Alteogen Inc

Korea (South)alteogen.com

Alteogen Inc is a South Korea–based biopharmaceutical company specializing in biologics R&D and enabling technologies for large‑molecule medicines. The company develops biosimilars and “biobetter” formulations, as well as platforms that improve delivery and pharmacokinetics of therapeutic proteins and antibodies.

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A core technology is its recombinant human hyaluronidase (also known as berahyaluronidase alfa/ALT‑B4), designed to facilitate high‑volume subcutaneous administration of biologics that are typically given intravenously. Alteogen also works on antibody–drug conjugate (ADC) technologies, long‑acting protein therapeutics, and ophthalmology and oncology biosimilar candidates. Its activities span protein engineering, cell line and process development, formulation science, and CMC analytics, with out‑licensing and collaborations with global pharmaceutical partners. The company is headquartered in Daejeon, South Korea.

Projects Alteogen Inc is involved in

None yet. When a new project in the record names Alteogen Inc as owner, partner or investor, it shows here.

Alteogen Inc in chemical industry news

21 September 2026
Merck’s KEYTRUDA QLEX approved in Japan for subcutaneous use across all KEYTRUDA indications

First subcutaneous immune‑checkpoint inhibitor in Japan; can be given in as little as one minute and showed comparable exposure and response to IV pembrolizumab in a phase‑3 trial.

19 November 2025
Merck's KEYTRUDA® Subcutaneous Form Approved by European Commission

KEYTRUDA SC, a subcutaneous immune checkpoint inhibitor, is approved in Europe for faster administration across all adult indications.

19 September 2025
FDA Approves Merck's Subcutaneous KEYTRUDA QLEX for Solid Tumors

KEYTRUDA QLEX, a subcutaneous immune checkpoint inhibitor, offers comparable efficacy to IV KEYTRUDA in treating metastatic NSCLC, with administration possible in one minute by healthcare providers.

19 September 2025
Merck Gains EU CHMP Support for KEYTRUDA SC and New Head and Neck Cancer Use

CHMP backs KEYTRUDA SC for all EU adult indications and a new use in LA-HNSCC. Awaiting European Commission's final decision.