Phase 1 First-in-Human Dose Escalation and Expansion Study to Assess Safety and Tolerability of Intravenous Administration of ICVB-1042 in Patients With Advanced Solid Tumors
Latest Information Update: 11 Apr 2025
At a glance
- Drugs ICVB-1042 (Primary)
- Indications Solid tumours
- Focus Adverse reactions; First in man
- Sponsors IconOVir Bio
- 08 Apr 2025 Status changed from active, no longer recruiting to discontinued due to lack of Demonstrated Clinical Activity..
- 10 Mar 2025 According to an IconOVir Bio media release, company hosted a webinar to discuss ICVB-1042 on 20 Feb 2025.
- 09 Jan 2025 Status changed from recruiting to active, no longer recruiting.