Motif Bio Invited to Present at Infectious Diseases Conference
22 Juin 2017 - 8:00AM
Motif Bio plc (NASDAQ:MTFB)(AIM:MTFB.LN), a clinical stage
biopharmaceutical company specializing in developing novel
antibiotics, today announced that Dr. David Huang, Chief Medical
Officer at Motif Bio, has been invited to present a clinical
development overview of iclaprim during the formal Symposia session
at IDWeek 2017 on October 5, 2017. In addition, Dr. Huang will lead
a “Meet-the-Professors Session” in a clinically oriented Q&A
session on October 6, 2017.
IDWeek is the combined annual meeting of the
Infectious Diseases Society of America, Society for Healthcare
Epidemiology of America, HIV Medicine Association and Pediatric
Infectious Diseases Society. The Symposia session is focused on
clinical programs in late clinical development and closest to
regulatory approval.
Commenting on the invitation David Huang, CMO at
Motif Bio said, “IDWeek is a major event for infectious diseases
professionals and I am delighted that the IDWeek Committee has
selected iclaprim for presentation. I look forward to
presenting the positive data from the REVIVE-1 trial. We
believe these data suggest iclaprim may serve as an important
differentiated antibiotic option in an era of emerging antibiotic
resistant infections.”
About Iclaprim
Iclaprim is a potential novel antibiotic, designed to be
effective against bacteria that have developed resistance to other
antibiotics. Iclaprim exhibits potent activity against
Gram-positive clinical isolates of many genera of staphylococci,
including methicillin-sensitive staphylococci (MSSA) and
methicillin-resistant staphylococci (MRSA). The MIC90 of iclaprim
was lower, demonstrating higher potency, than most comparators
including vancomycin and linezolid, standard of care therapies used
in serious and life-threatening Gram-positive hospital infections.
To date, iclaprim has been studied in over 1,000 patients and
healthy volunteers. No dosage adjustment is required in patients
with renal impairment, or in obese patients. The iclaprim fixed
dose may help reduce the resources required in hospitals since
dosage adjustment by health care professionals is avoided, and
overall hospital treatment costs may be lower, especially in
renally impaired patients.
About IDWeek
IDWeek is attended by over 6000 healthcare
professionals practicing or involved in infectious diseases and
healthcare epidemiology and prevention, including researchers,
clinicians, quality and patient safety practitioners,
epidemiologists. In addition, public health officials,
including those who see HIV and pediatric patients attend in
numbers. It is a meeting for professionals who want to stay
current and apply state-of-the art science to clinical care, and
excel in their own career.
About Motif Bio: www.motifbio.com
Motif Bio is a clinical-stage biopharmaceutical
company, engaged in the research and development of novel
antibiotics designed to be effective against serious and
life-threatening infections in hospitalized patients caused by
multi-drug resistant bacteria. Our lead product candidate,
iclaprim, is being developed for the treatment of acute bacterial
skin and skin structure infections (ABSSSI) and hospital acquired
bacterial pneumonia (HABP), including ventilator associated
bacterial pneumonia (VABP), infections often caused by MRSA
(methicillin-resistant Staphylococcus aureus). Having completed the
REVIVE-1 trial, patients are currently being enrolled and dosed in
a second global Phase 3 clinical trial (REVIVE-2) with an
intravenous formulation of iclaprim, for the treatment of ABSSSI.
Data readout for REVIVE-2 is expected in the second half of
2017.
Forward-Looking Statements
This press release contains forward-looking
statements. Words such as “expect,” “believe,” “intend,” “plan,”
“continue,” “may,” “will,” “anticipate,” and similar expressions
are intended to identify forward-looking statements.
Forward-looking statements involve known and unknown risks,
uncertainties and other important factors that may cause Motif
Bio’s actual results, performance or achievements to be materially
different from any future results, performance or achievements
expressed or implied by the forward-looking statements. Motif Bio
believes that these factors include, but are not limited to, (i)
the timing, progress and the results of clinical trials for Motif
Bio’s product candidates, (ii) the timing, scope or likelihood of
regulatory filings and approvals for Motif Bio’s product
candidates, (iii) Motif Bio’s ability to successfully commercialize
its product candidates, (iv) Motif Bio’s ability to effectively
market any product candidates that receive regulatory approval, (v)
Motif Bio’s commercialization, marketing and manufacturing
capabilities and strategy, (vi) Motif Bio’s expectation regarding
the safety and efficacy of its product candidates, (vii) the
potential clinical utility and benefits of Motif Bio’s product
candidates, (viii) Motif Bio’s ability to advance its product
candidates through various stages of development, especially
through pivotal safety and efficacy trials, (ix) Motif Bio’s
estimates regarding the potential market opportunity for its
product candidates, and (x) the factors discussed in the section
entitled “Risk Factors” in Motif Bio plc’s Annual Report on Form
20-F filed with the SEC on May 1, 2017, which is available on the
SEC’s web site, www.sec.gov. Motif Bio plc undertakes no obligation
to update or revise any forward-looking statements.
For further information, please contact:
Motif Bio plc Contact:
Graham Lumsden
Chief Executive Officer
ir@motifbio.com
Investor Contact:
Patricia L. Bank
Westwicke Partners
415-513-1284
patti.bank@westwicke.com
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