Country for PR: United States
Contributor: PR Newswire New York
Tuesday, May 25 2021 - 20:00
AsiaNet
Comparison of Advanced Aesthetic Technologies, Inc.'s 2.5% Agarose Gel with Hyaluronic Acid Filler for the Correction of Moderate to Severe Nasolabial Folds Reveals Equivalent Results
BROOKLINE, Mass., May 25, 2021 /PRNewswire-AsiaNet/ --

-- Results of Split-Face Study to Determine the Efficacy and Safety of 2.5% 
Agarose Gel Filler for the Correction of Nasolabial Folds Published in Peer 
Reviewed Journal


Advanced Aesthetic Technologies, Inc. (AAT), a leader in aesthetic gel implant 
technology, is proud to announce that Algeness(R) VL (2.5% Agarose Gel) 
demonstrated equivalent efficacy, safety, and usability compared to those of 
NASHA-L based on a split-face study published in the Journal of Cosmetic 
Dermatology. 

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"Agarose gel filler is a naturally occurring polymer gel with a 
three-dimensional structure similar to the extracellular matrix, which achieves 
its duration without the need for crosslinking. Our objective with this study 
of 66 patients was to determine the efficacy and safety of 2.5% agarose gel 
filler for the correction of nasolabial folds as compared with NASHA-L. Our 
assessments included assessment of the nasolabial fold (NLF), Wrinkle Severity 
Rating Scale (WSRS), Global Aesthetic Improvement Scale (GAIS [blinded 
investigator]), as well as subject satisfaction, adverse events, and 
usability," according to lead investigator Nicolò Scuderi MD of the Department 
of General and Plastic Surgery at the University of La Sapienza, Rome, Italy. 

Among the 66 participants in the study, 46 individuals or 66.7% were available 
for evaluation at 3 months, when mean change in WSRS was identical for both 
products ( -1.1(+_) 0.4 for 2.5% agarose; -1.1(+_) 0.4 for NASHA-L). Scores for 
each product remained similar across all time points and began to return to 
baseline between 7 and 8 months. GAIS score followed a similar pattern, rising 
between months 7 and 8 (2.7 (+_) 0.6 for 2.5% agarose at month 7 and 3.3 (+_) 
0.5 at month 8, vs.  2.7 (+_) 0.6 for NASHA-L at month 7-3.3 (+_) 0.5 at month 
8). The longevity of both fillers was confirmed by Ultrasound. All adverse 
events were transient in nature and resolved within 15 days, most events were 
mild in nature, and the number and severity of events was similar between the 
two fillers. According to Dr. Scuderi, "We continue to be impressed with the 
clinical outcomes of the novel Algeness(R) range of dermal fillers. This is the 
first 100% natural, biocompatible and biodegradable filler on the market to 
date, which differentiates it from other injectable products."

U.S. based investigator Brian Kinney, MD, FACS, Division of Plastic Surgery, 
University of Southern California, Keck School of Medicine, in Beverly Hills, 
CA, adds, "These results add to the growing body of evidence that confirms that 
Algeness(R) (2.5% agarose gel filler) has a high safety profile and is well 
tolerated by patients. We concluded that this unique dermal filler compound had 
a longevity which was equivalent to one of the most widely used fillers, 
NASHA-L a hyaluronic acid."

Doug Abel, CEO of AAT commented, "We are very pleased with the outcome of this 
important study which demonstrate that in this initial clinical study, the 
results with 2.5% agarose gel are equivalent to those of NASHA-L. This is 
another significant milestone demonstrating the efficacy and performance of our 
proprietary Algeness(R) technology. This notable recognition from three 
internationally respected plastic surgeons reconfirms the durability of the 
Algeness(R) technology and secures its place as a differentiator in the global 
dermal filler market.  We have begun the process to pursue both US FDA approval 
for Algeness® and, through our strategic Partner, registration in China."

Algeness(R) is a patented family of fully resorbable injectable gel implant 
dermal fillers that are 100% natural, providing advantages in terms of safety, 
skin rejuvenation, and natural looking results both at rest and during facial 
movement. Typical clinical advantages include minimal swelling upon injection 
and immediately visible results. Algeness(R) holds a CE Mark and is currently 
distributed in over 30 countries worldwide. 

About Advanced Aesthetic Technologies, Inc.

AAT is a fast growing, global corporation developing new technologies for 
aesthetic medicine. Our lead products, the Algeness(R) family of injectable 
implants, are the culmination of more than 10 years of scientific and clinical 
research and were developed with the goal of providing aesthetic injectors 
advances in the ability to achieve deep structural support, clean definition, 
and exceptional clinical outcomes where the result at the time of treatment is 
the final outcome. Algeness(R) is a 100% natural and biodegradable filler based 
on purified agarose with a differentiated clinical and safety performance 
profile. AAT continuously invests in research and product development to expand 
the scientific knowledge on Algeness(R) and agarose as well as in pursuit of 
new and innovative technologies to enhance aesthetic medicine and expand our 
portfolio. Algeness
(R) is CE Marked, has multiple additional country level registrations, and is 
currently available in over 30 countries. AAT is in the process of pursuing 
registration in the US through the FDA and also in China through the 
partnership with Lanzhou Biotechnique Development Co., LTD (Lanzhou) and their 
parent company China National Biotec Group Co., LTD (CNBG). 
http://www.algeness.com

References

Scuderi N, Fanelli B, Fino P, Kinney BM. Comparison of 2.5% agarose gel vs 
hyaluronic acid filler, for the correction of moderate to severe nasolabial 
folds. J Cosmet Dermatol. 2021;00:1– 8. https://doi.org/10.1111/jocd.13962

Contact: filler@algeness.com 





SOURCE: Advanced Aesthetic Technologies, Inc.
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