Antiretroviral Pregnancy Registry (APR): Multi-sponsor Registry to Detect Any Major Teratogenic Effect Involving Any of the Registry Drugs When Administered to Pregnant People.

NCT00404989 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 24258

Last updated 2025-04-01

No results posted yet for this study

Summary

The purpose of the Antiretroviral Pregnancy Registry (Registry) is to detect any major teratogenic effect involving any of the Registry drugs when administered to pregnant people. Registration is voluntary and confidential with information obtained from the health care provider. A Registry-assigned identifier allows for follow-up capability. Information on subjects is provided to the Registry prospectively (prior to the outcome of pregnancy being known) through their health care provider, with follow-up obtained from the health care provider after the outcome is determined. Providers are strongly urged to enroll their patients as early in pregnancy as possible to maximize the validity of the data. In addition, the Registry is very interested in assembling a group of providers who are willing to make a commitment to report all of their site's antiretroviral pregnancy exposures to the Registry, thereby assuring all cases can be considered prospective. Providers are encouraged to contact the Registry for more information about this group. The Registry is informed in its analysis by other data, for example, retrospective reports and clinical studies.

Given the increasing number of medications and more aggressive approach to therapy, more HIV- and hepatitis B-infected people may be treated during pregnancy or become pregnant while under treatment. The paucity of data on use and infant outcomes of antiretroviral therapies during pregnancy makes this Registry an essential component of the ongoing program of epidemiologic studies of the safety of these therapies.

Each year the Registry has enrolled approximately 1300-1700 pregnant people in the US exposed to antiretroviral drugs. This number represents approximately 15% of the 8,700 HIV positive people who give birth to live infants annually in the US.

Conditions

Sponsors & Collaborators

  • AbbVie

    collaborator INDUSTRY
  • Alvogen Inc.

    collaborator UNKNOWN
  • Amneal Pharmaceuticals, LLC

    collaborator INDUSTRY
  • Apotex Corp.

    collaborator UNKNOWN
  • Boehringer Ingelheim

    collaborator INDUSTRY
  • Bristol-Myers Squibb

    collaborator INDUSTRY
  • Cipla Ltd.

    collaborator INDUSTRY
  • Dr. Reddy's Laboratories Limited

    collaborator INDUSTRY
  • Gilead Sciences

    collaborator INDUSTRY
  • Hetero Labs

    collaborator UNKNOWN
  • Hikma Pharmaceuticals LLC

    collaborator INDUSTRY
  • i3 Pharmaceuticals, LLC

    collaborator UNKNOWN
  • Janssen Scientific Affairs, LLC

    collaborator INDUSTRY
  • Lannett Company, Inc.

    collaborator INDUSTRY
  • Laurus Labs Limited

    collaborator UNKNOWN
  • Lupin Pharmaceuticals, Inc.

    collaborator INDUSTRY
  • Macleods Pharmaceuticals Ltd

    collaborator INDUSTRY
  • Merck Sharp & Dohme LLC

    collaborator INDUSTRY
  • Mylan Laboratories

    collaborator INDUSTRY
  • Pharmascience Inc.

    collaborator INDUSTRY
  • Qilu Pharmaceutical Co., Ltd.

    collaborator INDUSTRY
  • Sigmapharm Laboratories

    collaborator UNKNOWN
  • Strides Pharma Science Limited

    collaborator UNKNOWN
  • Teva Pharmaceuticals USA

    collaborator INDUSTRY
  • ViiV Healthcare

    collaborator INDUSTRY
  • Yung Shin Pharm. Ind. Co., Ltd.

    collaborator INDUSTRY
  • Zydus Pharmaceuticals USA, Inc.

    collaborator INDUSTRY
  • Syneos Health

    lead OTHER

Principal Investigators

  • Jessica D Albano, PhD, MPH · Syneos Health

Eligibility

Min Age
12 Years
Max Age
60 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
1989-01-31
Primary Completion
2099-01-31
Completion
2099-01-31

Countries

  • United States

Study Locations

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Entities

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 NCT00404989 on ClinicalTrials.gov