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Multiple Ascending Dose Study of MHS552 in Adults With Type 1 Diabetes Mellitus - Trial NCT05272059

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.

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NCT05272059
Phase 1
Not yet recruiting
drug
Trial Details
ClinicalTrials.gov โ€ข NCT05272059
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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)

Study Focus

Type 1 Diabetes Mellitus

MHS552

Interventional

drug

Sponsor & Location

Novartis Pharmaceuticals

Novartis

Timeline & Enrollment

Phase 1

Feb 13, 2023

Apr 14, 2025

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 mellitus
Type 1 diabetes mellitus with unspecified complications
Type 1 diabetes mellitus with other specified complications
Type 1 diabetes mellitus without complications
Type 1 diabetes mellitus with multiple complications

Data Source

ClinicalTrials.gov

NCT05272059

Non-Device Trial