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Recruiting NCT07048496

NCT07048496 Intravesical Treatment of Bladder Cancer at Home, Multi-modal Treatment Support

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Clinical Trial Summary
NCT ID NCT07048496
Status Recruiting
Phase —
Sponsor Abramson Cancer Center at Penn Medicine
Condition Bladder Cancer
Study Type INTERVENTIONAL
Enrollment 50 participants
Start Date 2025-07-05
Primary Completion 2027-02-05

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
BCG delivery at home

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 50 participants in total. It began in 2025-07-05 with a primary completion date of 2027-02-05.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The proposed project will have two separate cohorts. The first will be to perform a more in-depth qualitative assessment of the barriers and facilitators for treatment compliance for non-muscle invasive bladder cancer. The second arm will be to create and test a BCG at home program. Participants in the second cohort will be enrolled in a conversational agent to measure patient symptoms and quality of life and improve self-efficacy.

Eligibility Criteria

Inclusion Criteria: Inclusion criteria for patients in Cohort 1 * Age 18 years or older; * completed intravesical treatment for non-muscle invasive bladder cancer within the past year Cohort 1 inclusion criteria for key stakeholders * Age 18 years or older; * experience with the delivery of BCG delivery for more than 2 years Cohort 2 inclusion criteria * Age 18 years or older; * diagnosed with non-muscle invasive bladder cancer and prescribed BCG for initial therapy Exclusion Criteria: Cohort 1 exclusion criteria • inability to provide informed consent Cohort 2 exclusion criteria * inability to provide informed consent * inability to undergo catheterization (i.e. - history of urethral stricture) * inability to receive BCG therapy (i.e. - previous reaction with BCG) * no access to mobile phone * inability to respond to written conversations in English

Contact & Investigator

Central Contact

Daniel Lee, PI, MD

✉ daniel.lee4@pennmedicine.upenn.edu

📞 215-615-3780

Frequently Asked Questions

Who can join the NCT07048496 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Bladder Cancer. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07048496 currently recruiting?

Yes, NCT07048496 is actively recruiting participants. Contact the research team at daniel.lee4@pennmedicine.upenn.edu for enrollment information.

Where is the NCT07048496 trial being conducted?

This trial is being conducted at Philadelphia, United States.

Who is sponsoring the NCT07048496 clinical trial?

NCT07048496 is sponsored by Abramson Cancer Center at Penn Medicine. The trial plans to enroll 50 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology