A Phase I/IB, First-Time-in-Human, Single Centre, Double-Blind, Randomized, Placebo-controlled, Dose Escalating Study of the Safety, Tolerability and Pharmacokinetics of Single and Repeat Doses of VB0004 Administered Orally to Healthy Volunteers; and to Patients With Mild to Moderate Hypertension With Low Cardiovascular Risk.
Latest Information Update: 01 Mar 2023
At a glance
- Drugs VB 0004 (Primary)
- Indications Hypertension
- Focus Adverse reactions; First in man
- 23 Feb 2023 Planned End Date changed from 23 Jan 2023 to 23 Jan 2024.
- 23 Feb 2023 Planned primary completion date changed from 16 Oct 2022 to 16 Dec 2023.
- 19 Apr 2022 Planned End Date changed from 23 May 2022 to 23 Jan 2023.