Evidence map›Paper›PMID 39873899›Full record

ArticleDrug safety2025

Antiretroviral Use for HIV Prevention During Pregnancy: The Need to Strengthen Regulatory and Surveillance Systems in Africa.

Robin Schaefer, L Donaldson, A Chigome, M Escudeiro Dos Santos, S Lamprianou, N Ndembi, J I Nwokike, P Nyambayo, V Palmi, F Renaud and 2 more

Abstract read
In one paragraph

Article in Drug safety, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Robin SchaeferForum for Collaborative Research, University of California, Berkeley, Washington, DC, USA. rschaefer@forumresearch.org.ORCID 0000-0003-4733-4692
L DonaldsonForum for Collaborative Research, University of California, Berkeley, Washington, DC, USA.
A ChigomeSouth African Health Products Regulatory Authority, Pretoria, South Africa.
M Escudeiro Dos SantosVaccines and Therapies for Infectious Diseases, Human Medicines Division, European Medicines Agency, Amsterdam, The Netherlands.
S LamprianouPharmacovigilance team, Department of Regulation and Prequalification, World Health Organization, Geneva, Switzerland.
N NdembiAfrica Centres for Disease Control and Prevention, Addis Ababa, Ethiopia.
J I NwokikeUnited States Agency for International Development (USAID)'s Promoting the Quality of Medicines Plus (PQM+) Program, United States Pharmacopeia, Rockville, MD, USA.
P NyambayoMedicines Control Authority of Zimbabwe, Harare, Zimbabwe.
V PalmiInternational Affairs, European Medicines Agency, Amsterdam, The Netherlands.
F RenaudGlobal HIV, Hepatitis, and STIs Programmes, World Health Organization, Geneva, Switzerland.
M Gonzalez TomeVaccines and Therapies for Infectious Diseases, Human Medicines Division, European Medicines Agency, Amsterdam, The Netherlands.
V MillerForum for Collaborative Research, University of California, Berkeley, Washington, DC, USA.

Funding

Bill and Melinda Gates Foundation INV-045445World Health Organization 001
6 · The paper itself

Abstract

HIV-prevention efforts focusing on women of child-bearing potential are needed to end the HIV epidemic in the African region. The use of antiretroviral drugs as pre-exposure prophylaxis (PrEP) is a critical HIV prevention tool. However, safety data on new antiretrovirals during pregnancy are often limited because pregnant people are excluded from drug development studies. Calls from communities, healthcare professionals, and regulators to improve the information supporting decision-making around the use of medical products during pregnancy have been increasing. Post-marketing safety surveillance is an essential tool for detecting adverse outcomes and evaluating real-world, longer-term effects of drugs. Detecting and evaluating uncommon pregnancy outcomes requires large sample sizes, highlighting the benefits of and need for safety surveillance. Surveillance systems vary widely across Africa, and the need for enhanced surveillance of PrEP use during pregnancy highlights the limitations of current regulatory and surveillance systems. Challenges include weak regulation and insufficient resources. Pooling of resources and regulatory harmonization could address resource challenges. The African Medicines Agency, as a specialized agency of the African Union, has the potential to improve African medical product regulation, including post-marketing safety surveillance. This can strengthen regulation and ensure that market authorization holders meet their responsibility to invest in post-marketing surveillance systems, such as pregnancy registries. At the same time, independent post-marketing studies are needed to ensure generation of essential safety data. The Forum for Collaborative Research has initiated a project to facilitate interactions between regulators in Africa, the USA, and Europe, as well as other stakeholders, and to work toward consensus on safety data generation from PrEP during pregnancy before and after marketing authorization.

Indexed as

Anti-HIV AgentsAnti-Retroviral AgentsHIV InfectionsPre-Exposure ProphylaxisPregnancy Complications, InfectiousProduct Surveillance, PostmarketingAfricaFemaleHumansPregnancyAnti-HIV AgentsAnti-Retroviral Agents

Identifiers

PMID39873899
PMCPMC11829904

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.