Non Muscle Invasive Bladder CancerPhase 3BOND-003NCT04452591
Study of Cretostimogene Given in Patients With Non-Muscle Invasive Bladder Cancer ,Unresponsive to Bacillus-Calmette-Guerin
A Phase 3 study testing Cretostimogene Grenadenorepvec and n-dodecyl-B-D-maltoside in people with Non Muscle Invasive Bladder Cancer and High-grade Ta/ T1 Papillary Disease Bladder Cancer, run by CG Oncology, Inc. at 86 sites in 6 countries.
Trial summary
This is a Phase 3, open-label, single arm trial designed to evaluate Cretostimogene patients with NMIBC who have failed prior BCG therapy. Up to approximately 115 CIS bladder cancer patients with or without HG Ta or HG T1 papillary disease will be enrolled under the original protocol through Amendment 4, which will… Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Non Muscle Invasive Bladder Cancer, High-grade Ta/ T1 Papillary Disease Bladder Cancer
- What is being tested?
- Cretostimogene Grenadenorepvec and n-dodecyl-B-D-maltoside
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 190 participants
- Where
- 86 sitesin 6 countries
- Study dates
- 27 Oct 2020to 24 Dec 2031
- Phase
- Phase 3
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Cohort C Inclusion Criteria
In order to be eligible for participation in this trial, the patient must:
- Be ≥18 years of age (or legal age of majority in the jurisdiction) on day of signing informed consent.
- Have Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2.
- Have pathologically confirmed (WHO grading system employed for tumor grading) (Compérat 2019) BCG unresponsive CIS. Patients with BCG unresponsive CIS are those unlikely to benefit from, and who will not be receiving, further intravesical BCG. There is no maximum limit to the amount of prior BCG treatment, but maintenance BCG should be administered on a schedule consistent with standard induction-maintenance protocols (e.g., BCG weekly × 6 then weekly × 3 weeks administered at Months 3, 6, 12, 18, 24, and 36). Specifically, the definition of BCG unresponsive CIS will also require the following:
- Pathologically confirmed relapsed or persistent CIS (with or without HG Ta or HG T1 disease) within 12 months of completion (last dose) of adequate BCG treatment for HGUC (e.g., CIS, HG Ta, HG T1, or a combination of these HGUC pathologies).
- Completion of qualifying BCG treatment (e.g., "5+2" minimum exposure) within 12 months of the initial qualifying dose of BCG (e.g., induction and initial maintenance or re-induction cycle must be completed over no more than a 12-month period of time).
- Pathological confirmation of BCG unresponsive CIS within 8 weeks of study enrollment.
- CIS specimen must be predominantly urothelial (transitional cell) and have less than 50% variant (e.g., sarcomatoid, squamous etc. component) histology.
- No maximum limit to the amount of BCG administered but maintenance BCG should be administered on a schedule consistent with the SWOG 8507 regimen (Lamm 2000).
- Have all Ta and/or T1 disease resected and all CIS resected or fulgurated, as feasible, prior to study treatment (e.g., prior to Day 1 treatment).
- Ineligible to receive radical cystectomy (medically unfit) or refusal of radical cystectomy according to Investigator assessment.
- Demonstrate adequate organ function
- Patients must be willing to comply with study mandated cystoscopies, urine cytology, urograms, biopsies, and other procedures (including TURBT or other resection for all Ta/T1 disease) for the duration of the study. Patients who withdraw consent for these procedures will be withdrawn from the trial
Cohort P Inclusion Criteria
- Be ≥18 years of age (or legal age of majority in the jurisdiction) on day of signing informed consent
- Have ECOG performance status of 0 to 2.
- Have pathologically confirmed (WHO grading system employed for tumor grading) (Compérat 2019) BCG-unresponsive HG Ta/T1 papillary disease without CIS. Patients with BCG-unresponsive HG Ta/T1 papillary disease are those unlikely to benefit from and who will not be receiving further IVE BCG. There is no maximum limit to the amount of prior BCG treatment, but maintenance BCG should be administered on a schedule consistent with standard induction-maintenance protocols. Specifically, the definition of BCG unresponsive HG Ta/T1 papillary disease without CIS will also require the following:
- Pathologically confirmed recurrent HG Ta/T1 papillary disease without CIS within 6 months of completion (last dose) of adequate BCG treatment for HGUC (e.g., CIS, HG Ta, HG T1, or a combination of these HGUC pathologies).
- Patients with HG Ta: Completion of qualifying BCG treatment (e.g., "5+2" minimum exposure) within 12 months of the initial qualifying dose of BCG (e.g., induction and initial maintenance or re-induction cycle must be completed over no more than a 12-month period of time).
- Patients with HG T1: Patients may be eligible after the initial induction alone (5 of 6 doses of an induction course) as the qualifying BCG treatment.
- Completion (last dose) of qualifying BCG treatment within 12 months of study enrollment.
- Pathological confirmation of BCG-unresponsive HG Ta/T1 papillary disease without CIS within 14 days of study enrollment.
- All pathology specimens must be predominantly urothelial (transitional cell) and have less than 50% variant (e.g., sarcomatoid, squamous etc. component) histology.
- No maximum limit to the amount of BCG administered; however, there should be no more than 12 months between cycles of BCG
- Have all Ta and/or T1 disease resected, prior to study treatment (e.g., prior to Day 1 treatment).
- Ineligible to receive radical cystectomy (medically unfit) or refusal of radical cystectomy based on Investigator assessment.
- Demonstrate adequate organ function,
- Patients must be willing to comply with study-mandated cystoscopies, urine cytology, imaging, biopsies, and other procedures for the duration of the trial
Cohort C and Cohort P Key Exclusion Criteria:
- Has current or past history of muscle invasive (T2 or higher stage) or locally advanced (T3/T4, any N) or metastatic bladder cancer.
- Any HGUC as T1, HG Ta, or CIS in the upper genitourinary tract or prostatic urethra (including CIS of the urethra) within 24 months prior to enrollment OR any history of T2 or higher stage urothelial carcinoma in the upper genitourinary tract (kidneys, renal collecting systems, ureters).
- Has received systemic anti-cancer therapy, including investigational agents, within 4 weeks of Day 1.
- Has had prior systemic treatment (with the exception of checkpoint inhibitor therapy), radiation therapy, or surgery for bladder cancer other than TURBT or bladder biopsies.
- Has any of the following within the 6 months prior to starting study treatment: myocardial infarction, severe/unstable angina, coronary/peripheral artery bypass graft, cerebrovascular accident, pulmonary embolus, uncontrolled hypertension, or uncontrolled congestive heart failure.
- Cannot tolerate study-related biopsies, IVE administration, or 1-hour bladder hold of cretostimogene.
- IVE therapy within 8 weeks prior to beginning study treatment with the exception of cytotoxic agents (e.g., Mitomycin C, gemcitabine, doxorubicin and epirubicin) when administered as a single instillation immediately following a TURBT procedure which is permitted 14 or more days prior to beginning study treatment
Trial locations and contacts
86 sites in 6 countries.
86 sites in 6 countries
United States45 sites
Emory University
Atlanta, Georgia, 30322
University of Colorado
Aurora, Colorado, 80045
Our Lady of Lourdes
Binghamton, New York, 13905
Brigham and Women's Hospital
Boston, Massachusetts, 02115
Duke University
Durham, North Carolina, 27710
New Jersey Premier Urology
Edison, New Jersey, 08837
Conrad Pearson Clinic
Germantown, Tennessee, 38138
Prisma Health - Regional Urology
Greenville, South Carolina, 29605
Urology Indiana LLC
Greenwood, Indiana, 46143
Chesapeake Urology
Hanover, Maryland, 21076
Urology Centers Alabama
Homewood, Alabama, 35209
Houston Metro Urology
Houston, Texas, 77027
University of California - Irvine
Irvine, California, 92868
Mayo Clinic - Jacksonville
Jacksonville, Florida, 32224
Southern Urology
Lafayette, Louisiana, 70508
Colorado Clinical Research
Lakewood, Colorado, 80228
Keystone Urology Specialists
Lancaster, Pennsylvania, 17601
Arkansas Urology
Little Rock, Arkansas, 72211
Urology Associates, Research Department
Lone Tree, Colorado, 80124
American Insititute of Research
Los Angeles, California, 90017
Carolina Urologic Research Center LLC
Myrtle Beach, South Carolina, 29572
Urology Associates- Nashville
Nashville, Tennessee, 37209
Vanderbilt University Medical Center, Dept of Urology
Nashville, Tennessee, 37232
University of Pennsylvania, Perelman School of Medicine
Philadelphia, Pennsylvania, 19104
BCG Oncology
Phoenix, Arizona, 85032
Mayo Clinic Cancer Center
Phoenix, Arizona, 85054
Mayo Rochester
Rochester, Minnesota, 55905
Urology San Antonio, PA
San Antonio, Texas, 78229
Chesapeake Urology
Severna Park, Maryland, 21076
Genesis Research
Sherman Oaks, California, 91411
Spokane Urology
Spokane, Washington, 99202
Mercy Medical Center
St Louis, Missouri, 63109
Washington University
St Louis, Missouri, 63130
Specialty Clinical Research of St. Louis
St Louis, Missouri, 63141
Stony Brook University
Stony Brook, New York, 11794
Moffit Cancer Center
Tampa, Florida, 33612
Baylor Scott & White Medical Center-Temple
Temple, Texas, 76508
Montifiore Medical Center
The Bronx, New York, 10461
University of Toledo
Toledo, Ohio, 43614
Genesis Research LLC
Torrance, California, 90505
Arizona Institute of Urology
Tucson, Arizona, 85704
MedStar Washington Hospital Center
Washington D.C., District of Columbia, 20010
The University of Kansas Cancer Center
Westwood, Kansas, 66205
Wichita Urology
Wichita, Kansas, 67226
Wake Forest
Winston-Salem, North Carolina, 27157
Japan25 sites
National Cancer Center Hospital East
Chiba
Nagoya University Hospital
Fujita
Hirosaki University Hospital
Hashimoto
Chugoku Rosai Hospital
Hiroshima
Shinshu University Hospital
Ishizuka
University of Tsukuba Hospital
Kandori, Ibaraki, 305-8576
Nara Medical University Hospital
Kashihara, Nara, 634-8522
The Jikei University Kashiwa Hospital
Kashiwa-shi, Chiba, 227-8567
St. Marianna University Hospital
Kawasaki, Kanagawa, 216-8511
National Hospital Organization Kyoto Medical Center
Kyoto, Kyoto, 6128555
Kagawa Rosai Hospital
Marugame, Kagawa-ken, 763-8502
Keio University Hospital
Matsumoto, Tokyo, 160-8582
Okayama University Hospital
Okayama, Okayama-ken, 700-8558
Osaka City University Hospital
Osaka, Osaka, 545-8586
Osaka Medical and Pharmaceutical University Hospital
Osaka, Osaka, 569-8686
Osaka International Cancer Institute
Osaka
Kitsato University Hospital
Sagamihara
Saitama City Hospital
Saitama, Saitama, 3368522
Sapporo Medical University Hospital
Sapporo, Hokkaido, 060-8543
Shizuoka General Hospital
Shizuoka, Shizuoka, 420-8527
Keio University Hospital
Tokyo, Tokyo, 160-8582
Ehime University Hospital
Tōon, Ehime, 791-0295
Toyama University Hospital
Toyama, Toyama, 930-0194
Wakayama Medical University Hospital
Wakayama, Wakayama, 6418510
National Hospital Organization Yokohama Medical Center
Yokohama, Kanagawa, 245-8575
South Korea7 sites
Pusan National University Hospital
Busan, 49241
National Cancer Center
Goyang-si, Gyeonggi-do, 10408
Pusan National University Yangsan Hospital
Gyeongsang, 50612
Chonnam National University Hwasun Hospital
Jeongnam, 58128
Korea University Anam Hospital
Seoul, 02841
Seoul National University Hospital
Seoul, 03080
The Catholic University of Korea
Seoul, 06591
Taiwan4 sites
Keelung Chang Gung Memorial Hospital
Keelung, 20401
China Medical University Hospital
Taichung, 40447
Taipei Veterans General Hospital
Taipei, 11217
National Taiwan University Hospital
Taipei
Australia3 sites
Barwon Health, University Hospital Geelong, Andrew love cancer center
Geelong
Royal Melbourne Hospital
Melbourne
Southside Cancer Care Center
Miranda, New South Wales, 2228
Canada2 sites
CHUM Center for Research
Montreal, Quebec, H2X0A9
MUHC Glen-Ceders Cancer Centre, Oncology Pharmacy
Montreal, Quebec, H4A 3JI
About this study
Official title: A Phase 3 Study of Cretostimogene Grenadenorepvec in Patients With Non-Muscle Invasive Bladder Cancer (NMIBC) Unresponsive to Bacillus-Calmette-Guerin (BCG)
This is a Phase 3, open-label, single arm trial designed to evaluate Cretostimogene patients with NMIBC who have failed prior BCG therapy. Up to approximately 115 CIS bladder cancer patients with or without HG Ta or HG T1 papillary disease will be enrolled under the original protocol through Amendment 4, which will comprise Cohort C. Cohort C is closed to enrollment.
Under Amendment 5-1, Cohort P was added to enroll up to 70 patients with HG Ta/T1 papillary bladder cancer.
Read more
Under Amendment 6, the target number of patients enrolled in Cohort P was increased to 75. Cohort P is open to enrollment
Cohort C and Cohort P will be analyzed and reported separately. Patients will have had to fail prior BCG therapy which is defined as having persistent or recurrent disease within 12 months (Cohort C) or 6 months (Cohort P) following the completion of adequate BCG therapy for HGUC
Read the detailed description
Cohort C(All Countries) :
An open-label trial designed to evaluate Cretostimogene + DDM in patients with NMIBC who have failed prior BCG therapy. Single treatment arm that enrolled 115 patients with carcinoma in situ with or without concomitant high-grade Ta or T1 papillary disease
BCG failure is defined as a persistent or recurrent disease within 12 months of completion of adequate BCG therapy.
Cohort P(Japan and the United States Only):
To determine the all-cause High Grade Event Free Survival (HG-EFS) of cretostimogene in up to 75 patients with BCG-unresponsive HG Ta/T1 papillary disease without CIS.
BCG failure is defined as a persistent or recurrent disease within 6 months of completion of adequate BCG therapy.
- Being tested
- Cretostimogene Grenadenorepvec, n-dodecyl-B-D-maltoside
- Keywords
- high-grade Ta papillary disease, high-grade T1 papillary disease, carcinoma in situ, Bacillus-Calmette-Guerin unresponsive
- Medical subject headings
- Non-Muscle Invasive Bladder Neoplasms, Carcinoma in Situ
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Cretostimogene GrenadenorepvecBiological
Engineered Oncolytic Adenovirus
n-dodecyl-B-D-maltosideOther
Also called DDM
Transduction-enhancing agent.
| Study group | Role | What they receive |
|---|---|---|
| Cohort C(All Countries):Enrollment Closed | Experimental | Patients with CIS with or without HG Ta/T1 papillary disease. Cretostimogene will be administered intravesically following a series of bladder washes with 5% DDM and normal saline. Cretostimogene will be administered weekly x 6 on Weeks 1, 2, 3, 4, 5, and 6. If the patient has disease recurrence at Week 13, they will receive another cycle of 6 weekly treatments. If there is no disease present at Week 13 then the patient will receive 3 weekly treatments. Cohort C(All Countries):Beginning at Week 25, patients will receive weekly x 3 treatments every 12 weeks through week 51 then every 6 months and then a last treatment at Weeks 73, 74, and 75 until the tumor returns or study treatment is completed at Week 97. Cohort C Extension( Japan and the US) At Week 25, patients will receive weekly x 3 treatments every 12 weeks through week 51 then every 6 months starting at Weeks 73, 74, and 75 through Weeks 157, 158, and 159 until the tumor returns or study treatment is completed at Week 159. Receives: Biological: Cretostimogene Grenadenorepvec; Other: n-dodecyl-B-D-maltoside |
| Cohort P(Japan and United States Only) :Open to Enrollment | Experimental | HG Ta/T1 papillary disease bladder cancer patients.
In Cohort P, cretostimogene will be administered at a dose of 1 × 1012vp IVE following instillation of 5% DDM. Cretostimogene will be administered every week for 6 treatments on Weeks 1, 2, 3, 4, 5, and 6. If the patient has recurrence at Week 13 or any timepoint, the patient will receive a second induction of 6 weekly treatments (Weeks 13, 14, 15, 16, 17, and 18.). If the tumor has not returned they will receive 3 weekly treatments every 12 weeks (approximately 3 months) starting Weeks 13, 14, and 15 through Week 51 (approximately 12 months), and then every 6 months starting at Weeks 73, 74, and 75 (approximately 18 months) through Month 36. Receives: Biological: Cretostimogene Grenadenorepvec; Other: n-dodecyl-B-D-maltoside |
What is being measured
The primary outcome is the main question the study is designed to answer.
Cohort C:
To determine the Complete Response rate at any time in patients with BCG-unresponsive CIS with or without concomitant HG Ta/T1 papillary disease.
Measured: 36 months
Cohort P:
To determine the high-grade EFS of cretostimogene in patients with BCG-unresponsive HG Ta/T1 papillary disease without CIS.Ta/T1 papillary disease without CIS.
Measured: 36 months
Secondary outcomes (8)
Cohort C: Duration of response (DOR)
Median duration of response in patients with a CR or PR in subjects
Measured: 36 months
Cohort C and Cohort P: Assess high-grade reoccurrence free survival (RFS)
Measured: up to 60 months
Cohort C and Cohort P: Assess progression free survival (PFS )
Measured: up to 60 months
Cohort C:Complete Response rate at 12 months
Measured: 12 months
Cohort C and Cohort P : Cystectomy free survival
Measured: up to 60 months
Cohort C and Cohort P: Evaluate the safety of Cretostimogene
Measured: 36 months
Cohort C: Assess overall survival
Measured: up to 60 months
Cohort C: Reoccurrence free survival
Measured: up to 60 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted30 Jun 2020
- Study start27 Oct 2020
- Primary completion16 Jun 2030 (estimated)
- Study completion24 Dec 2031 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Non Muscle Invasive Bladder CancerStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 3
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 190 participants (estimated)
Sponsor and investigators
- Lead sponsor
- CG Oncology, Inc.
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- CG Oncology, Study director, CG Oncology
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04452591
- Sponsor's protocol ID
- CG3002S
- Acronym
- BOND-003
- Status last verified
- Jul 2026
- First submitted
- 26 Jun 2020
- Last updated
- 10 Jul 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
- Individual data sharing
- No
- Expanded access
- Available
Publications
Tyson MD 2nd, Nam JK, Joshi SS, Uchio EM, Jung SI, Bivalacqua TJ, Steinberg GD, Shore ND, Burke JM, Kitamura H, Tran B, Li R. Intravesical cretostimogene grenadenorepvec oncolytic immunotherapy in high-risk, BCG-unresponsive, non-muscle-invasive bladder cancer with carcinoma in situ (BOND-003 Cohort C): a single-arm, phase 3 trial. Lancet Oncol. 2026 Aug;27(8):983-993. doi: 10.1016/S1470-2045(26)00194-4.
PubMed 42508433
Study at a glance
From the registry record, last updated by the sponsor on 10 Jul 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Phase 3 Study of Cretostimogene Grenadenorepvec in Patients With Non-Muscle Invasive Bladder Cancer (NMIBC) Unresponsive to Bacillus-Calmette-Guerin (BCG)
- ClinicalTrials.gov ID
- NCT04452591
- Acronym / sponsor ID
- BOND-003 / CG3002S
- Keywords
- high-grade Ta papillary disease, high-grade T1 papillary disease, carcinoma in situ, Bacillus-Calmette-Guerin unresponsive
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- Active, not recruiting
- Enrolment
- 190 participants (estimated)
- Lead sponsor
- CG Oncology, Inc.Industry (pharma, biotech, devices)
- Study start
- 27 Oct 2020 (actual)
- Primary completion
- 16 Jun 2030 (estimated)
- Study completion
- 24 Dec 2031 (estimated)
- First posted
- 30 Jun 2020 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This is a Phase 3, open-label, single arm trial designed to evaluate Cretostimogene patients with NMIBC who have failed prior BCG therapy. Up to approximately 115 CIS bladder cancer patients with or without HG Ta or HG T1 papillary disease will be enrolled under the original protocol through Amendment 4, which will comprise Cohort C. Cohort C is closed to enrollment.
Under Amendment 5-1, Cohort P was added to enroll up to 70 patients with HG Ta/T1 papillary bladder cancer.
Under Amendment 6, the target number of patients enrolled in Cohort P was increased to 75. Cohort P is open to enrollment
Cohort C and Cohort P will be analyzed and reported separately. Patients will have had to fail prior BCG therapy which is defined as having persistent or recurrent disease within 12 months (Cohort C) or 6 months (Cohort P) following the completion of adequate BCG therapy for HGUC
Detailed description
Cohort C(All Countries) :
An open-label trial designed to evaluate Cretostimogene + DDM in patients with NMIBC who have failed prior BCG therapy. Single treatment arm that enrolled 115 patients with carcinoma in situ with or without concomitant high-grade Ta or T1 papillary disease
BCG failure is defined as a persistent or recurrent disease within 12 months of completion of adequate BCG therapy.
Cohort P(Japan and the United States Only):
To determine the all-cause High Grade Event Free Survival (HG-EFS) of cretostimogene in up to 75 patients with BCG-unresponsive HG Ta/T1 papillary disease without CIS.
BCG failure is defined as a persistent or recurrent disease within 6 months of completion of adequate BCG therapy.
Study design
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Cohort C(All Countries):Enrollment Closed | Experimental | Biological: Cretostimogene Grenadenorepvec, Other: n-dodecyl-B-D-maltosidePatients with CIS with or without HG Ta/T1 papillary disease. Cretostimogene will be administered intravesically following a series of bladder washes with 5% DDM and normal saline. Cretostimogene will be administered weekly x 6 on Weeks 1, 2, 3, 4, 5, and 6. If the patient has disease recurrence at Week 13, they will receive another cycle of 6 weekly treatments. If there is no disease present at Week 13 then the patient will receive 3 weekly treatments. Cohort C(All Countries):Beginning at Week 25, patients will receive weekly x 3 treatments every 12 weeks through week 51 then every 6 months and then a last treatment at Weeks 73, 74, and 75 until the tumor returns or study treatment is completed at Week 97. Cohort C Extension( Japan and the US) At Week 25, patients will receive weekly x 3 treatments every 12 weeks through week 51 then every 6 months starting at Weeks 73, 74, and 75 through Weeks 157, 158, and 159 until the tumor returns or study treatment is completed at Week 159. |
| Cohort P(Japan and United States Only) :Open to Enrollment | Experimental | Biological: Cretostimogene Grenadenorepvec, Other: n-dodecyl-B-D-maltosideHG Ta/T1 papillary disease bladder cancer patients. In Cohort P, cretostimogene will be administered at a dose of 1 × 1012vp IVE following instillation of 5% DDM. Cretostimogene will be administered every week for 6 treatments on Weeks 1, 2, 3, 4, 5, and 6. If the patient has recurrence at Week 13 or any timepoint, the patient will receive a second induction of 6 weekly treatments (Weeks 13, 14, 15, 16, 17, and 18.). If the tumor has not returned they will receive 3 weekly treatments every 12 weeks (approximately 3 months) starting Weeks 13, 14, and 15 through Week 51 (approximately 12 months), and then every 6 months starting at Weeks 73, 74, and 75 (approximately 18 months) through Month 36. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Cretostimogene GrenadenorepvecEngineered Oncolytic Adenovirus | Biological | Cohort C(All Countries):Enrollment Closed, Cohort P(Japan and United States Only) :Open to Enrollment |
| n-dodecyl-B-D-maltosideAlso: DDMTransduction-enhancing agent. | Other | Cohort C(All Countries):Enrollment Closed, Cohort P(Japan and United States Only) :Open to Enrollment |
Primary outcome
Cohort C:
Time frame: 36 months
To determine the Complete Response rate at any time in patients with BCG-unresponsive CIS with or without concomitant HG Ta/T1 papillary disease.
Cohort P:
Time frame: 36 months
To determine the high-grade EFS of cretostimogene in patients with BCG-unresponsive HG Ta/T1 papillary disease without CIS.Ta/T1 papillary disease without CIS.
8 secondary outcomes
Cohort C: Duration of response (DOR)
Time frame: 36 months
Cohort C and Cohort P: Assess high-grade reoccurrence free survival (RFS)
Time frame: up to 60 months
Cohort C and Cohort P: Assess progression free survival (PFS )
Time frame: up to 60 months
Cohort C:Complete Response rate at 12 months
Time frame: 12 months
Cohort C and Cohort P : Cystectomy free survival
Time frame: up to 60 months
Cohort C and Cohort P: Evaluate the safety of Cretostimogene
Time frame: 36 months
Cohort C: Assess overall survival
Time frame: up to 60 months
Cohort C: Reoccurrence free survival
Time frame: up to 60 months
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 10 Jul 2026.
- Derived from this study: PubMed 42508433Tyson MD 2nd, Nam JK, Joshi SS, Uchio EM, Jung SI, Bivalacqua TJ, Steinberg GD, Shore ND, Burke JM, Kitamura H, Tran B, Li R. Intravesical cretostimogene grenadenorepvec oncolytic immunotherapy in high-risk, BCG-unresponsive, non-muscle-invasive bladder cancer with carcinoma in situ (BOND-003 Cohort C): a single-arm, phase 3 trial. Lancet Oncol. 2026 Aug;27(8):983-993. doi: 10.1016/S1470-2045(26)00194-4.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
CG Oncology study director
CG Oncology
86 sites in 6 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing Cretostimogene Grenadenorepvec and n-dodecyl-B-D-maltoside in people with Non Muscle Invasive Bladder Cancer and High-grade Ta/ T1 Papillary Disease Bladder Cancer, run by CG Oncology, Inc. at 86 sites in 6 countries.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: under way, not looking for participants, as of the sponsor's last update on 10 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 86 sites in United States, Japan, South Korea, Taiwan, Australia and 1 more country. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Cohort C: (time frame: 36 months). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT04452591, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Jul 2026.