Phase 2b, Trial of Intravesical DTA-H19/PEI in Patients With Intermediate-Risk Superficial Bladder Cancer

NCT00595088 | Completed Phase 2 Results

• 1 other identifier: BC-07-01.CTIL
• Study Type: interventional
• Target: 47
• Locations: 2 countries
• Sites: 6

Brief Summary

This study is designed to assess the efficacy and safety of DTA-H19/PEI given as six intravesical instillations of 20 mg of plasmid DNA complexed with PEI into the bladder of patients with intermediate risk superficial bladder cancer \[recurrent stages Ta (low or high grade)and T1, (low grade) transitional cell carcinoma (TCC)\] who have failed prior intravesical therapies including either Bacillus Calmette-Guérin (BCG) or chemotherapy. The primary efficacy objective is to determine the effect of DTA-H19/PEI on the prevention of new tumors after the induction course of 6 weekly intravesical administrations of investigational product assessed 8 to 10 weeks after the start of treatment. Secondary objectives include assessing the ablative effect of DTA-H19/PEI on a marker tumor, safety assessed by the incidence and severity of adverse events, determining the long-term (46 weeks) continued rates of absence of bladder cancer, and time to tumor recurrence in those patients who had a complete response (CR) after the induction course.

Conditions

Superficial Bladder Cancer

Keywords

Bladder Cancer; Refractory; inodiftagene vixteplasmid

Outcome Measures

Primary Outcomes (1)

• Complete Tumor Response Defined as the Absence of New Tumors

  Tumor response evaluated at week 9 (range 8-10 weeks) during the first post induction course treatment cystoscopy or TUR of suspiciaous lesions

  9 Weeks

Secondary Outcomes (2)

• Time to Tumor Recurrence

  46 Weeks

• Ablative Effect on a Marker Tumor

  9 weeks

Study Arms (1)

20 mg of BC-819/PEI

EXPERIMENTAL

Six intravesical instillations of 20 mg of plasmid DNA (BC-819) complexed with PEI into the bladder of patients with intermediate-risk superficial bladder cancer \[recurrent stages Ta (low or high grade) and T1 (low grade) TCC\] who have failed prior intravesical therapies including BCG and/or chemotherapy.

Biological: BC-819/PEI

Interventions

BC-819/PEI BIOLOGICAL

Papillary tumors will be resected with the exception of one marker tumor that will remain to examine the effects of the treatment on the remaining tumor. Study treatments will consist of an induction course of six weekly instillations of 20 mg of DTA-H19/PEI into the urinary bladder. Intravesical therapy will be delivered through a Foley catheter. Patients will be instructed to hold the dose in the bladder for two hours after administration. If the patient has a complete response, then she/he will be eligible to receive three additional courses of 3 weekly intravesical administrations of the same dose of investigational product every 12 weeks.

Also known as: DTA-H19

20 mg of BC-819/PEI

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• To be eligible to participate in this study, patients must:
• Provide written informed consent.
• Have intermediate-risk recurrent superficial TCC of the bladder defined as Stage Ta (low or high grade) or T1 (but with penetration into no more than ½ of the lamina propria), low grade (grade 1 or grade 2), as confirmed by histopathology, and have not recurred within 3-months of a complete course of a prior acceptable therapy (i.e., 6-weekly intravesical administrations of BCG or standard adjuvant treatment with thiotepa, doxorubicin, epirubicin, valrubicin, or mitomycin C).
• Have complete resection of all papillary tumors with the exception of a single superficial papillary tumor that is appropriate to be a marker tumor (\<1 cm in diameter).
• Have ≥ 2 tumor and ≤ 7 tumors visible during cystoscopy and no tumor larger than 3 cm in diameter. If only one tumor is present, it must be large enough to obtain a biopsy specimen adequate to determine the tumor stage and grade and leave a marker tumor.
• Have at least one tumor specimen resected before the start of the study that was positive for H19 expression by ISH. H19 expression positive is defined as \>= 60 % of the tumor cells in the specimen expressing H19 at a moderate staining intensity.
• Have failed at least one prior standard intravesical treatment including chemotherapy with mitomycin C, thiotepa, valrubicin, doxyrubicin, or epirubicin, or immunotherapy with BCG. Failure after treatment with chemotherapy is defined as recurrent disease after at least one intravesical instillation of drug. Failure after treatment with BCG is defined as intolerance to treatment such that treatment was discontinued or after having received 6 or more BCG instillations there is recurrent or persistent disease 3 or more months after initiation of BCG treatment.
• Have a Karnofsky's performance status of greater than or equal to 60%.
• Have adequate bone marrow reserve: Hemoglobin \> 10 g/dL, WBC greater than or equal to 3000/mm3, and platelets \> 100,000 /mm3.
• Have adequate renal function with serum creatinine \< 1.5 x the laboratory upper limit of normal (ULN).
• Have adequate liver function with serum biliru¬bin, AST/SGOT and ALT/SGPT \< 2 times the laboratory ULN.
• Be at least 18 years of age.
• If male, agree to use a condom, if sexually active, and if female, agree to practice one of the acceptable methods of birth control or be surgically sterile or postmenopausal (greater than 1 year post last menstrual cycle.

You may not qualify if:

• To be eligible to participate in this study, patients must not:
• Have current diagnosis or history of Stage T1 (high grade) or Stage T2 or higher or CIS.
• Have severe concomitant disease that might limit compliance or completion of the protocol.
• Have a tumor in a diverticulum, in the prostatic urethra, or covering the ureteral orifice.
• Have any other malignancy that might impact 5-year survival or might be potentially confused with TCC.
• Have congenital or acquired immune deficiencies.
• Be receiving cytotoxic drugs or corticosteroids.
• Have received intravesical therapy within 8 weeks prior to study entry.
• Have received radiation therapy for their bladder cancer at any time or any other conditions including pelvic irradiation for any condition within 4 months prior to study entry.
• Have active infections (including urinary tract infections) defined as viral, bacterial, or fungal infections requiring therapy, HIV-positive status, concurrent febrile illness, or gross hematuria.
• Have biopsy, TUR, or traumatic catheterization within 14 days of start of treatment.
• If female, be pregnant or breast feeding.
• Have participated in any therapeutic research study within the last 8 weeks.
• Have participated in any other gene therapy study including patients who have received DTA-H19/PEI in the past.

Sponsors & Collaborators

• Anchiano Therapeutics Israel Ltd.: lead

Study Sites (6)

BCG Oncology

Phoenix, Arizona, 85032, United States

Location

Bnai Zion Medical Center

Haifa, Israel

Location

Edith Wolfson Medical Center

Holon, Israel

Location

Hadassah and Hebrew University Medical Center

Jerusalem, Israel

Location

Meir Medical Center

Kfar Saba, Israel

Location

Assaf Harofeh

Zrifin, Israel

Location

MeSH Terms

Conditions

Non-Muscle Invasive Bladder Neoplasms; Urinary Bladder Neoplasms

Condition Hierarchy (Ancestors)

Carcinoma; Neoplasms, Glandular and Epithelial; Neoplasms by Histologic Type; Neoplasms; Urologic Neoplasms; Urogenital Neoplasms; Neoplasms by Site; Female Urogenital Diseases; Female Urogenital Diseases and Pregnancy Complications; Urogenital Diseases; Urinary Bladder Diseases; Urologic Diseases; Male Urogenital Diseases

Results Point of Contact

• Title: Dr. Sarel Halachmi
• Organization: Bnai Zion Medical Center

sarel.halachmi@b-zion.org.il

+97248359542

Study Officials

• Donald Lamm, MD

  University of Arizona and BCG Oncolgy

  PRINCIPAL INVESTIGATOR

Publication Agreements

• PI is Sponsor Employee: No
• Restrictive Agreement: No

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: January 7, 2008
• First Posted: January 16, 2008
• Study Start: January 1, 2008
• Primary Completion: January 1, 2013
• Study Completion: January 1, 2013
• Last Updated: April 30, 2019
• Results First Posted: August 21, 2013

Record last verified: 2019-04

Locations

US (1); IL (5)