Allgemeine Informationen
  • Krankheitskategorie Kopf- und Nackenkrebs (BASEC)
  • Rekrutierungsstatus Rekrutierung abgeschlossen (BASEC/ICTRP)
  • Studienstandort
    Lausanne, Zürich
    (BASEC)
  • Studienverantwortliche Medizinische Auskünfte swiss.medinfo@novartis.com (BASEC)
  • Datenquelle(n) BASEC: Import vom 17.02.2026 ICTRP: N/A
  • Letzte Aktualisierung 17.02.2026 15:35
HumRes58873 | SNCTP000005002 | BASEC2022-00431

A safety study of Lutathera in newly diagnosed glioblastoma patients in combination with currently approved treatments or in patients with recurrent glioblastoma as a single agent.

  • Krankheitskategorie Kopf- und Nackenkrebs (BASEC)
  • Rekrutierungsstatus Rekrutierung abgeschlossen (BASEC/ICTRP)
  • Studienstandort
    Lausanne, Zürich
    (BASEC)
  • Studienverantwortliche Medizinische Auskünfte swiss.medinfo@novartis.com (BASEC)
  • Datenquelle(n) BASEC: Import vom 17.02.2026 ICTRP: N/A
  • Letzte Aktualisierung 17.02.2026 15:35

Zusammenfassung der Studie

Glioblastoma (GB) is the most common malignant tumor of the central nervous system. Given the available data, GB could be a plausible target for targeted peptide receptor radionuclide therapy, Lutathera. Lutathera was approved in 2019 for the treatment of inoperable or metastatic, progressive gastroenteropancreatic neuroendocrine tumors (NET) with sufficient expression of somatostatin receptors on tumor cells in adults. A radioactive particle (Lutetium-177) is used, which is attached to a targeting ligand that specifically binds to somatostatin receptors (receptors for the hormone somatostatin) on the surface of tumor cells. Due to the presence of somatostatin receptors in GB samples, Lutathera could broadly irradiate tumor margins. This open-label, multicenter study aims to determine the recommended dose of Lutathera® in combination with standard treatment or as a single agent in three different groups of participants with glioblastoma. Eligible participants with newly diagnosed glioblastoma will be assigned to group 1 or group 2 based on the amounts of a form of biomarker (laboratory value of the MGMT biomarker). Participants with recurrent glioblastoma will be assigned to group 3. Furthermore, this study will investigate the safety of Netspot® as an imaging agent in participants with glioblastoma. Netspot® is already approved for imaging somatostatin receptors on NET cells using positron emission tomography (PET).

(BASEC)

Untersuchte Intervention

- All participants will be scanned during screening with Netspot® PET/CT (or PET/MRI) to check if we can use this examination as a new imaging method in patients with GB. - Participants in group 1 will receive treatment with Lutathera® in combination with standard treatment. Lutathera® will be administered in the nuclear medicine department every 4 weeks up to a total of 6 times. Radiation therapy and temozolomide will be administered 7 to 10 days after the first administration of Lutathera®. Radiation therapy will be conducted 5 days a week, followed by 2 rest days, over 6 consecutive weeks. Temozolomide will be administered orally, concurrently with radiation therapy. During the maintenance phase, the dosage of temozolomide may be increased. - Participants in group 2 will receive treatment with Lutathera® in combination with standard therapy. Lutathera® will be administered in the nuclear medicine department every 4 weeks for the first 3 doses, then every 3 weeks as a single agent, for a total of up to 6 times. Radiation therapy will be initiated 7 to 10 days after the first administration of Lutathera® and will be conducted with a dose of 2 Gy/day for 5 days a week, followed by 2 rest days, over 6 consecutive weeks. - Participants in group 3 will receive Lutathera® every 3 weeks as a single agent.

(BASEC)

Untersuchte Krankheit(en)

Recurrent and newly diagnosed glioblastoma (brain tumor)

(BASEC)

Kriterien zur Teilnahme
Common criteria: - Histologically confirmed glioblastoma - Appropriate blood values of bone marrow, electrolytes, and organ functions Newly diagnosed glioblastoma: - Presence of a gadolinium-enhanced tumor on MRI prior to surgery - Karnofsky performance status ≥ 70%. - Presence of representative tumor tissue for GB from a definitive surgery or biopsy Recurrent glioblastoma: - The participant has a first or second recurrence of their glioblastoma after standard or experimental therapy that includes prior radiation therapy. - Netspot® signal in the PET/CT or PET/MRI scan in the tumor region - Karnofsky performance status ≥ 60%. (BASEC)

Ausschlusskriterien
Common criteria: - The participant is receiving additional, concurrent active therapy for glioblastoma outside of the study - Extensive leptomeningeal disease - History of another active malignant disease in the last 3 years prior to study initiation Newly diagnosed glioblastoma: - Any prior treatment of a glioma of any grade Recurrent glioblastoma: - Early progression of disease before 3 months after completion of radiation therapy - More than 2 prior systemic therapies - Prior treatment with Bevacizumab (BASEC)

Studienstandort

Lausanne, Zürich

(BASEC)

nicht verfügbar

Sponsor

Novartis Pharma Schweiz AG

(BASEC)

Kontakt für weitere Auskünfte zur Studie

Kontaktperson Schweiz

Medizinische Auskünfte

+41 41 763 71 11

swiss.medinfo@novartis.com

Novartis Pharma Schweiz AG Medical Information

(BASEC)

Wissenschaftliche Auskünfte

nicht verfügbar

Name der bewilligenden Ethikkommission (bei multizentrischen Studien nur die Leitkommission)

Ethikkommission Zürich

(BASEC)

Datum der Bewilligung durch die Ethikkommission

28.06.2022

(BASEC)


ICTRP Studien-ID
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Offizieller Titel (Genehmigt von der Ethikkommission)
A Phase Ib Dose Finding Study Assessing Safety and Activity of [177Lu]Lu-DOTA-TATE in Newly Diagnosed Glioblastoma in Combination with Radiotherapy with or without Temozolomide and in Recurrent Glioblastoma as Single Agent (BASEC)

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Untersuchte Krankheit(en)
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Untersuchte Intervention
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Primäre und sekundäre Endpunkte
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Einschluss des ersten Teilnehmers
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Weitere Informationen zur Studie
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Ergebnisse der Studie

Zusammenfassung der Ergebnisse

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Link zu den Ergebnissen im Primärregister

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