Accelerating drug discovery for pregnant and lactating women living with HIV

Abstract

On International Women’s Day, we honour the incredible advancements in science and public health that have resulted in improved health for the more than 1.5 million women living with HIV who become pregnant each year, as well as for their children and families [1]. These achievements have been possible through the participation of countless women in clinical trials and the dedication of researchers, programme planners and community members who have been at the forefront of ensuring women’s health has remained a priority on the global HIV research agenda. However, despite these important gains, the pace of drug discovery and approval for pregnant and lactating women remains unacceptably slow, with an approximate six-year lag between antiretroviral licensure and any data in pregnancy [2]. Pregnant and lactating women are typically excluded from clinical trials in order to protect the mother and foetus from potential harm. However, excluding these women from trials instead shifts the risk of harm from occurring under trial settings in which informed consent and intensive monitoring are practiced, to occurring in routine care settings in which medications may be used despite a lack of data for evidence-based management decisions. Therefore, the strategy of excluding pregnant and lactating women from clinical trials to avoid harm in fact only serves to increase risk for larger numbers of women who are exposed to medications with uncertain dosing, safety and efficacy data. Advocacy for the women’s health research agenda has represented an important step towards future equity and includes leadership from the Task Force on Research Specific to Pregnant and Lactating Women (PRGLAC), sponsored by the National Institute of Child Health and Human Development (NICHD), and the Pregnancy and HIV/AIDS Seeking Equitable Study (PHASES) Working Group, sponsored by the National Institute of Allergy and Infectious Diseases (NIAID). These groups have outlined and are working to overcome barriers to research in pregnant and lactating women, which include liability concerns (legal, financial, reputational); lack of clarity on ethics; costs; a challenging regulatory environment; and a lack of timely preclinical reproductive toxicity and pharmacokinetic (PK) data [3,4]. The PHASES Working Group has proposed a conceptual shift that includes defining pregnant women as a complex population rather than a vulnerable population; protecting women through research rather than from research; and striving for fair inclusion in research rather than presumptive exclusion [4]. Actualizing this frameshift will require significant adaptations in the approach to research in the following areas: (1) reducing regulatory barriers; (2) leveraging innovations in study design; and (3) strengthening infrastructure for research with an emphasis on global collaborations and multisectoral partnerships. Below, we further elaborate on each of these areas with a focus on tangible steps towards more equitable and timely inclusion of pregnant and lactating women in clinical research. Reducing regulatory barriers is a critical step that can facilitate earlier enrolment of pregnant and lactating women in clinical trials to ensure PK, safety, and efficacy data for these populations are available when new drugs are approved. The majority of data for therapeutics in pregnancy arise from Phase IV studies; however, with more proactive planning, early preclinical reproductive toxicity data can allow for inclusion of pregnant women in Phase IIb/III studies. These studies can employ approaches to reduce risks, such as that used in the US Microbicide Trials Network’s DELIVER Study, in which women are enrolled in sequential cohorts, first in late pregnancy (36+ weeks) and, after safety is established for these women and their infants through interim data review, subsequent cohorts of women are enrolled in progressively earlier antepartum periods [5]. Additionally, requirements for women to stop study drug if they become pregnant during trial follow-up slows the pace of discovery. In order to address concerns about risk and allow inclusion of these women in licensure trials, appropriate re-consent language should be used, allowing women to weigh the risks and benefits of participation, assuming preclinical reproductive toxicity data do not suggest increased risk. Inclusion of Hoffman RM et al. Journal of the International AIDS Society 2021, 24:e25680 http://onlinelibrary.wiley.com/doi/10.1002/jia2.25680/full | https://doi.org/10.1002/jia2.25680