VIBATIV Pregnancy Registry

NCT01130324 · Status: WITHDRAWN · Type: OBSERVATIONAL

Last updated 2020-10-19

No results posted yet for this study

Summary

The purpose of this registry is to evaluate the outcome of pregnancy in women exposed to VIBATIV at any time during pregnancy. There are no mandated physician visits for the registry.

Conditions

  • Pregnancy

Interventions

DRUG

VIBATIV

Observational

Sponsors & Collaborators

  • Cumberland Pharmaceuticals

    lead INDUSTRY

Principal Investigators

  • Adam Haberle, PhD · Cumberland Pharmaceuticals, Inc.

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-11-30
Primary Completion
2020-10-31
Completion
2020-10-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01130324 on ClinicalTrials.gov