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HK inno.N and Kine Sciences to Jointly Develop Sarcopenia Treatment

HK inno.N and Kine Sciences to Jointly Develop Sarcopenia Treatment and Initiate Phase 2 Clinical Trial

 

Joint development of Sarcopenia drug candidate ‘KINE-101’ and accelerated plans for phase 2 clinical trial in Korea

Expansion of ‘KINE-101’ indications to Sarcopenia, following Rheumatoid Arthritis and Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)

Anticipated synergy with HK inno.N’s obesity treatment currently under development



 

Photo. HK inno.N CEO Darl-Won Kwak (front row, right) and Kine Sciences CEO Dae-Ho Cho (front row, left), along with researchers from both companies, are taking a commemorative photo to mark the signing of the joint R&D agreement.


HK inno.N is actively advancing the development of a Sarcopenia treatment, accelerating the expansion of its portfolio in aging-related and metabolic diseases.

 

On November 18, HK inno.N announced that it had recently signed a joint research and development agreement with Kine Sciences for ‘KINE-101,’ an inflammation-modulating peptide-based drug candidate for the treatment of Sarcopenia.

 

Under the agreement, HK inno.N will lead the phase 2 clinical trial in Korea for KINE-101, while Kine Sciences will handle the manufacturing of the investigational medicinal product and provide technical support. Both companies will collaborate closely to ensure a swift initiation of the clinical program and secure commercialization potential in Korea, with the goal of entering phase 2 next year.

 

KINE-101’ is a peptide derived from ERDR1 (Erythroid Differentiation Regulator 1), a key protein involved in regulating inflammatory responses. It is an innovative drug candidate with mechanisms that maintain immune homeostasis and alleviate inflammation.

 

The compound has completed a phase 1 clinical trial in the United States as a treatment for rheumatoid arthritis and a clinical study in Korea for chronic inflammatory demyelinating polyneuropathy (CIDP). It has also successfully completed preclinical studies for the Sarcopenia indication.

 

Sarcopenia is caused by various factors such as aging, obesity, and metabolic disorders, and the number of patients is rapidly increasing as global population aging accelerates. Among Koreans aged 65 years and older, the prevalence of Sarcopenia is approximately 9.5% in men and 9.3% in women, and the demand for related treatments continues to grow.

 

Under this joint development agreement, synergy in reducing muscle loss through combination use with ‘IN-B0009,’ HK inno.N’s obesity treatment currently in a domestic phase 3 clinical trial, is also anticipated. Most obesity treatments currently approved or under development have the limitation of causing muscle loss alongside weight reduction. KINE-101 is therefore considered to have differentiated value as a muscle-preserving therapy.

 

Dalwon Kwak, CEO of HK inno.N, stated, “In preparation for an aging society, we are continuously strengthening our portfolio of treatments for chronic diseases. We are fully committed to developing a Sarcopenia therapy in collaboration with Kine Sciences, aiming not only to secure leadership in the Korean market but also to actively pursue global technology out-licensing.”

 

Dae Ho Cho, CEO of Kine Sciences, stated, “KINE-101 is an innovative peptide drug candidate that restores immune homeostasis by activating regulatory T cells (Tregs). It has demonstrated therapeutic potential across various immune and inflammatory diseases. Through this collaboration, we expect to successfully advance the development of a Sarcopenia treatment for older adults.” (END)

 

(Reference Information)

CIDP: chronic inflammatory demyelinating polyneuropathy

 

Source of Sarcopenia prevalence in Korea: Press release “Results of the 2024 Korea National Health and Nutrition Examination Survey – Increase in Chronic Disease Prevalence, Improvement in Treatment Rates,” Korea Disease Control and Prevention Agency (KDCA), September 30, 2025.

Nari KIMManager(Communication team)
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nari.kim@inno-n.com
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