drugset / Trial / NCT05199090
Study to Assess Safety, Tolerability and Efficacy of SC Administered MBL949 in Obese Participants With or Without T2DM
RandomizedSingle-groupDouble-blindTreatment
Summary
This was a multi-center, randomized, placebo-controlled, participant-and-investigator-blinded, sponsor open-label study in obese participants with or without Type 2 Diabetes Mellitus.
Timeline
- Start
- 2022-02-10
- Primary completion
- 2023-05-11
- Completion
- 2023-05-11
Outcome
Outcome not reported
Stopped: “The tolerability to benefit ratio based on maximum weight loss observed was not considered favorable at the doses studied and the study was terminated early”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | MBL949 | Unknown | 2.2 mg | Subcutaneous |
| Comparator | MBL949 | Unknown | 4.5 mg | Subcutaneous |
| Comparator | MBL949 | Unknown | 7.5 mg | Subcutaneous |