Phase 1 study evaluating the safety, tolerability and pharmacokinetics of single-ascending doses (SAD) and multiple-ascending doses (MAD) of ORX142 in healthy volunteers
Latest Information Update: 23 Jun 2025
At a glance
- Drugs ORX 142 (Primary)
- Indications Hypersomnia
- Focus Adverse reactions; First in man
Most Recent Events
- 16 Jun 2025 According to a Centessa Pharmaceuticals media release, the U.S. Food and Drug Administration (FDA) has cleared the IND to initiate a Phase 1 clinical study of ORX142 in healthy volunteers, The Company plans to initiate the first-in-human Phase 1 clinical study imminently, with clinical data expected this year, which is expected to enable a dose selection for planned studies evaluating ORX142 in patients.
- 18 Nov 2024 New trial record
- 12 Nov 2024 According to a Centessa Pharmaceuticals media release, Clinical data in healthy volunteers planned for 2025.