- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT04810208
Intratumoural Injection of a Novel NanoZolid®-Docetaxel Depot Formulation in Patients With Advanced Solid Tumours
A Phase Ia/Ib, First-in-human, Open Label, Multicentre, Dose-escalation and Dose-expansion Study of a Novel NanoZolid®-Docetaxel Depot Formulation (NZ-DTX Depot) Given as an Intra-tumoural Injection in Patients With Advanced Solid Tumours
Aperçu de l'étude
Type d'étude
Inscription (Réel)
Phase
- La phase 1
Contacts et emplacements
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
Inclusion Criteria:
- Signed written informed consent granted before undertaking any study-specific procedures;
- Male or female patient ≥18 years of age on the day of consenting to the study;
- Histologically or cytologically confirmed diagnosis of solid cancer;
At least 1 advanced solid, palpable, cutaneous or subcutaneous tumour lesion with following characteristics:
- a cutaneous lesion with of thickness ≥4 mm and diameter ≥25 mm at the longest axis, or
- a subcutaneous lesion of diameter ≥20 mm at the longest and the shortest axis;
- Eastern Co-operative Oncology Group (ECOG) performance status (PS) 0-2;
Patient from one the following categories:
- Patient for whom no standard therapy exists, or standard therapy is contraindicated, or
- Patient who is scheduled for other anti-cancer treatment (e.g. radiotherapy, immunological treatment, surgery) which will start after completion of at least one treatment cycle of NZ-DTX, i.e after the end-of-study (EOS) visit.
Exclusion Criteria:
- Known hypersensitivity to any of the excipients in the NZ-DTX Depot formulation (docetaxel, calcium sulphate, sodium carboxymethylcellulose);
- Life expectancy <3 months;
- Bleeding deficiencies or ongoing anticoagulant therapy that would put the patient at increased risk of clinically significant bleeding, in the judgement of the Investigator. If the patient has an international normalised ratio (INR) below 1.2 the Investigator may judge if interruption of anticoagulant therapy is warranted;
Any of the following abnormal laboratory values at screening;
Bone marrow function:
- Absolute neutrophil count (ANC) <1.5 x 109/l;
- Platelet count <100 x 109/l;
- Haemoglobin <9.0 mg/dl.
Coagulation:
- International Normalized Ratio (INR) >1.2.
Hepatic, renal, and biochemistry parameters:
- Aspartate transaminase (AST) or alanine transaminase (ALT) >2.5 x upper limit of normal (ULN) (>5 x ULN if liver metastases present)*;
- Alkaline phosphatase (ALP) >2.5 x ULN;
- Total bilirubin >1.5 x ULN;
Estimated glomerular filtration rate (eGFR) <40 ml/min/1.73 m² using the Modified Cockcroft & Gault formula.
- For patients with liver impairment who have serum transaminase levels (ALT and/or AST) greater than 1.5 times x ULN - the doses will be restricted to max. 75mg/m2. In the event this is not possible the patient will not be included.
- Severe fluid retention, e.g. pulmonary oedema, pleural effusion, pericardial effusion or ascites;
- Clinically significant heart disease (i.e. heart failure or myocardial infarction within 6 months of screening, instable angina pectoris);
- History of thromboembolic or cerebrovascular events within 6 months of screening;
- Major surgery within 2 weeks of screening, or patient not recovered from major surgery;
- Known untreated or uncontrolled acute infection, including urinary tract infection, within 7 days of screening;
- Not recovered from Grade 2 or higher adverse events (AEs) due to previous treatments, excepting alopecia;
- Concurrent participation in another investigational study;
- Last investigational drug administration in a prior investigational study within 14 days of study treatment initiation or <5 times the half-life of the investigational drug, whichever is longer;
- Last administration of other anti-neoplastic drug within 14 days of study treatment initiation;
- Radiotherapy of lesion to be injected within 4 weeks of first treatment with NZ-DTX Depot, or irradiated lesion to be injected without signs of disease progression since irradiation;
- For men and women of childbearing potential: Unwillingness to follow contraception requirements;
- Female patients with planned or current pregnancy and/or currently breastfeeding;
- Any other severe, acute or chronical medical or psychiatric condition or laboratory abnormality that, in the judgement of the Investigator, would make the patient inappropriate for study participation.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: N / A
- Modèle interventionnel: Affectation à un seul groupe
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
---|---|
Expérimental: NZ-DTX Depot
|
Docetaxel in NanoZolid formulation, for intratumoural injection
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
---|---|---|
Maximum tolerated dose (MTD) of NZ-DTX Depot given as an intra-tumoural injection in solid, palpable, cutaneous or subcutaneous tumour lesions.
Délai: 5 weeks
|
The MTD will be determined by incidence of DLTs
|
5 weeks
|
The recommended Phase 2 dose (RP2D) of NZ-DTX Depot given as an intra-tumoural injection in a solid, palpable cutaneous or subcutaneous tumour lesion.
Délai: 5 weeks
|
The RP2D will be determined by frequency and severity of adverse events
|
5 weeks
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
---|---|---|
Frequency and severity of treatment-emergent adverse events [safety and tolerability] following an intratumoural injection of NZ-DTX Depot
Délai: 5 weeks
|
Frequency and severity of treatment-emergent adverse events
|
5 weeks
|
Plasma concentration of docetaxel, following an intratumoural injection of NZ-DTX Depot
Délai: 5 weeks
|
Plasma concentration of docetaxel
|
5 weeks
|
Anti-tumour effect following an intratumoural injection of NZ-DTX Depot
Délai: 5 weeks
|
Tumour response by RECIST
|
5 weeks
|
Autres mesures de résultats
Mesure des résultats |
Description de la mesure |
Délai |
---|---|---|
Presence of immune biomarkers in plasma, following an intratumoural injection of NZ-DTX Depot
Délai: 9 weeks
|
Analysis of cytokines in plasma
|
9 weeks
|
Presence of immune biomarkers in tissue, following an intratumoural injection of NZ-DTX Depot
Délai: 9 weeks
|
Immunohistochemistry analysis [PD-L1] in tissue
|
9 weeks
|
Collaborateurs et enquêteurs
Parrainer
Les enquêteurs
- Directeur d'études: Charlotta Gauffin, PhD, Lidds AB
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Réel)
Achèvement de l'étude (Réel)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- NZ-DTX-001
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Étudie un produit d'appareil réglementé par la FDA américaine
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .
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