Intratumoural Injection of a Novel NanoZolid®-Docetaxel Depot Formulation in Patients With Advanced Solid Tumours

LIDDS

Status and phase: Terminated; Phase 1

Conditions: Solid Tumor

Treatments: Drug: Docetaxel

Study type: Interventional

Funder types: Industry

Identifiers

NCT04810208

NZ-DTX-001

Details and patient eligibility

About

This is a multicentre, open-label, first in man, study of a novel NanoZolid®-docetaxel depot formulation (NZ-DTX Depot) given as an intra-tumoural injection in patients with advanced solid tumours. The study includes a dose escalation part and a dose expansion part.

Enrollment: 6 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Signed written informed consent granted before undertaking any study-specific procedures;

2. Male or female patient ≥18 years of age on the day of consenting to the study;

3. Histologically or cytologically confirmed diagnosis of solid cancer;

4. 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;

5. Eastern Co-operative Oncology Group (ECOG) performance status (PS) 0-2;

6. 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

1. Known hypersensitivity to any of the excipients in the NZ-DTX Depot formulation (docetaxel, calcium sulphate, sodium carboxymethylcellulose);

2. Life expectancy <3 months;

3. 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;

4. 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.

5. Severe fluid retention, e.g. pulmonary oedema, pleural effusion, pericardial effusion or ascites;

6. Clinically significant heart disease (i.e. heart failure or myocardial infarction within 6 months of screening, instable angina pectoris);

7. History of thromboembolic or cerebrovascular events within 6 months of screening;

8. Major surgery within 2 weeks of screening, or patient not recovered from major surgery;

9. Known untreated or uncontrolled acute infection, including urinary tract infection, within 7 days of screening;

10. Not recovered from Grade 2 or higher adverse events (AEs) due to previous treatments, excepting alopecia;

11. Concurrent participation in another investigational study;

12. 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;

13. Last administration of other anti-neoplastic drug within 14 days of study treatment initiation;

14. 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;

15. For men and women of childbearing potential: Unwillingness to follow contraception requirements;

16. Female patients with planned or current pregnancy and/or currently breastfeeding;

17. 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.

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

---

6 participants in 1 patient group

NZ-DTX Depot

Experimental group

Treatment:

Drug: Docetaxel