Status:
TERMINATED
Intratumoural Injection of a Novel NanoZolid®-Docetaxel Depot Formulation in Patients With Advanced Solid Tumours
Lead Sponsor:
Lidds AB
Conditions:
Solid Tumor
Eligibility:
All Genders
18+ years
Phase:
PHASE1
Brief Summary
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. Th...
Eligibility Criteria
Inclusion
- 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
- 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.
Key Trial Info
Start Date :
February 28 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 7 2021
Estimated Enrollment :
6 Patients enrolled
Trial Details
Trial ID
NCT04810208
Start Date
February 28 2019
End Date
October 7 2021
Last Update
December 30 2021
Active Locations (4)
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1
Herlev Hospital
Copenhagen, Denmark
2
Lithuanian University of Health Sciences
Kaunas, Lithuania
3
National Cancer Institute
Vilnius, Lithuania
4
Karolinska University Hospital
Stockholm, Sweden