drugset / Trial / NCT01472848

A Study Of Gastrointestinal Tolerability Of PF05212389 In Obese Subjects

NCT01472848 ↗

Phase 1 Withdrawn Pfizer
RandomizedParallel-groupDouble-blindTreatment

Summary

This study examines whether a gradual increase of dose improves the gastrointestinal tolerability (nausea and vomiting) of PF05212389

Timeline

Start
2011-04
Primary completion
2011-07
Completion
2011-08

Drugs

EvaluationDrugModalityDoseRoute
Comparator PF 05212389 Unknown — Subcutaneous

Indications