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NCT03552796
sEphB4-HSA in Treating Participants With BCG-Unresponsive or Refractory Bladder Cancer
Phase 1 trial testing Pharmacokinetic Study in Recurrent Bladder Carcinoma. Withdrawn.
1 August 2024
Quick facts
| Lead sponsor | University of Southern California |
|---|---|
| Phase | Phase 1 |
| Status | Withdrawn |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Start date | 1 August 2023 |
| Primary completion | 1 August 2024 |
| Estimated completion | 1 August 2025 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Pharmacokinetic Study
- Recombinant EphB4-HSA Fusion Protein — full drug profile →
Conditions studied
- Recurrent Bladder Carcinoma — all drugs for Recurrent Bladder Carcinoma →
- Bladder Cancer Stage 0 — all drugs for Bladder Cancer Stage 0 →
- Bladder Cancer Stage I — all drugs for Bladder Cancer Stage I →
Sponsor
University of Southern California
Who can join
Adults 18 to 80, any sex, with Recurrent Bladder Carcinoma or Bladder Cancer Stage 0. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This phase I trial studies the side effects and best dose of recombinant EphB4-HSA fusion protein (sEphB4-HSA), and to see how well it works in treating participants with bladder cancer that has come back or that isn't responding to bacillus Calmette-Guerin (BCG) vaccine treatment. sEphB4-HAS prevents tumor cells from multiplying and blocks several compounds that promote the growth of blood vessels that bring nutrients to the tumor. Giving sEphB4-HSA may work better in treating participants with bladder cancer.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Prognostic value of ephrin B receptors in breast cancer: An online survival analysis using the microarray data of 3,554 patients.
Mu X, Huang O, Jiang M, Xie Z, et al · · 2019 · cited 4× · PMID 31289549 · DOI 10.3892/ol.2019.10363
Verify or expand the search:
- PubMed search for NCT03552796
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT03552796 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by University of Southern California
- Last refreshed: 26 June 2023
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03552796.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing