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

Phase 2CompletedNCT02007005

Abnoba Gmbh37 enrolled

Overview

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.

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.

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Superficial Bladder Cancer

Interventions

abnobaVISCUM FraxiniDRUG

intravesical instillation 6 times, once weekly, in increasing dosages until dose-limiting-toxicity occurs

Eligibility

Sex: ALLMin age: 18 YearsMax age: 80 Years

Medical Language ↔ Plain English

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

Locations (2)

Theodor Bilharz Research Institute

Giza, Egypt

Clinic of Urology of the University Hospital of Essen

Essen, Germany

Outcomes

Primary Outcomes

Maximum tolerable concentration of abnobaVISCUM Fraxini for intravesical instillation

The primary objective is to investigate the maximum tolerable concentration of abnobaVISCUM Fraxini for intravesical instillation in patients with superficial bladder cancer. The treatment schedule included 6 weekly instillations.

Time frame: 6 weeks

Secondary Outcomes

Local and systemic tolerability of different concentrations of abnobaVISCUM Fraxini for intravesical instillation

Secondary objectives are to investigate the local and systemic tolerability of different concentrations of abnobaVISCUM Fraxini for intravesical instillation. Main variables of safety analysis are adverse events, vital signs and clinical laboratory tests.

Time frame: 6 weeks

Influence on remission and influence on the one year recurrence rate of abnobaVISCUM Fraxini for intravesical instillation

Secondary objectives are to investigate the influence on remission and influence on the one year recurrence rate measured by histological examination of biopsies of the marker lesion, cytology and cystoscopy.

Time frame: up to 1 year

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.