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OncoMatch/Clinical Trials/NCT07747740

Sequential Gemcitabine Plus Docetaxel Versus Gemcitabine Plus Mitomycin C for BCG-Unresponsive Non-Muscle-Invasive Bladder Cancer

Is NCT07747740 recruiting? Yes, currently enrolling (Sep 2026). This Phase 2 trial studies multiple treatments including Gemcitabin and Docetaxel for non-muscle-invasive bladder cancer.

Phase 2RecruitingBlokhin's Russian Cancer Research CenterNCT07747740Data as of Sep 2026Location: Russia

Treatment: Gemcitabin · Docetaxel · Mitomicin CThis prospective, randomized, open-label, phase II clinical trial compares two sequential intravesical chemotherapy regimens in patients with bacillus Calmette-Guérin (BCG)-unresponsive high-grade non-muscle-invasive bladder cancer (NMIBC) following complete transurethral resection of bladder tumor (TURBT). Participants are randomized in a 1:1 ratio to receive sequential intravesical gemcitabine plus docetaxel or sequential intravesical gemcitabine plus mitomycin C. The primary objective is to compare 12-month event-free survival between treatment groups. Secondary objectives include evaluation of cystectomy-free survival, progression-free survival, treatment safety, tolerability, and patient-reported quality of life.

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Extracted eligibility criteria

Treatments studied

Chemotherapy

Docetaxel

Other

GemcitabinMitomicin C

Cancer type

Urothelial Carcinoma

Disease stage

Required: Stage NON-MUSCLE-INVASIVE

Excluded: Stage MUSCLE-INVASIVE (≥T2), III, IV

Histologically confirmed BCG-unresponsive non-muscle-invasive urothelial bladder cancer (NMIBC)

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Lab requirements

Blood counts

Kidney function

Liver function

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT07747740 currently recruiting?

Yes, this trial is currently recruiting patients.

What disease stage is eligible?

Stage NON-MUSCLE-INVASIVE is required.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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