Combining two drugs may tackle bladder cancer that resists standard therapy
NCT ID NCT04179162
First seen Jun 27, 2026 · Last updated Aug 12, 2026 · Updated 2 times
Summary
This trial investigates whether combining two drugs—BCG and gemcitabine—can safely and effectively treat a type of bladder cancer called non-muscle invasive bladder cancer (NMIBC) that has come back after previous BCG treatment. Participants receive BCG directly into the bladder once a week for several weeks, along with gemcitabine twice a week in four cycles. The study first tests different doses of gemcitabine to find the safest level, then measures how many people are cancer-free six months after starting treatment.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- BCG (bacillus Calmette-Guérin) and gemcitabine
- What this could lead to
- If successful, this combination could offer a new treatment option for people whose bladder cancer has stopped responding to standard BCG therapy.
- What could go wrong
- This is an early-phase trial with a small number of participants, so the combination may not prove effective or may cause unexpected side effects.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 1/2
Runs two stages together: safety and dose first, then whether the treatment works.
- Participants
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54 people
The number who actually took part.
- Started
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Nov 2019
- Expected to finish
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Nov 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Recurrent for persistent high-grade NMIBC Ta/T1/Tis (Ta/T1 with CIS is preferred, but not required) within 24 months of the last treatment with BCG (with or without IFN) o Up to 26 months from the last BCG treatment is allowed for the treating physician to perform a transurethral resection of bladder tumor (TURBT) so long as there is evidence of recurrent disease (by positive cytology, imaging, or office cystoscopy) within 24 months of last BCG transurethral resection of bladder tumor (TURBT) * Pathologic confirmation of stage, grade, and urothelial histology by the Department of Pathology at MSK * All visible papillary lesions macroscopically resected within 60 days of treatment initiation * Absence of urothelial carcinoma involving the upper urinary tract (documented by radiological imaging or ureteroscopy) within 12 months from the start of treatment * Receipt of restaging transurethral resection (TUR) for any tumor with invasion into the lamina propria (HGT1) as part of standard care * Age ≥18 years * Karnofsky performance status ≥60% * Informed consent Exclusion Criteria: * Positive pregnancy test * Known contraindications to BCG * History of systemic hypersensitivity reaction or history of febrile systemic BCG reaction * Febrile illness or persistent gross hematuria * Active tuberculosis * Immunosuppression due to congenital or acquired immune deficiency, concurrent immune suppressive disease, systemic cancer therapy, or chronic immunosuppressive therapy other than topical or inhaled corticosteroids * History of or currently being treated for muscle-invasive (i.e., stage T2 or higher) or metastatic urothelial cell carcinoma * Evidence of concurrent extravesical (i.e., urethra, ureter, or renal pelvis) urothelial cell carcinoma * BCG-unresponsive NMIBC as defined by the FDA: * HGT1 within 3 months after an induction BCG course (received ≥5 of 6 doses) * Persistent or recurrent high-grade NMIBC (Tis, Ta, T1) within 6 months of ≥5 of 6 doses of induction BCG therapy and ≥2 of 3 doses of maintenance BCG therapy
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Hartford Healthcare (Data Collection)
Hartford, Connecticut, 06102, United States
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Memorial Sloan Kettering Basking Ridge (Limited Protocol Activities)
Basking Ridge, New Jersey, 07920, United States
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Memorial Sloan Kettering Bergen (Limited Protocol Activities)
Montvale, New Jersey, 07645, United States
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Memorial Sloan Kettering Cancer Center (All Protocol Activities)
New York, New York, 10065, United States
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Memorial Sloan Kettering Commack (Limited Protocol Activities)
Commack, New York, 11725, United States
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Memorial Sloan Kettering Monmouth (Limited Protocol Activities)
Middletown, New Jersey, 07748, United States
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Memorial Sloan Kettering Nassau (Limited Protocol Activities)
Uniondale, New York, 11553, United States
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Memorial Sloan Kettering Westchester (Limited Protocol Activities)
Harrison, New York, 10604, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can heated saline during bladder surgery stop tumors from coming back?
- Can a bladder rinse before surgery keep bladder cancer at bay?
- Can a home care plan ease bladder cancer treatment side effects?
- Can a new drug help keep bladder cancer at bay?
- Can heated chemotherapy beat bladder cancer without surgery?
- Could a simple urine test spare bladder cancer patients from chemotherapy?