TY - JOUR
T1 - Accelerating Generic Long-Acting Antiretrovirals for Global HIV Treatment
T2 - Workshop Findings and a Roadmap to Access
AU - Arshad, Usman
AU - Gaayeb, Lobna
AU - Pertinez, Henry
AU - Rajoli, Rajith K.R.
AU - Watkins, Melynda
AU - Nimbolkar, Parag
AU - Perazzolo, Simone
AU - Pagi, Bharat
AU - Wensing, Annemarie
AU - Khoo, Saye
AU - Boffito, Marta
AU - Holm, René
AU - Panos, Zack
AU - Mahaka, Imelda
AU - Venter, Francois
AU - Kottiri, Benny
AU - Crawford, Keith W.
AU - Ho, Rodney J.Y.
AU - Clayden, Polly
AU - Domanico, Paul
AU - Struble, Kimberly
AU - Owen, Andrew
AU - Flexner, Charles
N1 - Publisher Copyright:
© 2026 The Author(s). Clinical Pharmacology & Therapeutics published by Wiley Periodicals LLC on behalf of American Society for Clinical Pharmacology and Therapeutics.
PY - 2026/5
Y1 - 2026/5
N2 - The global HIV response aims for widespread availability of affordable, quality-assured long-acting antiretroviral (LA ARV) drugs to achieve sustained epidemic control, particularly in low- and middle-income countries. This report summarizes key discussion points, findings, and outcomes from an international workshop on generic LA ARVs, held in Liverpool, United Kingdom, and co-organized by the Long-Acting/Extended-Release Antiretroviral Resource Program (LEAP) and the Centre of Excellence for Long-acting Therapeutics (CELT). The workshop brought together experts from across disciplines to evaluate the multifaceted challenges and opportunities for faster development and regulatory approval of affordable and accessible generic LA ARVs. Key topics included the application of novel pharmacokinetic end points to reduce study duration, the integration of community preferences into practice-based research in resource-limited settings, intellectual property considerations, formulation and manufacturing complexities that affect cost, scalability and implementation, and the growing role of model-integrated evidence in streamlining bioequivalence assessments. To reach the goal of timely and equitable global access to long-acting medicines, this workshop emphasized the need for strategic public-private engagement to promote data sharing, enhance regulatory efficiencies, and develop robust in vitro–in vivo correlation strategies that meet regulatory guidance for LAI products.
AB - The global HIV response aims for widespread availability of affordable, quality-assured long-acting antiretroviral (LA ARV) drugs to achieve sustained epidemic control, particularly in low- and middle-income countries. This report summarizes key discussion points, findings, and outcomes from an international workshop on generic LA ARVs, held in Liverpool, United Kingdom, and co-organized by the Long-Acting/Extended-Release Antiretroviral Resource Program (LEAP) and the Centre of Excellence for Long-acting Therapeutics (CELT). The workshop brought together experts from across disciplines to evaluate the multifaceted challenges and opportunities for faster development and regulatory approval of affordable and accessible generic LA ARVs. Key topics included the application of novel pharmacokinetic end points to reduce study duration, the integration of community preferences into practice-based research in resource-limited settings, intellectual property considerations, formulation and manufacturing complexities that affect cost, scalability and implementation, and the growing role of model-integrated evidence in streamlining bioequivalence assessments. To reach the goal of timely and equitable global access to long-acting medicines, this workshop emphasized the need for strategic public-private engagement to promote data sharing, enhance regulatory efficiencies, and develop robust in vitro–in vivo correlation strategies that meet regulatory guidance for LAI products.
UR - https://www.scopus.com/pages/publications/105030472109
U2 - 10.1002/cpt.70238
DO - 10.1002/cpt.70238
M3 - Review article
C2 - 41704016
AN - SCOPUS:105030472109
SN - 0009-9236
VL - 119
SP - 1195
EP - 1204
JO - Clinical Pharmacology and Therapeutics
JF - Clinical Pharmacology and Therapeutics
IS - 5
ER -