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EnGeneIC

Full company profile

uuid00054bv

Namestring
EnGeneIC
Legal namestring
EnGeneIC Limited
Websiteurl
engeneic.com
Company typeenum
Private
Founded yearint
2001
Descriptiontext

EnGeneIC Limited is a clinical-stage biopharmaceutical company founded in 2001, incorporated in Bermuda, headquartered in Sydney, Australia, with a US subsidiary (EnGeneIC Inc) in New York. The company develops targeted cyto-immunotherapy for solid tumors using its proprietary EnGeneIC Dream Vector (EDV) nanocell platform — bacterially-derived 400nm nanocells that can carry up to approximately one million drug molecules, functional nucleic acids (siRNA, miRNA, plasmid DNA), or immune-stimulating adjuvants directly into tumor cells while bypassing normal tissue and the blood-brain barrier. The platform combines direct cytotoxic payload delivery with simultaneous activation of both innate and adaptive anti-tumor immune responses (macrophages, NK cells, dendritic cells, and CD8+ T-cells), and is modular across cancer types by changing the targeting antibody — including CD-19 for B-cell lymphoma, asialoglycoprotein for liver cancer, and anti-ganglioside G2 for melanoma and neuroblastoma.

The company's lead clinical programs target glioblastoma multiforme, pancreatic cancer, mesothelioma, and other EGFR-expressing solid tumors. EnGeneIC holds 435+ granted patents across 19 patent families, has received FDA Orphan Drug Designation for glioblastoma (March 2017) and FDA Fast-Track Designation for pancreatic cancer (December 2023), and has reported a 37.5% response rate across 133 patients in first-in-man safety studies, with a 41-week median survival in mesothelioma patients. Manufacturing is conducted at an in-house pilot facility and through CDMO partner BioCina, with a research collaboration with Takeda for EDV-based immunomodulatory therapies and a clinical partnership with the Asbestos Diseases Research Institute for the MesomiR-1 mesothelioma program.

As a pre-revenue clinical-stage company, EnGeneIC's business model centers on advancing investigational therapies through clinical trials toward regulatory approval, with future revenue expected from licensing deals, milestone payments, and ultimately product commercialization. The company currently operates with 11-50 employees, has raised approximately $14.1 million in disclosed funding across multiple rounds since 2011 (including a $10M Series B in January 2015 led by a US institutional investor, with co-investors Foley Ventures and Shepherd Kaplan Krochuk), and runs clinical trials in Australia with planned expansion to Singapore and the United States for a Phase IIa glioblastoma program. Leadership comprises Joint CEO and Founder Jennifer MacDiarmid, Co-Founder and Co-Managing Director Himanshu Brahmbhatt, COO David Seaton, and CFO William Harris, with independent directors Professor Bryan Williams and Dr. Mark Levitt.

Short descriptiontext

EnGeneIC is a clinical-stage biopharmaceutical company developing targeted cancer therapies via its proprietary EDV nanocell platform, which delivers chemotherapeutics and nucleic acids directly to tumors while stimulating anti-tumor immune responses. It serves patients with aggressive solid tumors, notably glioblastoma and pancreatic cancer.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersSydney, Australia
HQ citystring
Sydney
HQ countrystring
Australia
HQ regionstring
Oceania
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
targeted cancer therapy, nanocell drug delivery, cyto-immunotherapy platform, oncology drug development, brain tumor therapy
Industry3 codes
1Antibody-Drug Conjugates (ADCs) & Antibody Conjugates
CodeHLAAAAAEPrimaryYes
2Cell Therapy Enabling Technologies (gene editing, cell engineering, delivery methods)
CodeHLAAABALPrimaryNo
3Therapeutic Vaccines (e.g., Cancer/Chronic Infection)
CodeHLAIAEAGPrimaryNo
NAICS code3 codes
  • Biological Product (except Diagnostic) Manufacturing325414
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
  • Pharmaceutical and Medicine Manufacturing3254
SIC code3 codes
  • Biological Products, (No Disgnostic Substances)2836
  • Pharmaceutical Preparations2834
  • Services-Commercial Physical & Biological Research8731
Product category
Oncology Biopharmaceuticals
Social media profiles3 records
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model1 record
1Clinical-stage biopharmaceutical development
TypeLicensing Royalties
Description

EnGeneIC is a clinical-stage biopharmaceutical company developing novel cancer therapies based on its proprietary EDV nanocell platform. Revenue is derived from development milestones, licensing deals, and ultimately product commercialization as the company advances multiple clinical-stage programs through regulatory approval.

engeneic.com
Marketing channels3 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

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

Cost components5 values
Personnel, Technology or R&D, Operations, Supply Chain, Infrastructure
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

EnGeneIC researches, develops, and manufactures investigational targeted cancer therapies built on its proprietary EDV (EnGeneIC Dream Vector) nanocell platform — bacterially-derived 400nm nanocells that deliver chemotherapeutics and functional nucleic acids (siRNA/miRNA) directly to tumor cells while simultaneously stimulating anti-tumor immune responses. The pipeline includes EGFR-targeted EDV therapies for glioblastoma multiforme, doxorubicin-loaded EDVs, microRNA replacement therapies (e.g., miR-16a for mesothelioma), and a COVID-19 EDV vaccine, all delivered through clinical-stage trials at partnered hospitals.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 4 values shown
  • 37.5% response rate in first-in-man safety studies with 50/133 patients showing clinical benefit
+3 more records
Product overview1 text field

EnGeneIC is a clinical-stage biopharmaceutical company developing its proprietary EDV™ (EnGeneIC Dream Vector) nanocell platform, a first-in-class cyto-immunotherapy technology. The platform comprises targeted nanocells (400nm) derived from bacteria that deliver therapeutic payloads directly to tumors while activating anti-tumor immune responses. The core EDV platform supports multiple therapeutic applications including EGFR-targeted therapies for glioblastoma and other solid tumors, microRNA replacement therapies, and a COVID-19 EDV vaccine. The platform is designed to carry various payloads including chemotherapeutic drugs (doxorubicin, PNU159682), functional nucleic acids (siRNA, miRNA, plasmid DNA), and immune-stimulating adjuvants.

Product and service4 records
1EnGeneIC Dream Vector (EDV™) Nanocell Platform
CategoryNanocell Drug Delivery Platform
Description

First-in-class cyto-immunotherapy platform using antibody-targeted, non-living bacterially-derived nanocells (400nm) to deliver chemotherapeutics and functional nucleic acids directly into tumor cells, bypassing the blood-brain barrier and stimulating anti-tumor immune responses. The platform is versatile across cancer types — the targeting antibody can be changed (e.g., EGFR for solid tumors, CD-19 for B-cell lymphoma, asialo-glycoprotein for liver cancer, anti-ganglioside G2 for melanoma and neuroblastoma). Each nanocell carries up to ~1 million drug molecules and is lyophilizable for 2+ year shelf storage.

2EGFR-Targeted EDV Therapy
CategoryOncology Therapeutics — Targeted Cytotoxic-Immunotherapy
Description

Investigational targeted cyto-immunotherapy using EGFR-targeted EDV nanocells loaded with doxorubicin and an immune-modulating adjuvant, designed to treat patients with recurrent glioblastoma multiforme and other EGFR-expressing solid tumors. Demonstrated ability to bypass the blood-brain barrier and deliver therapeutic payloads directly to brain tumors.

3EDV Doxorubicin
CategoryOncology Therapeutics — Chemotherapeutic-loaded Nanocell
Description

Bacterially-derived nanocell particles loaded with the chemotherapeutic doxorubicin and an immune-modulating adjuvant, designed to directly target cancer cells while simultaneously activating an anti-tumor immune response. Used as the cytotoxic payload within EGFR-targeted EDV therapy for glioblastoma and other EGFR-expressing solid tumors.

4COVID-EDV Vaccine
CategoryViral Vaccine — EDV-based Therapeutic Vaccine
Description

World-first nanocellular anti-COVID-19 vaccine using EDV technology to deliver interferon-stimulating molecules together with COVID-19 spike protein, producing a therapeutic vaccine intended to be effective against all variants and designed for immune-compromised patients. Developed from the EDV nanocell platform and trialled in healthy volunteers.

Scale indicator7 records

Each record includes

Type, Value, Description, Source

Partnership4 partners
Strategic tierCoreTypeStrategic or Co-development Partner
Description

EnGeneIC selected BioCina as global CDMO (Contract Development and Manufacturing Organization) to advance their groundbreaking cancer treatment. BioCina will support manufacturing scale-up for EDV-based cancer therapeutics.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Research collaboration with Takeda to develop EDV-based immunomodulatory therapies for oncology. Collaboration announced October 2016.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Collaboration for MesomiR-1 Phase 1 trial in late stage mesothelioma patients. Joint initiative to advance microRNA-based treatment using EDV nanocells.

Strategic tierMinorTypeStrategic or Co-development Partner
Description

EnGeneIC provided support for Foundation for Sarcoidosis Research's first New York fundraiser.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

French clinical-stage nanomedicine company developing nanoparticle-based cancer therapeutics (Hafnium oxide nanoparticles, NBTXR3). Directly comparable to EnGeneIC as a nanoparticle-delivery oncology platform targeting solid tumors with externally validated IP and clinical data.

TypeDirect peer
Description

Developed exosome-based therapeutic delivery platforms (engEx) for cancer and other diseases. Comparable to EnGeneIC's EDV nanocell platform as a biologic nanocarrier enabling targeted payload delivery to specific cell types.

TypeDirect peer
Description

Acquired by Pfizer in 2016, Bind developed Accurins — targeted nanoparticle therapeutics for oncology. Highly comparable as a nanoparticle-platform company using targeted delivery to solid tumors with platform optionality across indications.

TypeDirect peer
Description

Developed tumor-targeted nanoparticle-drug conjugates (CRLX101, CRLX301) using a cyclodextrin-PEG-based nanoparticle platform. Closely aligned with EDV nanocells as a tumor-targeted nanocarrier for oncology payloads.

TypeDirect peer
Description

Developed tumor-targeted gold nanoparticle delivery platform (Aurimune) loaded with TNF-alpha. Closely parallel to EnGeneIC's antibody-targeted nanocell approach for delivering potent oncology payloads with reduced systemic toxicity.

TypeRegional player
Description

Australian-headquartered clinical-stage oncology biotech developing targeted radiopharmaceuticals. Comparable as a regionally-similar Australian oncology platform with multiple clinical programs and a similar commercialization pathway to US/European markets.

TypeEmerging player
Description

Clinical-stage biotech developing TCR-based immunotherapies for solid tumors. Comparable as an emerging-platform oncology company developing targeted cancer therapies with multiple clinical-stage programs in solid tumor indications.

TypeEmerging player
Description

Clinical-stage oncology company developing therapeutics for glioblastoma multiforme (VAL-083). Comparable as a small-cap clinical-stage peer sharing EnGeneIC's high-risk, high-unmet-need GBM focus with similar Phase II/III trajectory requirements.

TypeBroad incumbent
Description

Developed liposomal cancer therapeutics (Onivyde) using nanoliposomal delivery. Comparable as a broader oncology platform player using encapsulated delivery vehicles for cytotoxic payloads in solid tumor indications.

TypeEmerging player
Description

Clinical-stage cell therapy company developing engineered TCR therapies for solid tumors. Comparable as a clinical-stage oncology platform peer pursuing novel modalities against hard-to-treat solid tumor indications with platform optionality.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat3 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

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

Segment1 record

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

Feature5 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles6 records

Each record includes

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

Subsidiaries1 record

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

Compliance8 records

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds4 records

Each record includes

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

Investors2 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 →

EnGeneIC

Oncology Biopharmaceuticalsengeneic.com

EnGeneIC is a clinical-stage biopharmaceutical company developing targeted cancer therapies via its proprietary EDV nanocell platform, which delivers chemotherapeutics and nucleic acids directly to tumors while stimulating anti-tumor immune responses. It serves patients with aggressive solid tumors, notably glioblastoma and pancreatic cancer.

What EnGeneIC does

EnGeneIC Limited is a clinical-stage biopharmaceutical company founded in 2001, incorporated in Bermuda, headquartered in Sydney, Australia, with a US subsidiary (EnGeneIC Inc) in New York. The company develops targeted cyto-immunotherapy for solid tumors using its proprietary EnGeneIC Dream Vector (EDV) nanocell platform — bacterially-derived 400nm nanocells that can carry up to approximately one million drug molecules, functional nucleic acids (siRNA, miRNA, plasmid DNA), or immune-stimulating adjuvants directly into tumor cells while bypassing normal tissue and the blood-brain barrier. The platform combines direct cytotoxic payload delivery with simultaneous activation of both innate and adaptive anti-tumor immune responses (macrophages, NK cells, dendritic cells, and CD8+ T-cells), and is modular across cancer types by changing the targeting antibody — including CD-19 for B-cell lymphoma, asialoglycoprotein for liver cancer, and anti-ganglioside G2 for melanoma and neuroblastoma.

The company's lead clinical programs target glioblastoma multiforme, pancreatic cancer, mesothelioma, and other EGFR-expressing solid tumors. EnGeneIC holds 435+ granted patents across 19 patent families, has received FDA Orphan Drug Designation for glioblastoma (March 2017) and FDA Fast-Track Designation for pancreatic cancer (December 2023), and has reported a 37.5% response rate across 133 patients in first-in-man safety studies, with a 41-week median survival in mesothelioma patients. Manufacturing is conducted at an in-house pilot facility and through CDMO partner BioCina, with a research collaboration with Takeda for EDV-based immunomodulatory therapies and a clinical partnership with the Asbestos Diseases Research Institute for the MesomiR-1 mesothelioma program.

As a pre-revenue clinical-stage company, EnGeneIC's business model centers on advancing investigational therapies through clinical trials toward regulatory approval, with future revenue expected from licensing deals, milestone payments, and ultimately product commercialization. The company currently operates with 11-50 employees, has raised approximately $14.1 million in disclosed funding across multiple rounds since 2011 (including a $10M Series B in January 2015 led by a US institutional investor, with co-investors Foley Ventures and Shepherd Kaplan Krochuk), and runs clinical trials in Australia with planned expansion to Singapore and the United States for a Phase IIa glioblastoma program. Leadership comprises Joint CEO and Founder Jennifer MacDiarmid, Co-Founder and Co-Managing Director Himanshu Brahmbhatt, COO David Seaton, and CFO William Harris, with independent directors Professor Bryan Williams and Dr. Mark Levitt.

EnGeneIC firmographics

Firmographics
Name
EnGeneIC
Legal name
EnGeneIC Limited
Website
https://engeneic.com
Company type
Private
Founded year
2001
Operating status
Operating
Headcount range
11–50 employees
Short description
EnGeneIC is a clinical-stage biopharmaceutical company developing targeted cancer therapies via its proprietary EDV nanocell platform, which delivers chemotherapeutics and nucleic acids directly to tumors while stimulating anti-tumor immune responses. It serves patients with aggressive solid tumors, notably glioblastoma and pancreatic cancer.
Ownership category
akta.pro rank

EnGeneIC industry classification

Industry
Product category
Oncology Biopharmaceuticals
NAICS
Biological Product (except Diagnostic) Manufacturing (325414), Research and Development in Biotechnology (except Nanobiotechnology) (541714), Pharmaceutical and Medicine Manufacturing (3254)
SIC
Biological Products, (No Disgnostic Substances) (2836), Pharmaceutical Preparations (2834), Services-Commercial Physical & Biological Research (8731)
akta.pro primary industry
Antibody-Drug Conjugates (ADCs) & Antibody Conjugates (HLAAAAAE)
akta.pro secondary industries
Cell Therapy Enabling Technologies (gene editing, cell engineering, delivery methods) (HLAAABAL), Therapeutic Vaccines (e.g., Cancer/Chronic Infection) (HLAIAEAG)

Keywords

  • Targeted cancer therapy
  • Nanocell drug delivery
  • Cyto-immunotherapy platform
  • Oncology drug development
  • Brain tumor therapy

Where EnGeneIC is headquartered

Location

Headquarters

HQ city
Sydney
HQ country
Australia
HQ region
Oceania

Offices2 records

Markets served

EnGeneIC business model

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

Revenue model

  1. Clinical-stage biopharmaceutical development: EnGeneIC is a clinical-stage biopharmaceutical company developing novel cancer therapies based on its proprietary EDV nanocell platform. Revenue is derived from development milestones, licensing deals, and ultimately product commercialization as the company advances multiple clinical-stage programs through regulatory approval.

Go-to-market motion2 records

Distribution channels1 record

Marketing channels3 records

EnGeneIC product offering

Product offering

Core offering

EnGeneIC researches, develops, and manufactures investigational targeted cancer therapies built on its proprietary EDV (EnGeneIC Dream Vector) nanocell platform — bacterially-derived 400nm nanocells that deliver chemotherapeutics and functional nucleic acids (siRNA/miRNA) directly to tumor cells while simultaneously stimulating anti-tumor immune responses. The pipeline includes EGFR-targeted EDV therapies for glioblastoma multiforme, doxorubicin-loaded EDVs, microRNA replacement therapies (e.g., miR-16a for mesothelioma), and a COVID-19 EDV vaccine, all delivered through clinical-stage trials at partnered hospitals.

Product overview

EnGeneIC is a clinical-stage biopharmaceutical company developing its proprietary EDV™ (EnGeneIC Dream Vector) nanocell platform, a first-in-class cyto-immunotherapy technology. The platform comprises targeted nanocells (400nm) derived from bacteria that deliver therapeutic payloads directly to tumors while activating anti-tumor immune responses. The core EDV platform supports multiple therapeutic applications including EGFR-targeted therapies for glioblastoma and other solid tumors, microRNA replacement therapies, and a COVID-19 EDV vaccine. The platform is designed to carry various payloads including chemotherapeutic drugs (doxorubicin, PNU159682), functional nucleic acids (siRNA, miRNA, plasmid DNA), and immune-stimulating adjuvants.

Differentiator

Problem solved

Functional benefit

Products and services

  • EnGeneIC Dream Vector (EDV™) Nanocell Platform First-in-class cyto-immunotherapy platform using antibody-targeted, non-living bacterially-derived nanocells (400nm) to deliver chemotherapeutics and functional nucleic acids directly into tumor cells, bypassing the blood-brain barrier and stimulating anti-tumor immune responses. The platform is versatile across cancer types — the targeting antibody can be changed (e.g., EGFR for solid tumors, CD-19 for B-cell lymphoma, asialo-glycoprotein for liver cancer, anti-ganglioside G2 for melanoma and neuroblastoma). Each nanocell carries up to ~1 million drug molecules and is lyophilizable for 2+ year shelf storage.
  • EGFR-Targeted EDV Therapy Investigational targeted cyto-immunotherapy using EGFR-targeted EDV nanocells loaded with doxorubicin and an immune-modulating adjuvant, designed to treat patients with recurrent glioblastoma multiforme and other EGFR-expressing solid tumors. Demonstrated ability to bypass the blood-brain barrier and deliver therapeutic payloads directly to brain tumors.
  • EDV Doxorubicin Bacterially-derived nanocell particles loaded with the chemotherapeutic doxorubicin and an immune-modulating adjuvant, designed to directly target cancer cells while simultaneously activating an anti-tumor immune response. Used as the cytotoxic payload within EGFR-targeted EDV therapy for glioblastoma and other EGFR-expressing solid tumors.
  • COVID-EDV Vaccine World-first nanocellular anti-COVID-19 vaccine using EDV technology to deliver interferon-stimulating molecules together with COVID-19 spike protein, producing a therapeutic vaccine intended to be effective against all variants and designed for immune-compromised patients. Developed from the EDV nanocell platform and trialled in healthy volunteers.

Quantifiable outcome

  • 37.5% response rate in first-in-man safety studies with 50/133 patients showing clinical benefit
  • +3 more outcomes

Companies that use EnGeneIC

Customer profile

Named customers2 records

Segments1 record

Ideal customer profiles2 records

EnGeneIC technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature5 records

EnGeneIC partnerships and signals

Strategic signal

Partnerships

Four partnerships are on record, tiered core and minor.

  • BioCinacoreStrategic or Co-development PartnerEnGeneIC selected BioCina as global CDMO (Contract Development and Manufacturing Organization) to advance their groundbreaking cancer treatment. BioCina will support manufacturing scale-up for EDV-based cancer therapeutics.
  • TakedacoreStrategic or Co-development PartnerResearch collaboration with Takeda to develop EDV-based immunomodulatory therapies for oncology. Collaboration announced October 2016.
  • Asbestos Diseases Research InstitutecoreStrategic or Co-development PartnerCollaboration for MesomiR-1 Phase 1 trial in late stage mesothelioma patients. Joint initiative to advance microRNA-based treatment using EDV nanocells.
  • Foundation for Sarcoidosis ResearchminorStrategic or Co-development PartnerEnGeneIC provided support for Foundation for Sarcoidosis Research's first New York fundraiser.

Scale indicators7 records

Recent moves6 records

Expansion highlights6 records

EnGeneIC competitors and assessment

Company assessment

Direct peers

  • Nanobiotix: French clinical-stage nanomedicine company developing nanoparticle-based cancer therapeutics (Hafnium oxide nanoparticles, NBTXR3). Directly comparable to EnGeneIC as a nanoparticle-delivery oncology platform targeting solid tumors with externally validated IP and clinical data.
  • Codiak BioSciences: Developed exosome-based therapeutic delivery platforms (engEx) for cancer and other diseases. Comparable to EnGeneIC's EDV nanocell platform as a biologic nanocarrier enabling targeted payload delivery to specific cell types.
  • Bind Therapeutics: Acquired by Pfizer in 2016, Bind developed Accurins — targeted nanoparticle therapeutics for oncology. Highly comparable as a nanoparticle-platform company using targeted delivery to solid tumors with platform optionality across indications.
  • Cerulean Pharma: Developed tumor-targeted nanoparticle-drug conjugates (CRLX101, CRLX301) using a cyclodextrin-PEG-based nanoparticle platform. Closely aligned with EDV nanocells as a tumor-targeted nanocarrier for oncology payloads.
  • CytImmune Sciences: Developed tumor-targeted gold nanoparticle delivery platform (Aurimune) loaded with TNF-alpha. Closely parallel to EnGeneIC's antibody-targeted nanocell approach for delivering potent oncology payloads with reduced systemic toxicity.

Regional players

  • Telix Pharmaceuticals: Australian-headquartered clinical-stage oncology biotech developing targeted radiopharmaceuticals. Comparable as a regionally-similar Australian oncology platform with multiple clinical programs and a similar commercialization pathway to US/European markets.

Emerging players

  • Immatics: Clinical-stage biotech developing TCR-based immunotherapies for solid tumors. Comparable as an emerging-platform oncology company developing targeted cancer therapies with multiple clinical-stage programs in solid tumor indications.
  • Kintara Therapeutics: Clinical-stage oncology company developing therapeutics for glioblastoma multiforme (VAL-083). Comparable as a small-cap clinical-stage peer sharing EnGeneIC's high-risk, high-unmet-need GBM focus with similar Phase II/III trajectory requirements.
  • Adaptimmune Therapeutics: Clinical-stage cell therapy company developing engineered TCR therapies for solid tumors. Comparable as a clinical-stage oncology platform peer pursuing novel modalities against hard-to-treat solid tumor indications with platform optionality.

Broad incumbents

  • Merrimack Pharmaceuticals: Developed liposomal cancer therapeutics (Onivyde) using nanoliposomal delivery. Comparable as a broader oncology platform player using encapsulated delivery vehicles for cytotoxic payloads in solid tumor indications.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat3 records

Key risks6 records

Key highlights7 records

Customer concentration

EnGeneIC social profiles

Digital presence

EnGeneIC compliance and trust

Trust signal

Compliance8 records

EnGeneIC financial estimates

Financial estimate

Revenue estimate

Valuation estimate

EnGeneIC leadership team

Management profile

Number of profiles

Profiles6 records

EnGeneIC subsidiaries and ownership

Company hierarchy

Subsidiaries1 record

EnGeneIC funding detail

Funding detail

Funding overview

Funding rounds4 records

Investors2 records

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

EnGeneIC 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 EnGeneIC

What does EnGeneIC do?

EnGeneIC researches, develops, and manufactures investigational targeted cancer therapies built on its proprietary EDV (EnGeneIC Dream Vector) nanocell platform — bacterially-derived 400nm nanocells that deliver chemotherapeutics and functional nucleic acids (siRNA/miRNA) directly to tumor cells while simultaneously stimulating anti-tumor immune responses. The pipeline includes EGFR-targeted EDV therapies for glioblastoma multiforme, doxorubicin-loaded EDVs, microRNA replacement therapies (e.g., miR-16a for mesothelioma), and a COVID-19 EDV vaccine, all delivered through clinical-stage trials at partnered hospitals.

Is EnGeneIC a public or private company?

EnGeneIC is a private company. It is classified as venture growth investor backed and is currently operating.

When was EnGeneIC founded?

EnGeneIC was founded in 2001. It employs 11 to 50 people.

Where is EnGeneIC based?

EnGeneIC is headquartered in Sydney, Australia, in the Oceania region.

How does EnGeneIC make money?

One revenue line is on record: clinical-stage biopharmaceutical development.

Who are EnGeneIC's main competitors?

Direct peers on record are Nanobiotix, Codiak BioSciences, Bind Therapeutics, Cerulean Pharma and CytImmune Sciences. Telix Pharmaceuticals is listed as a regional player. Emerging players are Immatics, Kintara Therapeutics and Adaptimmune Therapeutics. Merrimack Pharmaceuticals is listed as a broad incumbent.

Does EnGeneIC have an API?

No public API is recorded for EnGeneIC.

What industry is EnGeneIC in?

EnGeneIC's product category is Oncology Biopharmaceuticals. Its primary akta.pro industry code is HLAAAAAE, Antibody-Drug Conjugates (ADCs) & Antibody Conjugates, with a secondary code of HLAAABAL, Cell Therapy Enabling Technologies (gene editing, cell engineering, delivery methods). Its NAICS code is 325414 and its SIC code is 2836.

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Live signals
GlobeNewswireEnGeneIC Honored with 2026 Breakthrough in Glioblastoma Biotech Award at Northwell Foundation Lenox Hill Neurosurgery Brain Cancer Gala in New YorkEnGeneIC Limited was awarded the Breakthrough in Glioblastoma Biotech Award 2026 at the Northwell Foundation Lenox Hill Neurosurgery Brain Tumor Center Gala in New York on June 4, 2026. The award recognizes the company's advancement of its proprietary EnGeneIC Dream Vector (EDV™) nanocell platform, designed to bypass the blood-brain barrier and deliver therapeutic payloads directly to tumors while activating anti-tumor immune responses. EnGeneIC is advancing multiple clinical-stage programs and is working toward initiating a Phase IIa glioblastoma trial in the United States.Business InsiderEnGeneIC Honored with 2026 Breakthrough in Glioblastoma Biotech Award at Northwell Foundation Lenox Hill Neurosurgery Brain Cancer Gala in New YorkEnGeneIC Limited received the 2026 Breakthrough in glioblastoma Biotech Award at the Northwell Foundation Gala in New York for its development of targeted cyto-immunotherapy using its EDV nanocell platform. The award recognizes advances that could significantly improve treatment options for glioblastoma and other cancers.GlobeNewswireEnGeneIC Announces First Patient Dosed in Recurrent Glioblastoma Clinical TrialEnGeneIC Limited announced that the first patient has been dosed in a clinical trial evaluating its investigational EGFR-targeted EDV therapy for recurrent glioblastoma multiforme, an aggressive and currently incurable form of brain cancer. The trial is being conducted at Australian sites including Westmead Hospital and the Kinghorn Cancer Centre, with planned expansion to clinical sites in Singapore. The therapy uses bacterially-derived nanocell particles loaded with doxorubicin and an immune-modulating adjuvant to target cancer cells while simultaneously activating an anti-tumour immune response.GlobeNewswireEnGeneIC Announces First Patient Dosed in Recurrent Glioblastoma Clinical TrialEnGeneIC announced the first patient dosed in its clinical trial of EGFR-targeted EDV therapy for recurrent glioblastoma, led by Dr. Mark Wong at Westmead Hospital. The trial evaluates the dual-payload EDVs, combining doxorubicin and α-GalCer, with recruitment planned at Australian and Singaporean sites.GlobeNewswireEnGeneIC and Singapore Institute of Advanced Medicine Holdings Forge Strategic Partnership to Revolutionise Cancer Treatment in AsiaEnGeneIC announced strategic partnerships with Singapore Institute of Advanced Medicine Holdings and Singapore Medical Incorporation to fund its clinical trials in Australia and the USA. The deal grants SAM exclusive rights to sell EnGeneIC's EDV therapeutics in Asia, with net profits shared and EnGeneIC receiving a majority. The companies will also collaborate on EDV-based theranostics.GlobeNewswireEnGeneIC’s breakthrough Armed Nanocell Drug Conjugate (ANDC) treatment shows promising results in Pancreatic cancer patients who have run out of treatment optionsEnGeneIC published trial results in Clinical Cancer Research showing its EDV nanocell drug conjugate (ANDC) treatment for pancreatic cancer. The study found 88% of patients surpassed double historical survival rates, with the longest survivor living 19.7 months and minimal toxicity. The company plans Phase IIa trials in Australia and the USA.GlobeNewswireNovember is Pancreatic Cancer Awareness MonthEnGeneIC's EDV nanocell therapy for pancreatic cancer has received FDA IND acceptance for a US Phase II trial. A Los Angeles patient with metastatic PDAC achieved complete remission after 15 months of treatment, with cancer disappearing and minimal side effects. The company is now entering Phase IIa trials for intractable cancers.GlobeNewswireEnGeneIC publishes the COVID-EDV vaccine’s novel mechanism of action in a leading Immunology journalEnGeneIC published its COVID-EDV vaccine's novel mechanism in Frontiers in Immunology, showing high-affinity antibodies neutralizing 90-100% of COVID variants in mice and human volunteers. The vaccine, stored at room temperature, has been tested in 80 volunteers with no side effects, and trials in immune-compromised patients are underway.GlobeNewswireEnGeneIC’s second generation COVID-19 vaccine protects against all variantsEnGeneIC's second-generation COVID-19 vaccine, tested in Sydney and Melbourne, showed high-affinity antibodies neutralizing all variants, including Omicron, in 27 of 32 healthy participants. The company plans trials for immune-compromised individuals and Australians over 75 in July/August.