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Asgard Therapeutics

Full company profile

uuid0000uie

Namestring
Asgard Therapeutics
Legal namestring
Asgard Therapeutics AB
Websiteurl
asgardthx.com
Company typeenum
Private
Founded yearint
2018
Descriptiontext

Asgard Therapeutics AB is a Swedish private biotechnology company incorporated in December 2018 as a spin-off from Lund University (with support from LU Holding AB), headquartered at Medicon Village in Lund. The company is developing AT-108, a first-in-class, off-the-shelf gene therapy candidate that uses a replication-deficient adenoviral vector to deliver three proprietary transcription factors that directly reprogram tumor cells into conventional type 1 dendritic cells (cDC1) in situ — a process the company brands as the TrojanDC platform. The intended effect is to convert the patient's own tumor into an antigen-presenting cell, triggering a personalized anti-tumor immune response while bypassing the manufacturing and logistical complexity of autologous cell therapies. The scientific work originated in the labs of co-founders Cristiana Pires, Filipe Pereira, and Fábio Rosa, with key proof-of-concept data published in Science in 2024 and follow-on mechanistic publications in Immunity (2025) and Cell Systems (2026).

The company is pre-revenue and preclinical, with AT-108 as its single lead program targeting solid tumors. AT-108 is being advanced toward IND-readiness by 2026 and Phase 1/2 clinical development, with preclinical data presented at AACR 2026 and ASGCT 2026 showing monotherapy activity and synergy with checkpoint blockade. Asgard's stated business model is to commercialize AT-108 either independently or through licensing, royalty, or co-development agreements with large pharmaceutical partners for global development and commercialization. To date the company has raised approximately €36 million across a €6 million seed round (November 2021, co-led by Novo Holdings) and a €30 million Series A (March 2024, co-led by RV Invest and Johnson & Johnson Innovation – JJDC, with Novo Holdings, Boehringer Ingelheim Venture Fund, and Industrifonden). The current go-to-market emphasis is on scientific publications, conference presentations, and strategic pharma partnering rather than direct sales.

Short descriptiontext

Asgard Therapeutics is a Swedish preclinical biotech, spun out of Lund University in 2018, developing AT-108 — a first-in-class, off-the-shelf gene therapy that uses an adenoviral vector to reprogram tumor cells into dendritic cells in situ for solid tumor immunotherapy, targeting licensing deals with pharmaceutical partners.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersLund, Sweden
HQ citystring
Lund
HQ countrystring
Sweden
HQ regionstring
Europe
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
cancer immunotherapy, cell reprogramming therapy, gene therapy oncology, dendritic cell therapy, immuno-oncology platform
Industry4 codes
1Dendritic Cell & Other APC-based Therapies
CodeHLAAABAFPrimaryYes
2Personalized Therapeutic Design (neoantigen vaccines, individualized cell/gene therapies)
CodeHLAAANAKPrimaryNo
3Therapeutic Vaccines (e.g., Cancer/Chronic Infection)
CodeHLAIAEAGPrimaryNo
4Oncology Gene Therapies (incl. oncolytic vectors & gene-modified approaches)
CodeHLAAACAFPrimaryNo
NAICS code2 codes
  • Biological Product (except Diagnostic) Manufacturing325414
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
SIC code2 codes
  • Biological Products, (No Disgnostic Substances)2836
  • Pharmaceutical Preparations2834
Product category
Cancer Immunotherapy / Gene Therapy
Social media profiles2 records
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1Future therapeutic product sales
TypeLicensing Royalties
Description

As a preclinical-stage biotech company, Asgard Therapeutics is pre-revenue. The company plans to generate revenue through commercialization of its lead program AT-108 (TrojanDC), either independently or through strategic partnerships and licensing agreements with pharmaceutical companies for global development and commercialization.

Marketing channels4 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

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

Cost components3 values
Technology or R&D, Personnel, Operations
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

Asgard Therapeutics is developing AT-108, a first-in-class off-the-shelf gene therapy that uses in vivo direct cell reprogramming to convert tumor cells into conventional type 1 dendritic cells (cDC1) within the patient's body, triggering personalized anti-tumor immune responses. The product is based on a replication-deficient adenoviral vector delivering three proprietary transcription factors, and is designed to overcome the manufacturing and logistical hurdles of conventional cell-based cancer therapies.

Differentiator
Functional benefit
Problem solved
Product overview1 text field

Asgard Therapeutics is developing AT-108, a first-in-class, off-the-shelf gene therapy product for cancer immunotherapy. The company's approach uses in vivo direct cell reprogramming technology to convert tumor cells into dendritic cells within the patient's body. AT-108 is designed as a single lead program that reprograms tumor cells to present their own antigens, triggering personalized anti-cancer immune responses while maintaining the manufacturing and logistical advantages of an off-the-shelf therapy.

Product and service1 record
1AT-108 (TrojanDC)
CategoryGene Therapy / Cancer Immunotherapy
Description

AT-108 is a first-in-class, off-the-shelf gene therapy that uses a replication-deficient adenoviral vector to deliver three proprietary transcription factors, directly reprogramming tumor cells in vivo into conventional type 1 dendritic cells (cDC1). This triggers personalized anti-tumor immune responses within the patient's tumor microenvironment, targeting solid tumors and overcoming tumor immune evasion. Intended for cancer patients with solid tumors.

Scale indicator3 records

Each record includes

Type, Value, Description, Source

Partnership1 partner
Strategic tierCoreTypeStrategic or Co-development Partner
Description

Asgard Therapeutics is a spin-out from Lund University, originating from the research labs of co-founders Cristiana Pires, Filipe Pereira, and Fábio Rosa. The company maintains ongoing academic collaborations with Lund University researchers in cell reprogramming and immunology.

Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Clinical-stage biotech developing viral vector-delivered immunotherapies that turn 'cold' solid tumors 'hot,' most directly comparable to Asgard's approach of using adenoviral vectors to reprogram the tumor microenvironment for immune activation.

TypeDirect peer
Description

Personalized cancer immunotherapy company developing clonal neoantigen-reactive T cell therapies for solid tumors. Both Asgard and Achilles pursue personalized tumor antigen-driven immune activation in solid tumor indications.

TypeDirect peer
Description

Commercial-stage cell therapy company developing engineered TCR-T cell therapies for solid tumors. Comparable in targeting solid tumor immune evasion with cellular engineering approaches distinct from but adjacent to Asgard's in vivo reprogramming.

TypeDirect peer
Description

Clinical-stage biotech engineering macrophages and other immune cells to treat cancer. Both Asgard and Carisma leverage cell engineering/reprogramming strategies to redirect myeloid lineage cells against solid tumors.

TypeDirect peer
Description

Clinical-stage company developing off-the-shelf iPSC-derived cell therapies for cancer immunotherapy. Comparable as a pioneer in off-the-shelf engineered immune cell therapies that avoid autologous manufacturing constraints.

TypeDirect peer
Description

Clinical-stage biotech developing next-generation engineered T cell therapies for solid tumors. Comparable in pursuing cell-based immunotherapy solutions for solid tumor indications with high unmet need.

TypeDirect peer
Description

Clinical-stage biotech pioneering allogeneic CAR-T cell therapies. Comparable in pursuing off-the-shelf cellular immunotherapies that can be manufactured at scale rather than patient-by-patient.

TypeBroad incumbent
Description

Commercial-stage mRNA immunotherapy leader with a broad oncology pipeline. As a broad incumbent in personalized cancer immunotherapy, BioNTech is comparable in pursuing patient-specific immune activation strategies but operates at vastly greater scale.

TypeBroad incumbent
Description

Commercial-stage biotech with a broad mRNA-based cancer immunotherapy pipeline. Comparable as a broad incumbent developing nucleic acid-based immunotherapies that activate patient immune responses against tumors.

TypeEmerging player
Description

Clinical-stage biotech developing non-viral gene therapy and cell therapy approaches for cancer. Comparable in the gene-therapy-driven oncology space, particularly for solid tumors, though at an earlier stage and with different delivery technology.

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

Segment1 record

Each record includes

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

Ideal customer profile1 record

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

Feature1 record

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles8 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 rounds3 records

Each record includes

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

Investors6 records

Each record includes

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

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

M&A

Each record includes

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

Investment

Each record includes

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

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

Asgard Therapeutics

Cancer Immunotherapy / Gene Therapyasgardthx.com

Asgard Therapeutics is a Swedish preclinical biotech, spun out of Lund University in 2018, developing AT-108 — a first-in-class, off-the-shelf gene therapy that uses an adenoviral vector to reprogram tumor cells into dendritic cells in situ for solid tumor immunotherapy, targeting licensing deals with pharmaceutical partners.

What Asgard Therapeutics does

Asgard Therapeutics AB is a Swedish private biotechnology company incorporated in December 2018 as a spin-off from Lund University (with support from LU Holding AB), headquartered at Medicon Village in Lund. The company is developing AT-108, a first-in-class, off-the-shelf gene therapy candidate that uses a replication-deficient adenoviral vector to deliver three proprietary transcription factors that directly reprogram tumor cells into conventional type 1 dendritic cells (cDC1) in situ — a process the company brands as the TrojanDC platform. The intended effect is to convert the patient's own tumor into an antigen-presenting cell, triggering a personalized anti-tumor immune response while bypassing the manufacturing and logistical complexity of autologous cell therapies. The scientific work originated in the labs of co-founders Cristiana Pires, Filipe Pereira, and Fábio Rosa, with key proof-of-concept data published in Science in 2024 and follow-on mechanistic publications in Immunity (2025) and Cell Systems (2026).

The company is pre-revenue and preclinical, with AT-108 as its single lead program targeting solid tumors. AT-108 is being advanced toward IND-readiness by 2026 and Phase 1/2 clinical development, with preclinical data presented at AACR 2026 and ASGCT 2026 showing monotherapy activity and synergy with checkpoint blockade. Asgard's stated business model is to commercialize AT-108 either independently or through licensing, royalty, or co-development agreements with large pharmaceutical partners for global development and commercialization. To date the company has raised approximately €36 million across a €6 million seed round (November 2021, co-led by Novo Holdings) and a €30 million Series A (March 2024, co-led by RV Invest and Johnson & Johnson Innovation – JJDC, with Novo Holdings, Boehringer Ingelheim Venture Fund, and Industrifonden). The current go-to-market emphasis is on scientific publications, conference presentations, and strategic pharma partnering rather than direct sales.

Asgard Therapeutics firmographics

Firmographics
Name
Asgard Therapeutics
Legal name
Asgard Therapeutics AB
Website
https://asgardthx.com
Company type
Private
Founded year
2018
Operating status
Operating
Headcount range
11–50 employees
Short description
Asgard Therapeutics is a Swedish preclinical biotech, spun out of Lund University in 2018, developing AT-108 — a first-in-class, off-the-shelf gene therapy that uses an adenoviral vector to reprogram tumor cells into dendritic cells in situ for solid tumor immunotherapy, targeting licensing deals with pharmaceutical partners.
Ownership category
akta.pro rank

Asgard Therapeutics industry classification

Industry
Product category
Cancer Immunotherapy / Gene Therapy
NAICS
Biological Product (except Diagnostic) Manufacturing (325414), Research and Development in Biotechnology (except Nanobiotechnology) (541714)
SIC
Biological Products, (No Disgnostic Substances) (2836), Pharmaceutical Preparations (2834)
akta.pro primary industry
Dendritic Cell & Other APC-based Therapies (HLAAABAF)
akta.pro secondary industries
Personalized Therapeutic Design (neoantigen vaccines, individualized cell/gene therapies) (HLAAANAK), Therapeutic Vaccines (e.g., Cancer/Chronic Infection) (HLAIAEAG), Oncology Gene Therapies (incl. oncolytic vectors & gene-modified approaches) (HLAAACAF)

Keywords

  • Cancer immunotherapy
  • Cell reprogramming therapy
  • Gene therapy oncology
  • Dendritic cell therapy
  • Immuno-oncology platform

Where Asgard Therapeutics is headquartered

Location

Headquarters

HQ city
Lund
HQ country
Sweden
HQ region
Europe

Offices1 record

Markets served

Asgard Therapeutics business model

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

Revenue model

  1. Future therapeutic product sales: As a preclinical-stage biotech company, Asgard Therapeutics is pre-revenue. The company plans to generate revenue through commercialization of its lead program AT-108 (TrojanDC), either independently or through strategic partnerships and licensing agreements with pharmaceutical companies for global development and commercialization.

Go-to-market motion1 record

Distribution channels1 record

Marketing channels4 records

Asgard Therapeutics product offering

Product offering

Core offering

Asgard Therapeutics is developing AT-108, a first-in-class off-the-shelf gene therapy that uses in vivo direct cell reprogramming to convert tumor cells into conventional type 1 dendritic cells (cDC1) within the patient's body, triggering personalized anti-tumor immune responses. The product is based on a replication-deficient adenoviral vector delivering three proprietary transcription factors, and is designed to overcome the manufacturing and logistical hurdles of conventional cell-based cancer therapies.

Product overview

Asgard Therapeutics is developing AT-108, a first-in-class, off-the-shelf gene therapy product for cancer immunotherapy. The company's approach uses in vivo direct cell reprogramming technology to convert tumor cells into dendritic cells within the patient's body. AT-108 is designed as a single lead program that reprograms tumor cells to present their own antigens, triggering personalized anti-cancer immune responses while maintaining the manufacturing and logistical advantages of an off-the-shelf therapy.

Differentiator

Problem solved

Functional benefit

Products and services

  • AT-108 (TrojanDC) AT-108 is a first-in-class, off-the-shelf gene therapy that uses a replication-deficient adenoviral vector to deliver three proprietary transcription factors, directly reprogramming tumor cells in vivo into conventional type 1 dendritic cells (cDC1). This triggers personalized anti-tumor immune responses within the patient's tumor microenvironment, targeting solid tumors and overcoming tumor immune evasion. Intended for cancer patients with solid tumors.

Companies that use Asgard Therapeutics

Customer profile

Segments1 record

Ideal customer profiles1 record

Asgard Therapeutics technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature1 record

Asgard Therapeutics partnerships and signals

Strategic signal

Partnerships

One partnership is on record.

  • Lund UniversitycoreStrategic or Co-development PartnerAsgard Therapeutics is a spin-out from Lund University, originating from the research labs of co-founders Cristiana Pires, Filipe Pereira, and Fábio Rosa. The company maintains ongoing academic collaborations with Lund University researchers in cell reprogramming and immunology.

Scale indicators3 records

Recent moves7 records

Expansion highlights6 records

Asgard Therapeutics competitors and assessment

Company assessment

Direct peers

  • Turnstone Biologics: Clinical-stage biotech developing viral vector-delivered immunotherapies that turn 'cold' solid tumors 'hot,' most directly comparable to Asgard's approach of using adenoviral vectors to reprogram the tumor microenvironment for immune activation.
  • Achilles Therapeutics: Personalized cancer immunotherapy company developing clonal neoantigen-reactive T cell therapies for solid tumors. Both Asgard and Achilles pursue personalized tumor antigen-driven immune activation in solid tumor indications.
  • Adaptimmune Therapeutics: Commercial-stage cell therapy company developing engineered TCR-T cell therapies for solid tumors. Comparable in targeting solid tumor immune evasion with cellular engineering approaches distinct from but adjacent to Asgard's in vivo reprogramming.
  • Carisma Therapeutics: Clinical-stage biotech engineering macrophages and other immune cells to treat cancer. Both Asgard and Carisma leverage cell engineering/reprogramming strategies to redirect myeloid lineage cells against solid tumors.
  • Fate Therapeutics: Clinical-stage company developing off-the-shelf iPSC-derived cell therapies for cancer immunotherapy. Comparable as a pioneer in off-the-shelf engineered immune cell therapies that avoid autologous manufacturing constraints.
  • Tmunity Therapeutics: Clinical-stage biotech developing next-generation engineered T cell therapies for solid tumors. Comparable in pursuing cell-based immunotherapy solutions for solid tumor indications with high unmet need.
  • Allogene Therapeutics: Clinical-stage biotech pioneering allogeneic CAR-T cell therapies. Comparable in pursuing off-the-shelf cellular immunotherapies that can be manufactured at scale rather than patient-by-patient.

Broad incumbents

  • BioNTech: Commercial-stage mRNA immunotherapy leader with a broad oncology pipeline. As a broad incumbent in personalized cancer immunotherapy, BioNTech is comparable in pursuing patient-specific immune activation strategies but operates at vastly greater scale.
  • Moderna: Commercial-stage biotech with a broad mRNA-based cancer immunotherapy pipeline. Comparable as a broad incumbent developing nucleic acid-based immunotherapies that activate patient immune responses against tumors.

Emerging players

  • Ziopharm Oncology: Clinical-stage biotech developing non-viral gene therapy and cell therapy approaches for cancer. Comparable in the gene-therapy-driven oncology space, particularly for solid tumors, though at an earlier stage and with different delivery technology.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat3 records

Key risks6 records

Key highlights7 records

Customer concentration

Asgard Therapeutics social profiles

Digital presence

Asgard Therapeutics financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Asgard Therapeutics leadership team

Management profile

Number of profiles

Profiles8 records

Asgard Therapeutics funding detail

Funding detail

Funding overview

Funding rounds3 records

Investors6 records

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

Asgard 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 Asgard Therapeutics

What does Asgard Therapeutics do?

Asgard Therapeutics is developing AT-108, a first-in-class off-the-shelf gene therapy that uses in vivo direct cell reprogramming to convert tumor cells into conventional type 1 dendritic cells (cDC1) within the patient's body, triggering personalized anti-tumor immune responses. The product is based on a replication-deficient adenoviral vector delivering three proprietary transcription factors, and is designed to overcome the manufacturing and logistical hurdles of conventional cell-based cancer therapies.

Is Asgard Therapeutics a public or private company?

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

When was Asgard Therapeutics founded?

Asgard Therapeutics was founded in 2018. It employs 11 to 50 people.

Where is Asgard Therapeutics based?

Asgard Therapeutics is headquartered in Lund, Sweden, in the Europe region.

How does Asgard Therapeutics make money?

One revenue line is on record: future therapeutic product sales.

Who are Asgard Therapeutics's main competitors?

Direct peers on record are Turnstone Biologics, Achilles Therapeutics, Adaptimmune Therapeutics, Carisma Therapeutics, Fate Therapeutics, Tmunity Therapeutics and Allogene Therapeutics. Broad incumbents are BioNTech and Moderna. Ziopharm Oncology is listed as an emerging player.

Does Asgard Therapeutics have an API?

No public API is recorded for Asgard Therapeutics.

What industry is Asgard Therapeutics in?

Asgard Therapeutics's product category is Cancer Immunotherapy / Gene Therapy. Its primary akta.pro industry code is HLAAABAF, Dendritic Cell & Other APC-based Therapies, with a secondary code of HLAAANAK, Personalized Therapeutic Design (neoantigen vaccines, individualized cell/gene therapies). Its NAICS code is 325414 and its SIC code is 2836.

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Live signals
BioWorldAsgard’s AT-108 shows promise as immunotherapeuticAsgard Therapeutics developed AT-108, a lead candidate for immunotherapy targeting defects in antigen presentation. The adenoviral vector reprograms tumor cells into cDC1-like cells and shows synergy with immune checkpoint blockade. The company aims for durable efficacy.PharmaTimesAsgard Therapeutics to present new preclinical data on AT‑108 at ASGCT 2026Asgard Therapeutics will present new preclinical data on its lead asset AT-108 at the ASGCT Annual Meeting in Boston from 11–15 May. The data show systemic, dose-dependent efficacy in mouse models, including abscopal effects, and identify biomarker parameters for future clinical studies.GlobeNewswireAsgard Therapeutics announces oral presentation at ASGCT 2026, showcasing advanced preclinical data on AT-108 – its first-in-class, off-the-shelf, gene-based cancer immunotherapyAsgard Therapeutics will present advanced preclinical data on its lead asset AT-108, a first-in-class off-the-shelf gene-based cancer immunotherapy, at the ASGCT Annual Meeting in Boston from May 11–15, 2026. The data shows that AT-108 doubled median survival as monotherapy in multiple mouse models and achieved 50% complete tumor regressions when combined with immune checkpoint blockade. The company is advancing AT-108 toward clinical development for solid tumors through IND-enabling studies and CMC development.BioSpaceAsgard Therapeutics to present preclinical data on lead asset AT-108, a personalized, off-the-shelf gene therapy, at AACR Annual Meeting 2026Asgard Therapeutics will present preclinical data on its lead asset AT-108 at the AACR Annual Meeting in San Diego, April 2026. The poster details systemic, dose-dependent efficacy and broad tumor activity, with key biomarkers identified for future clinical development.OncoDailyAsgard Therapeutics Reveals Promising Preclinical Data for First-in-Class In Situ Tumor Reprogramming Gene Therapy AT-108Asgard Therapeutics presented preclinical data for AT-108, a first-in-class in-vivo gene therapy that reprograms tumor cells into antigen-presenting dendritic cells within the tumor itself, at a major oncology conference. The data demonstrate systemic, dose-dependent antitumor activity, supporting advancement toward IND-enabling studies for solid tumors. If the preclinical efficacy and safety profile translates to patients, AT-108 could establish a mechanistically novel class of cancer therapy.GlobeNewswireAsgard Therapeutics to present preclinical data on lead asset AT-108, a personalized, off-the-shelf gene therapy, at AACR Annual Meeting 2026Asgard Therapeutics will present preclinical data on its lead asset AT-108, a first-in-class gene therapy for cancer immunotherapy, at the AACR Annual Meeting 2026 in San Diego. The poster will detail preclinical findings showing AT-108 induces systemic, dose-dependent efficacy with broad tumor activity by reprogramming tumor cells into dendritic cells. The company is advancing IND-enabling studies and CMC development as it progresses toward clinical development for solid tumors.Investing.comAsgard Therapeutics names Wolfram Brugger as chief medical officer By Investing.comAsgard Therapeutics appointed Prof Dr Wolfram Brugger as its new Chief Medical Officer, with Brugger joining from Autolus Therapeutics where he led the global clinical development of AUTO1, a CD19 CAR T therapy that received FDA approval in 2024 for relapsed/refractory B-cell acute lymphoblastic leukemia. Brugger brings experience from over 130 Phase I-III clinical oncology trials, as well as prior roles at MorphoSys and AstraZeneca, and will oversee the development of Asgard's AT-108, an off-the-shelf gene therapy currently in IND-enabling studies.GlobeNewswireAsgard Therapeutics appoints Professor Dr Wolfram Brugger as Chief Medical Officer as it advances transformative ‘personalized off-the-shelf’ immunotherapy toward clinical developmentAsgard Therapeutics announced the appointment of Professor Dr Wolfram Brugger as Chief Medical Officer as the company advances its lead asset AT-108 toward Phase 1 clinical development. Brugger brings over 20 years of experience in oncology drug development, having led clinical programs at Autolus Therapeutics, MorphoSys, and AstraZeneca, and has been involved in more than 130 Phase I-III clinical trials across various cancer types. The appointment strengthens Asgard's leadership as it progresses IND-enabling studies for AT-108, a first-in-class 'personalized off-the-shelf' immunotherapy that reprograms tumor cells to trigger personalized immune responses against cancer.BioSpaceAsgard Therapeutics appoints Professor Dr Wolfram Brugger as Chief Medical Officer as it advances transformative ‘personalized off-the-shelf’ immunotherapy toward clinical developmentAsgard Therapeutics appointed Prof Dr Wolfram Brugger as Chief Medical Officer to advance its lead asset AT-108 toward Phase 1 clinical development. AT-108 is a personalized off-the-shelf immunotherapy that reprograms tumor cells to present antigens, with IND-enabling studies currently underway. The company aims to transition to a clinical-stage biotech.PR NewswireAsgard Therapeutics appoints immunology expert Shane Olwill as Chief Development OfficerAsgard Therapeutics appointed Shane Olwill, an immunology drug development specialist with over two decades of experience, as Chief Development Officer. Olwill will lead IND-enabling studies and clinical trials planning for the company's lead asset AT-108, a first-in-class off-the-shelf cell reprogramming therapy for cancer immunotherapy currently progressing toward clinical development. The appointment comes as the company transitions from a research-focused to a drug development company, backed by investors including Johnson & Johnson Innovation, Novo Holdings, and Boehringer Ingelheim Venture Fund.