Pharos iBio Co., Ltd.
Pharos iBio is a KOSDAQ-listed biotech developing drugs for rare, intractable diseases including cancer using its AI platform Chemiverse.
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Business overview
Source: DART corporate disclosureFounded in 2016 and listed on KOSDAQ in 2023, Pharos iBio is a research and development company focused on innovative therapies for rare and intractable diseases, particularly oncology. Using its AI-driven drug discovery platform Chemiverse, the company has built a pipeline including the acute myeloid leukemia candidate Lasmotinib (PHI-101), the recurrent ovarian cancer candidate PHI-101-OC, the FAK inhibitor PHI-301, and the NRAS AML candidate PHI-501. Pharos iBio manufactures no marketed drug itself, instead pursuing conditional approval after Phase 2 trials and out-licensing of candidates as its business model, and Lasmotinib (PHI-101) received orphan drug designations from the US FDA in 2019, Korea's MFDS in 2024 (the country's 53rd such designation), and the EU EMA in 2025.
Products & technology
- Lasmotinib (PHI-101)Acute myeloid leukemia (AML) treatment targeting FLT3 mutations
- PHI-101-OCRecurrent ovarian cancer treatment
- PHI-301FAK inhibitor-based composition for enhancing radiosensitivity
- PHI-501NRAS AML treatment, indication expanded to refractory solid tumors
Regulatory approvals
1 Orphan Drug designations · 2024
- OrphanPHI-101(경구제)2024-09-03Orphan Drug designation · in development20240150685
Clinical trials
data.go.kr3 MFDS clinical trial authorisations · 2020–2025 (Phase 1 3)
- Phase 1PHI-5012025-06-25
6 trial sites
- Phase 1PHI-1012020-11-06
9 trial sites
- Phase 1PHI-1012020-02-07
21 trial sites
R&D and key agreements
Source: DART corporate disclosurePHI-101(라스모티닙) · 급성골수성백혈병(AML) · 임상 1상 완료, CSR 수령(2025.6.30) · Received orphan drug designations from the US FDA (2019), Korea MFDS (2024, the country's 53rd such designation), and EU EMA (2025); an investigator-initiated trial (IIT) is ongoing for minimal residual disease (MRD)
PHI-101-OC · 재발성 난소암 · 임상 1상 진행 중 · Preclinical evaluation showed efficacy in cell and in vivo models regardless of BRCA mutation status; Phase 1 trial initiated November 2020
PHI-301 · 방사선 민감성 증진(FAK 저해제) · 선도물질 단계 · Under development via an exclusive license from the Korea Institute of Radiological & Medical Sciences
PHI-501 · NRAS AML / 난치성 고형암 · 임상 1상 진행 중 · Patent acquired from the Korea Institute of Science and Technology; indication expanded to refractory solid tumors using the Chemiverse AI platform
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Sources and updates
- Company basics
- Korea Exchange · DART
- Business content
- Compiled from disclosure filings
- AI visibility
- Measured 2026-08-13
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