose administered does not exceed 10^5 TCR+ cells/kg of patient weight.

11. Negative pregnancy; routinely using a highly effective method of birth control.

Exclusion Criteria (Dose Expansion):

  1. Acute promyelocytic leukemia (t15;17) or myeloproliferative neoplasm (MPN) per WHO 2022 diagnostic criteria.
  2. AML with only extramedullary manifestations (e.g., chloroma, primary myeloid sarcoma).
  3. Active manifestation of AML in the central nervous system.
  4. Bone marrow failure syndromes.
  5. Cardiac disease: heart failure (New York Heart Association III or IV); unstable coronary artery disease, myocardial infarction, or serious cardiac ventricular arrhythmias requiring anti-arrhythmic therapy within the last 6 months prior to study entry.
  6. Active pulmonary disease with clinically relevant hypoxia (SpO₂ <92% on room air or daily need for supplemental oxygen).
  7. Parkinson's disease or epilepsy with clinical symptoms in the previous 6 months .
  8. Stroke, seizure, or intracranial hemorrhage in the past 12 months.
  9. History or presence of disseminated intravascular coagulation (DIC), deep vein thrombosis or thromboembolism within 3 months prior to start of treatment.
  10. Active infectious disease considered by investigator to be incompatible with protocol or being contraindications for lymphodepletion therapy
  11. Presence of hemorrhagic cystitis
  12. Other toxicity from prior anticancer treatment has not resolved to Grade ≤1 or baseline.
  13. Allogeneic stem cell transplantation within last 2 months or GvHD requiring systemic immunosuppressive therapy.
  14. Vaccination with live viruses < 2 weeks prior to lymphodepletion therapy.
  15. Major surgery within 28 days prior to start of R-TM123 infusion.
  16. Prior malignancy in the past 3 years or any malignancy requiring ongoing active therapy other than adjuvant endocrine therapy. Participants with malignancy within the last 3 years, but with resected or ablated tumors, such as basal cell carcinoma of skin, carcinoma-in-situ of the cervix, or other tumors considered cured may be considered for the study with Sponsor approval.
  17. Treatment with any investigational drug substance or experimental therapy within 4 weeks or 5 half-lives (whichever is shorter) of the substance prior to lymphodepletion.
  18. Treatment with anti-leukemic therapy within 4 weeks or 5 half-lives (whichever is shorter) prior to lymphodepletion.
  19. Prior treatment with gene modified cell products.
  20. Autoimmune diseases requiring systemic steroids or other systemic immunosuppressants.
  21. Pregnant or breastfeeding women.
  22. Psychologic disorders with treatment modifications required within the last 3 months, drug and/or significant active alcohol abuse as per investigator's medical judgement. Depression or anxiety due to presence of the underlying malignancy may be exempted with Sponsor approval.
  23. History of human immunodeficiency virus (HIV) or human T-lymphotropic virus (HTLV) or active/chronic infection with hepatitis C virus (HCV) or hepatitis B virus (HBV).
  24. Known presence of autoantibodies against lupus La protein (La)/ Sjögren syndrome type B antigen (SS-B) or presence or history of autoimmune diseases associated with such antibodies. (Results from recent sampling are not required for eligibility unless MH or other facts indicate La/SS-B would likely be positive.)
  25. Known hypersensitivity to cellular component (Allo-RevCAR01-T) and/or TM (R-TM123) excipients or to compounds of the lymphodepletion therapy, tocilizumab, or corticosteroids.
  26. Evidence that the participant is not likely or able to follow the study protocol (e.g., lacking compliance) in the judgment of the investigator.
  27. Participant unable to understand the informed consent and possible consequences of the participation in the clinical trial in the judgment of the investigator.

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: NVT
  • Interventioneel model: Opdracht voor een enkele groep
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: Allo-RevCAR01-T-CD123 treatment

Following lymphodepleting therapy (from Day -5 to Day -3), R-TM123 will be administered as continuous infusion from Cycle 1 Day 1 and then will continue for 20 days. Allo-RevCAR01-T will be administered on Day 1.

All participants who tolerate Cycle 1 of R-TM123 and Allo-RevCAR01-T without clear disease progression or safety or other contraindications after Cycle 1, will be considered for consolidation cycles of up to 12 consecutive days each of continuous IV infusion of R-TM123 until relapse, unacceptable toxicity, potentially curative treatment option (alloHSCT), consent withdrawal, or maximum one-year overall treatment time (whichever occurs first).
Ander: Cyclophosphamide (Non-IMP, Lymphodepletion)

Intravenous infusion over 3 days (d-5 to d-3)

Ander: Fludarabine (Non-IMP, Lymphodepletion)

Intravenous infusion over 3 days (d-5 to d-3)

Geneesmiddel: R-TM123

Intravenous infusion over 20 days

Andere namen:
  • R-TM123 is een onderdeel van de behandeling met Allo-RevCAR01-T-CD123
Geneesmiddel: Allo-RevCAR01-T

Allo-RevCAR01-T will be administered as IV infusion on Treatment Day 1

Andere namen:
  • Allo-RevCAR01-T is een onderdeel van de behandeling met Allo-RevCAR01-T-CD123

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Safety and tolerability
Tijdsspanne: At the end of cycle 1 (in total 28 days, given no treatment interruptions)

Incidence and intensity of adverse events (AEs) graded according to Common Terminology Criteria for Adverse Events (CTCAE) Version 5.0, except for cytokine release syndrome (CRS), immune effector cell associated neurotoxicity syndrome (ICANS), tumor lysis syndrome, and graft versus host disease (GvHD), which will be graded according to widely accepted specialized criteria
At the end of cycle 1 (in total 28 days, given no treatment interruptions)

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Response rate to consolidation treatment cycles
Tijdsspanne: At any timepoint until end of study (6 months after the end of last R-TM123 administration)
  • Complete remission (CR, CRc, CRh, CRi, CRMRDneg, CRMRDpos)
  • Morphologic leukemia free state (MLFS),
  • Partial remission (PR)
  • Overall response rate (ORR)
  • Best response rate
  • Duration of response
At any timepoint until end of study (6 months after the end of last R-TM123 administration)
Survival rates
Tijdsspanne: At end of study visit (6 months after the end of last R-TM123 administration)
  • Progression free survival
  • Overall survival
At end of study visit (6 months after the end of last R-TM123 administration)
Evidence of biological and clinical activity including best response rate
Tijdsspanne: At any timepoint until end of study (6 months after the end of last R-TM123 administration)
  • Complete remission (CR, CRh, CRi, CRMRDneg, CRMRDpos)
  • Morphologic leukemia free state (MLFS)
  • Partial remission (PR)
  • Overall response rate (ORR)
  • Best response rate
  • Duration of response
  • PFS
  • OS
At any timepoint until end of study (6 months after the end of last R-TM123 administration)

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Sponsor

AvenCell Europe GmbH

Medewerkers

Allucent (NL) BV

Onderzoekers

  • Studie directeur: Manfred Klevesath, MD, AvenCell Therapeutics, Inc.

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

3 januari 2024

Primaire voltooiing (Geschat)

1 mei 2027

Studie voltooiing (Geschat)

1 januari 2028

Studieregistratiedata

Eerst ingediend

23 juni 2023

Eerst ingediend dat voldeed aan de QC-criteria

14 juli 2023

Eerst geplaatst (Werkelijk)

17 juli 2023

Updates van studierecords

Laatste update geplaatst (Werkelijk)

24 september 2026

Laatste update ingediend die voldeed aan QC-criteria

21 september 2026

Laatst geverifieerd

1 september 2026

Meer informatie

Termen gerelateerd aan deze studie

Aanvullende relevante MeSH-voorwaarden

Andere studie-ID-nummers

  • AVC-201-01
  • 2022-501797-19-00 (Andere identificatie: EU CT Number)

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

Abonneren