Developer docs
API playgroundTry for free, no card

Search company profiles

Medicenna Therapeutics

Full company profile

uuid0002zgw

Namestring
Medicenna Therapeutics
Legal namestring
Medicenna Therapeutics Corp.
Websiteurl
medicenna.com
Company typeenum
Public
Founded yearint
2012
Descriptiontext

Medicenna Therapeutics is a clinical-stage immunotherapy company developing engineered interleukin-based therapies for cancer and immune-driven diseases. The company operates three proprietary platforms — Superkine (engineered IL-2, IL-4, and IL-13 variants optimized for receptor selectivity, potency, half-life, and tissue distribution), BiSKIT (Bi-functional SuperKine Immuno-Therapy fusing Superkines with antibodies or other proteins to modulate two signaling pathways simultaneously), and T-MASK (Targeted Metallo-protease Activated SuperKines that remain masked in healthy tissue and activate only at disease sites) — built on directed evolution and AI-driven rational design. The clinical pipeline is led by MDNA11, a long-acting beta-enhanced IL-2 Superkine in Phase 1/2 for advanced solid tumors that demonstrated a 36% objective response rate as monotherapy and 43% in combination with pembrolizumab; MDNA113, a first-in-class anti-PD-1 x IL-2 bifunctional Superkine advancing toward IND submission in H2 2026; and bizaxofusp (MDNA55), a Phase 3-ready IL-4-toxin fusion for recurrent glioblastoma that holds FDA Fast Track and Orphan Drug designations. The pipeline also includes preclinical autoimmune and inflammatory candidates MDNA209 and MDNA413.

Medicenna is pre-revenue and operates from Toronto, Canada, with additional offices in Houston, Texas. The company employs between 11 and 50 people and is publicly listed on the TSX under ticker MDNA:CA. Its go-to-market model is enterprise pharma partnering: it pursues co-development, out-licensing, and research collaborations (exemplified by a clinical trial collaboration and supply agreement with Merck for pembrolizumab in the ABILITY-1 study and an investigator-initiated trial with Fondazione Melanoma Onlus in Italy) rather than building its own commercial sales force. Clinical trials run globally across the US, Canada, Australia, Ireland, Portugal, Spain, and Italy. Revenue, when generated, is expected to flow from licensing royalties or partnership upfronts rather than direct product sales, as none of its candidates are approved or commercialized. The company has raised over US$40 million equivalent in equity financings since 2022, including a CA$20 million private placement from RA Capital Management in April 2024, while reporting an $18.4 million net loss for fiscal year 2026 and holding $6.3 million in cash as of March 2026.

Short descriptiontext

Medicenna Therapeutics is a clinical-stage immunotherapy company developing engineered interleukin-based therapies through its Superkine, BiSKIT, and T-MASK platforms for cancer, autoimmune, and inflammatory diseases, pursuing partnerships with pharmaceutical companies for development and commercialization.

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

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
engineered interleukin therapies, cancer immunotherapy drugs, superkine biologics platform, clinical-stage biopharmaceuticals, immuno-oncology pipeline
Industry3 codes
1Cytokines, Interferons & Immunomodulatory Proteins
CodeHLAAAAACPrimaryYes
2Immunology & Autoimmune Specialty Pharmaceuticals
CodeHLAIACABPrimaryNo
3Oncology & Hematology Pharmaceuticals
CodeHLAIAAACPrimaryNo
NAICS code2 codes
  • Biological Product (except Diagnostic) Manufacturing325414
  • Pharmaceutical Preparation Manufacturing325412
SIC code2 codes
  • Biological Products, (No Disgnostic Substances)2836
  • Pharmaceutical Preparations2834
Product category
Immuno-oncology biopharmaceuticals
Social media profiles1 record
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model1 record
1Therapeutic Product Development and Commercialization
TypeLicensing Royalties
Description

Medicenna is a pre-revenue clinical-stage immunotherapy company. Its revenue model is based on developing and commercializing proprietary interleukin-based therapies for cancer and autoimmune diseases. Revenue will be derived from product sales upon regulatory approval or from licensing/partnership deals with pharmaceutical companies for co-development and commercialization rights.

medicenna.com
Marketing channels5 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
Technology or R&D, Personnel, Operations, Marketing or Sales, Others
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 3 records shown
1Superkine
Description

Interleukins engineered to deliver properties that natural interleukins cannot achieve, optimized for receptor selectivity, potency, half-life and tissue distribution.

medicenna.com
+2 more records
Core offering1 text field

Medicenna Therapeutics is a clinical-stage immunotherapy company that develops engineered interleukin-based therapies (Superkines) for cancer and immune-driven diseases. It operates three proprietary platforms — Superkine, BiSKIT, and T-MASK — built on directed evolution and AI-driven rational design, and advances a pipeline of drug candidates including MDNA11 (IL-2 Superkine), MDNA113 (anti-PD-1 x IL-2 BiSKIT), bizaxofusp/MDNA55 (IL-4-toxin fusion for recurrent glioblastoma), MDNA209 and MDNA413 (super-antagonists for autoimmune/inflammatory diseases). Revenue is expected to be generated through product sales and out-licensing/co-development partnerships with pharmaceutical companies.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 4 values shown
  • MDNA11 achieved 36% objective response rate as monotherapy and 43% in combination with pembrolizumab in the ABILITY-1 study in patients with solid tumors following checkpoint therapy failure
+3 more records
Product overview1 text field

Medicenna Therapeutics is a clinical-stage immunotherapy company developing engineered interleukin-based therapies through three proprietary technology platforms: Superkine (IL-2, IL-4, IL-13 Superkines), BiSKIT (Bi-functional SuperKine Immuno-Therapy), and T-MASK (Targeted Metallo-protease Activated SuperKines). The lead clinical candidate MDNA11 is an IL-2 Superkine in Phase 1/2 for solid tumors, with MDNA113 (anti-PD-1-IL-2 BiSKIT) advancing toward IND submission. The pipeline includes MDNA209 and MDNA413 for autoimmune/inflammatory diseases, and bizaxofusp (MDNA55), a Phase 3-ready IL-4-toxin fusion for recurrent glioblastoma with FDA Fast Track and Orphan Drug designation. Medicenna utilizes directed evolution and AI-driven rational design to engineer interleukins for precision immune modulation.

Product and service5 records
1MDNA11
CategoryClinical-stage oncology drug candidate
Description

Long-acting, beta-enhanced IL-2 Superkine designed to selectively signal through the IL-2 beta receptor on cancer-fighting immune cells, enabling once-every-two-weeks dosing for advanced solid tumors as monotherapy and in combination with pembrolizumab.

2MDNA113
CategoryClinical-stage oncology drug candidate
Description

First-in-class tumor-anchored anti-PD-1 x IL-2 bifunctional Superkine (BiSKIT/T-MASK) being developed for solid tumors expressing IL-13Rα2, with a significantly wider therapeutic window than alpha-biased comparators that caused vascular leak syndrome.

3Bizaxofusp (MDNA55)
CategoryClinical-stage oncology drug candidate
Description

First-in-class IL-4-toxin fusion therapy that selectively targets IL-4R-expressing myeloid-derived suppressor cells in the tumor microenvironment of recurrent glioblastoma, inducing immunogenic cell death; Phase 3-ready with FDA Fast Track and Orphan Drug designations.

4MDNA209
CategoryPreclinical-stage autoimmune drug candidate
Description

IL-2/IL-15 pathway super antagonist Superkine in preclinical development for autoimmune diseases, designed to selectively dampen pathogenic immune signaling.

5MDNA413
CategoryPreclinical-stage inflammatory disease drug candidate
Description

IL-4/IL-13 pathway super antagonist Superkine in preclinical development for inflammatory diseases, designed to selectively modulate type 2 immune signaling.

Scale indicator9 records

Each record includes

Type, Value, Description, Source

Partnership3 partners
Strategic tierCoreTypeStrategic or Co-development Partner
Description

Medicenna has a clinical trial collaboration and supply agreement with Merck (known as MSD outside the US and Canada) to evaluate MDNA11 in combination with pembrolizumab (KEYTRUDA) in the Phase 1/2 ABILITY-1 study. Medicenna is the study sponsor and Merck supplies pembrolizumab. The collaboration explores combining MDNA11 with checkpoint inhibitors to enhance anti-tumor immune responses.

2Fondazione Melanoma Onlus — NEO-CYT Study
Strategic tierCoreTypeStrategic or Co-development Partner
Description

Medicenna is collaborating with Fondazione Melanoma Onlus, a leading Italian melanoma research organization, in an investigator-initiated trial assessing MDNA11 in combination with nivolumab with and without ipilimumab in high-risk, surgically resectable Stage III cutaneous melanoma in the neoadjuvant setting. Fondazione Melanoma is the study sponsor and Medicenna supplies study medication. Led by Professor Paolo A. Ascierto at the Istituto Nazionale Tumori Fondazione G. Pascale in Naples, Italy.

medicenna.com
Strategic tierCoreTypeChannel Partner/ Reseller/ Distributor
Description

Bloom Burton Securities Inc. acted as the sole agent for Medicenna's marketed public offering of units in May 2026, raising approximately CDN$4.44 million in gross proceeds. Bloom Burton received a 7% cash commission. The firm is a Canadian healthcare-focused investment bank.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Clinical-stage oncology company developing conditionally activated engineered cytokines (PREDATOR platform) including IL-2 and IL-12 variants for solid tumors. Most direct competitor to Medicenna's Superkine and T-MASK platforms, with a similar mask-based tumor-localization strategy.

TypeDirect peer
Description

Engineered cytokine company developing optimized IL-2, IL-15, and IL-21 therapeutics for cancer and autoimmune disease. Directly comparable to Medicenna in both cytokine engineering technology and oncology/autoimmune dual focus.

TypeDirect peer
Description

Clinical-stage biotech developing tumor-activated immunotherapies, including masked cytokines (IL-2, IL-12) and IL-15. Shares Medicenna's masked-cytokine (T-MASK-like) approach to localizing immune activation in the tumor microenvironment.

TypeDirect peer
Description

Clinical-stage company developing IL-2-based biologics (Immuno-STAT platform) that selectively modulate T cell activity for cancer and autoimmune disease. Comparable approach to Medicenna's BiSKIT bispecific cytokine fusions.

TypeDirect peer
Description

Developer of N-803 (nogapendekin alfa inbakicept-pmln), an IL-15 superagonist approved for BCG-unresponsive non-muscle invasive bladder cancer. Closest commercial-stage analog to Medicenna's engineered IL-2/IL-15 cytokine approach.

TypeDirect peer
Description

Developer of NKTR-358 (rezpegaldesleukin), a PEGylated IL-2 for autoimmune disease, and other cytokine-based therapies. Directly comparable to Medicenna's MDNA209 autoimmune program and broader IL-2 engineering pipeline.

TypeBroad incumbent
Description

Global pharmaceutical company that developed bempegaldesleukin (PEG-IL-2) and runs multiple IL-2, IL-12, and cytokine programs. Represents the incumbent competitive threat to Medicenna's IL-2 franchise in oncology.

TypeBroad incumbent
Description

Medicenna's clinical trial collaboration partner on MDNA11 + pembrolizumab (KEYTRUDA). As a broad incumbent with established checkpoint franchises and internal cytokine programs, Merck is both a validation partner and a potential long-term competitive threat.

TypeBroad incumbent
Description

Global pharmaceutical company with multiple engineered IL-2 variant programs in oncology and a leadership position in immuno-oncology. Represents the larger-platform incumbent competing in the same cytokine-engineering space as Medicenna.

TypeEmerging player
Description

Clinical-stage oncology company developing paxalisib for glioblastoma and other brain cancers. Relevant emerging peer given overlapping glioblastoma indication with Medicenna's bizaxofusp (MDNA55) program.

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 highlights6 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers3 records

Each record includes

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

Feature6 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles5 records

Each record includes

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

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds8 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 →

Medicenna Therapeutics

Immuno-oncology biopharmaceuticalsmedicenna.com

Medicenna Therapeutics is a clinical-stage immunotherapy company developing engineered interleukin-based therapies through its Superkine, BiSKIT, and T-MASK platforms for cancer, autoimmune, and inflammatory diseases, pursuing partnerships with pharmaceutical companies for development and commercialization.

What Medicenna Therapeutics does

Medicenna Therapeutics is a clinical-stage immunotherapy company developing engineered interleukin-based therapies for cancer and immune-driven diseases. The company operates three proprietary platforms — Superkine (engineered IL-2, IL-4, and IL-13 variants optimized for receptor selectivity, potency, half-life, and tissue distribution), BiSKIT (Bi-functional SuperKine Immuno-Therapy fusing Superkines with antibodies or other proteins to modulate two signaling pathways simultaneously), and T-MASK (Targeted Metallo-protease Activated SuperKines that remain masked in healthy tissue and activate only at disease sites) — built on directed evolution and AI-driven rational design. The clinical pipeline is led by MDNA11, a long-acting beta-enhanced IL-2 Superkine in Phase 1/2 for advanced solid tumors that demonstrated a 36% objective response rate as monotherapy and 43% in combination with pembrolizumab; MDNA113, a first-in-class anti-PD-1 x IL-2 bifunctional Superkine advancing toward IND submission in H2 2026; and bizaxofusp (MDNA55), a Phase 3-ready IL-4-toxin fusion for recurrent glioblastoma that holds FDA Fast Track and Orphan Drug designations. The pipeline also includes preclinical autoimmune and inflammatory candidates MDNA209 and MDNA413.

Medicenna is pre-revenue and operates from Toronto, Canada, with additional offices in Houston, Texas. The company employs between 11 and 50 people and is publicly listed on the TSX under ticker MDNA:CA. Its go-to-market model is enterprise pharma partnering: it pursues co-development, out-licensing, and research collaborations (exemplified by a clinical trial collaboration and supply agreement with Merck for pembrolizumab in the ABILITY-1 study and an investigator-initiated trial with Fondazione Melanoma Onlus in Italy) rather than building its own commercial sales force. Clinical trials run globally across the US, Canada, Australia, Ireland, Portugal, Spain, and Italy. Revenue, when generated, is expected to flow from licensing royalties or partnership upfronts rather than direct product sales, as none of its candidates are approved or commercialized. The company has raised over US$40 million equivalent in equity financings since 2022, including a CA$20 million private placement from RA Capital Management in April 2024, while reporting an $18.4 million net loss for fiscal year 2026 and holding $6.3 million in cash as of March 2026.

Medicenna Therapeutics firmographics

Firmographics
Name
Medicenna Therapeutics
Legal name
Medicenna Therapeutics Corp.
Website
https://medicenna.com
Company type
Public
Founded year
2012
Operating status
Operating
Headcount range
11–50 employees
Short description
Medicenna Therapeutics is a clinical-stage immunotherapy company developing engineered interleukin-based therapies through its Superkine, BiSKIT, and T-MASK platforms for cancer, autoimmune, and inflammatory diseases, pursuing partnerships with pharmaceutical companies for development and commercialization.
Ownership category
akta.pro rank

Medicenna Therapeutics industry classification

Industry
Product category
Immuno-oncology biopharmaceuticals
NAICS
Biological Product (except Diagnostic) Manufacturing (325414), Pharmaceutical Preparation Manufacturing (325412)
SIC
Biological Products, (No Disgnostic Substances) (2836), Pharmaceutical Preparations (2834)
akta.pro primary industry
Cytokines, Interferons & Immunomodulatory Proteins (HLAAAAAC)
akta.pro secondary industries
Immunology & Autoimmune Specialty Pharmaceuticals (HLAIACAB), Oncology & Hematology Pharmaceuticals (HLAIAAAC)

Keywords

  • Engineered interleukin therapies
  • Cancer immunotherapy drugs
  • Superkine biologics platform
  • Clinical-stage biopharmaceuticals
  • Immuno-oncology pipeline

Where Medicenna Therapeutics is headquartered

Location

Headquarters

HQ city
Toronto
HQ country
Canada
HQ region
North America

Offices2 records

Markets served

Medicenna Therapeutics business model

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

Revenue model

  1. Therapeutic Product Development and Commercialization: Medicenna is a pre-revenue clinical-stage immunotherapy company. Its revenue model is based on developing and commercializing proprietary interleukin-based therapies for cancer and autoimmune diseases. Revenue will be derived from product sales upon regulatory approval or from licensing/partnership deals with pharmaceutical companies for co-development and commercialization rights.

Go-to-market motion2 records

Distribution channels1 record

Marketing channels5 records

Medicenna Therapeutics product offering

Product offering

Core offering

Medicenna Therapeutics is a clinical-stage immunotherapy company that develops engineered interleukin-based therapies (Superkines) for cancer and immune-driven diseases. It operates three proprietary platforms — Superkine, BiSKIT, and T-MASK — built on directed evolution and AI-driven rational design, and advances a pipeline of drug candidates including MDNA11 (IL-2 Superkine), MDNA113 (anti-PD-1 x IL-2 BiSKIT), bizaxofusp/MDNA55 (IL-4-toxin fusion for recurrent glioblastoma), MDNA209 and MDNA413 (super-antagonists for autoimmune/inflammatory diseases). Revenue is expected to be generated through product sales and out-licensing/co-development partnerships with pharmaceutical companies.

Product overview

Medicenna Therapeutics is a clinical-stage immunotherapy company developing engineered interleukin-based therapies through three proprietary technology platforms: Superkine (IL-2, IL-4, IL-13 Superkines), BiSKIT (Bi-functional SuperKine Immuno-Therapy), and T-MASK (Targeted Metallo-protease Activated SuperKines). The lead clinical candidate MDNA11 is an IL-2 Superkine in Phase 1/2 for solid tumors, with MDNA113 (anti-PD-1-IL-2 BiSKIT) advancing toward IND submission. The pipeline includes MDNA209 and MDNA413 for autoimmune/inflammatory diseases, and bizaxofusp (MDNA55), a Phase 3-ready IL-4-toxin fusion for recurrent glioblastoma with FDA Fast Track and Orphan Drug designation. Medicenna utilizes directed evolution and AI-driven rational design to engineer interleukins for precision immune modulation.

Differentiator

Problem solved

Functional benefit

Brands

  • Superkine: Interleukins engineered to deliver properties that natural interleukins cannot achieve, optimized for receptor selectivity, potency, half-life and tissue distribution.
  • BiSKIT (Bi-functional SuperKine Immuno-Therapy)
  • T-MASK (Targeted Metallo-protease Activated SuperKines)

Products and services

  • MDNA11 Long-acting, beta-enhanced IL-2 Superkine designed to selectively signal through the IL-2 beta receptor on cancer-fighting immune cells, enabling once-every-two-weeks dosing for advanced solid tumors as monotherapy and in combination with pembrolizumab.
  • MDNA113 First-in-class tumor-anchored anti-PD-1 x IL-2 bifunctional Superkine (BiSKIT/T-MASK) being developed for solid tumors expressing IL-13Rα2, with a significantly wider therapeutic window than alpha-biased comparators that caused vascular leak syndrome.
  • Bizaxofusp (MDNA55) First-in-class IL-4-toxin fusion therapy that selectively targets IL-4R-expressing myeloid-derived suppressor cells in the tumor microenvironment of recurrent glioblastoma, inducing immunogenic cell death; Phase 3-ready with FDA Fast Track and Orphan Drug designations.
  • MDNA209 IL-2/IL-15 pathway super antagonist Superkine in preclinical development for autoimmune diseases, designed to selectively dampen pathogenic immune signaling.
  • MDNA413 IL-4/IL-13 pathway super antagonist Superkine in preclinical development for inflammatory diseases, designed to selectively modulate type 2 immune signaling.

Quantifiable outcome

  • MDNA11 achieved 36% objective response rate as monotherapy and 43% in combination with pembrolizumab in the ABILITY-1 study in patients with solid tumors following checkpoint therapy failure
  • +3 more outcomes

Companies that use Medicenna Therapeutics

Customer profile

Named customers3 records

Segments1 record

Ideal customer profiles2 records

Medicenna 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

Medicenna Therapeutics partnerships and signals

Strategic signal

Partnerships

Three partnerships are on record, tiered core.

  • Merck (MSD) — ABILITY-1 Clinical CollaborationcoreStrategic or Co-development PartnerMedicenna has a clinical trial collaboration and supply agreement with Merck (known as MSD outside the US and Canada) to evaluate MDNA11 in combination with pembrolizumab (KEYTRUDA) in the Phase 1/2 ABILITY-1 study. Medicenna is the study sponsor and Merck supplies pembrolizumab. The collaboration explores combining MDNA11 with checkpoint inhibitors to enhance anti-tumor immune responses.
  • Fondazione Melanoma Onlus — NEO-CYT StudycoreStrategic or Co-development PartnerMedicenna is collaborating with Fondazione Melanoma Onlus, a leading Italian melanoma research organization, in an investigator-initiated trial assessing MDNA11 in combination with nivolumab with and without ipilimumab in high-risk, surgically resectable Stage III cutaneous melanoma in the neoadjuvant setting. Fondazione Melanoma is the study sponsor and Medicenna supplies study medication. Led by Professor Paolo A. Ascierto at the Istituto Nazionale Tumori Fondazione G. Pascale in Naples, Italy.
  • Bloom Burton Securities Inc.coreChannel Partner/ Reseller/ DistributorBloom Burton Securities Inc. acted as the sole agent for Medicenna's marketed public offering of units in May 2026, raising approximately CDN$4.44 million in gross proceeds. Bloom Burton received a 7% cash commission. The firm is a Canadian healthcare-focused investment bank.

Scale indicators9 records

Recent moves6 records

Expansion highlights6 records

Medicenna Therapeutics competitors and assessment

Company assessment

Direct peers

  • Werewolf Therapeutics: Clinical-stage oncology company developing conditionally activated engineered cytokines (PREDATOR platform) including IL-2 and IL-12 variants for solid tumors. Most direct competitor to Medicenna's Superkine and T-MASK platforms, with a similar mask-based tumor-localization strategy.
  • Synthekine: Engineered cytokine company developing optimized IL-2, IL-15, and IL-21 therapeutics for cancer and autoimmune disease. Directly comparable to Medicenna in both cytokine engineering technology and oncology/autoimmune dual focus.
  • Xilio Therapeutics: Clinical-stage biotech developing tumor-activated immunotherapies, including masked cytokines (IL-2, IL-12) and IL-15. Shares Medicenna's masked-cytokine (T-MASK-like) approach to localizing immune activation in the tumor microenvironment.
  • Cue Biopharma: Clinical-stage company developing IL-2-based biologics (Immuno-STAT platform) that selectively modulate T cell activity for cancer and autoimmune disease. Comparable approach to Medicenna's BiSKIT bispecific cytokine fusions.
  • Altor BioScience (NantHealth): Developer of N-803 (nogapendekin alfa inbakicept-pmln), an IL-15 superagonist approved for BCG-unresponsive non-muscle invasive bladder cancer. Closest commercial-stage analog to Medicenna's engineered IL-2/IL-15 cytokine approach.
  • Nektar Therapeutics: Developer of NKTR-358 (rezpegaldesleukin), a PEGylated IL-2 for autoimmune disease, and other cytokine-based therapies. Directly comparable to Medicenna's MDNA209 autoimmune program and broader IL-2 engineering pipeline.

Broad incumbents

  • Bristol-Myers Squibb: Global pharmaceutical company that developed bempegaldesleukin (PEG-IL-2) and runs multiple IL-2, IL-12, and cytokine programs. Represents the incumbent competitive threat to Medicenna's IL-2 franchise in oncology.
  • Merck & Co. Medicenna's clinical trial collaboration partner on MDNA11 + pembrolizumab (KEYTRUDA). As a broad incumbent with established checkpoint franchises and internal cytokine programs, Merck is both a validation partner and a potential long-term competitive threat.
  • Roche: Global pharmaceutical company with multiple engineered IL-2 variant programs in oncology and a leadership position in immuno-oncology. Represents the larger-platform incumbent competing in the same cytokine-engineering space as Medicenna.

Emerging players

  • Kazia Therapeutics: Clinical-stage oncology company developing paxalisib for glioblastoma and other brain cancers. Relevant emerging peer given overlapping glioblastoma indication with Medicenna's bizaxofusp (MDNA55) program.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat5 records

Key risks6 records

Key highlights6 records

Customer concentration

Medicenna Therapeutics social profiles

Digital presence

Medicenna Therapeutics financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Medicenna Therapeutics leadership team

Management profile

Number of profiles

Profiles5 records

Medicenna Therapeutics funding detail

Funding detail

Funding overview

Funding rounds8 records

Investors2 records

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

Medicenna 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 Medicenna Therapeutics

What does Medicenna Therapeutics do?

Medicenna Therapeutics is a clinical-stage immunotherapy company that develops engineered interleukin-based therapies (Superkines) for cancer and immune-driven diseases. It operates three proprietary platforms — Superkine, BiSKIT, and T-MASK — built on directed evolution and AI-driven rational design, and advances a pipeline of drug candidates including MDNA11 (IL-2 Superkine), MDNA113 (anti-PD-1 x IL-2 BiSKIT), bizaxofusp/MDNA55 (IL-4-toxin fusion for recurrent glioblastoma), MDNA209 and MDNA413 (super-antagonists for autoimmune/inflammatory diseases). Revenue is expected to be generated through product sales and out-licensing/co-development partnerships with pharmaceutical companies.

Is Medicenna Therapeutics a public or private company?

Medicenna Therapeutics is a public company. It is currently operating.

When was Medicenna Therapeutics founded?

Medicenna Therapeutics was founded in 2012. It employs 11 to 50 people.

Where is Medicenna Therapeutics based?

Medicenna Therapeutics is headquartered in Toronto, Canada, in the North America region.

How does Medicenna Therapeutics make money?

One revenue line is on record: therapeutic Product Development and Commercialization.

Who are Medicenna Therapeutics's main competitors?

Direct peers on record are Werewolf Therapeutics, Synthekine, Xilio Therapeutics, Cue Biopharma, Altor BioScience (NantHealth) and Nektar Therapeutics. Broad incumbents are Bristol-Myers Squibb, Merck & Co. and Roche. Kazia Therapeutics is listed as an emerging player.

Does Medicenna Therapeutics have an API?

No public API is recorded for Medicenna Therapeutics.

What industry is Medicenna Therapeutics in?

Medicenna Therapeutics's product category is Immuno-oncology biopharmaceuticals. Its primary akta.pro industry code is HLAAAAAC, Cytokines, Interferons & Immunomodulatory Proteins, with a secondary code of HLAIACAB, Immunology & Autoimmune Specialty Pharmaceuticals. Its NAICS code is 325414 and its SIC code is 2836.

Unlock the full company data

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

Contact sales
Live signals
Ticker ReportMedicenna Therapeutics (TSE:MDNA) Stock Price Down 2.1% – Should You Sell?Medicenna Therapeutics stock fell 2.1% to C$0.46, with trading volume down 82% from average. The company reported a quarterly loss of C$0.05 per share, and analysts forecast a fiscal-year loss of C$0.37 per share.Financial PostMedicenna Therapeutics Reports First Quarter Fiscal 2027 Financial Results and Announces Oral Presentations at Upcoming ConferencesMedicenna Therapeutics reported first-quarter fiscal 2027 financial results, showing a net loss of $5.1 million and cash reserves of $5.7 million following proceeds from a public offering and Australian R&D incentives. The company also announced it has entered into a term sheet for a potential structured financing arrangement with Sorbie Bornholm LP and Sorbie Investments LLP that could provide up to $8.0 million in additional capital. Additionally, Medicenna plans to present updated clinical data for its drug bizaxofusp at upcoming medical conferences.Stock TitanMedicenna Q1 Fiscal 2027 Earnings: $5.1M LossMedicenna Therapeutics reported a net loss of $5.1 million for the first quarter of fiscal 2027, while securing additional capital through a public offering and an Australian R&D incentive. The company provided updates on its clinical pipeline, noting that enrolment in the ABILITY-1 study remains on track for completion in Q3 2026, with plans to engage the FDA regarding expedited development paths. Additionally, Medicenna is advancing MDNA113 towards an IND submission for a Phase 1 trial in 2027 and continues patient enrolment in the NEO-CYT melanoma study.BioSpaceMedicenna Therapeutics Reports First Quarter Fiscal 2027 Financial Results and Announces Oral Presentations at Upcoming ConferencesMedicenna reported Q1 2027 financial results, ending with $5.7 million in cash and a net loss of $5.1 million. The company plans to present updated MDNA11 and bizaxofusp data at upcoming conferences and expects ABILITY-1 enrolment completion in Q3 2026. It also plans an IND submission for MDNA113 in 2027.Ticker ReportMedicenna Therapeutics (TSE:MDNA) Reaches New 1-Year Low – What’s Next?Medicenna Therapeutics Corp. stock reached a new 52-week low of C$0.34 on Thursday, closing at C$0.35 with 54,128 shares traded. The company has a market capitalization of C$33.23 million and reported a loss of C($0.05) earnings per share for the quarter, with a negative P/E ratio of -1.64 and negative net margin of 533,640%. Medicenna is a Canada-based immuno-oncology company developing interleukin-4 empowered cytokines for cancer treatment targeting over-expressed receptors in 20 different cancers.Financial PostMedicenna Therapeutics Reports Fiscal Year 2026 Financial Results and Operational HighlightsMedicenna Therapeutics reported fiscal year 2026 financial results for the year ended March 31, 2026, with a net loss of $18.4 million ($0.22 loss per share) compared to $11.8 million the prior year, driven by increased R&D expenses of $16.9 million. The company exited the fiscal year with $6.3 million in cash and subsequently completed a $4.4 million public offering while executing a term sheet for up to $8 million in structured financing with Sorbie Bornholm LP and Sorbie Investments LLP. Medicenna is pursuing partnership opportunities for its Phase 3-ready asset bizaxofusp (for recurrent glioblastoma) and anticipates multiple clinical milestones for fiscal 2027 including completing enrollment in the ABILITY-1 study for MDNA11 and filing an IND application for MDNA113.FinancialContent Business PageMedicenna Therapeutics Reports Fiscal Year 2026 Financial Results and Operational HighlightsMedicenna Therapeutics reported fiscal year 2026 financial results, posting a net loss of $18.4 million with cash and cash equivalents of $6.3 million as of March 31, 2026, compared to a net loss of $11.8 million in the prior year. The company announced clinical progress for its MDNA11 IL-2 Superkine, with ABILITY-1 enrollment expected to complete in Q3 2026 and key data readouts in Q4 2026, alongside preclinical data for MDNA113 presented at AACR 2026. Subsequent to year end, Medicenna closed a $4.4 million public offering and executed a term sheet for structured financing with Sorbie, extending projected cash runway through Q1 calendar 2027.Stock TitanMedicenna posts $18.4M loss, MDNA11 readouts due Q4Medicenna Therapeutics Corp. reported fiscal year 2026 financial results ended March 31, 2026, posting a net loss of $18.4 million compared to an $11.8 million loss in the prior year, with total operating costs increasing to $22.4 million from $20.4 million. The company announced that its MDNA11 Superkine demonstrated compelling anti-tumor activity with response rates in the 30-40% range in difficult-to-treat solid tumors, with key data readouts from the ABILITY-1 study expected in Q4 2026. Medicenna expects its cash runway to extend through Q1 calendar 2027, pending completion of planned financings including a structured financing arrangement with Sorbie.GlobeNewswireMedicenna Therapeutics Reports Fiscal Year 2026 Financial Results and Operational HighlightsMedicenna Therapeutics reported fiscal 2026 results, ending with $6.3 million in cash and a net loss of $18.4 million. The company plans to complete ABILITY-1 enrollment in Q3 2026 and file an IND for MDNA113 in Q4 2026, with financing expected to extend its runway through Q1 2027.BioSpaceMedicenna Strengthens U.S. Patent Estate with Newly Issued and Allowed Patents Across its IL-2, IL-4 and IL-13 Superkine PlatformsMedicenna Therapeutics announced the issuance of two U.S. patents and allowance of one for its IL-2, IL-4, and IL-13 Superkine platforms, including bizaxofusp. The patents cover cellular immunotherapy and combination therapy for CNS tumors, expanding its global portfolio to over 100 active patents and applications.