Charles Eric Mowbray

Dr. Charles Eric Mowbray

orcid

Research Focus & Metrics

Academic Career Length

37Years (1990-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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5 October 2015 in Nature Reviews Drug Discovery
Verified
Journal Article
Closed access
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KKKei Katsuno
Kei Katsuno
JBJeremy N. Burrows
Jeremy N. Burrows
KDKen Duncan
Ken Duncan
RHRob Hooft van Huijsduijnen
Rob Hooft van Huijsduijnen
TKTakushi Kaneko
Takushi Kaneko
BSB. T. Slingsby
B. T. Slingsby

1 October 2018 in Clinical Microbiology Reviews
Verified
Journal Article
Open access
PDF file
FAFabiana Alves
Fabiana Alves
GBGraeme Bilbe
Graeme Bilbe
SBSéverine Blesson
Séverine Blesson
VGVishal Goyal
Vishal Goyal
SMSéverine Monnerat
Séverine Monnerat
JAJorge Alvar
Jorge Alvar
Research in visceral leishmaniasis in the last decade has been focused on how better to use the existing medicines as monotherapy or in combination. Systematic research by geographical regions has shown that a universal treatment is far from today's reality.

15 February 2022 in Nature Communications
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Journal Article
Open access
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RARana Abdelnabi
Rana Abdelnabi
CFCaroline Shi-Yan Foo
Caroline Shi-Yan Foo
DJDIRK JOCHMANS
DIRK JOCHMANS
LVLaura Vangeel
Laura Vangeel
SJSteven De Jonghe
Steven De Jonghe
JNJohan Hendrik Neyts
Johan Hendrik Neyts
There is an urgent need for potent and selective antivirals against SARS-CoV-2. Pfizer developed PF-07321332 (PF-332), a potent inhibitor of the viral main protease (Mpro, 3CLpro) that can be dosed orally and that is in clinical development. We here report that PF-332 exerts equipotent in vitro activity against the four SARS-CoV-2 variants of concerns (VoC) and that it can completely arrest replication of the alpha variant in primary human airway epithelial cells grown at the air-liquid interface. Treatment of Syrian Golden hamsters with PF-332 (250 mg/kg, twice daily) completely protected the animals against intranasal infection with the beta (B.1.351) and delta (B.1.617.2) SARS-CoV-2 variants. Moreover, treatment of SARS-CoV-2 (B.1.617.2) infected animals with PF-332 completely prevented transmission to untreated co-housed sentinels.

13 December 2018 in ACS Infectious Diseases
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Journal Article
Open access
SRSrinivasa Rao
Srinivasa Rao
MBMichael P. Barrett
Michael P. Barrett
GDGlenn Dranoff
Glenn Dranoff
CFChristopher J. Faraday
Christopher J. Faraday
CGClaudio R. Gimpelewicz
Claudio R. Gimpelewicz
TDThierry T. Diagana
Thierry T. Diagana
Kinetoplastid parasites have caused human disease for millennia. Significant achievements have been made toward developing new treatments for leishmaniasis (particularly on the Indian subcontinent) and for human African trypanosomiasis (HAT). Moreover, the sustained decrease in the incidence of HAT has made the prospect of elimination a tantalizing reality. Despite the gains, no new chemical or biological entities to treat kinetoplastid diseases have been registered in more than three decades, and more work is needed to discover safe and effective therapies for patients with Chagas disease and leishmaniasis. Advances in tools for drug discovery and novel insights into the biology of the host–parasite interaction may provide opportunities for accelerated progress. Here, we summarize the output from a gathering of scientists and physicians who met to discuss the current status and future directions in drug discovery for kinetoplastid diseases.

10 September 2014 in Expert Review of Anti-infective Therapy
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Journal Article
Open access
GEGilles Eperon
Gilles Eperon
MBManica Balasegaram
Manica Balasegaram
JPJulien Potet
Julien Potet
CMCharles Eric Mowbray
Charles Eric Mowbray
OVOlaf Valverde
Olaf Valverde
FCFrançois Chappuis
François Chappuis
Treatment of second-stage gambiense human African trypanosomiasis relied on toxic arsenic-based derivatives for over 50 years. The availability and subsequent use of eflornithine, initially in monotherapy and more recently in combination with nifurtimox (NECT), has drastically improved the prognosis of treated patients. However, NECT logistic and nursing requirements remain obstacles to its deployment and use in peripheral health structures in rural sub-Saharan Africa. Two oral compounds, fexinidazole and SCYX-7158, are currently in clinical development. The main scope of this article is to discuss the potential impact of new oral therapies to improve diagnosis-treatment algorithms and patients' access to treatment, and to contribute to reach the objectives of the recently launched gambiense human African trypanosomiasis elimination program.

1 October 1998 in The Journal of Organic Chemistry
Verified
Journal Article
Closed access
RJRichard F. W. Jackson
Richard F. W. Jackson
RMRebecca J. Moore
Rebecca J. Moore
CDCharles S. Dexter
Charles S. Dexter
JEJason Elliott
Jason Elliott
CMCharles Eric Mowbray
Charles Eric Mowbray