NCT05272059

Multiple Ascending Dose Study of MHS552 in Adults With Type 1 Diabetes Mellitus

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)
Novartis Pharmaceuticals·Phase 1·ClinicalTrials.gov·drugNot yet recruiting
View on ClinicalTrials.gov
Study focus
Disease/Condition
Type 1 Diabetes Mellitus
Drug/Device/Intervention
MHS552
Study type
Interventional
Intervention type
drug
Sponsor & location
Primary sponsor
Novartis Pharmaceuticals
Funder
Novartis
Timeline & enrollment
Phase
Phase 1
Start date
Feb 13, 2023
End date
Apr 14, 2025
Enrollment
28 participants
Primary outcome

Number of participants with Adverse events (AEs) and Serious Adverse events (SAEs)

Summary

The purpose of this two-part multiple ascending dose study is to evaluate the safety and
 tolerability of multiple doses of MHS552 in adults with type 1 diabetes mellitus.
 Participants will be treated for 4 or 12 weeks followed by an 8 week follow-up period

ICD-10 classifications
Type 1 diabetes mellitusType 1 diabetes mellitus with unspecified complicationsType 1 diabetes mellitus with other specified complicationsType 1 diabetes mellitus without complicationsType 1 diabetes mellitus with multiple complications
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT05272059
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT05272059 through Pure Global AI's free database. This Phase 1 trial is sponsored by Novartis Pharmaceuticals and is currently Not yet recruiting. The study focuses on Type 1 Diabetes Mellitus. Target enrollment is 28 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.