An Expanded Access Program of Cretostimogene Grenadenorepvec for Treatment of NMIBC for Patients Unresponsive to BCG
An Expanded Access Program of Cretostimogene Grenadenorepvec in Patients With Non-Muscle Invasive Bladder Cancer (NMIBC) Unresponsive to Bacillus Calmette-Guerin (BCG)
Sponsor: CG Oncology, Inc.
A observational or N/A phase clinical study on Bladder Cancer and Non-Muscle Invasive Bladder Cancer, this trial is ongoing. The trial is conducted by CG Oncology, Inc. and has accumulated 12 data snapshots since 2026. Oncology trials at this stage typically focus on safety, tolerability, and early efficacy signals.
Study Description(click to expand)All participants will be assigned the same treatment schedule. Participants will receive an induction course of 6 weekly treatments, and, if there is no disease recurrence at Week 13, participants will receive a cycle of 3 weekly treatments up to Week 15. If there is persistent HG Ta and/or CIS at Week 13, participants may receive a second induction cycle. If the participant has persistent but improved HG Ta and/or CIS at Week 25 or a later timepoint, the participant may receive a cycle of 3 weekly treatments of cretostimogene at the discretion of the Investigator provided that T1 or higher stage of urothelial carcinoma is not present. If there is no disease present at Week 25 or a later timepoint, participants will receive a cycle of 3 weekly treatments every 12 weeks through Month 12. After Month 12, participants will receive a cycle of 3 weekly treatments every 6 months through the last treatment cycle at Month 24, or until discontinuation from the study treatment. Disease status will be assessed based on local standard of care (which may include urine cytology, cystoscopy, and directed TURBT/biopsy) every 12 weeks. CTU/MRU can be done per standard of care evaluation at investigator's...
All participants will be assigned the same treatment schedule. Participants will receive an induction course of 6 weekly treatments, and, if there is no disease recurrence at Week 13, participants will receive a cycle of 3 weekly treatments up to Week 15.
If there is persistent HG Ta and/or CIS at Week 13, participants may receive a second induction cycle.
If the participant has persistent but improved HG Ta and/or CIS at Week 25 or a later timepoint, the participant may receive a cycle of 3 weekly treatments of cretostimogene at the discretion of the Investigator provided that T1 or higher stage of urothelial carcinoma is not present.
If there is no disease present at Week 25 or a later timepoint, participants will receive a cycle of 3 weekly treatments every 12 weeks through Month 12.
After Month 12, participants will receive a cycle of 3 weekly treatments every 6 months through the last treatment cycle at Month 24, or until discontinuation from the study treatment.
Disease status will be assessed based on local standard of care (which may include urine cytology, cystoscopy, and directed TURBT/biopsy) every 12 weeks. CTU/MRU can be done per standard of care evaluation at investigator's discretion.
Status Flow
Change History
12 versions recorded-
Apr 16, 2026 — Present [daily]
Available
-
Mar 2026 — Apr 2026 [monthly]
Available
-
Jan 2026 — Mar 2026 [monthly]
Available
-
Dec 2025 — Jan 2026 [monthly]
Available
-
Nov 2025 — Dec 2025 [monthly]
Available
▶ Show 7 earlier versions
-
Oct 2025 — Nov 2025 [monthly]
Available
-
Sep 2025 — Oct 2025 [monthly]
Available
-
Aug 2025 — Sep 2025 [monthly]
Available
-
Jul 2025 — Aug 2025 [monthly]
Available
-
May 2025 — Jul 2025 [monthly]
Available
-
Sep 2024 — May 2025 [monthly]
Available
-
Jul 2024 — Sep 2024 [monthly]
Available
First recorded
Eligibility Summary
This is an open-label, expanded access trial designed to provide access to cretostimogene in patients with NMIBC (specifically CIS with or without HG Ta/T1) unresponsive to BCG.
Contact Information
- CG Oncology, Inc.
For direct contact, visit the study record on ClinicalTrials.gov .