Developer docs
API playgroundTry for free, no card

Search company profiles

Medipost

Full company profile

uuid00026qn

Namestring
Medipost
Legal namestring
MEDIPOST, Inc.
Websiteurl
medi-post.com
Company typeenum
Private
Founded yearint
2000
Descriptiontext

Medipost (KOSDAQ: 078160), founded in 2000 and headquartered in Seongnam, South Korea, is a clinical-stage and commercial biotechnology company specializing in stem cell therapeutics and cord blood banking, with US operations conducted through its wholly owned subsidiary MEDIPOST, Inc. in Cambridge, Massachusetts. The company's flagship product is CARTISTEM, an allogeneic umbilical cord blood-derived mesenchymal stem cell (hUCB-MSC) therapy for knee osteoarthritis that became the world's first regulatory-approved allogeneic stem cell therapy product when launched in South Korea in 2012 and has since been administered to over 36,000 patients domestically. The underlying platform leverages immune-privileged MSCs that are isolated, expanded under GMP standards, cryopreserved at drug substance stage, and validated through potency assays confirming cell viability for up to 72 hours at 2–10°C, enabling off-the-shelf administration without patient matching.

Medipost operates a vertically integrated regenerative medicine ecosystem spanning cord blood collection, processing, cryopreservation, and therapeutic development, which underpins both its cord blood banking services and the CARTISTEM therapeutic pipeline. The company is currently advancing CARTISTEM through Phase 3 trials in the United States and Japan, with patient enrollment in the US expected in the first half of 2026 following an FDA-agreed confirmatory evidence BLA pathway that leverages existing Korean and Japanese Phase 3 data plus real-world evidence from approximately 550 patients; US market approval is targeted by 2031. Manufacturing capacity for global clinical and commercial supply is being built through partnerships with OmniaBio (Toronto) and Charles River Laboratories (Asia-Pacific and North America), while a partnership with RMDC Co., Ltd. is developing Physical AI autonomous cell culture robots to standardize quality and minimize contamination risk.

The business model combines direct hospital and clinic sales in South Korea (one-time treatment pricing managed through the healthcare system), licensing and milestone-based revenue from the exclusive Japanese commercialization partnership with Teikoku Seiyaku ($8M upfront and $10M short-term regulatory milestone already secured plus undisclosed sales milestones), and planned US commercialization contingent on FDA approval. Strategic investors include Skylake Equity Partners, Crescendo Equity Partners, Woori Private Equity Asset Management, and NH Private Equity, which together provided $140 million in growth capital via convertible bonds in January 2026. The leadership team is anchored by founder Dr. Yang Yoon-Sun (Forbes Asia Women Powerlist honoree) and CEO Ed Ahn of MEDIPOST Inc.

Short descriptiontext

Medipost is a South Korean clinical-stage biotech that develops and commercializes allogeneic umbilical cord blood-derived mesenchymal stem cell therapies, anchored by CARTISTEM — the world's first approved allogeneic stem cell therapy — for knee osteoarthritis patients, with over 36,000 treated in Korea since 2012 and Phase 3 trials underway in the US and Japan.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
251–500
akta.pro rankint
HeadquartersSeongnam, South Korea
HQ citystring
Seongnam
HQ countrystring
South Korea
HQ regionstring
Asia
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
stem cell therapy, regenerative medicine, cell therapy products, cord blood banking, mesenchymal stem cells
Industry4 codes
1Cell Therapy Developers (Allogeneic/Off-the-shelf)
CodeHLAAABABPrimaryYes
2Stem Cell Therapies (MSC/iPSC/HSC-derived)
CodeHLAAABAEPrimaryNo
3Cartilage, Bone & Musculoskeletal Regeneration
CodeHLAAAGAHPrimaryNo
4Cell Therapy Manufacturing Services (GMP, autologous/allogeneic)
CodeHLAAAKACPrimaryNo
NAICS code2 codes
  • Biological Product (except Diagnostic) Manufacturing325414
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
SIC code1 code
  • Biological Products, (No Disgnostic Substances)2836
Product category
Cell Therapy / Regenerative Medicine
Social media profiles1 record
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model3 records
1CARTISTEM Product Sales (Korea)
TypeOne Time License
Description

Commercial sales of CARTISTEM in South Korea where the product has been approved since 2012, treating over 36,000 patients. Revenue generated from direct hospital/clinic sales to healthcare providers treating knee osteoarthritis patients.

bdapartners.com
2Japan Commercialization Licensing
TypeLicensing Royalties
Description

Multi-year partnership with Teikoku Seiyaku for exclusive commercialization of CARTISTEM in Japan. MEDIPOST receives upfront payment ($8M), regulatory milestones ($10M short-term), and additional undisclosed sales-based milestones. MEDIPOST supplies drug substance and retains manufacturing rights.

prnewswire.com
3US Market Entry (Future)
TypeOne Time License
Description

Planned US commercialization following FDA approval of CARTISTEM for knee osteoarthritis. Phase 3 trials ongoing with patient enrollment expected in first half of 2026 and market approval targeted by 2031.

businesswire.com
Marketing channels5 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels3 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Technology or R&D, Operations, Personnel, Supply Chain, Marketing or Sales
Pricing details1 tier
1CARTISTEM is prescribed through healthcare providers and hospitals
ModelOtherBilling cadencePay-as-you-go
Notes

Pricing not publicly disclosed; treatment costs are managed through healthcare systems and insurance coverage in applicable markets.

bdapartners.com
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

Medipost develops, manufactures, and commercializes allogeneic umbilical cord blood-derived mesenchymal stem cell (hUCB-MSC) therapies. Its flagship product CARTISTEM is the world's first regulatory-approved allogeneic stem cell therapy, indicated for knee osteoarthritis and commercialized in South Korea since 2012 with over 36,000 patients treated. The company also operates cord blood banking and a vertically integrated pipeline for inflammation-driven degenerative diseases.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 3 values shown
  • Over 36,000 patients treated with CARTISTEM in South Korea since 2012
+2 more records
Product overview1 text field

MEDIPOST operates as a vertically integrated stem cell therapeutics company offering two interconnected product lines: (1) CARTISTEM, the company's flagship allogeneic umbilical cord blood-derived MSC therapy for knee osteoarthritis, which received regulatory approval in South Korea in 2012 and has treated over 36,000 patients, with ongoing Phase 3 trials in the US and Japan; and (2) cord blood banking services that form the foundational raw material source for the therapeutic pipeline. The company functions as a total solution provider for regenerative medicine, encompassing collection, processing, cryopreservation, and therapeutic development within a unified ecosystem.

Product and service3 records
1CARTISTEM
CategoryCell Therapy / Regenerative Medicine
Description

Allogeneic umbilical cord blood-derived mesenchymal stem cell (hUCB-MSC) therapy for adult patients with symptomatic knee osteoarthritis. Administered off-the-shelf without patient matching, leveraging immune-privileged cells to reduce inflammation and promote cartilage repair. Sold to hospitals and clinics via direct sales in South Korea and through Teikoku Seiyaku in Japan.

2Cord Blood Banking
CategoryCord Blood Banking
Description

Collection, processing, and cryopreservation of umbilical cord blood as the raw material feedstock for Medipost's allogeneic stem cell therapeutic pipeline and as a banking service for families.

3Degenerative Disease Stem Cell Pipeline
CategoryCell Therapy Pipeline
Description

Investigational stem cell therapy pipeline applying the hUCB-MSC platform to inflammation-driven degenerative diseases beyond osteoarthritis, including neurological, cardiovascular, and pulmonary indications.

Scale indicator4 records

Each record includes

Type, Value, Description, Source

Partnership4 partners
Strategic tierCoreTypeTechnology or IntegrationAnnounced on2026-05-13
Description

Non-exclusive Memorandum of Understanding for collaboration on GMP-compliant testing and commercial efforts for cell therapy development. Partnership leverages Charles River's biologics and cell therapy GMP testing expertise to support MEDIPOST's global pipeline, beginning with Asia-Pacific and North America markets.

Strategic tierMinorTypeStrategic or Co-development PartnerAnnounced on2026-03-01
Description

Business partnership to jointly develop 'Physical AI' autonomous cell culture robots. RMDC's automated stem cell culture device serves as foundation for collaborative innovation project aimed at accelerating sales cooperation in overseas markets. The device features closed-system automation to minimize contamination risk and standardize quality through algorithm-based management.

Strategic tierCoreTypeChannel Partner/ Reseller/ DistributorAnnounced on2025-12-01
Description

Multi-year partnership for exclusive commercialization of CARTISTEM in Japan. MEDIPOST receives $8M upfront payment, $10M short-term regulatory milestone, and additional sales-based milestones. MEDIPOST supplies drug substance and retains manufacturing rights. Teikoku Seiyaku manages exclusive market rights and sales through its orthopedic hospital and clinic network with dedicated medical representatives.

Strategic tierCoreTypeTechnology or Integration
Description

Partnership with cell and gene therapy CDMO based in Toronto, Canada. Expands manufacturing capacity and strengthens delivery to North American clinical trial sites. Ensures manufacturing continuity and cost visibility ahead of US Phase III trial.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Mesoblast develops allogeneic mesenchymal stem cell therapies (remestemcel-L) for inflammatory and degenerative diseases, including a Phase 3 program for chronic low back pain and acute graft-versus-host disease. Direct competitor in the allogeneic MSC space with comparable regulatory pathway and manufacturing model.

TypeDirect peer
Description

Vericel markets MACI (autologous cultured chondrocytes on porcine collagen membrane) for cartilage repair of the knee — a direct disease-modifying competitor to CARTISTEM in knee osteoarthritis/cartilage defects, also targeting orthopedic surgeons in the US.

TypeDirect peer
Description

BrainStorm develops NurOwn, an autologous MSC-based cell therapy for neurodegenerative diseases (ALS, MS). Comparable stem cell platform with similar regulatory pathway and target indications in the broader MSC regenerative medicine space.

TypeDirect peer
Description

Capricor develops CAP-1002, an allogeneic cardiosphere-derived cell therapy for Duchenne muscular dystrophy and other inflammatory diseases. Comparable allogeneic cell therapy developer with similar manufacturing complexity and regulatory pathway.

TypeEmerging player
Description

Stempeutics commercializes Stempeucel, a pooled allogeneic bone marrow-derived MSC therapy approved in India for critical limb ischemia, with development in osteoarthritis. Comparable MSC platform addressing similar regenerative indications in emerging markets.

TypeDirect peer
Description

Athersys developed MultiStem, an allogeneic bone marrow-derived multipotent adult progenitor cell therapy for stroke, ARDS, and trauma, with partner Helios (now Athersys KK) in Japan. Direct competitor in allogeneic off-the-shelf cell therapy with parallel Japan commercialization pathway.

TypeEmerging player
Description

Holostem commercializes Holoclar, the first EMA-approved stem cell therapy (autologous limbal stem cells for corneal regeneration). Comparable stem cell therapeutic developer with EU regulatory approval and similar first-in-class positioning.

TypeBroad incumbent
Description

Smith+Nephew acquired Osiris Therapeutics' cartilage and wound care portfolio (including Cartiform and Grafix) and competes in sports medicine and regenerative medicine broadly. Incumbent competitor in orthopedic regenerative medicine with established hospital sales channels.

TypeBroad incumbent
Description

Takeda acquired TiGenix and its allogeneic adipose-derived stem cell therapy Cx601 (darvadstrocel) for complex perianal fistulas in Crohn's disease. Incumbent competitor in allogeneic stem cell therapy with global commercialization capability.

TypeDirect peer
Description

Corestemchemon is a South Korean clinical-stage biotech developing autologous bone marrow-derived MSCs (NeuroNata-R) for ALS, with KOSDAQ listing. Comparable Korean MSC developer in the regenerative medicine space targeting the same investor base and regulatory pathway.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat5 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers2 records

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment2 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile3 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature3 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles3 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

Subsidiaries3 records

Each record includes

Name, Acquired on, Relationship type, Type, Business focus

No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds3 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors5 records

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Medipost

Cell Therapy / Regenerative Medicinemedi-post.com

Medipost is a South Korean clinical-stage biotech that develops and commercializes allogeneic umbilical cord blood-derived mesenchymal stem cell therapies, anchored by CARTISTEM — the world's first approved allogeneic stem cell therapy — for knee osteoarthritis patients, with over 36,000 treated in Korea since 2012 and Phase 3 trials underway in the US and Japan.

What Medipost does

Medipost (KOSDAQ: 078160), founded in 2000 and headquartered in Seongnam, South Korea, is a clinical-stage and commercial biotechnology company specializing in stem cell therapeutics and cord blood banking, with US operations conducted through its wholly owned subsidiary MEDIPOST, Inc. in Cambridge, Massachusetts. The company's flagship product is CARTISTEM, an allogeneic umbilical cord blood-derived mesenchymal stem cell (hUCB-MSC) therapy for knee osteoarthritis that became the world's first regulatory-approved allogeneic stem cell therapy product when launched in South Korea in 2012 and has since been administered to over 36,000 patients domestically. The underlying platform leverages immune-privileged MSCs that are isolated, expanded under GMP standards, cryopreserved at drug substance stage, and validated through potency assays confirming cell viability for up to 72 hours at 2–10°C, enabling off-the-shelf administration without patient matching.

Medipost operates a vertically integrated regenerative medicine ecosystem spanning cord blood collection, processing, cryopreservation, and therapeutic development, which underpins both its cord blood banking services and the CARTISTEM therapeutic pipeline. The company is currently advancing CARTISTEM through Phase 3 trials in the United States and Japan, with patient enrollment in the US expected in the first half of 2026 following an FDA-agreed confirmatory evidence BLA pathway that leverages existing Korean and Japanese Phase 3 data plus real-world evidence from approximately 550 patients; US market approval is targeted by 2031. Manufacturing capacity for global clinical and commercial supply is being built through partnerships with OmniaBio (Toronto) and Charles River Laboratories (Asia-Pacific and North America), while a partnership with RMDC Co., Ltd. is developing Physical AI autonomous cell culture robots to standardize quality and minimize contamination risk.

The business model combines direct hospital and clinic sales in South Korea (one-time treatment pricing managed through the healthcare system), licensing and milestone-based revenue from the exclusive Japanese commercialization partnership with Teikoku Seiyaku ($8M upfront and $10M short-term regulatory milestone already secured plus undisclosed sales milestones), and planned US commercialization contingent on FDA approval. Strategic investors include Skylake Equity Partners, Crescendo Equity Partners, Woori Private Equity Asset Management, and NH Private Equity, which together provided $140 million in growth capital via convertible bonds in January 2026. The leadership team is anchored by founder Dr. Yang Yoon-Sun (Forbes Asia Women Powerlist honoree) and CEO Ed Ahn of MEDIPOST Inc.

Medipost firmographics

Firmographics
Name
Medipost
Legal name
MEDIPOST, Inc.
Website
https://medi-post.com
Company type
Private
Founded year
2000
Operating status
Operating
Headcount range
251–500 employees
Short description
Medipost is a South Korean clinical-stage biotech that develops and commercializes allogeneic umbilical cord blood-derived mesenchymal stem cell therapies, anchored by CARTISTEM — the world's first approved allogeneic stem cell therapy — for knee osteoarthritis patients, with over 36,000 treated in Korea since 2012 and Phase 3 trials underway in the US and Japan.
Ownership category
akta.pro rank

Medipost industry classification

Industry
Product category
Cell Therapy / Regenerative Medicine
NAICS
Biological Product (except Diagnostic) Manufacturing (325414), Research and Development in Biotechnology (except Nanobiotechnology) (541714)
SIC
Biological Products, (No Disgnostic Substances) (2836)
akta.pro primary industry
Cell Therapy Developers (Allogeneic/Off-the-shelf) (HLAAABAB)
akta.pro secondary industries
Stem Cell Therapies (MSC/iPSC/HSC-derived) (HLAAABAE), Cartilage, Bone & Musculoskeletal Regeneration (HLAAAGAH), Cell Therapy Manufacturing Services (GMP, autologous/allogeneic) (HLAAAKAC)

Keywords

  • Stem cell therapy
  • Regenerative medicine
  • Cell therapy products
  • Cord blood banking
  • Mesenchymal stem cells

Where Medipost is headquartered

Location

Headquarters

HQ city
Seongnam
HQ country
South Korea
HQ region
Asia

Offices2 records

Markets served

Medipost business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Technology or R&D, Operations, Personnel, Supply Chain, Marketing or Sales

Revenue model

  1. CARTISTEM Product Sales (Korea): Commercial sales of CARTISTEM in South Korea where the product has been approved since 2012, treating over 36,000 patients. Revenue generated from direct hospital/clinic sales to healthcare providers treating knee osteoarthritis patients.
  2. Japan Commercialization Licensing: Multi-year partnership with Teikoku Seiyaku for exclusive commercialization of CARTISTEM in Japan. MEDIPOST receives upfront payment ($8M), regulatory milestones ($10M short-term), and additional undisclosed sales-based milestones. MEDIPOST supplies drug substance and retains manufacturing rights.
  3. US Market Entry (Future): Planned US commercialization following FDA approval of CARTISTEM for knee osteoarthritis. Phase 3 trials ongoing with patient enrollment expected in first half of 2026 and market approval targeted by 2031.

Pricing tiers

ModelBillingPrice
OtherPay-as-you-goCARTISTEM is prescribed through healthcare providers and hospitals

Go-to-market motion2 records

Distribution channels3 records

Marketing channels5 records

Medipost product offering

Product offering

Core offering

Medipost develops, manufactures, and commercializes allogeneic umbilical cord blood-derived mesenchymal stem cell (hUCB-MSC) therapies. Its flagship product CARTISTEM is the world's first regulatory-approved allogeneic stem cell therapy, indicated for knee osteoarthritis and commercialized in South Korea since 2012 with over 36,000 patients treated. The company also operates cord blood banking and a vertically integrated pipeline for inflammation-driven degenerative diseases.

Product overview

MEDIPOST operates as a vertically integrated stem cell therapeutics company offering two interconnected product lines: (1) CARTISTEM, the company's flagship allogeneic umbilical cord blood-derived MSC therapy for knee osteoarthritis, which received regulatory approval in South Korea in 2012 and has treated over 36,000 patients, with ongoing Phase 3 trials in the US and Japan; and (2) cord blood banking services that form the foundational raw material source for the therapeutic pipeline. The company functions as a total solution provider for regenerative medicine, encompassing collection, processing, cryopreservation, and therapeutic development within a unified ecosystem.

Differentiator

Problem solved

Functional benefit

Products and services

  • CARTISTEM Allogeneic umbilical cord blood-derived mesenchymal stem cell (hUCB-MSC) therapy for adult patients with symptomatic knee osteoarthritis. Administered off-the-shelf without patient matching, leveraging immune-privileged cells to reduce inflammation and promote cartilage repair. Sold to hospitals and clinics via direct sales in South Korea and through Teikoku Seiyaku in Japan.
  • Cord Blood Banking Collection, processing, and cryopreservation of umbilical cord blood as the raw material feedstock for Medipost's allogeneic stem cell therapeutic pipeline and as a banking service for families.
  • Degenerative Disease Stem Cell Pipeline Investigational stem cell therapy pipeline applying the hUCB-MSC platform to inflammation-driven degenerative diseases beyond osteoarthritis, including neurological, cardiovascular, and pulmonary indications.

Quantifiable outcome

  • Over 36,000 patients treated with CARTISTEM in South Korea since 2012
  • +2 more outcomes

Companies that use Medipost

Customer profile

Named customers2 records

Segments2 records

Ideal customer profiles3 records

Medipost technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature3 records

Medipost partnerships and signals

Strategic signal

Partnerships

Four partnerships are on record, tiered core and minor.

  • Charles River LaboratoriescoreTechnology or Integration · 13 May 2026Non-exclusive Memorandum of Understanding for collaboration on GMP-compliant testing and commercial efforts for cell therapy development. Partnership leverages Charles River's biologics and cell therapy GMP testing expertise to support MEDIPOST's global pipeline, beginning with Asia-Pacific and North America markets.
  • RMDC Co., Ltd.minorStrategic or Co-development Partner · 1 March 2026Business partnership to jointly develop 'Physical AI' autonomous cell culture robots. RMDC's automated stem cell culture device serves as foundation for collaborative innovation project aimed at accelerating sales cooperation in overseas markets. The device features closed-system automation to minimize contamination risk and standardize quality through algorithm-based management.
  • Teikoku SeiyakucoreChannel Partner/ Reseller/ Distributor · 1 December 2025Multi-year partnership for exclusive commercialization of CARTISTEM in Japan. MEDIPOST receives $8M upfront payment, $10M short-term regulatory milestone, and additional sales-based milestones. MEDIPOST supplies drug substance and retains manufacturing rights. Teikoku Seiyaku manages exclusive market rights and sales through its orthopedic hospital and clinic network with dedicated medical representatives.
  • OmniaBiocoreTechnology or IntegrationPartnership with cell and gene therapy CDMO based in Toronto, Canada. Expands manufacturing capacity and strengthens delivery to North American clinical trial sites. Ensures manufacturing continuity and cost visibility ahead of US Phase III trial.

Scale indicators4 records

Recent moves6 records

Expansion highlights6 records

Medipost competitors and assessment

Company assessment

Direct peers

  • Mesoblast: Mesoblast develops allogeneic mesenchymal stem cell therapies (remestemcel-L) for inflammatory and degenerative diseases, including a Phase 3 program for chronic low back pain and acute graft-versus-host disease. Direct competitor in the allogeneic MSC space with comparable regulatory pathway and manufacturing model.
  • Vericel: Vericel markets MACI (autologous cultured chondrocytes on porcine collagen membrane) for cartilage repair of the knee — a direct disease-modifying competitor to CARTISTEM in knee osteoarthritis/cartilage defects, also targeting orthopedic surgeons in the US.
  • BrainStorm Cell Therapeutics: BrainStorm develops NurOwn, an autologous MSC-based cell therapy for neurodegenerative diseases (ALS, MS). Comparable stem cell platform with similar regulatory pathway and target indications in the broader MSC regenerative medicine space.
  • Capricor Therapeutics: Capricor develops CAP-1002, an allogeneic cardiosphere-derived cell therapy for Duchenne muscular dystrophy and other inflammatory diseases. Comparable allogeneic cell therapy developer with similar manufacturing complexity and regulatory pathway.
  • Athersys: Athersys developed MultiStem, an allogeneic bone marrow-derived multipotent adult progenitor cell therapy for stroke, ARDS, and trauma, with partner Helios (now Athersys KK) in Japan. Direct competitor in allogeneic off-the-shelf cell therapy with parallel Japan commercialization pathway.
  • Corestemchemon: Corestemchemon is a South Korean clinical-stage biotech developing autologous bone marrow-derived MSCs (NeuroNata-R) for ALS, with KOSDAQ listing. Comparable Korean MSC developer in the regenerative medicine space targeting the same investor base and regulatory pathway.

Emerging players

  • Stempeutics Research: Stempeutics commercializes Stempeucel, a pooled allogeneic bone marrow-derived MSC therapy approved in India for critical limb ischemia, with development in osteoarthritis. Comparable MSC platform addressing similar regenerative indications in emerging markets.
  • Holostem Terapie Avanzate: Holostem commercializes Holoclar, the first EMA-approved stem cell therapy (autologous limbal stem cells for corneal regeneration). Comparable stem cell therapeutic developer with EU regulatory approval and similar first-in-class positioning.

Broad incumbents

  • Smith+Nephew (Regenerative Medicine portfolio): Smith+Nephew acquired Osiris Therapeutics' cartilage and wound care portfolio (including Cartiform and Grafix) and competes in sports medicine and regenerative medicine broadly. Incumbent competitor in orthopedic regenerative medicine with established hospital sales channels.
  • Takeda Pharmaceutical (TiGenix heritage): Takeda acquired TiGenix and its allogeneic adipose-derived stem cell therapy Cx601 (darvadstrocel) for complex perianal fistulas in Crohn's disease. Incumbent competitor in allogeneic stem cell therapy with global commercialization capability.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat5 records

Key risks6 records

Key highlights7 records

Customer concentration

Medipost social profiles

Digital presence

Medipost financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Medipost leadership team

Management profile

Number of profiles

Profiles3 records

Medipost subsidiaries and ownership

Company hierarchy

Subsidiaries3 records

Medipost funding detail

Funding detail

Funding overview

Funding rounds3 records

Investors5 records

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Medipost M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Medipost

What does Medipost do?

Medipost develops, manufactures, and commercializes allogeneic umbilical cord blood-derived mesenchymal stem cell (hUCB-MSC) therapies. Its flagship product CARTISTEM is the world's first regulatory-approved allogeneic stem cell therapy, indicated for knee osteoarthritis and commercialized in South Korea since 2012 with over 36,000 patients treated. The company also operates cord blood banking and a vertically integrated pipeline for inflammation-driven degenerative diseases.

Is Medipost a public or private company?

Medipost is a private company. It is classified as public and is currently operating.

When was Medipost founded?

Medipost was founded in 2000. It employs 251 to 500 people.

Where is Medipost based?

Medipost is headquartered in Seongnam, South Korea, in the Asia region.

How does Medipost make money?

Three revenue lines are on record. CARTISTEM Product Sales (Korea) is the primary driver. The others are japan Commercialization Licensing and US Market Entry (Future).

Who are Medipost's main competitors?

Direct peers on record are Mesoblast, Vericel, BrainStorm Cell Therapeutics, Capricor Therapeutics, Athersys and Corestemchemon. Emerging players are Stempeutics Research and Holostem Terapie Avanzate. Broad incumbents are Smith+Nephew (Regenerative Medicine portfolio) and Takeda Pharmaceutical (TiGenix heritage).

Does Medipost have an API?

No public API is recorded for Medipost.

What industry is Medipost in?

Medipost's product category is Cell Therapy / Regenerative Medicine. Its primary akta.pro industry code is HLAAABAB, Cell Therapy Developers (Allogeneic/Off-the-shelf), with a secondary code of HLAAABAE, Stem Cell Therapies (MSC/iPSC/HSC-derived). Its NAICS code is 325414 and its SIC code is 2836.

Unlock the full company data

50 free credits on sign-up, no credit card required.

Contact sales
Live signals
PR NewswireStem Cells Market to Reach US$ 32.57 Bn by 2031, Growing at 11.5% CAGR: Wissen ResearchThe global stem cells market is projected to grow from USD 18.9 billion in 2026 to USD 32.57 billion by 2031, a CAGR of 11.5%, driven by regenerative medicine and cell-based therapies. Adult stem cells led product revenue in 2025, and North America held the largest regional share. Asia-Pacific is the fastest-growing region.NateMedipost, first half consolidated operating loss of 41.2 billion won... Global clinical costs increase: Nate NewsMedipost reported a consolidated operating loss of 41.2 billion won for the first half of the year, driven by increased research and development costs associated with global clinical trials in the United States and Japan. Despite the operational deficit, the company achieved a net profit surplus due to significant derivative evaluation profits that boosted financial income.Business Wire BlogMEDIPOST Inc. Treats First U.S. Participant in Phase III Trial of Umbilical Cord Stem Cell Therapy for Symptomatic Cartilage Defects Due to Knee OsteoarthritisMEDIPOST Inc. treated the first U.S. participant in its Phase III trial of an umbilical cord stem cell therapy for knee osteoarthritis. The FDA agreed the single pivotal study, with prior Phase 3 data from South Korea and Japan, can support a U.S. BLA filing. The trial is enrolling adults 18-75 with knee cartilage lesions.Investing.comMedipost secures FDA agreement for single phase 3 cartilage study By Investing.comMedipost announced that the U.S. Food and Drug Administration agreed to allow the company to conduct a single pivotal Phase 3 study for its knee osteoarthritis treatment Cartistem in the United States, using existing clinical data from South Korea and Japan plus real-world evidence from approximately 550 patients. The streamlined regulatory pathway is expected to reduce the company's U.S. clinical development timeline and costs, potentially enabling an earlier Biologics License Application filing than previously anticipated. Cartistem, approved in South Korea in 2012, has been used by more than 36,000 patients, and Medipost holds more cash than debt on its balance sheet.AijournMEDIPOST Secures FDA Agreement on Single Pivotal Phase 3 Study with Confirmatory Evidence BLA Filing Strategy for CARTISTEM® in the U.S.MEDIPOST announced it has secured the FDA's agreement to conduct a single pivotal Phase 3 study for its knee osteoarthritis treatment CARTISTEM® in the U.S., leveraging existing Phase 3 data from South Korea and Japan along with Real-World Evidence from approximately 550 South Korean patients. The agreement is expected to significantly reduce the company's overall U.S. clinical development timeline and costs, enabling an earlier BLA filing and expedited market entry. The milestone accelerates MEDIPOST's U.S. commercialization strategy and supports global partnership discussions.PR NewswireMEDIPOST Secures FDA Agreement on Single Pivotal Phase 3 Study with Confirmatory Evidence BLA Filing Strategy for CARTISTEM® in the U.S.MEDIPOST announced FDA agreement to conduct a single pivotal Phase 3 study for CARTISTEM® in the U.S., leveraging existing Phase 3 data from South Korea and Japan along with real-world evidence from approximately 550 South Korean patients. The company expects this agreement to significantly reduce its U.S. clinical development timeline and costs while enabling an earlier BLA filing and expedited market entry in the U.S. and Canada. MEDIPOST, which commercialized the world's first regulatory-approved allogeneic stem cell therapy product in 2012, has treated over 36,000 patients with CARTISTEM® in South Korea to date.BioSpaceMEDIPOST Secures FDA Agreement on Single Pivotal Phase 3 Study with Confirmatory Evidence BLA Filing Strategy for CARTISTEM® in the U.S.MEDIPOST secured FDA agreement for a single pivotal Phase 3 study of CARTISTEM in the U.S., using data from South Korea and Japan. The company expects reduced development costs and an earlier BLA filing, potentially accelerating U.S. commercial entry. It will also include RWE from about 550 patients treated three years ago as confirmatory evidence.PR Newswire APACMEDIPOST's CARTISTEM® Meets All Primary and Secondary Endpoints in Japan Phase 3 Trial and Demonstrates Statistically Significant Efficacy Gains Versus Active ControlMEDIPOST's CARTISTEM knee osteoarthritis treatment met all primary and secondary efficacy endpoints in a Japan Phase 3 trial, showing statistically significant improvements over hyaluronic acid control. The company plans to file a biologics license application in Japan later this year, with regulatory approval targeted by end of 2027.Stock TitanCharles River, MEDIPOST sign GMP testing MOUCharles River Laboratories and MEDIPOST Co., Ltd. have signed a non-exclusive Memorandum of Understanding to collaborate on GMP-compliant testing and commercial efforts for cell therapy development. The partnership will leverage Charles River's biologics and cell therapy GMP testing expertise to support MEDIPOST's global pipeline, beginning with Asia-Pacific and North America markets. MEDIPOST, which has over 14 years of commercial-stage experience treating more than 36,000 patients in South Korea with its CARTISTEM product, is now expanding into global markets with regulatory Phase 3 studies ongoing in Japan and the United States.Asiae'Drugs to Prevent Aging' Enter Their First Target Year... First Patient Dosed in the US [New Path for Bio, Anti-Aging] ①2026 has become the first year in which aging itself became a direct target for new drug development, with U.S.-based Life Biosciences receiving FDA IND approval for its epigenetic reprogramming therapy ER-100 and beginning to dose the first patients in March — the first time in history a drug designed to reverse aging has been administered to humans. Global anti-aging biotech funding reached $3.74 billion in Q1 2026, up 56% year-over-year, with cumulative disclosed big pharma investment surpassing $11 billion, including a landmark $2.75 billion partnership between Eli Lilly and Insilico Medicine for an AI-discovered preclinical oral drug candidate. Korean pharmaceutical companies Hanmi Pharm and Medipost, alongside the Ministry of Health and Welfare, have launched anti-aging drug development initiatives, positioning Korea to enter this emerging global market as industry experts forecast that clinical data over the next one to two years will determine big pharma's growth trajectory post-GLP-1.