QUÉBEC CITY, June 26, 2012 /CNW Telbec/ - Aeterna Zentaris Inc. (NASDAQ:
AEZS) (TSX: AEZ) (the "Company") today announced that final Phase 3
results for its oral ghrelin agonist, AEZS-130, show that the drug is
safe and effective in diagnosing adult growth hormone deficiency
(AGHD). Jose M. Garcia, MD, PhD, of the Baylor College of Medicine and
the Michael E. DeBakey VA Medical Center, disclosed these data during
an oral presentation yesterday at the 94th ENDO Annual Meeting and Expo currently being held in Houston, Texas.
This multicenter open label study was originally designed as a
cross-over trial of AEZS-130 vs growth hormone-releasing hormone
(GHRH)+L-Arginine (ARG) in AGHD patients and in controls, matched for
body mass index (BMI), estrogen status, gender and age. After 43 AGHD
patients and 10 controls had been tested, GHRH became unavailable. The
study was completed by testing 10 more AGHD patients and 38 controls
with AEZS-130 alone.
Of the 53 AGHD subjects enrolled, 52 received AEZS-130, and 50 who had
confirmed AGHD prior to study entry were included in this analysis,
along with 48 controls. Two AGHD subjects could not be matched due to
the combination of young age, high body mass index (BMI) and estrogen
use. The objective of this clinical trial was to determine the efficacy
and safety of AEZS-130 in the diagnosis of AGHD.
Mean peak growth hormone (GH) levels in AGHD patients and controls
following AEZS-130 administration were 2.36ng/mL (range 0.03-33) and
17.71ng/mL (range 10.5-94), respectively. The receiver operating
characteristic (ROC) plot analysis yielded an optimal GH cut-point of
2.7ng/mL, with 82% sensitivity, 92% specificity and a 13%
misclassification rate. Obesity (BMI>30) was present in 58% of cases
and controls, and peak GH levels were inversely associated with BMI in
Adverse events (AE) were seen in 37% of AGHD patients and in 21% of
controls following AEZS-130. In contrast, 61% of AGHD subjects and 30%
of controls experienced AEs with L-ARG+GHRH. The most common AEs after
AEZS-130 were unpleasant taste (19.2%) and diarrhea (3.8%) for the AGHD
patients and unpleasant taste (4.2%) and diarrhea (4.2%) for the
matched controls. AEs were generally mild or moderate in severity.
Data are available on preference of the two tests for 50 subjects. Of
these, 70% expressed a preference for AEZS-130 over L-ARG+GHRH.
Data show AEZS-130 to be safe and effective in diagnosing AGHD.
The abstract titled, "AEZS-130 (Macimorelin) - Stimulated GH Test: Validation of a Novel Test
for the Diagnosis of Adult Growth Hormone Deficiency (AGHD)", J. M. Garcia, R. Swerdloff, C. Wang, M. Kyle, M. Kipnes, B. Biller, D.
Cook, K. Yuen, V. Bonert, A. Dobs, M. Molitch, G. Merriam, is available
through this link.
AEZS-130, a ghrelin agonist, is a novel orally-active small molecule
that stimulates the secretion of growth hormone. The Company has
completed a Phase 3 trial for use as an oral diagnostic test for AGHD.
AEZS-130 has been granted orphan drug designation by the FDA for use in
this indication. AEZS-130 is also in a Phase 2A trial as a treatment
for cancer induced cachexia. Aeterna Zentaris owns the worldwide rights
About Aeterna Zentaris
Aeterna Zentaris is an oncology and endocrinology drug development
company currently investigating treatments for various unmet medical
needs. The Company's pipeline encompasses compounds at all stages of
development, from drug discovery through to marketed products. For more
information please visit www.aezsinc.com.
SOURCE AETERNA ZENTARIS INC.
For further information:
Ginette Beaudet Vallières
Investor Relations Coordinator
(418) 652-8525 ext. 265
Director of Communications
(418) 652-8525 ext. 406