Press Release
G2GBio has the best experts in the field of innovative improved injectable drug development.
G2GBio has been selected for a government-supported project by the Ministry of SMEs and Startups, receiving 11.4 billion won in funding over three years
2024.04.30
HIT 220
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G2GBio has been selected for a
government-supported project by the Ministry of SMEs and Startups, receiving
11.4 billion won in funding over three years. - Research and development project for a one-month sustained-release
schizophrenia treatment - The goal is to replace once-daily oral administration with a formulation
that enhances therapeutic effects.
Based
on G2GBio's patented platform technology, research on a sustained-release
schizophrenia treatment has been selected as a new supported project under the
Small and Medium Venture Business Department's 2024 Small Business Technology
Innovation Development Project (Market Expansion Type, Scale-up TIPS). G2GBio
announced on the 30th that it will receive exclusive government funding of 11.4
billion won for the next three years. The
Small and Medium Venture Business Department's Scale-up TIPS (Technology
Innovation Development Project for SMEs) is a national project aimed at
fostering challenges, innovations, and scale-ups of manufacturing,
hardware-based, and technology-intensive SMEs by connecting private investment
with government funds. The
research selected for this national project aims to develop a schizophrenia
treatment that lasts for one month using G2G Bio's drug delivery technology,
InnoLAMP. While
there is a growing trend in long-acting injectable drugs that offer convenience
and increased therapeutic effects, commercialized injectables require
improvements such as reducing discomfort associated with high dosages. G2GBio
aims to develop high-dose products to significantly reduce dosage and address
unmet patient needs, thereby improving medication adherence. Seol
Eun-young, the research director for this project at G2G Bio, stated, "We
have already confirmed in preliminary testing that it is possible to control
the pharmacokinetic profile with high-dose formulations." She added,
"Now that we have been selected for the national project, our plan is to
secure the final candidate formulation and proceed with comprehensive animal
efficacy testing, toxicity testing, and scale-up research."
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