A Phase I, First-in-human, Two-part, Randomized, Placebo-controlled, Double-blind, Single and Repeated Dose Escalation Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Subcutaneous Doses of SAR442501 in Healthy Adult Subjects
Latest Information Update: 11 Jan 2024
At a glance
- Drugs SAR 442501 (Primary)
- Indications Achondroplasia; Osteochondrodysplasias
- Focus Adverse reactions; First in man
- Sponsors Sanofi
- 11 May 2023 Status changed from recruiting to completed.
- 11 Feb 2021 New trial record