17
Participants
Start Date
September 13, 2016
Primary Completion Date
December 22, 2016
Study Completion Date
December 22, 2016
(+)-SJ000557733
(+)-SJ000557733 (SJ733), in short SJ733, will be the second PfATP4 inhibitor to enter clinical development after KAE609 (Novartis) which is currently in Phase 2 stage. KAE609 (cipargamin; previously known as NITD609) is a spirotetrahydro-β-carbolines (spiroindolone). KAE609 inhibits QP15C20\_SJ733\_Challenge Protocol\_v2.0\_26July2016 Page 28 of 110 PfATP4, which results in a disruption of parasite sodium homeostasis. Compared to KAE609, SJ733 has the potential to be a very fast acting, antimalarial drug for human therapeutic application and may have a different safety profile in human participants. Finally, SJ733 blocks parasite transmission in vivo at potencies close to those where it is efficacious in blood stages, indicating its potential for transmission blockade in humans.
Q-Pharm Clinics, Royal Brisbane and Women's Hospital, Brisbane
Q-Pharm Clinics, Herston
Collaborators (1)
QIMR Berghofer Medical Research Institute
OTHER
Q-Pharm Pty Limited
INDUSTRY
Clinical Network Services (CNS) Pty Ltd
INDUSTRY
Medicines for Malaria Venture
OTHER