A Phase 1, Randomized, Double-blind, Placebo-controlled, Single-center, First-in-human Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single and Multiple Ascending Doses of CC-97489 in Healthy Adult Subjects
Latest Information Update: 20 Dec 2023
At a glance
- Drugs CC-97489 (Primary)
- Indications Neurological disorders
- Focus Adverse reactions; First in man
- Sponsors Celgene Corporation
- 08 Dec 2023 Status changed from recruiting to discontinued (Business objectives changed).
- 03 Mar 2023 Planned End Date changed from 30 Dec 2022 to 26 Oct 2023.
- 03 Mar 2023 Planned primary completion date changed from 30 Dec 2022 to 26 Oct 2023.