A Phase 1, Single-Center, Open-Label, Single-Arm, Dose-Escalation, Positron Emission Tomography Study to Assess the Safety and Tolerability, Immunogenicity, Pharmacokinetics, Dosimetry and Biodistribution Following GEH200521 (18F) Injection Co-Administered With GEH200520 Injection in Healthy Volunteers
Latest Information Update: 26 Jun 2025
At a glance
- Drugs GEH-200520/GEH-200521 (Primary)
- Indications Solid tumours
- Focus Adverse reactions
- Sponsors GE Healthcare
Most Recent Events
- 22 Jun 2025 Planned End Date changed from 1 May 2025 to 1 Jan 2026.
- 22 Jun 2025 Planned primary completion date changed from 1 May 2025 to 1 Jan 2026.
- 06 Aug 2024 Last checked against ClinicalTrials.gov: US National Institutes of Health record.