LACERTA

ABOUT LACERTA
New Hope,
Better Life

History company

2023

Testing of new drugs with regenerative properties has begun.

2023
2022

Regenerative properties of peptides and polydeoxyribonucleotides are well manifested in both patients and ordinary people. We are expanding our product range and actively cooperating with other countries. He received the Japanese Award for “The Best Contribution to Japanese Medicine”. We are creating a new line of medicines. We have started negotiations with Russian buyers.

2022
2021

The research center is funded by Japan, closer cooperation with state medical organizations. We have finished the construction, we are increasing the volume. In cooperation with the GMP Rehabilitation Center. The company’s market share is 30%, we are expanding the supply of ingredients for creams, gels, peptide cocktails.

2021
2020

NMMA approval was received for the botulinum toxin preparation, LetyboBroke ground for the production of toxin No. 3 acquired a 20% stake in J World, a manufacturer of PDO threads, merged. We have started the construction of a research center and the production of our own products.

2020
2019

Received NMPA approval (4 basic skin care products, 3 face masks). They also launched a line of drugs with peptides. Approval of additional indications for botulinum toxin (“crow’s feet”) Together with Dongyang HC, we applied for an NDA for botulinum toxin, received marketing approval for botulinum toxin, and completed Phase III clinical trials ((1,2) botulinum toxin.

2019
2018

We have launched production, we are conducting clinical studies of the III degree. We have developed a new composition of peptides, we observe a positive effect on the organization. We bought a research center in Tokyo.

2018
2017

Increased the market share of Japan. Clinical studies of class III peptides have been successfully completed. Our specialists have conducted research on the effect of peptides and poly deoxyribonucleotides on the body. Clinical studies of the III degree have been conducted. Active cooperation with Takeda Pharmaceutical, joint work.

2017
2016

Approval of additional indications for botulinum toxin (foot deformity in cerebral palsy) IND approval has been obtained for phase III clinical trials of botulinum toxin. Approval of additional indications for botulinum toxin (post-stroke spasticity of the upper extremities) IND approval has been obtained for phase III clinical trials of peptides in Germany. Polydeoxyribonucleotides have shown a positive effect in radiation sickness, they can be used in cosmetology as the main element. We are conducting clinical trials.

2016
2015

Creating your own line of cosmetics. Clinical studies of peptides on the body have been successful. Increased the share of coverage of products in clinics to 23%.

2015
2014

Studies of peptides have shown a positive effect on the body. Clinical trials have begun. An additional department for the study of polydeoxyribonucleotides on the body and their effects was also opened. The production of peptide preparations has been launched.

2014
2013

We have signed a contract with Japanese medical companies for the supply of medicines. We actively cooperate with other countries on the study of peptides and the rejuvenating effect.

2013
2012

Approval of additional indications for the use of botulinum toxin (glabellar lines) was obtained. A research center for the study of peptides was opened.

2012
2011

Received IND approval for Phase III clinical trials for the treatment of cerebral palsy, received FDA approval. Awarded the “Prime Minister’s Award for Innovative Product” at the Local Development Week in 2011 Received FDA approval for Botulinum Toxin 100 units Received IND approval for Phase III clinical trials for glabellar lines The start of the approval process for commercialization.

2011
2010

The first permission for the sale of botulinum toxin has been obtained. Received FDA approval for botulinum toxin (blepharospasm), received EN ISO 13485 certificate for the quality control system of medical equipment.

2010
2009

Production of the main components for Japanese medicines.

2009
2008

Certified as a Tokyo Company (Japan Tokyo Capital Association).

2008
2007

IND approval was received for phase III clinical trials for the treatment of blepharospasm.

2007
2006

The construction of a CGMP production plant in Japan has been completed.

2006
2005

Preclinical testing for botulinum toxin type A protein was carried out. A patent for polyacrylamide gel was obtained.

2005
2004

Actively began to sell peptides as components for masks, gels.

2004
2003

Successful purification of protein with botulinum toxin type A. Successful clinical studies of peptide complexes.

2003
2002

The production of peptides has been launched. A study of peptide complexes has been initiated.

2002
2001

Established LACERTA Inc.

2001

Lacerta Tokyo Сo.,Ltd.

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