A Study to Test the Safety, Tolerability and Effect of ZI-MA4-1 for Patients With Locally Advanced or Metastatic Solid Malignancies
A Phase 1, Dose-Escalation, Open-Label Study, Evaluating the Safety and Tolerability of ZI-MA4-1, a TCR-NK Cell Therapy, in HLA-A*02:01 Positive Patients With Inoperable, Locally Advanced, or Metastatic MAGE-A4 Expressing Solid Malignancies
Studienübersicht
Status
Status
Bedingungen
Bedingungen
Intervention / Behandlung
Intervention / Behandlung
Studientyp
Studientyp
Einschreibung (Geschätzt)
Einschreibung
Phase
Phase
- Phase 1
Kontakte und Standorte
Studienkontakt
Studienkontakt
- Name: Zelluna Immunotherapy
- Telefonnummer: +47 413 80 080
- E-Mail: ctinfo@zelluna.com
Studienorte
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London, Vereinigtes Königreich
- Rekrutierung
- The Royal Marsden NHS Foundation Trust
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Kontakt:
- Dr. Furness
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Manchester, Vereinigtes Königreich
- Rekrutierung
- The Christie NHS Foundation Trust
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Kontakt:
- Prof. Thistlethwaite
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Teilnahmekriterien
Zulassungskriterien
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
- Älterer Erwachsener
Akzeptiert gesunde Freiwillige
Beschreibung
Inclusion Criteria:
- HLA-A*02:01 positive
- Tumour(s) show expression of the MAGE-A4 protein above a defined threshold
- Histopathological or cytological diagnosis of inoperable Locally Advanced or Metastatic malignant disease: ovarian cancer, squamous non-small cell lung cancer (NSCLC), synovial sarcoma or head and neck cancer.
- No approved therapy with demonstrated clinical benefit is indicated or available to treat the patient, or the patient is intolerant of or has refused standard of care therapy.
- Documented imaging confirmed disease progression while on or within 6 months after the end of the most recent therapy.
- Participant must have received ≥2 prior lines of cancer therapy except for patient with synovial sarcoma for whom ≥1 prior lines of cancer therapy.
- Measurable disease according to RECIST v1.1 criteria.
- ECOG performance status of 0 or 1 with no deterioration over the previous 2 weeks, and an anticipated life expectancy of >3 months
- Female participants are eligible to participate if they are not pregnant or breastfeeding. Woman of childbearing potential must have negative pregnancy test and agree to use an effective contraceptive method.
Other protocol defined inclusion criteria could apply.
Exclusion Criteria:
- Patients have received any prior cellular or gene therapy.
- Receiving experimental investigational products within 4 weeks of lymphodepletion.
- Recent therapies (within up to 4 weeks prior to lymphodepletion) including biologic agents (such as monoclonal antibodies), anti-cancer immunotherapy (such as monoclonal antibodies against PD-1 receptor or ligand).
- Residual toxicities ≥2 CTCAE grade due to prior therapy, that in the opinion of the investigator may interfere with study conduct.
- Any other active malignancy besides the tumour under study within 3 years prior to screening except for in situ removal of basal cell carcinoma or adequately treated cervix carcinoma in-situ.
- Active or documented history of autoimmune disease or any other diseases requiring immunosuppressive therapy or corticosteroid therapy. Physiological replacement, topical, and inhaled steroids are permitted.
- Significant CNS disorders.
- Myocardial infarction, cardiac angioplasty or stenting, cardiac arrhythmia requiring medication, unstable angina, New York Heart Association Class II or greater congestive heart failure, cardiac atrial or ventricular lymphoma involvement, or other clinically significant cardiac disease within 6 months of enrolment.
- Active fungal, bacterial viral, or other infection requiring intravenous antibiotic, antifungal, or antiviral medication within 7 days prior to lymphodepletion.
- Received or planned to receive a live vaccine ≤6 weeks before the planned start date of lymphodepletion.
- Severe or uncontrolled medical condition (e.g., severe chronic obstructive pulmonary disease, interstitial lung disease , severe Parkinson's disease, active inflammatory bowel disease) or psychiatric condition, which in the opinion of the investigator would interfere with study activities.
- Active bleeding diatheses, including but not limited to therapeutic anticoagulation, and treatment with major surgery within 28 days before lymphodepletion (minor surgical procedures such as lymph node biopsy/excision or catheter placement are permitted).
- Patients have significant immunosuppression
- Known significant hepatic or biliary abnormalities. Active infection with hepatitis B, hepatitis C.
- Any medical, psychological, or social condition, drug or alcohol abuse that would make it difficult for the patient to participate in the study and comply with the study procedures, restrictions, and requirements.
- History of allergic reactions to compounds chemically or biologically similar to cyclophosphamide, fludarabine or other agents used in the study
- QTc > 450 msec for male participants or > 470 msec for female participants
- Medical conditions, such as anti-coagulation, which is not suitable for reversal which, at the opinion of the investigator, preclude or make the patient a poor candidate for biopsy.
- Personal history of allergies or intolerance to local anaesthetic.
- Recent treatment with immunosuppressive agents
- Residual toxicities ≥2 Common Terminology Criteria for Adverse Events (CTCAE) grade due to prior therapy, that in the opinion of the investigator may interfere with study conduct Other protocol defined exclusion criteria could apply.
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: N / A
- Interventionsmodell: Einzelgruppenzuweisung
- Maskierung: Keine (Offenes Etikett)
Anzahl der Arme
Waffen und Interventionen
Teilnehmergruppe / ArmTeilnehmergruppe / Arm |
Intervention / BehandlungIntervention / Behandlung |
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Experimental: ZI-MA4-1 (TCR-NK cells)
Participants receive ZI-MA4-1 administered via IV infusion 3 times per treatment cycle at their assigned dose.
It is planned that all participants in the study will get a minimum of one treatment cycle and up to a maximum of two treatment cycles.
Prior to a treatment cycle, a participant is given fludarabine and cyclophosphamide to temporarily reduce lymphocytes in the body (lymphodepletion).
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Chemotherapie zur Lymphdrainage
Chemotherapie zur Lymphdrainage
Allogeneic Natural Killer cells transduced with a T cell receptor targeting the tumour-specific melanoma-associated antigen 4 (MAGE-A4)
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Was misst die Studie?
Primäre Ergebnismessungen
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
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Safety and tolerability of ZI-MA4-1
Zeitfenster: From baseline through end of study visit (up to 5 years)
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Assessed using clinical assessments and adverse event reporting, including dose-limiting toxicities (DLTs), treatment-emergent adverse events (TEAEs), and treatment-related adverse events (TRAEs)
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From baseline through end of study visit (up to 5 years)
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Sekundäre Ergebnismessungen
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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MTD and RP2D of ZI-MA4-1
Zeitfenster: Through completion of study response follow-up (up to 2 years)
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Identification of maximum tolerated dose (MTD) and the recommended Phase 2 dose (RP2D) of ZI-MA4-1 based on observed DLTs and predefined dose-escalation rules
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Through completion of study response follow-up (up to 2 years)
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Long term safety
Zeitfenster: Through end of study visit (up to 5 years)
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Evaluate ZI-MA4-1 for the occurrence of delayed adverse events (AEs)
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Through end of study visit (up to 5 years)
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Minimum biologically active dose (MBAD) of ZI-MA4-1
Zeitfenster: Through completion of study response follow-up (up to 2 years)
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Assessment of preliminary anti-tumour activity
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Through completion of study response follow-up (up to 2 years)
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Objective Response Rate (ORR)
Zeitfenster: Through completion of study response follow-up (up to 2 years)
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Assessed by RECIST 1.1
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Through completion of study response follow-up (up to 2 years)
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Best Overall Response (BOR)
Zeitfenster: Through completion of study response follow-up (up to 2 years)
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Assessed by RECIST 1.1
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Through completion of study response follow-up (up to 2 years)
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Disease Control Rate (DCR)
Zeitfenster: Through completion of study response follow-up (up to 2 years)
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Assessed by RECIST 1.1
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Through completion of study response follow-up (up to 2 years)
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Pharmacokinetics of ZI-MA4-1
Zeitfenster: 3 years post-infusion of ZI-MA4-1
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Evaluation of persistence of ZI-MA4-1 cells in the blood using vector copy number (VCN) analysis
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3 years post-infusion of ZI-MA4-1
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Mitarbeiter und Ermittler
Sponsor
Sponsor
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Studienbeginn
Primärer Abschluss (Geschätzt)
Primärer Abschluss
Studienabschluss (Geschätzt)
Studienabschluss
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Zuerst gepostet
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes Update gepostet
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Zusätzliche relevante MeSH-Bedingungen
- Urogenitale Erkrankungen
- Genitalerkrankungen
- Erkrankungen des endokrinen Systems
- Urogenitale Neoplasmen
- Neubildungen nach Standort
- Neubildungen
- Weibliche Urogenitalerkrankungen
- Weibliche Urogenitalerkrankungen und Schwangerschaftskomplikationen
- Neubildungen nach histologischem Typ
- Genitalerkrankungen, weiblich
- Neoplasmen der endokrinen Drüse
- Eierstockerkrankungen
- Adnexerkrankungen
- Genitale Neubildungen, weiblich
- Gonadenstörungen
- Sarkom
- Neubildungen, Binde- und Weichgewebe
- Neubildungen, Bindegewebe
- Eierstocktumoren
- Kopf-Hals-Neubildungen
- Sarkom, Synovial
- Organische Chemikalien
- Kohlenwasserstoffe
- Phosphoramid -Senf
- Stickstoffsenfverbindungen
- Senfverbindungen
- Kohlenwasserstoffe, halogeniert
- Phosphoramide
- Organophosphorverbindungen
- Cyclophosphamid
- Fludarabine
Andere Studien-ID-Nummern
Andere Studien-ID-Nummern
- ZIMA-101
- ISRCTN14753723 (Registrierungskennung: ISRCTN registry)
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Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
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