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Pharma & CDMOKOSDAQ 1876603 trials

Penetrium Bioscience Inc.

Official website

A Hyundai Bioscience-affiliated biotech developing cancer drugs via its Penetrium(TM) platform, alongside CRO services.

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Business overview

Source: DART corporate disclosure

Founded in 2003 and listed on KOSDAQ in 2021, Penetrium Bioscience is a biotech drug developer acquired by Hyundai Bioscience Co., Ltd. in May 2024. It builds its pipeline around Penetrium(TM), a drug-delivery platform, while providing CRO services. Its bio TF team licensed drug-delivery tech from Hyundai Bioscience for breast/lung cancer drugs via a June 26, 2024 deal worth KRW 9.1bn upfront plus milestones.

Products & technology

  • Contract Research Organization (CRO) ServiceClinical trial design, operation/management, data management and statistics, pharmacovigilance (PV), regulatory affairs (RA), and quality assurance (QA) for pharmaceutical/biotech clients across Phase 1-3 trials

Clinical trials

data.go.kr

3 MFDS clinical trial authorisations · 2020–2025 (Phase 1 1 · Phase 2a 1 · Phase 2 1)

  • Phase 1Penetrium(TM)2025-12-09

    1 trial site

  • Phase 2aAP-1012021-12-29

    1 trial site

  • Phase 2CDA-012020-07-08

    4 trial sites

R&D and key agreements

Source: DART corporate disclosure

유방암 항암제 (약물전달체 기반) · 유방암 · Acquired a portion of exclusive patent license (Patent 10-2378590, held by C&Pharm and We Biotree) from Hyundai Bioscience under a June 26, 2024 Exclusive License Transfer Agreement: KRW 9.1bn upfront, KRW 6.5bn on US Phase 2 success, KRW 5.0bn on US Phase 3 success, KRW 5.0bn on US approval, plus running royalties of 3-10% of net sales by tier

폐암 항암제 (약물전달체 기반) · 폐암(비소세포폐암 등 고형암) · Exclusive license acquired from Hyundai Bioscience under the same June 26, 2024 agreement; prepared mass production of clinical-grade drug in cooperation with Daegu-Gyeongbuk Medical Innovation Foundation (K-Medi Hub) and Yuyoung Pharm

고형암 치료제 (약물전달체 기반, IND 1상) · 고형암(유방암·폐암 등) · IND 1상 승인(2025.12.09, 식품의약품안전처) · Received Investigational New Drug (IND) Phase 1 approval from the Ministry of Food and Drug Safety on December 9, 2025 (source sentence is truncated beyond this point)

Key disclosures

KRX KIND via OpenDART
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Sources and updates

Counts on this page are not company-reported figures. MAA matched records from DART, the Korean MFDS, the US FDA, ClinicalTrials.gov, PubMed and KIPRIS to this company itself, by business registration number or registered name, never by name similarity. They may differ from figures the company publishes.

Company basics
Korea Exchange · DART
Business content
Compiled from disclosure filings
Approvals & clinical trials
Korean MFDS (data.go.kr) · US FDA openFDA — updated weekly
Key disclosures
KRX KIND via OpenDART exchange filings — updated daily
Global clinical trials
ClinicalTrials.gov (US NIH) — sponsor-matched, updated weekly
Financials
DART corporate disclosure filings — annual
Publications
PubMed (US National Library of Medicine) — affiliation-matched, updated daily
Patents
KIPRIS (Korea Institute of Patent Information) — applicant-matched, updated monthly
AI reads
Our server logs, IP-verified every 6 hours
AI visibility
Measured 2026-10-01

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