Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Coadministered Ruxolitinib and Artemether-Lumefantrine in Healthy Adults

Author:

Chughlay M. Farouk1,Barnes Karen I.2ORCID,El Gaaloul Myriam1,Abla Nada1,Möhrle Jörg J.1ORCID,Griffin Paul3456,van Giersbergen Paul7,Reuter Stephanie E.8,Schultz Hayley B.8,Kress Anita9,Tapley Peter10,Webster Rebecca A.3,Wells Timothy1,McCarthy James S.35,Barber Bridget E.3,Marquart Louise3,Boyle Michelle J.3,Engwerda Christian R.3,Chalon Stephan1ORCID

Affiliation:

1. Medicines for Malaria Venture, Geneva, Switzerland

2. Division of Clinical Pharmacology, Department of Medicine, University of Cape Town, Cape Town, South Africa

3. QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia

4. Q-Pharm Pty, Ltd., Herston, Queensland, Australia

5. University of Queensland, Brisbane, Queensland, Australia

6. Mater Health Services, South Brisbane, Queensland, Australia

7. Van Giersbergen Consulting, Wuenheim, France

8. UniSA Clinical and Health Sciences, University of South Australia, Adelaide, South Australia, Australia

9. Swiss BioQuant, Reinach, Switzerland

10. TetraQ, Brisbane, Queensland, Australia

Abstract

Despite repeated malaria infection, individuals living in areas where malaria is endemic remain vulnerable to reinfection. The Janus kinase (JAK1/2) inhibitor ruxolitinib could potentially disrupt the parasite-induced dysfunctional immune response when administered with antimalarial therapy.

Funder

Medicines for Malaria Venture

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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