Trial · NCT07908979
Risk-Enabled Therapy After Initiating EV/Pembro for Bladder Cancer
NCT07908979, Phase 2, Recruiting, Fox Chase Cancer Center
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Risk-Enabled Therapy After Initiating EV/Pembro for Bladder Cancer. Trials, record NCT07908979. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07908979
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Risk-Enabled Therapy After Initiating EV/Pembro for Bladder Cancer
- NCT number
- NCT07908979
- Status
- Recruiting
- Phases
- Phase 2
- Enrollment
- 70 participants, estimated
- Lead sponsor
- Fox Chase Cancer Center
- Conditions
- Bladder Cancer, Urothelial Carcinoma, Muscle-Invasive Bladder Carcinoma, Muscle-invasive Bladder Urothelial Carcinoma
- Interventions
- Enfortumab vedotin, Pembrolizumab, Cisplatin, Gemcitabine, Fluorouracil, Mitomycin c, Radical cystectomy, Radiation therapy
- First posted
- 2026-11-02
- Last updated
- 2026-11-02
Source ClinicalTrials.gov
Registered outcomes9
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | 2-Year Metastasis-Free Survival (MFS) | 2 years | Metastasis-free survival is defined as the time from initiation of neoadjuvant therapy to metastatic urothelial carcinoma or death from any cause, whichever occurs first. |
| Secondary | Bladder-intact metastasis-free survival in active surveillance patients | 2 years | |
| Secondary | Pathologic complete response (pT0) rate among participants undergoing cystectomy | At cystectomy | |
| Secondary | Clinical complete response rate | Up to 5 years | |
| Secondary | Rate of urothelial carcinoma recurrence in active surveillance participants | Up to 5 years | |
| Secondary | Overall survival (OS) | Up to 5 years | |
| Secondary | Rate of distant recurrence among post-treatment ctDNA-positive participants undergoing definitive local therapy | Up to 5 years | |
| Secondary | Proportion of participants undergoing cystectomy | Up to 5 years | |
| Secondary | Bladder-intact metastasis-free survival in all evaluable participants | 2 years |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07908979
GET https://conductscience.org/api/trials/v1/NCT07908979/registered