Allgemeine Informationen
  • Studienphase Phase 1/Phase 2 (ICTRP)
  • Rekrutierungsstatus Rekrutierung läuft (BASEC/ICTRP)
  • Studienstandort
    Vereinigte Staaten, Spanien, Schweiz
    (ICTRP)
  • Studienverantwortliche Study Director;Debiopharm International S.A clinicaltrials@debiopharm.com (ICTRP) Study DirectorDebiopharm International S.A clinicaltrials@debiopharm.com (ICTRP)
  • Datenquelle(n) ICTRP: Import vom 16.10.2026
  • Letzte Aktualisierung 16.10.2026 02:00
HumRes62503 | NCT05765812

A Study of Debio 0123 in Combination With Temozolomide in Adult Participants With Recurrent or Progressive Glioblastoma and of Debio 0123 in Combination With Temozolomide and Radiotherapy in Adult Participants With Newly Diagnosed Glioblastoma

  • Studienphase Phase 1/Phase 2 (ICTRP)
  • Rekrutierungsstatus Rekrutierung läuft (BASEC/ICTRP)
  • Studienstandort
    Vereinigte Staaten, Spanien, Schweiz
    (ICTRP)
  • Studienverantwortliche Study Director;Debiopharm International S.A clinicaltrials@debiopharm.com (ICTRP) Study DirectorDebiopharm International S.A clinicaltrials@debiopharm.com (ICTRP)
  • Datenquelle(n) ICTRP: Import vom 16.10.2026
  • Letzte Aktualisierung 16.10.2026 02:00

Studientyp

Interventional

(ICTRP)

Untersuchte Intervention

Drug: Debio 0123Drug: TemozolomideRadiation: Radiotherapy

(ICTRP)

Untersuchte Krankheit(en)

Glioblastoma IDH (Isocitrate Dehydrogenase) WildtypeAstrocytoma, Grade III

(ICTRP)

Kriterien zur Teilnahme

Screening Inclusion Criteria for Phase 1 and Phase 2:

  • Signed written informed consent approved before undertaking any study-specific procedures.
  • Age >=18 years of age.
  • Willing to provide archived or fresh tumor sample, if available. Receipt of tumor sample is not required for the start of study treatment.
  • Adequate bone marrow, hepatic, and renal function.
  • Willingness and ability to comply with scheduled visits, treatment plans, laboratory tests, and other study procedures.
  • Willing to practice highly effective methods of contraception.
  • Life expectancy of at least 3 months in the best judgment of the Investigator.
  • Measurable or non-measurable disease as per RANO criteria by gadolinium (Gd)-based contrast-enhanced brain magnetic resonance imaging (MRI).
  • Participants receiving corticosteroids must be on a stable or decreasing dose of <=4 mg daily dexamethasone (or <=25 mg prednisone) for the 7 days prior to the start of study treatment.
  • Participants with seizures must be adequately controlled on a stable regimen of anti-epileptic drugs.

Additional specific inclusion criteria for Phase 1 and Phase 2:

A maximum of 1 [for Phase 1 (Dose Expansion) and phase 2] or 2 (Phase 1 Arm A) prior
treatment lines of which first-line must be treatment with TMZ-based chemoradiotherapy
(TMZ concomitantly with RT).

Note: Only 1 prior line of systemic therapy is allowed combination therapy with TMZ and
RT with or without subsequent TMZ maintenance treatment is considered as 1 systemic line.
Prior surgery, radiation, or localized delivery of therapeutic agents (i.e.,
carmustine-containing wafers [GLIADEL]) for first recurrence is allowed.

  • Documented disease recurrence or progression by diagnostic biopsy or Gd-based contrast-enhanced brain MRI as per RANO criteria.
  • KPS >=60.

Additional specific inclusion criteria for Phase 1 Arm A:

  • Participants must have one of the following histopathologically proven diagnoses (WHO 2021):
  • GBM Isocitrate dehydrogenase (IDH)-wildtype Grade 4 which may include secondary GBMs (i.e., those that progress from low-grade gliomas).
  • Astrocytoma, IDH-mutant, Grade 3

Additional specific inclusion criteria for Phase 1 Arm B and C:

  • Participants must have a new, histopathologically proven diagnosis of GBM, IDH-wildtype, Grade 4 (based on WHO 2021), which may include secondary GBMs (i.e., those that progress from low-grade gliomas) if the prior treatment included surgery only.
  • KPS >=70.

Additional specific inclusion criteria for Phase 1 dose expansion and Phase 2:

Participants must have a histopathologically proven diagnosis of GBM, IDH-wildtype
Grade 4 WHO 2021

Additional specific exclusion criteria for Phase 1 Arm A Prior treatment with more than
2 lines of therapy for GBM, IDH-wildtype, Grade 4, or for astrocytoma, IDH-mutant, Grade
3

Additional specific exclusion criteria for Phase 1 and Phase 2

  • Known contraindication to undergoing for Gd-based, contrast-enhanced MRI.
  • Any anticancer treatment, monoclonal antibodies/biologics, investigational treatment, or RT with curative intent within 28 days prior to starting study treatment.
  • Hypersensitivity to Debio 0123, TMZ, dacarbazine, or any of the excipients found in the formulation for Debio 0123 or TMZ.
  • Prior exposure to any WEE1 inhibitor.
  • History of other malignancies requiring active treatment in the last 2 years prior to the first dose of study treatment except for superficial bladder cancers, adequately treated low-risk prostate cancer under active surveillance, ductal carcinoma in situ or other carcinomas in situ, and non-melanoma skin cancers (basal cell/squamous cell skin cancer) that have been treated with curative intent.
  • Left ventricular ejection fraction (LVEF) below 55%.

Additional specific exclusion criteria for Phase 1 Arm B and C:

  • Prior radiation, chemotherapy, biological therapy, interstitial brachytherapy, implanted chemotherapy, therapeutics delivered by local injection or convection-enhanced delivery for GBM.
  • Prior therapy that would result in an overlap of the radiation fields.

Additional specific exclusion criteria for Phase 1 dose expansion and Phase 2

Prior treatment with more than 1 line of systemic therapy for GBM, IDH-wildtype, Grade
4 (based on WHO 2021). Combination therapy with TMZ and RT with or without subsequent TMZ
maintenance treatment is considered as 1 systemic line.

[Note: Other inclusion/exclusion criteria mentioned in the protocol may apply.]

(ICTRP)


Ausschlusskriterien
nicht verfügbar

Studienstandort

Vereinigte Staaten, Spanien, Schweiz

(ICTRP)

Allgemeine Auskünfte

Debiopharm International SA,

+41 21 321 01 11

clinicaltrials@debiopharm.com

(ICTRP)

Allgemeine Auskünfte

Debiopharm International SA

+41 21 321 01 11

clinicaltrials@debiopharm.com

(ICTRP)

Wissenschaftliche Auskünfte

Debiopharm International SA,

+41 21 321 01 11

clinicaltrials@debiopharm.com

(ICTRP)


Wissenschaftlicher Titel
A Phase 1/2 Open-label Study of Debio 0123 in Combination With Temozolomide in Adult Participants With Recurrent or Progressive Glioblastoma and of Debio 0123 in Combination With Temozolomide and Radiotherapy in Adult Participants With Newly Diagnosed Glioblastoma (ICTRP)

Studiendesign

Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: None (Open Label).

(ICTRP)



Primäre und sekundäre Endpunkte

Phase 1 (Dose Escalation): Number of Participants Experiencing Dose-limiting Toxicities (DLTs);Phase 1 (Dose Escalation): Number of Participants With At Least One Treatment-emergent Adverse Event (TEAE);Phase 1 (Dose Escalation): Number of Participants With Clinically Significant Abnormalities in Laboratory, Vital Signs, Electrocardiogram (ECG), and Echocardiogram (ECHO) Parameters;Phase 1 (Dose Escalation): Change From Baseline in Karnofsky Performance Status (KPS) Score;Phase 1 (Dose Expansion): Number of Participants With At Least One Treatment-emergent Adverse Event (TEAE);Phase 1 (Dose Expansion): Change from Baseline in Tumor Size Assessed by Objective Response (OR) as per Response Assessment in Neuro-oncology (RANO) Criteria;Phase 1 (Dose Expansion): Plasma Concentration of Debio 0123 and its Metabolite;Phase 1 (Dose Expansion): Pharmacodynamic(s) PDy, Change from baseline in Phosphorylated Cell Division Cycle (pCDC2);Phase 2: Overall Survival (OS)

(ICTRP)



Phase 1 (Dose Expansion): OS;Phase 1 (Dose Escalation): Plasma Concentration of Temozolomide;Phase 1 (Dose Expansion): Number of Participants With Clinically Significant Abnormalities In Laboratory, Vital Signs, ECG, and (ECHO Parameters);Phase 1 (Dose Expansion): Number of Participants With At Least one TEAE;Phase 1 (Dose Expansion): Change From Baseline in KPS Score;Phase 2: Change From Baseline in KPS Score;Phase 2: Number of Participants With Clinically Significant Abnormalities in Laboratory, Vital Signs, and ECG Parameters;Phase 2: Number of Participants With At Least One TEAE;Phases 1 and 2: Plasma Concentration of Debio 0123 and its Metabolite;Phases 1 and 2: Percentage of Participants With Best Overall Response (BOR) Assessed As Per Response Assessment in Neuro-oncology (RANO) Criteria;Phases 1 and 2: Percentage of Participants with Objective Response (OR) Assessed As Per RANO Criteria;Phases 1 and 2: Percentage of Participants With Disease Control (DC) Assessed As Per RANO Criteria;Phases 1 and 2: Duration of Response (DOR) Assessed As Per RANO Criteria;Phases 1 and 2: Progression Free Survival (PFS) Assessed As Per RANO Criteria

(ICTRP)



Registrierungsdatum
nicht verfügbar

Einschluss des ersten Teilnehmers
nicht verfügbar

Sekundäre Sponsoren
nicht verfügbar

Weitere Kontakte
Study Director;Debiopharm International S.A, clinicaltrials@debiopharm.com, +41 21 321 01 11, Debiopharm International SA, (ICTRP)

Sekundäre IDs
2022-502156-31, U1111-1283-6423, Debio 0123-GBM-105 (ICTRP)

Angaben zur Verfügbarkeit von individuellen Teilnehmerdaten
nicht verfügbar

Weitere Informationen zur Studie
https://clinicaltrials.gov/study/NCT05765812 (ICTRP)

Ergebnisse der Studie

Zusammenfassung der Ergebnisse

nicht verfügbar

Link zu den Ergebnissen im Primärregister

nicht verfügbar