drugset / Trial / NCT04890873

ERX1000 - Safety, Tolerability, Pharmacokinetic, and Pharmacodynamic Study in Male and Female Subjects With Obesity

NCT04890873 ↗

Phase 1 Completed 48 enrolled ERX Pharmaceuticals
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary objective is to assess the safety and tolerability of single and multiple oral doses of ERX1000 in obese subjects.

Timeline

Start
2019-10-17
Primary completion
2023-07-03
Completion
2023-07-03

Drugs

EvaluationDrugModalityDoseRoute
Subject ERX1000 Unknown 4 mg Oral
Subject ERX1000 Unknown 8 mg Oral

Indications