Mass Drug Administration of Dihydroartemisinin-piperaquine + Single Low-dose Primaquine to Accelerate Toward Elimination Activities
Launched by UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · Apr 26, 2021
Trial Information
Current as of June 24, 2025
Completed
Keywords
ClinConnect Summary
Over the past two decades in Senegal, the scale-up of malaria control measures \[e.g., access to prompt testing and case management, LLINs, and SMC\] has led to a 78% reduction in malaria incidence. However, gains have not been uniform, with lower transmission areas in the north implementing pre-elimination activities and higher transmission areas in the south implementing control interventions (including SMC). The purpose of this study is determine whether MDA will be able to rapidly reduce malaria incidence in areas of moderate-to-low malaria transmission of southern Senegal (where contro...
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Age ≥3 months
- • Willingness to comply with trial procedures and written informed consent to be obtained at the beginning of the study
- Exclusion Criteria:
- • Severe illness or self-reported chronic illness (e.g., HIV, tuberculosis, heart/liver/kidney disease, and severe malnutrition)
- • Known hypersensitivity to study drug
- Additional exclusion criteria for DHA-PPQ:
- • First trimester pregnancy assessed by history and/or urine pregnancy testing
- • Concurrent artemisinin-based combination therapy (ACT) use
- • Taking drugs that influence cardiac function or prolong QTc interval
- Additional exclusion criteria for PQ:
- • Pregnancy (any trimester) or currently breastfeeding an infant \<6 months of age assessed by history and/or urine pregnancy testing
- • \<2 years of age
About University Of California, San Francisco
The University of California, San Francisco (UCSF) is a leading academic institution renowned for its commitment to advancing healthcare through innovative research and clinical trials. With a focus on translating scientific discoveries into effective therapies, UCSF collaborates with a diverse array of stakeholders, including healthcare professionals, industry partners, and patient communities. The university's research programs emphasize interdisciplinary approaches and leverage cutting-edge technology to address complex medical challenges. As a sponsor of clinical trials, UCSF is dedicated to maintaining the highest standards of ethical conduct and scientific rigor, ensuring the safety and well-being of participants while contributing to the broader medical knowledge base.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Tambacounda, , Senegal
Patients applied
Trial Officials
Jean Louis Ndiaye, MD PhD
Principal Investigator
Université de Thiès
Michelle Hsiang, MD MSc
Principal Investigator
University of California, San Francisco
Doudou Séne, MD
Principal Investigator
Senegal Programme National de Lutte contre le Paludisme (PNLP)
Katharine Sturm-Ramirez, PhD
Principal Investigator
US President's Malaria Initiative/CDC
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
Similar Trials