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OncoMatch/Clinical Trials/NCT06493552

Modular Trial of sEphB4-HSA in EphrinB2-High Solid Tumors

Is NCT06493552 recruiting? Yes, currently enrolling (May 2026). This Phase 2/3 trial studies multiple treatments for muscle-invasive bladder carcinoma.

Phase 2/3RecruitingVasgene Therapeutics, IncNCT06493552Data as of May 2026

Treatment: SEphB4-HSA · Pembrolizumab · Gemcitabine · Cisplatin · Enfortumab vedotinPatients with solid tumors that have high expression levels of EphrinB2 are treated with regimens that include EphrinB2 inhibitor, sEphB4-HSA. The primary objective of this study is to demonstrate additive therapeutic benefit for sEphB4-HSA. The secondary objectives are to determine whether the sEphB4-HSA containing regimen is safe and whether the oncological endpoints of importance in each cohort improve as a result of treatment with sEphB4-HSA containing regimen relative to a predefined threshold or to a control arm in the cohort where available. Treatment continues until progression of disease or unacceptable toxicities arise.

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Extracted eligibility criteria

Cancer type

Urothelial Carcinoma

Biomarker criteria

Required: EFNB2 overexpression

Tumor must express EphrinB2 as assessed by USC Norris Core Lab.

Required: NECTIN4 non-amplified

Tumor must be Nectin4 non-amplified- testing performed during pre-screening assessment.

Required: PD-L1 (CD274) any tested (testing required; no eligibility threshold specified)

Tumor tissue must be submitted for molecular profile through a commercial service such as Tempus, CARIS, Foundation One, etc. This must include a PD-L1 assay.

Performance status

ZUBROD 0–1

Prior therapy

No prior treatment (treatment-naive required)
Max 0 prior lines

Cannot have received: systemic therapy

Exception: no systemic therapy for cancer in the previous 12 months

No systemic therapy for cancer in the previous 12 months.

Lab requirements

Blood counts

wbc ≥2000/ul; neutrophils ≥1500/ul; platelets ≥100x103/ul; hemoglobin ≥9g/dl

Kidney function

measured or calculated creatinine clearance (crcl) greater than or equal to 30 ml/min using the cockcroft-gault formula using actual weight

Liver function

ast ≤3 x uln; alt ≤3 x uln; bilirubin ≤1.5 x uln

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

US trial sites

  • Sarcoma Oncology Center · Santa Monica, California

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

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