Maximum Tolerable Concentration of abnobaVISCUM Fraxini Intravesically in Patients With Superficial Bladder Cancer

Abnoba

Status and phase

Completed

Phase 2

Phase 1

Conditions

Superficial Bladder Cancer

Treatments

Drug: abnobaVISCUM Fraxini

Study type

Interventional

Funder types

Industry

Identifiers

NCT02007005

AB01

Details and patient eligibility

About

The aim of this phase Ib/IIa study is to investigate the maximum tolerable concentration of abnobaVISCUM® Fraxini for intravesical instillation in patients with superficial bladder cancer. Secondary objectives are the local and systemic tolerability, the influence on tumor remission and the influence on the one-year recurrence rate.

Full description

A dose-escalation-study according ICH/GCP (International Conference on Harmonisation/Good Clinical Practice) with different concentrations of abnobaVISCUM® Fraxini is conducted in two hospitals in Germany and Egypt. Patients with superficial bladder cancer TaG1/G2 or T1G1/G2 are enclosed after TUR-B (transurethral resection bladder). The tolerability of the different concentrations is assessed after weekly instillations into the urinary bladder for 6 weeks. A direct antitumoral effect is assessed on a single marker tumor left in the bladder after a complete TUR of all other lesions according a study design established by the EORTC-GENITO-URINARY GROUP (European Organisation for Research and Treatment of Cancer). A re-TUR is conducted after 12 weeks. Tumor response is measured by biopsy of the marker lesion and by cytology. Safety of the instillations is measured by analysis of adverse events, vital signs and clinical laboratory tests. After treatment of a cohort is finished a safety evaluation is conducted to decide about the increase to the next dosage.

Enrollment

37 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients with clinically proved superficial bladder cancer (Ta G1/G2 or T1G1/G2) 2 - 7 weeks before transurethral resection
Written informed consent for study participation and for documentation of disease data including further distribution of these data

Exclusion criteria

Muscle invasive bladder carcinoma and/or carcinoma in situ (CIS)
Intravesical instillation therapy within 6 months prior to study enrolment
Radiotherapy of the bladder prior to study enrolment
Contracted bladder (capacity less than 100 ml)
Non treated acute or chronic urinary tract infection
Allergy against mistletoe extract preparations
Subvesical obstructions (e. g. prostate hyperplasia, urethral stenosis, residual urine volume more than 80 ml)
Severe illnesses and circumstances not permitting study participation (e. g. alcoholism or substance abuse)
Pregnancy or lactation (pregnancy test if required) as well as women without sufficient contraception
Participation in another clinical study within 30 days prior to this study
Administration of immunotherapeutic and/or cytostatic drugs within 4 weeks prior to study enrolment
Chronic progressive infections (e. g. tuberculosis)
Pre-treatment with mistletoe extracts/mistletoe lectins