Trial abstract · §3
AOD-PH2B-OBESITY — results
Primary endpoint, absolute and relative effect where derivable, and harms as reported.
§3Results
§3.1Primary endpoint
Table 3. Primary endpoint as reported.
| Endpoint | Result as reported | Certainty |
|---|---|---|
| Percentage change in body weight from baseline to week 12 | No separation from placebo. Development in obesity was discontinued | Not rated |
| Reproduced from the published report. Where the report states a confidence interval the Institute reproduces it; where it does not, none is constructed. | ||
§3.2Endpoint hierarchy
§3.3Harms as reported
Table 5. Adverse events for AOD-9604 from the safety tables the Institute holds for this compound. Where a row names a different trial as its source, the figure is from that trial and not from this one.
| Event | Active, % | Comparator, % | Source trial |
|---|---|---|---|
| Injection-site reaction | — | — | Reported in research contexts |
| Headache | — | — | Reported |
| No effect on IGF-1 | — | — | Consistently reported and consistent with the design intent |
| No effect on glucose tolerance | — | — | Consistently reported |
Compound Evidence Institute · CEI-TR-0108/3 · https://compoundevidence.com/trials/aod-ph2b-obesity/results/ · retrieved 30 July 2026