A Randomized, Single Blind, Placebo Controlled, Single Center Phase I Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Pharmacodynamics of Single and Multiple Ascending Doses of Subcutaneously Administered RBD7022 in Participants With Normal or Elevated LDL-c Cholesterol
Latest Information Update: 29 Jul 2024
At a glance
- Drugs RBD-7022 (Primary)
- Indications Hyperlipidaemia
- Focus Adverse reactions; First in man
- Sponsors Suzhou Ribo Life Science
- 26 Jul 2024 Planned End Date changed from 31 Mar 2025 to 17 Feb 2025.
- 26 Jul 2024 Planned primary completion date changed from 30 Nov 2024 to 17 Feb 2025.
- 26 Jul 2024 Status changed from recruiting to active, no longer recruiting.