GI Dynamics Appoints Vice President of Clinical and Regulatory Affairs
January 03 2019 - 8:24PM
Business Wire
GI Dynamics® Inc. (ASX:GID), a medical device company that is
developing EndoBarrier® for patients with type 2 diabetes and
obesity, is pleased to announce the appointment of Stephen Linhares
to the position of vice president of clinical and regulatory
affairs.
Linhares’ role with GI Dynamics will focus on the pivotal trial
of EndoBarrier in the United States (GID 18-1) and the clinical
trial of EndoBarrier in India with Apollo Sugar. He will also lead
the company’s efforts with its notified body, Intertek, to seek a
CE mark for EndoBarrier.
Linhares brings over 30 years of experience in development,
regulatory, preclinical and clinical operations, quality and
resource management with a focus on medical devices. Prior to
joining GI Dynamics, Linhares held the positions of vice president
of regulatory, clinical affairs and quality assurance at Neograft
Technologies Inc. and leadership roles at Insulet Corporation,1
Boston Scientific Corporation Inc. and Phase Forward Inc. as well
as vice president roles at PLC Medical Systems.
Linhares brings deep knowledge of the diabetes disease space,
and the medical device space, where he has led 10 clinical trials,
multiple CE mark approvals and numerous 510(k) clearances. Linhares
holds nearly 20 United States and international patents and
co-author of two peer-reviewed publications.2
“GI Dynamics is preparing to launch clinical studies on a
product that could disrupt the conventional approaches for the
treatment of type 2 diabetes and obesity, and I am very honored and
excited to be involved,” said Linhares.
“On behalf of the GI Dynamics board of directors, I am pleased
to announce the appointment of Stephen Linhares,” said Scott
Schorer, president and chief executive officer of GI Dynamics.
“Stephen will join Charles Carter and I on our senior leadership
team. Together we are focused on stage 1 of GID 18-1, the clinical
trial in India and gaining the EndoBarrier CE mark. Stephen will
help lead the company with the necessary expertise, and I am
pleased to welcome him to the team.”
About GI Dynamics
GI Dynamics®, Inc. (ASX:GID) is the developer of EndoBarrier®,
the first endoscopically-delivered device therapy for the treatment
of type 2 diabetes and obesity. EndoBarrier is not approved for
sale and is limited by federal law to investigational use only.
Founded in 2003, GI Dynamics is headquartered in Boston,
Massachusetts. For more information please visit
www.gidynamics.com.
Forward-Looking Statements
This announcement may contain forward-looking statements. These
statements are based on GI Dynamics management’s current estimates
and expectations of future events as of the date of this
announcement. Furthermore, the estimates are subject to several
risks and uncertainties that could cause actual results to differ
materially and adversely from those indicated in or implied by such
forward-looking statements.
These risks and uncertainties include, but are not limited to,
risks associated with our ability to continue to operate as a going
concern; our ability to raise sufficient additional funds to
continue operations and to conduct the pivotal trial of EndoBarrier
in the United States (GID 18-1); our ability to execute GID 18-1
under FDA’s Investigational Device Exemption; our ability to enlist
clinical trial sites and enroll patients in accordance with GID
18-1; the risk that the FDA stops GID 18-1 early as a result of the
occurrence of certain safety events or does not approve an
expansion of GID 18-1; our ability to maintain compliance with our
obligations under our existing convertible note and warrant
agreements executed with Crystal Amber Fund Limited, including our
obligations to make payment on the relevant note that is due in
March 2019; our ability to restructure the terms of the convertible
note with Crystal Amber Fund Limited that is due in March 2019 if
we are unable to raise sufficient funds to enable us to fully repay
such note when due; obtaining and maintaining regulatory approvals
required to market and sell our products; the possibility that
future clinical trials will not be successful or confirm earlier
results; the timing and costs of clinical trials; the timing of
regulatory submissions; the timing, receipt and maintenance of
regulatory approvals; the timing and amount of other expenses; the
timing and extent of third-party reimbursement;
intellectual-property risk; risks related to excess inventory;
risks related to assumptions regarding the size of the available
market; the benefits of our products; product pricing; timing of
product launches; future financial results; and other factors,
including those described in our filings with the U.S. Securities
and Exchange Commission.
Given these uncertainties, one should not place undue reliance
on these forward-looking statements. We do not assume any
obligation to publicly update or revise any forward-looking
statements, whether as a result of new information or future events
or otherwise, unless we are required to do so by law.
1 Insulet Corporation, a medical device company specializing in
state-of-the-art insulin delivery devices.2 Z. Drozdowicz, R.I
Rudko, S.J. Linhares and B. Lax, “High Gain 4.3 to 4.5 um Optically
Pumped CO2 Laser,” IEEE Quantum Electron, vol. QE-17, pp. 574-1580,
1987.R.I. Rudko, A. Drozdowicz and S.J. Linhares, “High
Repetition-Rate, Recirculating Hydrogen Fluoride/Deuterium Fluoride
Laser,” Rev. Sci. Instruments, vol. 53, pp. 452-457, 1982.
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Investor RelationsUnited States:Janell Shields+1 (781)
357-3280investor@gidynamics.com
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