Nivolumab
DrugBiological, monoclonal antibody
NCT Number: NCT06059547
This is a multi-center, stratified and single-blinded Phase 2 trial of neoadjuvant immunotherapy in combination with the anti-GDF15 antibody visugromab (CTL-002) for the treatment of participants with MIBC set to undergo radical Cystectomy (RC)/Re-TURBT who cannot receive or refuse to receive cisplatin-based chemotherapy.
This study is active but is not currently recruiting participants.
Notify Me18 year and older
All sexes
Interventional
Phase 2
Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Main Inclusion Criteria:
Main Exclusion Criteria:
Biological, monoclonal antibody
Biological, monoclonal antibody
Placebo (NaCl) for Visugromab (CTL-002)
Time frame: min. 4 months
Rate of participants with complete pathological responses after IMP treatment as determined by local pathologist review
Time frame: min. 4 months
Rate of participants with radiological responses according to RECIST 1.1 prior Radical Cystectomy/Re-TURBT as assessed by the Investigator/Radiologist
Time frame: min. 6 months
Incidence of adverse events (related or unrelated to IMPs)
Time frame: min. 6 months
Treatment related delay of Radical Cystectomy/Re-TURBT > 8 weeks after last dose of IMP
Time frame: 1 day
PK parameter from serum Visugromab (CTL-002) levels
Time frame: 28 days
PK parameter from serum Visugromab (CTL-002) levels
Time frame: min. 3 months
PK parameter from serum Visugromab (CTL-002) levels
Time frame: 1 day
Measurement of concentration in peripheral blood
Time frame: min. 4 months
Rate of participants with complete pathological responses after IMP treatment as determined by central independent pathological review
Time frame: Min. 4 months
Rate of participants with radiological responses according to RECIST 1.1 prior Radical Cystectomy/Re-TURBT as assessed by the central independent review
Time frame: Min. 4 months
Rate of participants with major pathological responses after IMP treatment as determined by local pathologist review or central independent pathological review
Time frame: 12 months after Radical Cystectomy/Re-TURBT
Event-free survival will be defined as the time from first IMP administration to one of the following:
Radiographic disease progression precluding a curative intent surgery per RECIST v1.1 prior to RC/Re-TURBT.
Initiation of neoadjuvant chemotherapy preceding RC/Re-TURBT as per Investigator decision.
Inability to undergo RC/Re-TURBT due to the onset of treatment-related side effects.
Inability to complete a curative intent surgery determined by the urologist at the time of RC/Re-TURBT (e.g., unresectable tumor, metastases discovered at RC).
Local or distant recurrence assessed by cross-sectional imaging and/or biopsy after RC/Re-TURBT.
Death from any cause. In this trial, participant refusal to undergo RC due to the evidence of complete or near-complete clinical response (assessed on cross-sectional imaging as previously described) will not be considered an event.
Time frame: 15 months
Overall survival is defined as the time from the first IMP administration to the date of death, regardless of the cause of death.
Participants who were alive at the time of the analysis will be censored at the date the participant was last known to be alive.
Time frame: 12 months after Radical Cystectomy/Re-TURBT
Time to relapse will be measured from the time of RC/Re-TURBT until the day of documented relapse.
Time frame: min. 5 months
The number and percentage of participants with any detectable ADA after first IMP administration
Time frame: min. 3 months
Time frame: min. 3 months
CatalYm GmbH
Industry
A Multi-center Phase 2 Study of Neoadjuvant Immunotherapy in Combination With the Anti-GDF-15 Antibody Visugromab (CTL-002) for the Treatment of Muscle Invasive Bladder Cancer
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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