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OncoMatch/Clinical Trials/NCT06493370

Intravenous Ascorbate Plus Gemcitabine/Carboplatin: A Novel and Cost-Effective Alternative With Evident Efficacy in Patients With Muscle Invasive Bladder Cancer

Is NCT06493370 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies Intravenous ascorbic acid/vitamin C for bladder cancer.

Phase 2RecruitingUniversity of Kansas Medical CenterNCT06493370Data as of Jun 2026

Treatment: Intravenous ascorbic acid/vitamin CThis is a phase II, single arm, Simon two-stage design, trial, enrolling patients with cisplatin ineligible MIBC and/or those patients who decline cisplatin based NAC. Assess rates of pathologic downstaging and quality of life in MIBC cisplatin-ineligible/declined patients when IVC is added to gemcitabine-carboplatin NAC.

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Extracted eligibility criteria

Treatments studied

Other

Intravenous ascorbic acid/vitamin C

Cancer type

Urothelial Carcinoma

Biomarker criteria

Required: G6PD normal (normal)

Normal Glucose-6-phosphate dehydrogenase (G6PD) status

Excluded: G6PD deficiency

History of G6PD deficiency

Performance status

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

Lab requirements

Blood counts

Absolute Neutrophil Count >1.5K/UL (patients with benign neutropenia eligible with ANC 1000-1500 at physician discretion); Platelets >100K/UL; Hemoglobin ≥ 9 g/dL

Kidney function

Serum creatinine ≤ 1.5 x ULN or calculated creatinine clearance ≥ 30 mL/min using the Cockcroft-Gault equation

Liver function

Total bilirubin ≤ 2.0 x ULN; AST (SGOT) and ALT (SGPT) ≤ 2.5 x ULN unless liver metastases are present, in which case they must be ≤ 5 x ULN

Adequate organ function, defined as follows: Absolute Neutrophil Count >1.5K/UL... Platelets >100K/UL; Hemoglobin ≥ 9 g/dL; Serum creatinine ≤ 1.5 x ULN or calculated creatinine clearance ≥ 30 mL/min... Total bilirubin ≤ 2.0 x ULN; AST (SGOT) and ALT (SGPT) ≤ 2.5 x ULN unless liver metastases are present, in which case they must be ≤ 5 x ULN; Normal Glucose-6-phosphate dehydrogenase (G6PD) status

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

US trial sites

  • Holden Comprehensive Cancer Center - The University of Iowa · Iowa City, Iowa
  • The University of Kansas Cancer Center · Kansas City, Kansas

Showing up to 5 US sites.

See all sites on ClinicalTrials.gov →

Frequently asked questions

Is NCT06493370 currently recruiting?

Yes, this trial is currently recruiting patients.

Does this trial require G6PD?

Yes, G6PD normal is a required biomarker for enrollment.

Are patients with G6PD alterations eligible?

No. G6PD deficiency is an exclusion criterion.

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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