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Recruiting Phase 3

A Trial to Evaluate Intravesical Nadofaragene Firadenovec Alone or in Combination With Chemotherapy or Immunotherapy in Participants With High-grade BCG Unresponsive Non-muscle Invasive Bladder Cancer

NCT06545955 · tracked via the Priya Life Science South Korea tracker
Phase
Phase 3
Started
2024-10-01
Last updated
2026-09-25

Condition(s) studied

Non-muscle Invasive Bladder Cancer With Carcinoma in Situ

Investigational drug(s) / intervention(s)

Nadofaragene Firadenovec →Gemcitabine →Docetaxel →Pembrolizumab →

Nadofaragene Firadenovec: vector-based gene therapy for NMIBC treatment to potentiate durable therapeutic responses by interferon (IFN) alfa-2b (IFN-α2b) amplification. It is a non-replicating recombinant adenovirus serotype 5 vector containing a transgene encoding the human IFN-α2b gene.

Gemcitabine: Intravesical Gemcitabine chemotherapy, used in combination with Docetaxel.

Docetaxel: Intravesical Docetaxel chemotherapy, used in combination with Gemcitabine.

Pembrolizumab: Pembrolizumab is an FDA approved immune checkpoint inhibitor which restores the anti-tumour immune response by blocking the programmed cell death protein 1 (PD-1). Pembrolizumab is administered via intravenous (IV) infusion.

Study summary

The pivotal phase 3 trial (rAd-IFN-CS 003) evaluating the efficacy of nadofaragene firadenovec showed that 55 (53.4%) of 103 subjects with CIS ± high-grade Ta/T1 achieved a complete response (CR) at 3 months. In this trial, the safety and efficacy of intravesical instillation of nadofaragene firadenovec alone or in combination with chemotherapy or immunotherapy will be evaluated in participants with NMIBC CIS (± high-grade Ta/T1).

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Diagnosed, as documented, with carcinoma in situ (CIS) ±Ta/T1 high-grade disease. * For T1 disease biopsies should contain muscle fibres. * Unresponsive to ≥2 courses of Bacillus Calmette-Guerin (BCG) therapy within the last 12 months. BCG-unresponsive refers to participants with high-grade non-muscle invasive bladder cancer (NMIBC) who are unlikely to benefit from and who will not be receiving further intravesical BCG. The term "BCG-Unresponsive" includes participants who did not respond to BCG treatment and have a persistent high-grade recurrence within 12 months after BCG was initiated, and those who despite an initial complete response to BCG, relapse with CIS within 12 months of their last intravesical treatment with BCG or relapse with high-grade Ta/T1 NMIBC within 6 months of their last intravesical treatment with BCG. The following criteria define the participants who may be included in the trial: * Have received at least 2 courses of BCG within a 12 month period - defined as at least 5 of 6 induction BCG instillations and at least 2 of 3 instillations of maintenance BCG, or at least 2 of 6 instillations of a second induction course, where maintenance BCG is not given. o Exception: those who have T1 high-grade disease at 1st evaluation after induction BCG alone (at least 5 of 6 doses) may qualify in the absence of disease progression * At the time of tumour recurrence, participants with CIS alone or high-grade Ta/T1 with CIS should be within 12 months of last exposure to BCG * No maximum limit to the amount of BCG administered * All visible papillary tumours must be resected and those with persistent T1 disease on transurethral resection of bladder tumour (TURBT) should undergo an additional re-TURBT within 14 to 70 days prior to beginning trial treatment. Obvious areas of CIS should also be fulgurated * Eastern Cooperative Oncology Group (ECOG) status ≤2 * Aged ≥18 years at the time of consent * Available for the whole duration of the trial * Life expectancy \>2 years, in the opinion of the investigator * Absence of concomitant upper tract urothelial carcinoma or urothelial carcinoma within the prostatic urethra. Freedom from upper tract disease (if clinically indicated) as indicated by no evidence of upper tract tumour by either intravenous pyelogram, retrograde pyelogram, computed tomography (CT) scan with or without urogram, or magnetic resonance imaging (MRI) with or without urogram performed within 6 months of enrolment. Absence of locally advanced disease as assessed by CT scan or MRI * Participants who elect not to undergo cystectomy * Participants with prostate cancer on active surveillance at low risk for progression are permitted to be included into the trial at the discretion of the investigator * Females of reproductive potential must have a negative highly sensitive urine or serum pregnancy test upon entry into this trial and be willing to use highly effective contraception during treatment with the investigational medicinal product and for 6 months following the last dose. Otherwise, female participants must be post-menopausal (no menstrual period for a minimum of 12 months, as confirmed by follicle-stimulating hormone levels) or surgically sterile * Male subjects must be willing to use a male condom and effective contraception during sex throughout the treatment period and for 3 months following the last dose. Exclusion Criteria: * Current or previous evidence of muscle-invasive (muscularis propria) or metastatic disease presented at the screening visit. Examples of increased risk of muscle-invasive disease include but are not limited to: * Presence of lymphovascular invasion and / or micropapillary, sarcomatoid, plasmacytoid and / or neuroendocrine disease as shown in the histology of the biopsy sample * Participants with CIS+T1 disease accompanied by the presence of hydronephrosis secondary to the primary tumour * Current systemic therapy for bladder cancer other than investigational medicinal products used in randomisation arm * Current or prior investigational treatment for BCG-unresponsive NMIBC or any other investigational drug (drug used in a clinical trial, i.e drug used in a Ferring sponsored non interventional study does not apply) within 1 month prior to screening * Current or prior pelvic external beam radiotherapy within 2 years of screening * Prior treatment with nadofaragene firadenovec at any time * Prior systemic therapy for bladder cancer at any time * Prior intravesical chemotherapy for the treatment of BCG-unresponsive NMIBC

Primary outcome measure(s)

  • Complete response — up to 6 months
    Complete response (CR) at any time from first treatment (defined as absence of high-grade (HG) recurrence).

Trial sites (80)

FacilityCityRegionStatus
Center for Neurosciences Tucson Arizona Recruiting
Arkansas Urology, North Little Rock Little Rock Arkansas Recruiting
American Institute of Research Los Angeles California Recruiting
USC Kenneth Norris Jr Cancer Hospital Los Angeles California Recruiting
University of California, Irvine Orange California Recruiting
Genesis Research, LLC - San Diego San Diego California Recruiting
Advent Health Denver Colorado Recruiting
Colorado Urology - St. Anthony Hospital Campus Lakewood Colorado Recruiting
Yale School of Medicine New Haven Connecticut Recruiting
Medstar Georgetown University Hospital Washington D.C. District of Columbia Recruiting
Sarasota Memorial Healthcare System Sarasota Florida Recruiting
Emory University Atlanta Georgia Recruiting
Georgia Urology Atlanta Georgia Recruiting
Boise VA Medical Center Boise Idaho Recruiting
NextStage Clinical Research Lisle Illinois Recruiting
Indiana University Indianapolis Indiana Recruiting
Wichita Urology Group Wichita Kansas Recruiting
Anne Arundel Urology, PA Annapolis Maryland Recruiting
Chesapeake Urology Research Associates Hanover Maryland Recruiting
The Urology Group P.C. Southhaven Mississippi Recruiting
Atlantic Health Morristown New Jersey Recruiting
Roswell Park Cancer Institute Buffalo New York Recruiting
Great Lakes Physician PC d/b/a Western new York Urology Associates Cheektowaga New York Recruiting
Northwell Health -The Arthur Smith Institute for Urology Lake Success New York Recruiting
Veterans Affairs New York Harbor Healthcare System - Manhattan VA Medical Center New York New York Recruiting
James J. Peters VA Medical Center The Bronx New York Recruiting
University of Cincinnati Cincinnati Ohio Recruiting
OSU Arthur James Cancer Hospital Columbus Ohio Recruiting
MidLantic Urology Bala-Cynwyd Pennsylvania Recruiting
Keystone Urology Specialists Lancaster Pennsylvania Recruiting
University of Pennsylvania - Perelman Center for Advanced Medicine - Penn Urology Philadelphia Pennsylvania Recruiting
University of Pittsburgh Medical Center - Shadyside Medical Building Pittsburgh Pennsylvania Recruiting
Carolina Urologic Research Center Myrtle Beach South Carolina Recruiting
The Conrad Pearson Clinic - Wolf River Office (Urology Center of the South) Germantown Tennessee Recruiting
Urology Associates, P.C. Nashville Tennessee Recruiting
Urology Austin Austin Texas Recruiting
Urology Clinics of North Texas PLLC (Dallas) Dallas Texas Recruiting
University of Texas Southwestern Medical Center - Urology Clinic Dallas Texas Recruiting
Houston Methodist Hospital (Houston) Houston Texas Recruiting
Virginia Mason Medical Center Seattle Washington Recruiting

+ 40 more sites — see the full list on the official registry below.

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06545955 on ClinicalTrials.gov ↗ ← All trials in South Korea