Working…
ClinicalTrials.gov
ClinicalTrials.gov Menu

Mycobacterial Cell Wall-DNA Complex in Treatment of BCG-refractory Patients With Non-muscle Invasive Bladder Cancer

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT00406068
Recruitment Status : Completed
First Posted : December 4, 2006
Last Update Posted : July 28, 2016
Sponsor:
Information provided by (Responsible Party):
Bioniche Life Sciences Inc.

Tracking Information
First Submitted Date  ICMJE December 1, 2006
First Posted Date  ICMJE December 4, 2006
Last Update Posted Date July 28, 2016
Study Start Date  ICMJE November 2006
Actual Primary Completion Date July 2011   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures  ICMJE
 (submitted: June 13, 2007)
One year disease-free survival rate [ Time Frame: Prospective ]
Original Primary Outcome Measures  ICMJE
 (submitted: December 1, 2006)
One year disease-free survival rate
Change History
Current Secondary Outcome Measures  ICMJE
 (submitted: June 13, 2007)
  • The 3, 6 and 24 month disease-free survival rate [ Time Frame: Prospective ]
  • Duration of disease-free survival in all patients [ Time Frame: Prospective ]
  • Time to progression to muscle invasive disease [ Time Frame: Prospective ]
  • Overall survival in all patients [ Time Frame: Prospective ]
  • Rate of overall drug-related adverse events leading to two consecutive treatment delays of one week each or to the discontinuation of treatment. [ Time Frame: Prospective ]
Original Secondary Outcome Measures  ICMJE
 (submitted: December 1, 2006)
  • The 3, 6 and 24 month disease-free survival rate
  • Duration of disease-free survival in all patients
  • Time to progression to muscle invasive disease
  • Overall survival in all patients
  • Rate of overall drug-related adverse events leading to two consecutive treatment delays of one week each or to the discontinuation of treatment.
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title  ICMJE Mycobacterial Cell Wall-DNA Complex in Treatment of BCG-refractory Patients With Non-muscle Invasive Bladder Cancer
Official Title  ICMJE Open-label, Multi-center Study of the Efficacy and Safety of MCC in the Treatment of Patients With Non-muscle Invasive (Superficial) Bladder Cancer at High Risk of Progression and Who Are Refractory to BCG
Brief Summary The purpose of this study is to determine the efficacy and safety of intravesical Mycobacterial Cell Wall-DNA Complex (MCC) in patients with non-muscle invasive transitional cell carcinoma (papillary tumors and/or carcinoma in situ) of the urinary bladder at high risk of progression who are refractory to therapy with bacillus Calmette-Guerin (BCG).
Detailed Description

The study will be divided into 3 phases: Induction, Maintenance, and Follow-up.

The Induction Phase will cover a period of 6 weeks. During this time, patients will receive 6 weekly intravesical instillations of 8 mg MCC. The patients will be evaluated at month 3, at which time the patients will enter the Maintenance Phase. The Maintenance Phase will last from month 3 to month 24, and during this time, patients will receive weekly MCC instillations for three weeks at months 3, 6, 12, 18, and 24 and evaluations will be performed at months 3, 6, 9, 12, 15, 18, 21 and 24.

At month 3, the patient will be evaluated to assure that the disease is not progressing. Cytology, cystoscopy and biopsies will be performed to obtain adequate staging (if residual tumor persists). If the patient is disease-free, maintenance therapy will be initiated. Patients with non-muscle invasive tumors at month 3 will, at the discretion of the investigator, receive either a second 6-week induction course or a 3-week maintenance course. Patients who show progression to muscle invasive disease will be referred to other treatments.

At month 6 and thereafter at each evaluation visit, patients will be evaluated and managed according to the following results:

  • Patients who are disease-free will continue on maintenance treatment.
  • Patients who are not disease-free (evidence of papillary lesions, CIS or muscle invasive disease) will be withdrawn from further study treatment and will be referred to other therapies at the discretion of the investigator.

The final 36 months of the study is the Follow-up Phase. Evaluations will be performed at months 30, 36, 42, 48, 54 and 60.

Efficacy evaluations will include standard cystoscopy, biopsies and urine cytology. During the Maintenance Phase, standard cystoscopies will be performed at months 3, 6, 9, 12, 15, 18, 21 and 24 for the surveillance of bladder tumors. During the months that instillations will be performed, cystoscopies will be conducted only once at each of these months. During the Follow-up Phase, cystoscopies will be performed at months 30, 36, 42, 48, 54 and 60.

Mandatory bladder biopsies will be done for all patients at month 6.

During the course of the study, biopsies will be taken only if evident or suspicious lesions are seen during cystoscopy or in case of negative cystoscopy but positive cytology.

Study Type  ICMJE Interventional
Study Phase  ICMJE Phase 2
Phase 3
Study Design  ICMJE Allocation: N/A
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Condition  ICMJE Bladder Neoplasms
Intervention  ICMJE Drug: Mycobacterial cell wall-DNA complex
8 mg MCC, intravesical - Induction Phase (6 weekly intravesical instillations) and Maintenance Phase (3 weekly instillations at months 3, 6, 12, 18 and 24).
Other Name: MCC - Urocidin
Study Arms  ICMJE Experimental: Mycobacterial cell wall-DNA complex
Mycobacterial cell wall-DNA complex
Intervention: Drug: Mycobacterial cell wall-DNA complex
Publications * Morales A, Herr H, Steinberg G, Given R, Cohen Z, Amrhein J, Kamat AM. Efficacy and safety of MCNA in patients with nonmuscle invasive bladder cancer at high risk for recurrence and progression after failed treatment with bacillus Calmette-Guérin. J Urol. 2015 Apr;193(4):1135-43. doi: 10.1016/j.juro.2014.09.109. Epub 2014 Oct 5.

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status  ICMJE Completed
Actual Enrollment  ICMJE
 (submitted: August 13, 2012)
129
Original Enrollment  ICMJE
 (submitted: December 1, 2006)
105
Actual Study Completion Date  ICMJE July 2011
Actual Primary Completion Date July 2011   (Final data collection date for primary outcome measure)
Eligibility Criteria  ICMJE

Inclusion Criteria:

  • Patients refractory to BCG therapy;
  • Patients with histologically confirmed diagnosis of high grade lesions;
  • Diagnosis of high grade lesion must be within 56 days prior to beginning of study treatment;
  • Have had all visible papillary lesion(s) resected by TURBT within 56 days prior to beginning of study treatment;
  • Available for the whole duration of the study including follow-up (60 months);
  • Life expectancy of > 5 years;
  • Patients with an ECOG performance status grade of 2 or less;
  • Absence of urothelial carcinoma involving the upper urinary tract or prostatic urethra within 12 months from beginning of study treatment;
  • Able to understand and give written informed consent;
  • In the investigator's judgment, the patient is able to participate in the study.

Exclusion Criteria:

  • Current or previous history of muscle invasive tumors;
  • Current or previous history of lymph node or distant metastases from bladder cancer;
  • Current systemic cancer therapy;
  • Current or prior pelvic external beam radiotherapy;
  • Pelvic brachytherapy within 2 years of study entry;
  • Prior treatment with MCC;
  • Patients with existing urinary tract infection or recurrent severe bacterial cystitis;
  • Clinically significant and unexplained elevations of liver or renal function tests;
  • White blood cell count below 3 x109/L (3,000/mm3) or platelet count below 100 x 109/L(100,000/mm3);
  • Severe cardiovascular disease;
  • Women who are pregnant or lactating;
  • Congenital or acquired immune deficiency;
  • With history of malignancy of any organ system, treated or untreated, within the past 5 years (with the exception of adequately treated basal cell or squamous cell carcinoma of the skin, stage T1 prostate cancer, carcinoma in situ of the cervix or colon polyps);
  • Previous investigational treatment within 3 months from beginning of study treatment;
  • Patients who cannot hold the instillation for one hour;
  • Patients who cannot tolerate intravesical administration or intravesical surgical manipulation (cystoscopy or biopsy);
  • Clinically significant active infections;
  • Any medical or psychiatric condition which, in the opinion of the investigator, would preclude the participant from adhering to the protocol or completing the trial per protocol.
Sex/Gender  ICMJE
Sexes Eligible for Study: All
Ages  ICMJE 18 Years and older   (Adult, Older Adult)
Accepts Healthy Volunteers  ICMJE No
Contacts  ICMJE Contact information is only displayed when the study is recruiting subjects
Listed Location Countries  ICMJE Canada,   United States
Removed Location Countries  
 
Administrative Information
NCT Number  ICMJE NCT00406068
Other Study ID Numbers  ICMJE HIS-0611-0602
Has Data Monitoring Committee Yes
U.S. FDA-regulated Product Not Provided
IPD Sharing Statement  ICMJE Not Provided
Responsible Party Bioniche Life Sciences Inc.
Study Sponsor  ICMJE Bioniche Life Sciences Inc.
Collaborators  ICMJE Not Provided
Investigators  ICMJE
Principal Investigator: Alvaro Morales, MD Centre for Applied Urological Research, Kingston General Hospital/Queen's University
PRS Account Bioniche Life Sciences Inc.
Verification Date July 2016

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP