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Immuno-positron Emission Tomography Study of 89Zr-S095012 in Patients With Advanced Solid Tumours

Code de protocole Servier: CL1-95012-002 Sponsor: Institut de Recherches Internationales Servier Identifiant Clinicaltrials.gov: NCT05638334 Numéro EudraCT: 2021-001764-20

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Comment participer à l'étude ?
Si vous pensez être éligible pour cette étude (voir
critères d'éligibilité
ci-dessous), vous pouvez identifier le site le plus proche de chez vous et le contacter directement. Si vous ne trouvez pas de site près de chez vous, veuillez contacter l'Institut de Recherches Internationales Servier (I.R.I.S.).
Nom: Institut de Recherches Internationales Servier, Département des études cliniques
Numéro de téléphone: +33 1 55 72 60 00
L'étude a 1 centre

Description de l'étude

The purpose of this study is to assess the whole-body biodistribution and tumour uptake of 89Zr-S095012 in participants with solid tumours treated with S095012 (PD-L1x4-1BB bispecific antibody)
Titre officiel: An Open Label, Multicentre, Positron Emission Tomography (PET) Imaging Study Using Zirconium-89 to Investigate the Biodistribution and Tumour Uptake of a PD-L1x4-1BB Bispecific Antibody (S095012) in Patients With Advanced Solid Tumours
Indications
Advanced Solid Tumor
Interventions / Traitements
  • 89Zr-S095012 tracer and S095012 will be administered via an IV infusion
Autres numéros d'identification
  • CL1-95012-002

Critères d'éligibilité

Age éligible pour l’étude

18 ans et plus (Adulte, Adulte plus âgé)

Sexes

Homme/Femme

Accepte les volontaires en bonne santé

Non

  • * Histologically confirmed diagnosis of unresectable, locally advanced or metastatic solid tumour, for which standard treatment options are not available, no longer effective, or not tolerated
  • * At least one measurable target lesion as per RECIST 1.1
  • * Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
  • * Royal Marsden Prognosis score of 0 to 1 (score based on lactate dehydrogenase (LDH) value, albumin value and number of sites of metastasis)
  • * Adequate organ function as assessed by laboratory tests (especially adequate hepatic function)
  • * Negative test results for cytomegalovirus (CMV), Epstein-Barr virus (EBV), Hepatitis B virus (HBV), and Hepatitis C virus (HCV) infection, according to local standards.

  • * Participants with no available archived material and no tumour lesions amenable to biopsy
  • * Participants with primary central nervous system malignancies, with Child-Pugh Class B8 or higher, or C liver cirrhosis
  • * Participants with active auto-immune disease or immune-related adverse event currently requiring systemic anti-inflammatory agent (more than 10mg/day prednisone or equivalent)
  • * Participants with a history of an opportunistic infection within a year before the administration of first study drug dose are excluded.
  • * Participants who received either systemic corticosteroids (> 10 mg per day of prednisone or equivalent) or other immunosuppressive medication during the 2 months prior to the first dose of the study drug are excluded.
  • * Participants with prior history of Grade ≥ 3 immune-related pneumonitis, colitis, hepatitis, or myocarditis
  • * Participants with a history of progressive multifocal leukoencephalopathy
  • * Participants must not have a history of active tuberculosis requiring treatment within 3 years prior to the start of treatment or a suspicion of latent tuberculosis by the investigator.

Comment l'étude est-elle conçue ?

Allocation
N/A
Modèle d'étude interventionnelle
Groupe unique
Groupe de participants / Bras de traitement
Expérimental: 89Zr-S095012 tracer with S095012
Intervention / Traitement
Traitement: 89Zr-S095012 tracer and S095012 will be administered via an IV infusion
Imaging period 1 (Part A and Part B): The tracer will be administered with S095012 at non-therapeutic mass dose. The optimal mass dose of S095012 will be investigated in part A, and used in part B. Treatment period (Part A to C): S095012 will be administered with multiple 28 days- cycles in a Q2W schedule. Imaging period 2 (Part C): A second tracer dose will be administered at 1st treatment dose of S095012 in part C.