A Phase 1/2a Study of STM-416 Administered Intraoperatively (Bladder Cancer)

Purpose of this Study

We are doing this study to find out if an experimental drug called STM-416 (the study drug) is a safe and effective option for patients with a history of high grade, non-muscle invasive bladder cancer (cancer only within the bladder) whose disease has returned and who require an operation to remove cancer from the bladder.

Who Can Participate?

Eligibility

Adults ages 18+ who:
  • Have a history of pathologically confirmed high grade Ta or T1 NMIBC without carcinoma in situ
  • Have recurrent papillary disease seen on cystoscopy and are undergoing TURBT without perioperative intravesical chemotherapy
  • Are considered high risk for recurrence
  • Are not able to become pregnant
For more information, contact the study team at shawna.pochan@duke.edu.

Age Range

18-110

Sex/Genders

Male (cisgender)
Female (cisgender)
Non-binary or gender fluid
Transgender male
Transgender female
Looking for Healthy Participants
No

What is Involved?

Description

After the screening process, patients will receive a one time dose of the study drug during their bladder removal surgery. They will then be followed closely for the first two days after their procedure and then at regular intervals for the next two years.

Locations

Duke University Hospital

Visit Timing

Weekdays

Compensation

Yes

Spanish Materials Available

No

Study Details

Full Title

SURGE Therapeutics/ “A Phase 1/2a Study of STM-416 Administered Intraoperatively to Patients Undergoing Transurethral Resection of Bladder Tumor (TURBT) for Recurrent High-Grade Papillary Bladder Cancer”

Principal Investigator

Michael
Abern

Protocol Number

PRO00114565

NCT ID

NCT05710848

Phase

I/II

Enrollment Status

Open to Enrollment