To Evaluate the Effects of Cevostamab in Participants With Systemic Lupus Erythematosus With or Without Active Lupus Nephritis
An Open-Label, Multicenter, Phase Ib Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Cevostamab in Patients With Systemic Lupus Erythematosus With or Without Active Lupus Nephritis
Studienübersicht
Status
Status
Bedingungen
Bedingungen
Intervention / Behandlung
Intervention / Behandlung
Studientyp
Studientyp
Einschreibung (Geschätzt)
Einschreibung
Phase
Phase
- Phase 1
Kontakte und Standorte
Studienkontakt
Studienkontakt
- Name: Fastest response: use the inquiry form. https://www.gene.com/contact-us/submit-medical-inquiry
Studieren Sie die Kontaktsicherung
- Name: Reference Study ID Number: GA46280 https://forpatients.roche.com/ No attachments to email below.
- Telefonnummer: 888-662-6728
- E-Mail: global-roche-genentech-trials@gene.com
Studienorte
-
-
-
Seville, Spanien, 41009
- Rekrutierung
- Hospital Universitario Virgen Macarena
-
-
Teilnahmekriterien
Zulassungskriterien
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
- Älterer Erwachsener
Akzeptiert gesunde Freiwillige
Beschreibung
Inclusion Criteria:
- Diagnosis of SLE according to the 2019 European League Against Rheumatism (EULAR)/American College of Rheumatology (ACR) Classification Criteria at least 6 months prior to the first screening visit
- Active biopsy-proven LN established within 9 months of screening, demonstrating LN per 2018 Revised International Society of Nephrology/Renal Pathology Society (ISN/RPS) criteria
- Diagnosis of active SLE disease, as demonstrated by the Systemic Lupus Erythematosus Disease Activity Index 2000 (SLEDAI-2K) score
- Inadequate response or intolerance to, in the investigator's judgement, standard of care regimens for active SLE with or without LN
Exclusion Criteria:
- Pregnant or breastfeeding, or intending to become pregnant during the study or within the timeframe in which contraception is required
- Treatment with investigational or non-investigational biologic therapies that directly deplete B cells (e.g., anti-CD20 or anti-CD19 monoclonal antibodies) (or blinded comparators) is prohibited within 6 months or 5 drug elimination half-lives, whichever is longer, prior to screening and during the study
- Treatment with investigational biologic therapies that do not directly deplete B cells (or blinded comparators) is prohibited within 90 days or 5 drug elimination half-lives, whichever is longer, prior to initiation of study drug and during the study
- Treatment of SLE/LN with non-investigational biologic therapies that do not directly deplete B cells (e.g., belimumab, anifrolumab) is prohibited within 4 weeks prior to screening and during the study
- Treatment with CYC within 3 months prior to screening or during the study
- History of known or suspected allergic reaction or anaphylactic reaction to cevostamab or its excipients
- Major surgery requiring hospitalization during the 4 weeks prior to screening or during screening, or any planned surgery or procedure requiring hospitalization during the 12 weeks following study drug administration
- Alcohol or substance abuse within the 12 months prior to screening
- Active infection of any kind, excluding fungal infection of the nail beds
- History of serious recurrent or chronic infection
- Tuberculosis (TB) infection
- Active overlap syndrome with mixed connective tissue disease or systemic sclerosis within the 12 months prior to screening or during screening
- Catastrophic or severe antiphospholipid syndrome within the 12 months prior to screening or during screening
- High risk for clinically significant bleeding or any condition requiring plasmapheresis, IV immunoglobulin, or acute blood product transfusions
- Active severe or unstable lupus-associated neuropsychiatric disease, which, in the opinion of the investigator, is likely to require treatment with protocol-prohibited therapies
- Non-SLE related CNS disease such as stroke, epilepsy, CNS vasculitis, or neurodegenerative disease
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: N / A
- Interventionsmodell: Sequenzielle Zuweisung
- Maskierung: Keine (Offenes Etikett)
Anzahl der Arme
Waffen und Interventionen
Teilnehmergruppe / ArmTeilnehmergruppe / Arm |
Intervention / BehandlungIntervention / Behandlung |
|---|---|
|
Experimental: Dose Escalation and Expansion
The study consists of a dose-escalation stage followed by an expansion stage.
Participants in both stages will receive Cevostamab in a step-up dosing regimen, followed by a target dose.
|
Die Teilnehmer erhalten Cevostamab intravenös gemäß dem im Protokoll festgelegten Zeitplan.
Andere Namen:
Tocilizumab may be used as rescue medication for participants who experience a cytokine release syndrome (CRS) event.
Andere Namen:
|
Was misst die Studie?
Primäre Ergebnismessungen
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Zeitfenster |
|---|---|
|
Percentage of Participants with Adverse Events (AEs)
Zeitfenster: Up to approximately 52 weeks
|
Up to approximately 52 weeks
|
Sekundäre Ergebnismessungen
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Zeitfenster |
|---|---|
|
Serum Concentration of Cevostamab
Zeitfenster: Up to approximately 52 weeks
|
Up to approximately 52 weeks
|
|
Area Under the Concentration-Time Curve (AUC) of Cevostamab
Zeitfenster: Up to approximately 52 weeks
|
Up to approximately 52 weeks
|
|
Maximum Observed Serum Concentration (Cmax) of Cevostamab
Zeitfenster: Up to approximately 52 weeks
|
Up to approximately 52 weeks
|
|
Minimum Observed Serum Concentration (Cmin) of Cevostamab
Zeitfenster: Up to approximately 52 weeks
|
Up to approximately 52 weeks
|
|
Clearance (CL) of Cevostamab
Zeitfenster: Up to approximately 52 weeks
|
Up to approximately 52 weeks
|
|
Volume of Distribution at Steady State (Vdss) of Cevostamab
Zeitfenster: Up to approximately 52 weeks
|
Up to approximately 52 weeks
|
|
Change from Baseline in the Presence Anti-Drug Antibodies (ADAs)
Zeitfenster: Up to approximately 52 weeks
|
Up to approximately 52 weeks
|
Mitarbeiter und Ermittler
Sponsor
Sponsor
Publikationen und hilfreiche Links
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Geschätzt)
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
Andere Studien-ID-Nummern
Andere Studien-ID-Nummern
- GA46280
- 2025 (US NIH Stipendium/Vertrag: Faculty of Social Sciences Scientific Grant at the University of Gdańsk)
- 2025-522904-26-00 (Ctis)
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Produkt, das in den USA hergestellt und aus den USA exportiert wird
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 .