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Pharma & CDMOKOSDAQ 220100Orphan Drug11 approvals10 trials

FutureChem Co., Ltd.

Official website

Develops the PSMA-targeted prostate cancer diagnostic FC303 and therapeutic FC705 radiopharmaceuticals.

As of 2026-10-11, FutureChem Co., Ltd. has 3 Korean MFDS device approvals, 7 Korean MFDS drug approvals, 25 PubMed-indexed papers on record (counted by the MAA Company Index from its own matching of public databases).

Price

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Market cap

Business overview

Source: DART corporate disclosure

Founded in 2001 and listed on KOSDAQ in 2016, FutureChem is a company specializing in radiopharmaceutical drug development. In 2008 it commercialized the lung cancer diagnostic [18F]FLT and the Parkinson's disease diagnostic Fidewe ([18F]FP-CIT), and obtained marketing approval for Alzaview ([18F]Florapronol), Korea's 29th domestically developed new drug, for Alzheimer's diagnosis; it also holds a pipeline including the prostate cancer diagnostic FC303, brain tumor diagnostic [18F]FMT, cardio-cerebrovascular disease diagnostic [18F]FC505, Alzheimer's diagnostic [18F]FC211, and the PSMA-targeted prostate cancer therapeutics FC705 ([LU-177]FC705, [AC-225]FC705). FC303 has completed domestic trials and is under marketing approval review, completed US Phase 1, and is in Phase 3 trials in Europe and China through overseas partners, while FC705 received a Korean Phase 2 clinical study report in April 2025, is seeking Phase 3 approval, and is in FDA Phase 2a trials in the US.

Products & technology

  • Fidewe ([18F]FP-CIT)Parkinson's disease diagnosis
  • [18F]FLTLung cancer diagnosis
  • Alzaview ([18F]Florapronol)Alzheimer's disease diagnosis
  • FC303Prostate cancer diagnosis
  • FC705 ([LU-177]FC705, [AC-225]FC705)PSMA-targeted prostate cancer treatment

Regulatory approvals

data.go.kr

1 Orphan Drug designations · 2024 / 7 Korean MFDS drug approvals · 2005–2026 / 3 Korean MFDS device approvals · 2004–2005

  • Orphan[177Lu]루도타다이펩2024-07-12
    Orphan Drug designation · in development20240119325
  • MFDS drugProstavue(Florastamin(18F)) injection2026-04-30
    Drug · Prescription · Approval202601314
  • MFDS drug퓨쳐켐에프디지주사액(2-데옥시-2-플루오로-D-글루코스(18F)액)2020-08-21
    Drug · Prescription · Approval202005943
  • MFDS drug알자뷰주사액(플로라프로놀(18F)액)2018-02-02
    Drug · Prescription · Approval201800667
  • MFDS drug피디뷰주사(플루오로프로필씨아이티(18F))2014-11-18
    Drug · Prescription · Approval201405355
  • MFDS drugSubsidiary: 주식회사 퓨쳐켐헬스케어퓨쳐켐소듐플루오라이드F-18주사액Revoked2014-11-07
    Drug · Prescription · Approval201405200
  • MFDS drugSubsidiary: 주식회사 퓨쳐켐헬스케어퓨쳐켐암모니아N13주사액Revoked2014-10-28
    Drug · Prescription · Approval201404987
  • MFDS drugSubsidiary: 주식회사 퓨쳐켐헬스케어메타트레이스에프디지-10(2-데옥시-2-플루오로-D-글루코스(18F))액2005-06-01
    Drug · Prescription · Approval200503741
  • MFDSSubsidiary: 주식회사 퓨쳐켐헬스케어양전자방출전산화단층촬영장치Revoked2005-04-29
    Product approval · Class 3수허 05-378 호
  • MFDSSubsidiary: 주식회사 퓨쳐켐헬스케어양전자방출전산화단층촬영장치Revoked2004-06-14
    Product approval · Class 2수허 04-773 호
  • MFDSSubsidiary: 주식회사 퓨쳐켐헬스케어양전자방출전산화단층촬영장치Revoked2004-03-06
    Product approval · Class 2수허 04-308 호

Clinical trials

data.go.kr

10 MFDS clinical trial authorisations · 2013–2025 (Phase 3 5 · Phase 1 4 · Phase 2 1)

  • Phase 3[177Lu]루도타다이펩2025-09-04

    9 trial sites

  • Phase 3[F-18]Florastamin2024-10-18

    5 trial sites

  • Phase 3[F-18]Florastamin2022-12-26

    22 trial sites

  • Phase 2[177Lu]루도타다이펩2022-05-13

    1 trial site

  • Phase 3[F-18]Florastamin2020-11-30

    10 trial sites

  • Phase 1[177Lu]루도타다이펩2020-05-27

    1 trial site

  • Phase 1[F-18]Florastamin2019-09-23

    1 trial site

  • Phase 1[F-18]Florastamin2019-07-29

    1 trial site

  • Phase 3[18F]FC119S2014-09-05

    1 trial site

  • Phase 1[18F]FC119S2013-07-12

    1 trial site

Global clinical trials

ClinicalTrials.gov · sponsor-matched

R&D and key agreements

Source: DART corporate disclosure

FC303 · 전립선암 진단 · 국내 품목허가신청, 미국임상1상완료, 유럽·중국임상3상진행 · Approved for European (Austria) Phase 3 via overseas partner in May 2021; China Phase 3 also underway via overseas partner

FC705 · PSMA 전립선암 치료 · 국내임상3상승인신청, 미국FDA임상2a상진행 · Received Korean Phase 2 CSR in April 2025; US FDA Phase 1/2a approved May 2022, Phase 1 completed May 2023 (CSR received September), currently in Phase 2a

Key disclosures

KRX KIND via OpenDART
Show 11 more events

Publications

PubMed · affiliation-matched
Show 15 more publications

Patents

KIPRIS · applicant-matched
Show 41 more patents

AI reads

MAA server logs · IP-verified
77
Times AI engines pulled FutureChem Co., Ltd.'s records

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Times an AI needed something not yet in its index and fetched this page fresh while answering. Citations served from the index leave no trace here.

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Last 7 days
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Last 30 days
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Measured since Aug 27, 2026 · 5 AI engines · last read Oct 10, 2026

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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

This page is compiled from public sources without the company's involvement. If anything is inaccurate or incomplete, please let us know. Materials provided by the company are labelled as such.

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