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ME Therapeutics

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uuid0002z1z

Namestring
ME Therapeutics
Legal namestring
ME Therapeutics Holdings, Inc.
Company typeenum
Public
Founded yearint
2014
Descriptiontext

ME Therapeutics Holdings, Inc. is a preclinical-stage biotechnology company founded in 2014 in Vancouver, Canada, focused on discovering and developing next-generation immuno-oncology therapeutics that reprogram immune cells in vivo to recognize and fight cancer. The company's core technological premise is that myeloid-cell-driven immune suppression is a central barrier in many solid tumors and certain hematologic malignancies, and that targeting myeloid biology can unlock durable anti-tumor responses where existing T-cell-directed therapies fail.

The pipeline spans five distinct modalities anchored on the company's in vivo reprogramming platform. The lead asset is a humanized anti-G-CSF monoclonal antibody (h1B11-12) designed to neutralize immune suppression in the tumor microenvironment; it has shown safety in non-human primate toxicology studies and is protected by granted patents in the US and China. Second, myeloid-targeted prodrug candidates (D094, D099) selectively interfere with suppressive myeloid pathways. Third, therapeutic mRNAs (STING activators) delivered via NanoVation Therapeutics' long-circulating lipid nanoparticle (lcLNP) platform have demonstrated synergy with PD-1 checkpoint inhibitors in preclinical colorectal cancer models. Fourth, an in vivo CAR-T and CAR-M program delivers genetic instructions directly into patients to reprogram immune cells in situ, potentially avoiding the ~$500,000-per-patient cost of ex vivo CAR-T manufacturing. Fifth, an exclusively licensed nanobody-based CD22 binder from the National Research Council of Canada extends the in vivo CAR approach into relapsed/refractory B-cell cancers.

ME Therapeutics is publicly listed on the Canadian Securities Exchange (METX) since October 2023 and on the Frankfurt Stock Exchange (Q9T) since December 2023, and is pursuing an uplisting to Nasdaq or NYSE American. The company has no commercial products and generates no product revenue; funding to date consists of small non-brokered private placements totaling approximately CAD $2 million and non-dilutive NRC IRAP grants totaling approximately CAD $190,000. The business model is entirely pre-commercial: value is expected to be realized through future pharmaceutical partnerships, licensing transactions, or acquisition, with first-in-human clinical trials targeted for late 2026 or early 2027. The company employs 11-50 people, is led by founder-CEO Dr. Salim Dhanji, and supplements its scientific team with senior commercial leadership including CBO Karim Lalji.

Short descriptiontext

ME Therapeutics is a preclinical Vancouver-based biotechnology company developing in vivo immune-cell reprogramming therapeutics, including an anti-G-CSF antibody, mRNA-LNP therapies, and in vivo CAR-T and CAR-M programs, targeting myeloid-driven immune suppression in solid and hematologic cancers.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersVancouver, Canada
HQ citystring
Vancouver
HQ countrystring
Canada
HQ regionstring
North America
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
immuno-oncology therapeutics, myeloid cell therapy, cancer immunotherapy drugs, mRNA lipid nanoparticles, monoclonal antibody development
Industry5 codes
1Antibody Discovery & Engineering Platforms (display tech, bispecifics, Fc engineering)
CodeHLAAAIABPrimaryYes
2CAR-T & TCR-T Therapies
CodeHLAAABACPrimaryNo
3Cytokines, Interferons & Immunomodulatory Proteins
CodeHLAAAAACPrimaryNo
4Bispecific & Multispecific Antibodies
CodeHLAAAAAFPrimaryNo
5Therapeutic Vaccines (e.g., Cancer/Chronic Infection)
CodeHLAIAEAGPrimaryNo
NAICS code3 codes
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
  • Scientific Research and Development Services5417
  • Biological Product (except Diagnostic) Manufacturing325414
SIC code2 codes
  • Biological Products, (No Disgnostic Substances)2836
  • Services-Commercial Physical & Biological Research8731
Product category
Immuno-oncology Therapeutics
GTM motion3 records

Each record includes

Type, Description, Source

Revenue model4 records
1Private Placement Financing
TypeOne Time License
Description

The company raises capital through non-brokered private placement offerings of units (common shares + warrants) to institutional and retail investors. This is the primary funding mechanism for preclinical development.

biospace.com
2Government Grants and Support
TypeSubscription Recurring
Description

Funding and advisory services from National Research Council of Canada Industrial Research Assistance Program (NRC IRAP) to support mRNA therapeutic program and preclinical testing. This is non-dilutive funding.

techcouver.com
3Future Licensing and Partnership Revenue
TypeLicensing Royalties
Description

Potential licensing deals and partnerships for drug candidates. The company is exploring strategic transactions and has engaged banks toward potential U.S. listing on Nasdaq or NYSE American.

businesswire.com
4Equity Listing and Trading
TypeSubscription Recurring
Description

Publicly listed on Canadian Securities Exchange (CSE: METX) and Frankfurt Stock Exchange (FSE: Q9T). Market-based valuation provides liquidity for investors and potential access to broader capital markets.

businesswire.com
Marketing channels10 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
Personnel, Technology or R&D, Operations, Marketing or Sales
GTM typeB2B
B2B
Offering typeServices
Services
Core offering1 text field

ME Therapeutics is a preclinical-stage biotechnology company discovering and developing next-generation immuno-oncology therapeutics that reprogram immune cells in vivo to recognize and fight cancer. Its pipeline includes a humanized anti-G-CSF antibody (h1B11-12), myeloid-targeted small molecule prodrugs (D094, D099), STING-activating therapeutic mRNAs delivered via lipid nanoparticles, and in vivo CAR cell therapy programs (CAR-T and CAR-M) using a licensed CD22 nanobody binder. The company does not yet sell commercial products and is advancing toward first-in-human clinical trials targeted for late 2026 or early 2027.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 5 values shown
  • STING activator demonstrated synergy with PD-1 checkpoint inhibitors in preclinical colorectal cancer models
+4 more records
Product overview1 text field

ME Therapeutics is developing a multi-modality immuno-oncology pipeline focused on reprogramming immune cells to fight cancer. The company's portfolio includes: (1) G-CSF Antibody Candidate (h1B11-12), a humanized monoclonal antibody targeting immune suppression in tumors; (2) Myeloid Targeted Prodrug Candidates (D094 and D099), small molecule drugs targeting suppressive myeloid cells; (3) Therapeutic mRNA Candidates encoding immune-modulating proteins delivered via LNP technology from NanoVation Therapeutics; (4) In Vivo CAR Cell Therapy Program using genetic engineering to reprogram immune cells directly in the body; and (5) CD22 Nanobody-based CAR Binder licensed from NRC for next-generation CAR-T and CAR-M therapies. The company leverages lipid nanoparticle (LNP) delivery technology as a core enabling platform across multiple programs.

Product and service5 records
1G-CSF Antibody Candidate (h1B11-12)
CategoryMonoclonal antibody therapeutic
Description

A humanized, high-affinity monoclonal antibody that binds to and blocks granulocyte colony-stimulating factor (G-CSF) to overcome immune suppression in the tumor microenvironment. The company's most advanced preclinical asset, intended for cancer treatment indications including solid tumors.

2Myeloid Targeted Prodrug Candidates (D094 and D099)
CategorySmall molecule prodrug therapeutic
Description

Small molecule prodrug candidates designed to specifically target suppressive myeloid cells in the tumor environment, with the active component interfering with key pathways involved in immune suppression and cancer growth.

3Therapeutic mRNA Candidates (STING activators)
CategorymRNA cancer immunotherapy
Description

mRNA-based drug candidates encoding immune-modulating proteins that activate the STING pathway to stimulate anti-cancer immune responses, delivered via lipid nanoparticle technology from NanoVation Therapeutics. Demonstrated synergy with PD-1 checkpoint inhibitors in preclinical colorectal cancer models.

4In Vivo CAR Cell Therapy Program
CategoryIn vivo cell therapy platform
Description

Next-generation immunotherapy program that delivers genetic instructions directly into a patient's body to reprogram immune cells (T cells and macrophages) within the tumor microenvironment using CAR technology, including in vivo CAR-T and CAR-M approaches, eliminating the need for ex vivo cell manufacturing.

5CD22 Nanobody-based CAR Binder
CategoryLicensed therapeutic binder
Description

Nanobody-based CD22 binder exclusively licensed from the National Research Council of Canada for use in CAR therapy applications including in vivo CAR-T and CAR-M approaches, providing an alternative target for relapsed/refractory B-cell cancers where CD22 expression is often maintained after CD19 CAR-T failure.

Scale indicator8 records

Each record includes

Type, Value, Description, Source

Partnership7 partners
Strategic tierSupportingTypeImplementation/ SI/ Consulting PartnerAnnounced on2026-01-30
Description

Corporate and securities law firm engaged to assist ME Therapeutics in evaluating and pursuing a potential listing on Nasdaq or NYSE American, working alongside investment banks toward this goal.

Strategic tierCoreTypeTechnology or IntegrationAnnounced on2025-10-15
Description

Technology license agreement dated October 15, 2025 granting ME Therapeutics exclusive commercial rights to NRC's proprietary nanobody-based CD22 binder for use in CAR therapy applications including in vivo CAR-T and CAR-M approaches. The license covers multiple territories (Australia, Brazil, Canada, China, Europe, India, Israel, Japan, New Zealand, Singapore, South Korea, and the United States). The CD22 nanobody is currently being evaluated in an investigator-driven Phase 1 clinical trial (NCT06208735).

Strategic tierSupportingTypeImplementation/ SI/ Consulting PartnerAnnounced on2025-03-03
Description

Distinguished corporate finance and securities law firm retained to assist in evaluating an uplisting to senior national securities exchanges such as Nasdaq Capital Market or NYSE. The firm brings extensive experience in corporate finance, mergers and acquisitions, and securities law.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2024-07-18
Description

Ongoing collaboration with Dr. Kenneth Harder's laboratory at UBC for joint research on G-CSF in cancer and novel LNP formulation discovery. Dr. Harder is an Associate Professor in Dept. of Microbiology and Immunology and member of Networks of Centres of Excellence (NCE) Nanomedicine Innovation Network (NMIN).

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2024-07-08
Description

Strategic collaboration announced July 2024 to test delivery and efficacy of mRNA-based drug candidates targeted to myeloid cells using NanoVation's cutting-edge lipid nanoparticle (LNP) technologies. The partnership leverages NanoVation's long-circulating LNP (lcLNP) technology for efficient nucleic acid delivery to immune cells. Initial stage involves testing delivery of two undisclosed target mRNAs to tumor-associated myeloid cells in vivo in mouse colon cancer models. The companies share expertise in myeloid-focused immuno-oncology and RNA delivery.

6Dr. Kate Hanham (Clinical Consultant)
Strategic tierSupportingTypeOthersAnnounced on2024-05-29
Description

Clinical trial consultant with strategic input experience ranging from startup biotechnology to top ten pharmaceutical companies. Brings expertise in clinical, regulatory and manufacturing strategies from early development through NDA, with experience in FDA and international regulatory agency communications.

metherapeutics.com
7Dr. Katherine Morris (Clinical Consultant)
Strategic tierSupportingTypeOthersAnnounced on2024-05-29
Description

Surgical oncologist and solid tumor immunologist with over 20 years of experience, specializing in gastrointestinal cancers. Completed training at Memorial Sloan Kettering Cancer Center with research focus on G-CSF role in cancer. Member of NIH Cellular Immunotherapy of Cancer study section.

metherapeutics.com
Recent move8 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Market position
Competitive moat4 records

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Type, Details

Key risks6 records

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Headline, Details, Source

Key highlights7 records

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Headline, Details, Source

Customer concentration

Classification, Details

Segment3 records

Each record includes

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

Ideal customer profile2 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

Feature6 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles6 records

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

Subsidiaries1 record

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No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds3 records

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

Investors1 record

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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 →

ME Therapeutics

Immuno-oncology Therapeuticsmetherapeutics.com

ME Therapeutics is a preclinical Vancouver-based biotechnology company developing in vivo immune-cell reprogramming therapeutics, including an anti-G-CSF antibody, mRNA-LNP therapies, and in vivo CAR-T and CAR-M programs, targeting myeloid-driven immune suppression in solid and hematologic cancers.

What ME Therapeutics does

ME Therapeutics Holdings, Inc. is a preclinical-stage biotechnology company founded in 2014 in Vancouver, Canada, focused on discovering and developing next-generation immuno-oncology therapeutics that reprogram immune cells in vivo to recognize and fight cancer. The company's core technological premise is that myeloid-cell-driven immune suppression is a central barrier in many solid tumors and certain hematologic malignancies, and that targeting myeloid biology can unlock durable anti-tumor responses where existing T-cell-directed therapies fail.

The pipeline spans five distinct modalities anchored on the company's in vivo reprogramming platform. The lead asset is a humanized anti-G-CSF monoclonal antibody (h1B11-12) designed to neutralize immune suppression in the tumor microenvironment; it has shown safety in non-human primate toxicology studies and is protected by granted patents in the US and China. Second, myeloid-targeted prodrug candidates (D094, D099) selectively interfere with suppressive myeloid pathways. Third, therapeutic mRNAs (STING activators) delivered via NanoVation Therapeutics' long-circulating lipid nanoparticle (lcLNP) platform have demonstrated synergy with PD-1 checkpoint inhibitors in preclinical colorectal cancer models. Fourth, an in vivo CAR-T and CAR-M program delivers genetic instructions directly into patients to reprogram immune cells in situ, potentially avoiding the ~$500,000-per-patient cost of ex vivo CAR-T manufacturing. Fifth, an exclusively licensed nanobody-based CD22 binder from the National Research Council of Canada extends the in vivo CAR approach into relapsed/refractory B-cell cancers.

ME Therapeutics is publicly listed on the Canadian Securities Exchange (METX) since October 2023 and on the Frankfurt Stock Exchange (Q9T) since December 2023, and is pursuing an uplisting to Nasdaq or NYSE American. The company has no commercial products and generates no product revenue; funding to date consists of small non-brokered private placements totaling approximately CAD $2 million and non-dilutive NRC IRAP grants totaling approximately CAD $190,000. The business model is entirely pre-commercial: value is expected to be realized through future pharmaceutical partnerships, licensing transactions, or acquisition, with first-in-human clinical trials targeted for late 2026 or early 2027. The company employs 11-50 people, is led by founder-CEO Dr. Salim Dhanji, and supplements its scientific team with senior commercial leadership including CBO Karim Lalji.

ME Therapeutics firmographics

Firmographics
Name
ME Therapeutics
Legal name
ME Therapeutics Holdings, Inc.
Website
https://metherapeutics.com
Company type
Public
Founded year
2014
Operating status
Operating
Headcount range
11–50 employees
Short description
ME Therapeutics is a preclinical Vancouver-based biotechnology company developing in vivo immune-cell reprogramming therapeutics, including an anti-G-CSF antibody, mRNA-LNP therapies, and in vivo CAR-T and CAR-M programs, targeting myeloid-driven immune suppression in solid and hematologic cancers.
Ownership category
akta.pro rank

ME Therapeutics industry classification

Industry
Product category
Immuno-oncology Therapeutics
NAICS
Research and Development in Biotechnology (except Nanobiotechnology) (541714), Scientific Research and Development Services (5417), Biological Product (except Diagnostic) Manufacturing (325414)
SIC
Biological Products, (No Disgnostic Substances) (2836), Services-Commercial Physical & Biological Research (8731)
akta.pro primary industry
Antibody Discovery & Engineering Platforms (display tech, bispecifics, Fc engineering) (HLAAAIAB)
akta.pro secondary industries
CAR-T & TCR-T Therapies (HLAAABAC), Cytokines, Interferons & Immunomodulatory Proteins (HLAAAAAC), Bispecific & Multispecific Antibodies (HLAAAAAF), Therapeutic Vaccines (e.g., Cancer/Chronic Infection) (HLAIAEAG)

Keywords

  • Immuno-oncology therapeutics
  • Myeloid cell therapy
  • Cancer immunotherapy drugs
  • MRNA lipid nanoparticles
  • Monoclonal antibody development

Where ME Therapeutics is headquartered

Location

Headquarters

HQ city
Vancouver
HQ country
Canada
HQ region
North America

Offices1 record

Markets served

ME Therapeutics business model

Business model
GTM type
B2B
Offering type
Services
Cost components
Personnel, Technology or R&D, Operations, Marketing or Sales

Revenue model

  1. Private Placement Financing: The company raises capital through non-brokered private placement offerings of units (common shares + warrants) to institutional and retail investors. This is the primary funding mechanism for preclinical development.
  2. Government Grants and Support: Funding and advisory services from National Research Council of Canada Industrial Research Assistance Program (NRC IRAP) to support mRNA therapeutic program and preclinical testing. This is non-dilutive funding.
  3. Future Licensing and Partnership Revenue: Potential licensing deals and partnerships for drug candidates. The company is exploring strategic transactions and has engaged banks toward potential U.S. listing on Nasdaq or NYSE American.
  4. Equity Listing and Trading: Publicly listed on Canadian Securities Exchange (CSE: METX) and Frankfurt Stock Exchange (FSE: Q9T). Market-based valuation provides liquidity for investors and potential access to broader capital markets.

Go-to-market motion3 records

Distribution channels4 records

Marketing channels10 records

ME Therapeutics product offering

Product offering

Core offering

ME Therapeutics is a preclinical-stage biotechnology company discovering and developing next-generation immuno-oncology therapeutics that reprogram immune cells in vivo to recognize and fight cancer. Its pipeline includes a humanized anti-G-CSF antibody (h1B11-12), myeloid-targeted small molecule prodrugs (D094, D099), STING-activating therapeutic mRNAs delivered via lipid nanoparticles, and in vivo CAR cell therapy programs (CAR-T and CAR-M) using a licensed CD22 nanobody binder. The company does not yet sell commercial products and is advancing toward first-in-human clinical trials targeted for late 2026 or early 2027.

Product overview

ME Therapeutics is developing a multi-modality immuno-oncology pipeline focused on reprogramming immune cells to fight cancer. The company's portfolio includes: (1) G-CSF Antibody Candidate (h1B11-12), a humanized monoclonal antibody targeting immune suppression in tumors; (2) Myeloid Targeted Prodrug Candidates (D094 and D099), small molecule drugs targeting suppressive myeloid cells; (3) Therapeutic mRNA Candidates encoding immune-modulating proteins delivered via LNP technology from NanoVation Therapeutics; (4) In Vivo CAR Cell Therapy Program using genetic engineering to reprogram immune cells directly in the body; and (5) CD22 Nanobody-based CAR Binder licensed from NRC for next-generation CAR-T and CAR-M therapies. The company leverages lipid nanoparticle (LNP) delivery technology as a core enabling platform across multiple programs.

Differentiator

Problem solved

Functional benefit

Products and services

  • G-CSF Antibody Candidate (h1B11-12) A humanized, high-affinity monoclonal antibody that binds to and blocks granulocyte colony-stimulating factor (G-CSF) to overcome immune suppression in the tumor microenvironment. The company's most advanced preclinical asset, intended for cancer treatment indications including solid tumors.
  • Myeloid Targeted Prodrug Candidates (D094 and D099) Small molecule prodrug candidates designed to specifically target suppressive myeloid cells in the tumor environment, with the active component interfering with key pathways involved in immune suppression and cancer growth.
  • Therapeutic mRNA Candidates (STING activators) mRNA-based drug candidates encoding immune-modulating proteins that activate the STING pathway to stimulate anti-cancer immune responses, delivered via lipid nanoparticle technology from NanoVation Therapeutics. Demonstrated synergy with PD-1 checkpoint inhibitors in preclinical colorectal cancer models.
  • In Vivo CAR Cell Therapy Program Next-generation immunotherapy program that delivers genetic instructions directly into a patient's body to reprogram immune cells (T cells and macrophages) within the tumor microenvironment using CAR technology, including in vivo CAR-T and CAR-M approaches, eliminating the need for ex vivo cell manufacturing.
  • CD22 Nanobody-based CAR Binder Nanobody-based CD22 binder exclusively licensed from the National Research Council of Canada for use in CAR therapy applications including in vivo CAR-T and CAR-M approaches, providing an alternative target for relapsed/refractory B-cell cancers where CD22 expression is often maintained after CD19 CAR-T failure.

Quantifiable outcome

  • STING activator demonstrated synergy with PD-1 checkpoint inhibitors in preclinical colorectal cancer models
  • +4 more outcomes

Companies that use ME Therapeutics

Customer profile

Segments3 records

Ideal customer profiles2 records

ME Therapeutics technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature6 records

ME Therapeutics partnerships and signals

Strategic signal

Partnerships

Seven partnerships are on record, tiered supporting and core.

  • Luckosky Brookman LLPsupportingImplementation/ SI/ Consulting Partner · 30 January 2026Corporate and securities law firm engaged to assist ME Therapeutics in evaluating and pursuing a potential listing on Nasdaq or NYSE American, working alongside investment banks toward this goal.
  • National Research Council of Canada (NRC)coreTechnology or Integration · 15 October 2025Technology license agreement dated October 15, 2025 granting ME Therapeutics exclusive commercial rights to NRC's proprietary nanobody-based CD22 binder for use in CAR therapy applications including in vivo CAR-T and CAR-M approaches. The license covers multiple territories (Australia, Brazil, Canada, China, Europe, India, Israel, Japan, New Zealand, Singapore, South Korea, and the United States). The CD22 nanobody is currently being evaluated in an investigator-driven Phase 1 clinical trial (NCT06208735).
  • Lucosky Brookman LLPsupportingImplementation/ SI/ Consulting Partner · 3 March 2025Distinguished corporate finance and securities law firm retained to assist in evaluating an uplisting to senior national securities exchanges such as Nasdaq Capital Market or NYSE. The firm brings extensive experience in corporate finance, mergers and acquisitions, and securities law.
  • University of British Columbia (Dr. Kenneth Harder Lab)coreStrategic or Co-development Partner · 18 July 2024Ongoing collaboration with Dr. Kenneth Harder's laboratory at UBC for joint research on G-CSF in cancer and novel LNP formulation discovery. Dr. Harder is an Associate Professor in Dept. of Microbiology and Immunology and member of Networks of Centres of Excellence (NCE) Nanomedicine Innovation Network (NMIN).
  • NanoVation Therapeutics Inc.coreStrategic or Co-development Partner · 8 July 2024Strategic collaboration announced July 2024 to test delivery and efficacy of mRNA-based drug candidates targeted to myeloid cells using NanoVation's cutting-edge lipid nanoparticle (LNP) technologies. The partnership leverages NanoVation's long-circulating LNP (lcLNP) technology for efficient nucleic acid delivery to immune cells. Initial stage involves testing delivery of two undisclosed target mRNAs to tumor-associated myeloid cells in vivo in mouse colon cancer models. The companies share expertise in myeloid-focused immuno-oncology and RNA delivery.
  • Dr. Kate Hanham (Clinical Consultant)supportingOthers · 29 May 2024Clinical trial consultant with strategic input experience ranging from startup biotechnology to top ten pharmaceutical companies. Brings expertise in clinical, regulatory and manufacturing strategies from early development through NDA, with experience in FDA and international regulatory agency communications.
  • Dr. Katherine Morris (Clinical Consultant)supportingOthers · 29 May 2024Surgical oncologist and solid tumor immunologist with over 20 years of experience, specializing in gastrointestinal cancers. Completed training at Memorial Sloan Kettering Cancer Center with research focus on G-CSF role in cancer. Member of NIH Cellular Immunotherapy of Cancer study section.

Scale indicators8 records

Recent moves8 records

Expansion highlights6 records

ME Therapeutics competitors and assessment

Company assessment

Market position

Competitive moat4 records

Key risks6 records

Key highlights7 records

Customer concentration

ME Therapeutics social profiles

Digital presence

ME Therapeutics financial estimates

Financial estimate

Revenue estimate

Valuation estimate

ME Therapeutics leadership team

Management profile

Number of profiles

Profiles6 records

ME Therapeutics subsidiaries and ownership

Company hierarchy

Subsidiaries1 record

ME Therapeutics funding detail

Funding detail

Funding overview

Funding rounds3 records

Investors1 record

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

ME Therapeutics 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 ME Therapeutics

What does ME Therapeutics do?

ME Therapeutics is a preclinical-stage biotechnology company discovering and developing next-generation immuno-oncology therapeutics that reprogram immune cells in vivo to recognize and fight cancer. Its pipeline includes a humanized anti-G-CSF antibody (h1B11-12), myeloid-targeted small molecule prodrugs (D094, D099), STING-activating therapeutic mRNAs delivered via lipid nanoparticles, and in vivo CAR cell therapy programs (CAR-T and CAR-M) using a licensed CD22 nanobody binder. The company does not yet sell commercial products and is advancing toward first-in-human clinical trials targeted for late 2026 or early 2027.

Is ME Therapeutics a public or private company?

ME Therapeutics is a public company. It is classified as public and is currently operating.

When was ME Therapeutics founded?

ME Therapeutics was founded in 2014. It employs 11 to 50 people.

Where is ME Therapeutics based?

ME Therapeutics is headquartered in Vancouver, Canada, in the North America region.

How does ME Therapeutics make money?

Four revenue lines are on record. Private Placement Financing is the primary driver. The others are government Grants and Support, future Licensing and Partnership Revenue and equity Listing and Trading.

Does ME Therapeutics have an API?

No public API is recorded for ME Therapeutics.

What industry is ME Therapeutics in?

ME Therapeutics's product category is Immuno-oncology Therapeutics. Its primary akta.pro industry code is HLAAAIAB, Antibody Discovery & Engineering Platforms (display tech, bispecifics, Fc engineering), with a secondary code of HLAAABAC, CAR-T & TCR-T Therapies. Its NAICS code is 541714 and its SIC code is 2836.

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Live signals
MarketScreenerME Therapeutics Raises C$0.58 Million Via Non-Brokered Private PlacementME Therapeutics Holdings Inc., a preclinical stage biotechnology company focused on immune oncology therapeutics, has raised C$0.58 million through a non-brokered private placement. The company is developing antibody drug candidates and small molecule prodrugs targeting suppressive myeloid cells in cancer treatment, and has also initiated work on mRNA-based cancer therapeutic candidates. The private placement represents a modest capital raise typical for early-stage biotech companies developing oncology programs.Investing.comME Therapeutics closes $576,500 private placement financing By Investing.comME Therapeutics Holdings Inc. closed a non-brokered private placement raising $576,500.60 through the issuance of 339,118 units at $1.70 per unit, each consisting of one common share and one warrant exercisable at $2.00 for three years. Company director John Priatel acquired 294,118 units for $500,000.60 in the financing, increasing his ownership from 13.89% to 16.21%. The company also granted 2,047,500 stock options to directors, officers, employees, and consultants, with proceeds earmarked for research and development, strategic transactions, pursuing a U.S. listing, marketing, investor relations, and working capital.YahooME Therapeutics Closes Over-Subscribed Private PlacementME Therapeutics Holdings Inc. announced the closing of a non-brokered private placement financing, raising aggregate proceeds of $576,500.60 through the issuance of 339,118 units at $1.70 per unit, each unit consisting of one common share and one warrant exercisable at $2.00 for three years. The proceeds are intended for advancing research and development, evaluating strategic transactions, pursuing a U.S. listing, investor relations, working capital, and general corporate purposes. The company also granted an aggregate of 2,047,500 stock options to its directors, officers, employees, and consultants, with 1,925,000 options granted to insiders exercisable at C$1.99 per share.Investing.comME Therapeutics announces private placement for up to $500,000 By Investing.comME Therapeutics Holdings Inc. announced plans to raise up to $500,000 through a non-brokered private placement, issuing up to 294,117 units at $1.70 per unit, each consisting of one common share and one warrant exercisable at $2.00 per share for three years. The biotech company, focused on developing immune cell reprogramming therapeutics for cancer treatment, stated proceeds will be used for R&D, strategic transactions, pursuing a U.S. listing, and general corporate purposes. The offering remains subject to Canadian Securities Exchange compliance and applicable securities laws.The Canadian Press NewsME Therapeutics Announces Private PlacementME Therapeutics announced a non-brokered private placement to raise up to $500,000 by issuing up to 294,117 units at $1.70 each. Proceeds will fund research, development, strategic transactions, and a U.S. listing. The company may increase the offering to $1,000,000 if investor interest warrants.Business Wire BlogME Therapeutics to Pitch at CSE Capital Tech Connect During Web Summit VancouverME Therapeutics will pitch at CSE Capital Tech Connect during Web Summit Vancouver on May 13. CEO Dr. Salim Dhanji will present its in vivo immune reprogramming approaches for cancer, including CARs and a CD22 nanobody binder. The event highlights the company's science and investment opportunity.Business Wire BlogME Therapeutics Provides Scientific Update on In Vivo CAR and Therapeutic mRNA ProgramsME Therapeutics provided an update on its in vivo CAR and therapeutic mRNA programs, including a dual CD19/CD22-targeted CAR and a STING-targeting mRNA candidate. The STING candidate showed dose-dependent efficacy in a mouse colorectal cancer model, and both programs aim to target leukemia, lymphoma, and solid tumors.Business Wire BlogME Therapeutics Scientific and Corporate UpdateME Therapeutics Holdings Inc., a Vancouver-based publicly listed biotechnology company, provided a corporate update on its pipeline of cancer therapeutics, including therapeutic mRNAs targeting STING and an in vivo CAR therapy program. In preclinical testing, the company's STING activator demonstrated synergy with PD-1 checkpoint inhibitors in colorectal cancer models, and the company plans to initiate in vivo testing of its optimized CAR constructs using lipid nanoparticle delivery systems. The company also disclosed it is working with Luckosky Brookman LLP and investment banks toward a potential listing on Nasdaq or NYSE American.PharmiWeb.comME Therapeutics Granted Licence for CD22 Nanobody Asset to Expand Next-Gen In Vivo CAR Cell Therapy ProgramME Therapeutics Holdings Inc., through its subsidiary ME Therapeutics Inc., entered into a technology license agreement with the National Research Council of Canada on October 15, 2025, securing exclusive commercial rights to the NRC's proprietary nanobody-based CD22 binder for use in Chimeric Antigen Receptor (CAR) therapy applications including in vivo CAR-T and CAR-M approaches. The CD22 binder, currently being evaluated in an investigator-driven Phase 1 clinical trial (NCT06208735), offers potential advantages in stability, synthesis, and design flexibility compared to traditional antibody formats for treating relapsed/refractory B-cell cancers. The license covers exclusive rights in Australia, Brazil, Canada, China, Europe, India, Israel, Japan, New Zealand, Singapore, South Korea, and the United States, with ME Therapeutics agreeing to pay an upfront license fee, milestone payments tied to clinical trial phases, and royalties on product sales.PharmiWeb.comME Therapeutics Added to CSE25 IndexME Therapeutics Holdings Inc., a Vancouver-based biotechnology company focused on immuno-oncology drug development, has been added to the CSE25 Index, which comprises the 25 largest companies by market capitalization listed on the Canadian Securities Exchange. The index holds over 75% of the total market capitalization of the CSE Composite Index. CEO Salim Dhanji stated that the company is honored by the recognition and remains focused on advancing its pipeline of immuno-oncology therapies that reprogram the tumour microenvironment.