ATLANTA, Sept. 13, 2018 /PRNewswire/ -- Alimera
Sciences, Inc. (NASDAQ: ALIM) (Alimera), a leader in the
commercialization and development of prescription ophthalmic
pharmaceuticals, today announced that two presentations will be
delivered, and one poster presented, on ILUVIEN® during
the 2018 Annual Meeting of the Retina Society being held
September 12-15 at The Palace Hotel
in San Francisco.
"We are pleased with the presentations and poster being shared
this year at Retina Society," said Dan
Myers, CEO of Alimera. "We are particularly excited to share
new data from the USER (U.S. Retrospective Chart Review in Patients
Receiving ILUVIEN) Study in one of the presentations that we
believe is relevant in the management of DME. This presentation
will discuss the benefit of ILUVIEN's CONTINUOUS MICRODOSING™
delivery to reduce both the recurrence of edema and retinal
thickness variability to maintain a consistently drier retina."
Scheduled to be presented at the podium on September 14th are:
- 8:41 a.m. – "Effect of
Fluocinolone Acetonide (FAc) 0.2µg/day Implant on the Decision to
Drive in Patients with Diabetic Macular Edema," by Ivan Suner, M.D.
- 8:51 a.m. – "USER Study Real
World Outcomes: Reduction in Retinal Thickness Variability with the
Fluocinolone Acetonide (ILUVIEN®) Implant for Diabetic Macular
Edema," by Christopher Riemann,
M.D.
- 8:56 a.m. – "The Effect of DME
Duration on Visual and Anatomical Response to the Fluocinolone
Acetonide Implant — a Subgroup Analysis from the 3-year RETRO-IDEAL
Study in Germany," by Albert Augustin, M.D.
The following poster is included in Poster Session II –
Saturday, September 15, 12:28 p.m. – 1:22
p.m.:
- "Consecutive Series of Long Term Outcomes with the Fluocinolone
Acetonide 0.2 ug/day (ILUVIEN 0.19 mg) Implant for Diabetic Macular
Edema," by Daniel Kiernan, M.D.
About ILUVIEN
www.ILUVIEN.com.
ILUVIEN'S U.S. Indication
ILUVIEN (fluocinolone acetonide intravitreal implant) 0.19 mg is
a sustained release intravitreal implant approved in the U.S. to
treat diabetic macular edema in patients who have been previously
treated with a course of corticosteroids and did not have a
clinically significant rise in intraocular pressure. Each ILUVIEN
implant is designed to release submicrogram levels of fluocinolone
acetonide, a corticosteroid, for 36 months.
About Diabetic Macular Edema (DME)
DME, the primary cause of vision loss associated with diabetic
retinopathy, is a disease affecting the macula, the part of the
retina responsible for central vision. When the blood vessel
leakage associated with diabetic retinopathy results in swelling of
the macula, the condition is called DME. The onset of DME is
painless and may go unreported by the patient until it manifests
with the blurring of central vision or acute vision loss. The
severity of this blurring may range from mild to profound loss of
vision. The Wisconsin Epidemiologic Study of Diabetic Retinopathy
found that over a 10-year period approximately 19% of people with
diabetes included in the study were diagnosed with DME. All people
with type 1 or type 2 diabetes are at risk of developing DME.
About Alimera Sciences, Inc.
www.alimerasciences.com
Alimera Sciences (NASDAQ:ALIM), founded in June 2003,
is a pharmaceutical company that specializes in the
commercialization and development of prescription ophthalmic
pharmaceuticals. Alimera is presently focused on diseases affecting
the back of the eye, or retina, because these diseases are not well
treated with current therapies and will affect millions of people
in our aging populations. Alimera's commitment to retina
specialists and their patients is manifest in Alimera's product
portfolio. For more information, please
visit www.alimerasciences.com.
For press
inquiries:
|
For investor
inquiries:
|
Katie
Brazel
|
CG Capital
|
for Alimera
Sciences
|
for Alimera
Sciences
|
404-317-8361
|
877-889-1972
|
kbrazel@bellsouth.net
|
investorrelations@cg.capital
|
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SOURCE Alimera Sciences, Inc.