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Human Life CORD

Full company profile

uuid0003erg

Namestring
Human Life CORD
Legal namestring
ヒューマンライフコード株式会社
Company typeenum
Private
Founded yearint
2017
Descriptiontext

Human Life CORD is a clinical-stage Japanese biotechnology company founded in April 2017 by Masamitsu Harata and headquartered in Nihonbashi, Tokyo. The company develops regenerative cell therapies based on umbilical cord-derived mesenchymal stromal cells (UC-MSCs), positioning itself as a first-in-class developer of UC-MSCs as a regenerative medicine product. Its core proprietary platform covers UC-MSC isolation, expansion, and quality control, originally licensed from Tokyo University of Medical Science (Prof. Tokiko Nagamura) and further developed through collaborations with Nagoya University and others. The lead asset, HLC-001, is being developed for non-infectious pulmonary complications after hematopoietic stem cell transplantation and entered Phase III clinical trials in February 2026 following orphan regenerative medicine product designation in August 2025; Phase II data showed a 71.4% 56-day survival rate versus an estimated 24.5% with existing treatment. The company is also pursuing additional indications including sarcopenia (with a granted Japan patent in January 2026), autoimmune diseases, and newborn chronic lung disease. A new sarcopenia biomarker study was completed in Brazil in September 2025.

The company operates a virtual pharma model rather than building a direct commercial sales force. Revenue is expected to be generated through one-time licensing arrangements and royalties on HLC-001 and follow-on UC-MSC products. In Japan, Mochida Pharmaceutical holds exclusive development and commercialization rights, Rohto Pharmaceutical serves as CDMO partner, and Alfresa handles distribution. International expansion is executed through partnership-based CDMO and clinical translation arrangements: New York Blood Center Enterprises is the exclusive US CDMO (MOU October 2025), Abu Dhabi Biobank and M42 support UAE/MENA localization (May 2026 partnership), HLC-MENA Ltd. is a joint venture with Hayat Capital in Abu Dhabi Global Market (September 2025), and UFRGS supports Brazil-based sarcopenia research. Total disclosed funding to date exceeds 2.7 billion yen (~$18M) across Series A/B/C rounds, with the Series C final close in November 2025 led by Rohto Pharmaceutical. Customer segments are vertically defined by indication: rare and intractable disease patients (primary, anchored by NIPCs), elderly patients with age-related conditions (sarcopenia), and academic medical institutions collaborating on autoimmune disease research.

The headcount of 11-50 employees and the activation of a formal CxO structure in October 2025 (CEO Harata, COO Matsushita, CFO Kidachi, CTrO Nakata, CPO Yamada) reflect an organization scaling from a clinical-stage R&D team toward a pre-commercial company with multi-region supply chain responsibilities. Marketing is conducted through corporate website, Japanese business media (Nikkei, Nikkei Biotech, Nikkei Business), industry events (BioJapan, JHVS, Regenerative Medicine JAPAN), international expos (Osaka-Kansai Expo, Global Startup EXPO), equity crowdfunding via FUNDINNO PLUS+, and active engagement with government-backed startup programs (J-Startup by METI, SusHi Tech Global Startups by Tokyo Metropolitan Government). The company has not yet launched a commercial product and is therefore pre-revenue, with revenue inflection contingent on Phase III completion and regulatory approval of HLC-001 in Japan.

Short descriptiontext

Human Life CORD is a clinical-stage Japanese biotechnology company developing umbilical cord-derived mesenchymal stromal cell (UC-MSC) therapies, with lead asset HLC-001 in Phase III trials for non-infectious pulmonary complications after stem cell transplantation and additional programs in sarcopenia and autoimmune diseases.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersTokyo, Japan
HQ citystring
Tokyo
HQ countrystring
Japan
HQ regionstring
Asia
Markets served

Serves global market

Offices4 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
regenerative medicine products, cell therapy biotechnology, mesenchymal stromal cells, umbilical cord-derived cells, clinical-stage biopharmaceuticals
Industry3 codes
1Stem Cell Therapies (MSC/iPSC/HSC-derived)
CodeHLAAABAEPrimaryYes
2Cell Processing & Ancillary Materials (media, cytokines, beads, vectors, disposables)
CodeHLAAABAHPrimaryNo
3Cell & Tissue Banking (biobanking, cord blood/tissue)
CodeHLAAAGAEPrimaryNo
NAICS code1 code
  • Biological Product (except Diagnostic) Manufacturing325414
SIC code1 code
  • Biological Products, (No Disgnostic Substances)2836
Product category
Regenerative Medicine
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model2 records
1Regenerative Medicine Product Sales
TypeOne Time License
Description

Revenue from sale of HLC-001 and future UC-MSC-based regenerative medicine products for treatment of non-infectious pulmonary complications and other indications. The company serves as the manufacturing and marketing authorization holder.

humanlifecord.com
2Partnership Milestones and Royalties
TypeLicensing Royalties
Description

Development and sales milestones plus royalties from partners such as Mochida Pharmaceutical for HLC-001 development and commercialization rights in Japan.

humanlifecord.com
Marketing channels6 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels4 records

Each record includes

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

Cost components4 values
Technology or R&D, Personnel, Supply Chain, Operations
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

Human Life CORD is a clinical-stage Japanese biotechnology company developing regenerative cell therapy products based on umbilical cord-derived mesenchymal stromal cells (UC-MSCs). Its core asset, HLC-001, is being advanced through Phase III clinical trials for non-infectious pulmonary complications after hematopoietic stem cell transplantation, with additional UC-MSC programs targeting sarcopenia, autoimmune diseases, and newborn chronic lung disease. The company operates a virtual-pharma model, holding manufacturing and marketing authorization while partnering for commercialization and distribution.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 3 values shown
  • 71.4% 56-day survival rate in Phase II trial for NIPCs (vs 24.5% historical)
+2 more records
Product overview1 text field

Human Life CORD is a clinical-stage Japanese biotechnology company developing regenerative cell therapies based on umbilical cord-derived mesenchymal stromal cells (UC-MSCs). The company's core product is HLC-001, a UC-MSC product targeting non-infectious pulmonary complications after hematopoietic stem cell transplantation, currently in Phase III clinical trials. The company is building a global ecosystem for sustainable cell therapy, with products targeting multiple indications including sarcopenia, autoimmune diseases, and newborn chronic lung disease. Their technology platform focuses on isolating, expanding, and quality-controlling UC-MSCs for therapeutic applications.

Product and service2 records
1HLC-001
CategoryCell Therapy / Regenerative Medicine
Description

Umbilical cord-derived mesenchymal stromal cell (UC-MSC) product in development for non-infectious pulmonary complications (NIPCs) following hematopoietic stem cell transplantation. Designated as a Rare Disease Regenerative Medicine Product by Japan's Ministry of Health, Labour and Welfare in August 2025, and currently in Phase III clinical trials with Mochida Pharmaceutical as co-development partner.

2UC-MSCs (Umbilical Cord-Derived Mesenchymal Stromal Cells) Pipeline Products
CategoryCell Therapy / Regenerative Medicine
Description

Cell therapy products derived from domestically sourced and stockpiled umbilical cords, targeting various rare and refractory diseases beyond NIPCs, including sarcopenia, autoimmune diseases, and newborn chronic lung disease. Underlying platform technology licensed from Tokyo University of Medical Science.

Scale indicator5 records

Each record includes

Type, Value, Description, Source

Partnership10 partners
1Abu Dhabi Biobank (Department of Health - Abu Dhabi and M42)
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-03-23
Description

Strategic partnership to localize UC-MSC manufacturing and clinical translation in UAE and MENA region. Abu Dhabi Biobank provides large-scale biobanking infrastructure, data, and translational research capabilities, while HLC contributes proprietary MSC technology and clinical development expertise.

humanlifecord.com
Strategic tierCoreTypeTechnology or IntegrationAnnounced on2025-10-28
Description

MOU for manufacturing collaboration in the USA. NYBCe serves as exclusive CDMO for manufacturing UC-MSC products, with facilities in Rye, New York. Partnership includes technology harmonization for standardized manufacturing between Japan and USA.

Strategic tierMinorTypeStrategic or Co-development PartnerAnnounced on2025-10-14
Description

MOU for cross-border clinical trials between Korea and Japan in the pharma R&D cooperation framework established by Korea's MSS with Japanese pharmaceutical companies.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-09-05
Description

Joint venture partnership to establish HLC-MENA Ltd. in Abu Dhabi Global Market (ADGM) for manufacturing, supplying, and commercializing UC-MSC products in Middle East and North Africa region.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-01-30
Description

Clinical research collaboration for sarcopenia in Brazil. Joint biomarker discovery study with 70 subjects completed in September 2025. Research conducted with Prof. Emilio Hideyuki Moriguchi.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2024-07-01
Description

Joint research course 'Lifespan Immunity Medical Implementation Course' for research on autoimmune diseases. Collaboration with Prof. Mori Masahiro for early diagnosis and optimal treatment of refractory autoimmune diseases.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2023-03-27
Description

Joint commercialization agreement for HLC-001 in Japan. HLC maintains manufacturing and marketing authorization holder status while Mochida handles development, sales, distribution, and post-marketing safety for specified diseases including NIPCs.

Strategic tierCoreTypeTechnology or IntegrationAnnounced on2022-02-14
Description

Manufacturing contract for HLC-001 products. Rohto serves as CDMO partner for cell processing and formulation using master cells provided by HLC, supporting Phase III clinical trial supply.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2020-11-17
Description

Exclusive global license for UC-MSC technology from Professor Tokiko Nagamura. Joint research for continued technology development and IMSUT-HLC Cell Processing Facility operation.

Strategic tierCoreTypeChannel Partner/ Reseller/ DistributorAnnounced on2020-04-02
Description

Capital and business partnership for stable supply chain construction. Alfresa handles distribution and logistics for cell products in Japan.

Recent move8 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight8 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Japanese specialty pharma with regenerative medicine capabilities (e.g., TEMCELL HS for acute GvHD) and a biologics manufacturing footprint. Comparable as a Japan-based, publicly listed cell therapy company operating in similar regulatory and reimbursement environments.

TypeDirect peer
Description

Clinical-stage developer of iPSC-derived MSC therapies for GvHD, osteoarthritis, and critical limb ischemia. Direct comparability on MSC modality, allogeneic manufacturing approach, and rare-disease focus overlapping HLC's NIPCs and autoimmune ambitions.

TypeBroad incumbent
Description

Global Japanese-headquartered pharma with a growing cell therapy franchise (post-TiGenix acquisition, ALLO-501 programs) and established CDMO/biologics capabilities. Comparable as the dominant Japanese incumbent with the resources and distribution to compete in regenerative medicine if it invests behind MSC or allogeneic platforms.

TypeEmerging player
Description

Tokyo-based clinical-stage biotech developing iPSC-derived cardiomyocyte cell therapy for heart failure. Comparable as a Japanese, venture-stage regenerative medicine company pursuing PMDA approval with similar technology-transfer and GMP manufacturing challenges.

TypeDirect peer
Description

Commercial-stage MSC therapy developer with remestemcel-L approved for pediatric SR-aGvHD and a pipeline across inflammatory and immune diseases. Direct comparability: same core modality (allogeneic MSC-based cell therapy) and overlapping rare/immune indications including graft-versus-host complications.

TypeDirect peer
Description

Developer of MultiStem (multipotent adult progenitor cell) therapies, partnered with Healios in Japan for ischemic stroke and ARDS. Direct comparability on allogeneic, off-the-shelf cell therapy for inflammatory/pulmonary indications, with shared regulatory pathway challenges.

TypeDirect peer
Description

Developer of placenta-derived, off-the-shelf cell therapy products (PLX cells) targeting muscle injury, hematopoietic recovery, and inflammatory indications. Comparable on placenta/tissue-derived MSC-like cell therapy platform and similar allogeneic manufacturing model.

TypeOthers
Description

Japanese pharma and HLC's contracted CDMO/manufacturing partner for HLC-001. Relevant as an ecosystem enabler—Rohto's cell processing capability materially supports HLC's manufacturing pathway and signals strategic adjacency for investor diligence.

TypeBroad incumbent
Description

Japan-headquartered global pharma with active cell and gene therapy programs (e.g., AT132 for XLMTM, Universal Cells platform acquisition). Comparable as a large incumbent with regenerative medicine ambitions that could overlap with HLC's pipeline through internal programs or M&A.

TypeDirect peer
Description

Japan-listed regenerative medicine company developing stem cell therapies for ARDS, ischemic stroke and acute GvHD through its MultiStem partnership. Highly comparable as a Japanese cell therapy company navigating the same PMDA regulatory pathway and orphan designation framework.

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

Segment3 records

Each record includes

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

Ideal customer profile4 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
Profiles1 record

Each record includes

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

Subsidiaries1 record

Each record includes

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

Compliance3 records

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds7 records

Each record includes

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

Investors6 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 →

Human Life CORD

Regenerative Medicinehumanlifecord.com

Human Life CORD is a clinical-stage Japanese biotechnology company developing umbilical cord-derived mesenchymal stromal cell (UC-MSC) therapies, with lead asset HLC-001 in Phase III trials for non-infectious pulmonary complications after stem cell transplantation and additional programs in sarcopenia and autoimmune diseases.

What Human Life CORD does

Human Life CORD is a clinical-stage Japanese biotechnology company founded in April 2017 by Masamitsu Harata and headquartered in Nihonbashi, Tokyo. The company develops regenerative cell therapies based on umbilical cord-derived mesenchymal stromal cells (UC-MSCs), positioning itself as a first-in-class developer of UC-MSCs as a regenerative medicine product. Its core proprietary platform covers UC-MSC isolation, expansion, and quality control, originally licensed from Tokyo University of Medical Science (Prof. Tokiko Nagamura) and further developed through collaborations with Nagoya University and others. The lead asset, HLC-001, is being developed for non-infectious pulmonary complications after hematopoietic stem cell transplantation and entered Phase III clinical trials in February 2026 following orphan regenerative medicine product designation in August 2025; Phase II data showed a 71.4% 56-day survival rate versus an estimated 24.5% with existing treatment. The company is also pursuing additional indications including sarcopenia (with a granted Japan patent in January 2026), autoimmune diseases, and newborn chronic lung disease. A new sarcopenia biomarker study was completed in Brazil in September 2025.

The company operates a virtual pharma model rather than building a direct commercial sales force. Revenue is expected to be generated through one-time licensing arrangements and royalties on HLC-001 and follow-on UC-MSC products. In Japan, Mochida Pharmaceutical holds exclusive development and commercialization rights, Rohto Pharmaceutical serves as CDMO partner, and Alfresa handles distribution. International expansion is executed through partnership-based CDMO and clinical translation arrangements: New York Blood Center Enterprises is the exclusive US CDMO (MOU October 2025), Abu Dhabi Biobank and M42 support UAE/MENA localization (May 2026 partnership), HLC-MENA Ltd. is a joint venture with Hayat Capital in Abu Dhabi Global Market (September 2025), and UFRGS supports Brazil-based sarcopenia research. Total disclosed funding to date exceeds 2.7 billion yen (~$18M) across Series A/B/C rounds, with the Series C final close in November 2025 led by Rohto Pharmaceutical. Customer segments are vertically defined by indication: rare and intractable disease patients (primary, anchored by NIPCs), elderly patients with age-related conditions (sarcopenia), and academic medical institutions collaborating on autoimmune disease research.

The headcount of 11-50 employees and the activation of a formal CxO structure in October 2025 (CEO Harata, COO Matsushita, CFO Kidachi, CTrO Nakata, CPO Yamada) reflect an organization scaling from a clinical-stage R&D team toward a pre-commercial company with multi-region supply chain responsibilities. Marketing is conducted through corporate website, Japanese business media (Nikkei, Nikkei Biotech, Nikkei Business), industry events (BioJapan, JHVS, Regenerative Medicine JAPAN), international expos (Osaka-Kansai Expo, Global Startup EXPO), equity crowdfunding via FUNDINNO PLUS+, and active engagement with government-backed startup programs (J-Startup by METI, SusHi Tech Global Startups by Tokyo Metropolitan Government). The company has not yet launched a commercial product and is therefore pre-revenue, with revenue inflection contingent on Phase III completion and regulatory approval of HLC-001 in Japan.

Human Life CORD firmographics

Firmographics
Name
Human Life CORD
Legal name
ヒューマンライフコード株式会社
Website
https://humanlifecord.com
Company type
Private
Founded year
2017
Operating status
Operating
Headcount range
11–50 employees
Short description
Human Life CORD is a clinical-stage Japanese biotechnology company developing umbilical cord-derived mesenchymal stromal cell (UC-MSC) therapies, with lead asset HLC-001 in Phase III trials for non-infectious pulmonary complications after stem cell transplantation and additional programs in sarcopenia and autoimmune diseases.
Ownership category
akta.pro rank

Human Life CORD industry classification

Industry
Product category
Regenerative Medicine
NAICS
Biological Product (except Diagnostic) Manufacturing (325414)
SIC
Biological Products, (No Disgnostic Substances) (2836)
akta.pro primary industry
Stem Cell Therapies (MSC/iPSC/HSC-derived) (HLAAABAE)
akta.pro secondary industries
Cell Processing & Ancillary Materials (media, cytokines, beads, vectors, disposables) (HLAAABAH), Cell & Tissue Banking (biobanking, cord blood/tissue) (HLAAAGAE)

Keywords

  • Regenerative medicine products
  • Cell therapy biotechnology
  • Mesenchymal stromal cells
  • Umbilical cord-derived cells
  • Clinical-stage biopharmaceuticals

Where Human Life CORD is headquartered

Location

Headquarters

HQ city
Tokyo
HQ country
Japan
HQ region
Asia

Offices4 records

Markets served

Human Life CORD business model

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

Revenue model

  1. Regenerative Medicine Product Sales: Revenue from sale of HLC-001 and future UC-MSC-based regenerative medicine products for treatment of non-infectious pulmonary complications and other indications. The company serves as the manufacturing and marketing authorization holder.
  2. Partnership Milestones and Royalties: Development and sales milestones plus royalties from partners such as Mochida Pharmaceutical for HLC-001 development and commercialization rights in Japan.

Go-to-market motion1 record

Distribution channels4 records

Marketing channels6 records

Human Life CORD product offering

Product offering

Core offering

Human Life CORD is a clinical-stage Japanese biotechnology company developing regenerative cell therapy products based on umbilical cord-derived mesenchymal stromal cells (UC-MSCs). Its core asset, HLC-001, is being advanced through Phase III clinical trials for non-infectious pulmonary complications after hematopoietic stem cell transplantation, with additional UC-MSC programs targeting sarcopenia, autoimmune diseases, and newborn chronic lung disease. The company operates a virtual-pharma model, holding manufacturing and marketing authorization while partnering for commercialization and distribution.

Product overview

Human Life CORD is a clinical-stage Japanese biotechnology company developing regenerative cell therapies based on umbilical cord-derived mesenchymal stromal cells (UC-MSCs). The company's core product is HLC-001, a UC-MSC product targeting non-infectious pulmonary complications after hematopoietic stem cell transplantation, currently in Phase III clinical trials. The company is building a global ecosystem for sustainable cell therapy, with products targeting multiple indications including sarcopenia, autoimmune diseases, and newborn chronic lung disease. Their technology platform focuses on isolating, expanding, and quality-controlling UC-MSCs for therapeutic applications.

Differentiator

Problem solved

Functional benefit

Products and services

  • HLC-001 Umbilical cord-derived mesenchymal stromal cell (UC-MSC) product in development for non-infectious pulmonary complications (NIPCs) following hematopoietic stem cell transplantation. Designated as a Rare Disease Regenerative Medicine Product by Japan's Ministry of Health, Labour and Welfare in August 2025, and currently in Phase III clinical trials with Mochida Pharmaceutical as co-development partner.
  • UC-MSCs (Umbilical Cord-Derived Mesenchymal Stromal Cells) Pipeline Products Cell therapy products derived from domestically sourced and stockpiled umbilical cords, targeting various rare and refractory diseases beyond NIPCs, including sarcopenia, autoimmune diseases, and newborn chronic lung disease. Underlying platform technology licensed from Tokyo University of Medical Science.

Quantifiable outcome

  • 71.4% 56-day survival rate in Phase II trial for NIPCs (vs 24.5% historical)
  • +2 more outcomes

Companies that use Human Life CORD

Customer profile

Named customers2 records

Segments3 records

Ideal customer profiles4 records

Human Life CORD technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature3 records

Human Life CORD partnerships and signals

Strategic signal

Partnerships

Ten partnerships are on record, tiered core and minor.

  • Abu Dhabi Biobank (Department of Health - Abu Dhabi and M42)coreStrategic or Co-development Partner · 23 March 2026Strategic partnership to localize UC-MSC manufacturing and clinical translation in UAE and MENA region. Abu Dhabi Biobank provides large-scale biobanking infrastructure, data, and translational research capabilities, while HLC contributes proprietary MSC technology and clinical development expertise.
  • New York Blood Center Enterprises (NYBCe)coreTechnology or Integration · 28 October 2025MOU for manufacturing collaboration in the USA. NYBCe serves as exclusive CDMO for manufacturing UC-MSC products, with facilities in Rye, New York. Partnership includes technology harmonization for standardized manufacturing between Japan and USA.
  • Youth Bio Global (Korea)minorStrategic or Co-development Partner · 14 October 2025MOU for cross-border clinical trials between Korea and Japan in the pharma R&D cooperation framework established by Korea's MSS with Japanese pharmaceutical companies.
  • Hayat Capital Limited (Tawasol Holding Group)coreStrategic or Co-development Partner · 5 September 2025Joint venture partnership to establish HLC-MENA Ltd. in Abu Dhabi Global Market (ADGM) for manufacturing, supplying, and commercializing UC-MSC products in Middle East and North Africa region.
  • Federal University of Rio Grande do Sul (UFRGS)coreStrategic or Co-development Partner · 30 January 2025Clinical research collaboration for sarcopenia in Brazil. Joint biomarker discovery study with 70 subjects completed in September 2025. Research conducted with Prof. Emilio Hideyuki Moriguchi.
  • Tokyo University of Science (formerly Tokyo Medical and Dental University)coreStrategic or Co-development Partner · 1 July 2024Joint research course 'Lifespan Immunity Medical Implementation Course' for research on autoimmune diseases. Collaboration with Prof. Mori Masahiro for early diagnosis and optimal treatment of refractory autoimmune diseases.
  • Mochida PharmaceuticalcoreStrategic or Co-development Partner · 27 March 2023Joint commercialization agreement for HLC-001 in Japan. HLC maintains manufacturing and marketing authorization holder status while Mochida handles development, sales, distribution, and post-marketing safety for specified diseases including NIPCs.
  • Rohto PharmaceuticalcoreTechnology or Integration · 14 February 2022Manufacturing contract for HLC-001 products. Rohto serves as CDMO partner for cell processing and formulation using master cells provided by HLC, supporting Phase III clinical trial supply.
  • Tokyo University of Medical Science (Institute of Medical Science)coreStrategic or Co-development Partner · 17 November 2020Exclusive global license for UC-MSC technology from Professor Tokiko Nagamura. Joint research for continued technology development and IMSUT-HLC Cell Processing Facility operation.
  • Alfresa Holdings / Alfresa CorporationcoreChannel Partner/ Reseller/ Distributor · 2 April 2020Capital and business partnership for stable supply chain construction. Alfresa handles distribution and logistics for cell products in Japan.

Scale indicators5 records

Recent moves8 records

Expansion highlights8 records

Human Life CORD competitors and assessment

Company assessment

Direct peers

  • JCR Pharmaceuticals: Japanese specialty pharma with regenerative medicine capabilities (e.g., TEMCELL HS for acute GvHD) and a biologics manufacturing footprint. Comparable as a Japan-based, publicly listed cell therapy company operating in similar regulatory and reimbursement environments.
  • Cynata Therapeutics: Clinical-stage developer of iPSC-derived MSC therapies for GvHD, osteoarthritis, and critical limb ischemia. Direct comparability on MSC modality, allogeneic manufacturing approach, and rare-disease focus overlapping HLC's NIPCs and autoimmune ambitions.
  • Mesoblast: Commercial-stage MSC therapy developer with remestemcel-L approved for pediatric SR-aGvHD and a pipeline across inflammatory and immune diseases. Direct comparability: same core modality (allogeneic MSC-based cell therapy) and overlapping rare/immune indications including graft-versus-host complications.
  • Athersys: Developer of MultiStem (multipotent adult progenitor cell) therapies, partnered with Healios in Japan for ischemic stroke and ARDS. Direct comparability on allogeneic, off-the-shelf cell therapy for inflammatory/pulmonary indications, with shared regulatory pathway challenges.
  • Pluristem Therapeutics: Developer of placenta-derived, off-the-shelf cell therapy products (PLX cells) targeting muscle injury, hematopoietic recovery, and inflammatory indications. Comparable on placenta/tissue-derived MSC-like cell therapy platform and similar allogeneic manufacturing model.
  • Healios KK: Japan-listed regenerative medicine company developing stem cell therapies for ARDS, ischemic stroke and acute GvHD through its MultiStem partnership. Highly comparable as a Japanese cell therapy company navigating the same PMDA regulatory pathway and orphan designation framework.

Broad incumbents

  • Takeda Pharmaceutical: Global Japanese-headquartered pharma with a growing cell therapy franchise (post-TiGenix acquisition, ALLO-501 programs) and established CDMO/biologics capabilities. Comparable as the dominant Japanese incumbent with the resources and distribution to compete in regenerative medicine if it invests behind MSC or allogeneic platforms.
  • Astellas Pharma: Japan-headquartered global pharma with active cell and gene therapy programs (e.g., AT132 for XLMTM, Universal Cells platform acquisition). Comparable as a large incumbent with regenerative medicine ambitions that could overlap with HLC's pipeline through internal programs or M&A.

Emerging players

  • Heartseed Inc. Tokyo-based clinical-stage biotech developing iPSC-derived cardiomyocyte cell therapy for heart failure. Comparable as a Japanese, venture-stage regenerative medicine company pursuing PMDA approval with similar technology-transfer and GMP manufacturing challenges.

Others

  • Rohto Pharmaceutical: Japanese pharma and HLC's contracted CDMO/manufacturing partner for HLC-001. Relevant as an ecosystem enabler—Rohto's cell processing capability materially supports HLC's manufacturing pathway and signals strategic adjacency for investor diligence.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat5 records

Key risks6 records

Key highlights7 records

Customer concentration

Human Life CORD social profiles

Digital presence

Human Life CORD compliance and trust

Trust signal

Compliance3 records

Human Life CORD financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Human Life CORD leadership team

Management profile

Number of profiles

Profiles1 record

Human Life CORD subsidiaries and ownership

Company hierarchy

Subsidiaries1 record

Human Life CORD funding detail

Funding detail

Funding overview

Funding rounds7 records

Investors6 records

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

Human Life CORD 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 Human Life CORD

What does Human Life CORD do?

Human Life CORD is a clinical-stage Japanese biotechnology company developing regenerative cell therapy products based on umbilical cord-derived mesenchymal stromal cells (UC-MSCs). Its core asset, HLC-001, is being advanced through Phase III clinical trials for non-infectious pulmonary complications after hematopoietic stem cell transplantation, with additional UC-MSC programs targeting sarcopenia, autoimmune diseases, and newborn chronic lung disease. The company operates a virtual-pharma model, holding manufacturing and marketing authorization while partnering for commercialization and distribution.

Is Human Life CORD a public or private company?

Human Life CORD is a private company. It is classified as venture growth investor backed and is currently operating.

When was Human Life CORD founded?

Human Life CORD was founded in 2017. It employs 11 to 50 people.

Where is Human Life CORD based?

Human Life CORD is headquartered in Tokyo, Japan, in the Asia region.

How does Human Life CORD make money?

Two revenue lines are on record. Regenerative Medicine Product Sales are the primary driver. The others are partnership Milestones and Royalties.

Who are Human Life CORD's main competitors?

Direct peers on record are JCR Pharmaceuticals, Cynata Therapeutics, Mesoblast, Athersys, Pluristem Therapeutics and Healios KK. Broad incumbents are Takeda Pharmaceutical and Astellas Pharma. Heartseed Inc. is listed as an emerging player. Rohto Pharmaceutical is listed as an others.

Does Human Life CORD have an API?

No public API is recorded for Human Life CORD.

What industry is Human Life CORD in?

Human Life CORD's product category is Regenerative Medicine. Its primary akta.pro industry code is HLAAABAE, Stem Cell Therapies (MSC/iPSC/HSC-derived), with a secondary code of HLAAABAH, Cell Processing & Ancillary Materials (media, cytokines, beads, vectors, disposables). Its NAICS code is 325414 and its SIC code is 2836.

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Prtimesヒューマンライフコード、UAE・アブダビに中東・北アフリカ地域の事業会社「Human Life CORD MENA」を設立Human Life Code established Human Life CORD MENA in Abu Dhabi's Masdar City Free Zone on August 12, 2026. The company will promote technology transfer, GMP-compliant local manufacturing, clinical development, and commercialization of umbilical cord-derived stem cell products in the MENA region. It plans to collaborate with Abu Dhabi Biobank and local partners to build a regional hub.GulfNewsAbu Dhabi Biobank, Human Life CORD Japan Partner to Advance Umbilical Cord Stem Cell Therapies in UAEAbu Dhabi Biobank has announced a strategic partnership with Human Life CORD Japan Inc. to support the development of umbilical cord-derived stem cell therapies in the UAE. The collaboration aims to establish one of the UAE's first local manufacturing and clinical pathways for these therapies, which are being explored for conditions including diabetes complications, age-related diseases, and musculoskeletal disorders. The partnership reflects growing scientific cooperation between the UAE and Japan while strengthening Abu Dhabi's position as a global healthcare and life sciences hub.NikkeibpNotice regarding the submission of the clinical trial application for the Phase III clinical trial of human life code, umbilical cord-derived mesenchymal stromal cells "HLC-001" for non-infectious pulmonary complications after hematopoietic stem cell transplantation.Mochida Pharmaceutical Co., Ltd. and Human Life Code Co., Ltd. announced that Mochida Pharmaceutical has submitted a clinical trial plan to initiate a Phase III clinical trial for cord-derived mesenchymal stromal cells product "HLC-001". The trial is intended to evaluate the product for non-infectious pulmonary complications following hematopoietic stem cell transplantation.PrtimesA total of 1.57 billion yen was raised in the Series C second close.Human Life Code Co., Ltd., a Tokyo-based biotech startup, completed an additional fundraising of approximately 800 million yen through the equity crowdfunding platform FUNDINNO PLUS+, bringing its total Series C fundraising to 1.57 billion yen. The capital will advance clinical development of umbilical cord-derived mesenchymal stem cell (UC-MSC) products targeting non-infectious pulmonary complications after hematopoietic stem cell transplantation. The company aims to accelerate the establishment of a global cell manufacturing and supply network while pursuing early practical application of its regenerative medicine pipeline.NikkeibpHuman Life Code has raised a total of 1.57 billion yen in the Series C second close, accelerating global expansion along with the preparation for the start of Phase III clinical trials.Human Life Code Co., Ltd. has raised a total of 1.57 billion yen in Series C second close funding, with approximately 800 million yen coming through the FUNDINNO PLUS investor platform operated by equity crowdfunding service FUNDINNO. The Tokyo-based biotechnology company is developing umbilical cord-derived mesenchymal stem cell (UC-MSCs) regenerative medicine products and plans to use the funding to accelerate global expansion and prepare for Phase III clinical trials. The company aims to commercialize these products ahead of global competitors.