A Randomized, Investigator and Participant Blinded, Placebo Controlled, Multiple Ascending Dose, Two Part Design Study to Assess the Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Effects of MHS552 in Adults With Type 1 Diabetes Mellitus (T1DM)
Latest Information Update: 10 Apr 2023
At a glance
- Drugs MHS 552 (Primary)
- Indications Type 1 diabetes mellitus
- Focus Adverse reactions
- Sponsors Novartis Pharmaceuticals
- 05 Apr 2023 Status changed from not yet recruiting to withdrawn prior to enrolment on sponsor's decision.
- 15 Mar 2023 Planned initiation date changed from 13 Feb 2023 to 1 Sep 2023.
- 28 Sep 2022 Planned End Date changed from 30 Dec 2024 to 14 Apr 2025.