Developer docs
API playgroundTry for free, no card

Search company profiles

MetrioPharm

Full company profile

uuid00025cr

Namestring
MetrioPharm
Legal namestring
MetrioPharm AG
Websiteurl
metriopharm.com
Company typeenum
Private
Founded yearint
2007
Descriptiontext

MetrioPharm AG is a clinical-stage biopharmaceutical company developing MP1032, a first-in-class oral small molecule positioned as a self-regulating immunomodulator. Founded in 2007, the company is headquartered in Zurich, Switzerland with research and development operations in Berlin, Germany, and operates as a privately held entity with 11-50 employees. Its lead clinical indication is Duchenne muscular dystrophy (DMD), supported by both FDA Orphan Drug Designation (May 2023) and EMA Orphan Drug Designation (July 2025), alongside a broader inflammatory disease pipeline targeting rheumatoid arthritis, multiple sclerosis, psoriasis, IBD, and sepsis.

The company's core technology centers on MP1032, a small molecule designed to modulate immune responses in a self-regulating manner, reducing pro-inflammatory signaling without inducing broad immunosuppression. Substance patents for MP1032 have been granted in more than nine countries, and the company has also received FDA Rare Pediatric Disease Designation for the DMD program, providing multiple layers of regulatory and intangible-asset protection around the lead asset. The company has explored COVID-19 as a proof-of-mechanism indication, with Phase IIa positive results published in Lancet Regional Health Europe (2024), providing clinical validation of the immunomodulatory mechanism.

MetrioPharm's business model is typical of clinical-stage biotech: the company is pre-revenue and depends on equity financings and non-dilutive grants to advance its pipeline, including a EUR 7.9 million EU HERA Incubator award secured in November 2021. Future revenue is expected to come through licensing transactions, partnerships, or eventual commercialization of MP1032 across multiple inflammatory indications. The company has undergone leadership transitions including a new CEO (Thomas Christély, October 2021) and CMO/CSO appointments in 2025-2026 to support late-stage clinical development.

Short descriptiontext

MetrioPharm AG is a Zurich-based, privately held, clinical-stage biopharmaceutical company developing MP1032, a first-in-class oral self-regulating immunomodulator. Its lead indication is Duchenne muscular dystrophy, with a broader pipeline targeting inflammatory conditions including arthritis and psoriasis.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersZürich, Switzerland
HQ citystring
Zürich
HQ countrystring
Switzerland
HQ regionstring
Europe
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
clinical-stage biopharmaceutical, small molecule immunomodulators, corticosteroid-sparing therapy, orphan disease drug development, anti-inflammatory therapeutics
Industry2 codes
1Immunology & Autoimmune Specialty Pharmaceuticals
CodeHLAIACABPrimaryYes
2Neurology & CNS Specialty Pharmaceuticals
CodeHLAIACACPrimaryNo
NAICS code2 codes
  • Pharmaceutical and Medicine Manufacturing3254
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
SIC code1 code
  • Biological Products, (No Disgnostic Substances)2836
Product category
Clinical-Stage Biopharmaceuticals
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1Drug Development and Licensing
TypeLicensing Royalties
Description

As a clinical-stage biopharmaceutical company, MetrioPharm generates no current revenue. The company's business model centers on developing its lead compound MP1032 through clinical stages (Phase I completed, Phase IIa completed in Psoriasis and COVID-19) toward market authorization. Revenue is expected to be generated through out-licensing partnerships with large pharmaceutical companies for commercialization across multiple indications, and through potential co-development arrangements. The company is also exploring Fixed-Dose Combination therapies combining MP1032 with lower doses of generic standard therapies to create novel medications with improved efficacy, fewer side effects, and renewed or extended patent protection.

metriopharm.com
Marketing channels9 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

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

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

MetrioPharm AG is a clinical-stage biopharmaceutical company developing MP1032, a first-in-class oral small molecule self-regulating immunomodulator (ROS scavenger) that normalizes pathologically reprogrammed mitochondrial energy metabolism in macrophages without causing immunosuppression. The company focuses on advancing MP1032 through clinical development for rare/orphan indications such as Duchenne Muscular Dystrophy (DMD), with the intent to out-license or co-develop the compound with larger pharmaceutical partners for commercialization across multiple indications including psoriasis, COVID-19, rheumatoid arthritis, multiple sclerosis, inflammatory bowel disease, and sepsis.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 4 values shown
  • Average 2.4 days earlier hospital discharge and 4 days shorter ICU stay for COVID-19 patients treated with MP1032 vs. placebo in Phase IIa study
+3 more records
Product overview1 text field

MetrioPharm AG is a clinical-stage biopharmaceutical company developing first-in-class self-regulating immunomodulators for inflammatory and infectious diseases. The company's product portfolio consists of two main offerings: the MP1000 Platform (a proprietary technology platform of oral small molecule immune modulators) and its lead compound MP1032 (the primary drug candidate developed on this platform). MP1032 is a first-in-class ROS scavenger that normalizes pathologically reprogrammed cellular/mitochondrial energy metabolism in inflammatory immune cells without causing immunosuppression. The platform enables corticosteroid-sparing therapies with efficacy comparable to corticosteroids but without serious side effects. The company is currently focused on rare diseases including Duchenne Muscular Dystrophy, with additional development in psoriasis, COVID-19, rheumatoid arthritis, multiple sclerosis, and sepsis.

Product and service2 records
1MP1032
CategoryLead drug candidate / small molecule immunomodulator
Description

MP1032 is MetrioPharm's lead drug candidate — an oral small molecule that acts as a self-regulating reactive oxygen species (ROS) scavenger, normalizing pathologically reprogrammed mitochondrial energy metabolism in inflammatory immune cells (e.g., macrophages) without causing immunosuppression. It is being developed as a corticosteroid-sparing therapy for Duchenne Muscular Dystrophy and other inflammatory/autoimmune and infectious diseases, with demonstrated efficacy in Phase IIa studies in Psoriasis and COVID-19.

2MP1000 Platform
CategoryProprietary drug discovery platform
Description

The MP1000 Platform is MetrioPharm's proprietary technology platform of oral small molecule immune modulators that target the pathologically dysregulated (reprogrammed) mitochondrial metabolism in macrophages and other immune cells. The platform enables development of self-regulating immunomodulators without immunosuppressive effects and serves as the foundation for the company's pipeline including MP1032.

Scale indicator7 records

Each record includes

Type, Value, Description, Source

Partnership1 partner
1iMPact Consortium Partners (ImmunoLogik, Catalyze, MC Toxicology Consulting)
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2021-01-01
Description

MetrioPharm leads the iMPact project consortium consisting of three additional partners: ImmunoLogik, Catalyze, and MC Toxicology Consulting. The consortium was formed to conduct the international COVID-19 research project including the Phase II clinical trial and preclinical studies on SARS-CoV-2 variants.

metriopharm.com
Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

U.S.-listed commercial-stage biotech focused on Duchenne Muscular Dystrophy with approved gene therapies (Elevidys) and antisense oligonucleotides. Directly comparable DMD franchise with orphan designations and rare disease regulatory pathway; serves as a commercial benchmark for what a successful DMD asset can become.

TypeDirect peer
Description

U.S.-listed rare disease company with multiple DMD assets (Translarna, Emflaza) and a broader pipeline in inflammation and metabolic disorders. Closely comparable business model of orphan drug development, EMA/FDA regulatory navigation, and pipeline diversification from a DMD anchor.

TypeDirect peer
Description

Swiss-listed rare disease company developing therapies for Duchenne Muscular Dystrophy (e.g., vamorolone) and other neuromuscular disorders. Highly comparable as a small-cap European clinical-stage DMD specialist pursuing similar orphan regulatory pathways and out-licensing economics.

TypeDirect peer
Description

Established rare disease specialty pharma with multiple approved orphan drugs across neuromuscular and metabolic conditions. Comparable in pursuing small-molecule and biologic therapies for rare inflammatory/genetic diseases via accelerated regulatory pathways.

TypeDirect peer
Description

Clinical-to-commercial rare disease company developing small-molecule therapies targeting inflammation and mitochondrial dysfunction (Skyclarys for Friedreich's ataxia). Highly comparable mechanistic and therapeutic-area overlap with MetrioPharm's ROS/mitochondrial platform.

TypeDirect peer
Description

European clinical-stage biotech developing first-in-class anti-inflammatory therapeutics (e.g., vilobelimab) targeting the complement system. Comparable as a small-cap inflammation-focused company pursuing novel mechanisms for rare and chronic inflammatory diseases.

TypeDirect peer
Description

European clinical-stage biotech historically focused on small-molecule immunology (JAK1 inhibitor filgotinib). Comparable as a mid-sized European inflammation-focused drug developer with similar out-licensing and partnership business model.

8Catabasis Pharmaceuticals
TypeDirect peer
Description

Clinical-stage rare disease company developing small molecules for DMD (edasalonexent) and inflammatory conditions. Direct comparable in targeting inflammatory pathways for Duchenne Muscular Dystrophy with novel mechanisms, and a cautionary tale on clinical execution.

TypeBroad incumbent
Description

Large incumbent immunology pharma with Humira, Rinvoq, and Skyrizi dominating anti-inflammatory markets. Represents the competitive standard-of-care and a likely out-licensing/acquisition counterparty for MP1032 in autoimmune indications.

TypeBroad incumbent
Description

Specialty rare and inflammatory disease pharma (now part of Amgen) with assets in gout, thyroid eye disease, and autoimmune conditions. Comparable as a rare/inflammatory disease-focused commercial-stage player and potential BD partner for orphan-designated assets.

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 risks7 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment3 records

Each record includes

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

Ideal customer profile3 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

Feature4 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles9 records

Each record includes

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

Subsidiaries1 record

Each record includes

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

No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds2 records

Each record includes

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

Investors1 record

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 →

MetrioPharm

Clinical-Stage Biopharmaceuticalsmetriopharm.com

MetrioPharm AG is a Zurich-based, privately held, clinical-stage biopharmaceutical company developing MP1032, a first-in-class oral self-regulating immunomodulator. Its lead indication is Duchenne muscular dystrophy, with a broader pipeline targeting inflammatory conditions including arthritis and psoriasis.

What MetrioPharm does

MetrioPharm AG is a clinical-stage biopharmaceutical company developing MP1032, a first-in-class oral small molecule positioned as a self-regulating immunomodulator. Founded in 2007, the company is headquartered in Zurich, Switzerland with research and development operations in Berlin, Germany, and operates as a privately held entity with 11-50 employees. Its lead clinical indication is Duchenne muscular dystrophy (DMD), supported by both FDA Orphan Drug Designation (May 2023) and EMA Orphan Drug Designation (July 2025), alongside a broader inflammatory disease pipeline targeting rheumatoid arthritis, multiple sclerosis, psoriasis, IBD, and sepsis.

The company's core technology centers on MP1032, a small molecule designed to modulate immune responses in a self-regulating manner, reducing pro-inflammatory signaling without inducing broad immunosuppression. Substance patents for MP1032 have been granted in more than nine countries, and the company has also received FDA Rare Pediatric Disease Designation for the DMD program, providing multiple layers of regulatory and intangible-asset protection around the lead asset. The company has explored COVID-19 as a proof-of-mechanism indication, with Phase IIa positive results published in Lancet Regional Health Europe (2024), providing clinical validation of the immunomodulatory mechanism.

MetrioPharm's business model is typical of clinical-stage biotech: the company is pre-revenue and depends on equity financings and non-dilutive grants to advance its pipeline, including a EUR 7.9 million EU HERA Incubator award secured in November 2021. Future revenue is expected to come through licensing transactions, partnerships, or eventual commercialization of MP1032 across multiple inflammatory indications. The company has undergone leadership transitions including a new CEO (Thomas Christély, October 2021) and CMO/CSO appointments in 2025-2026 to support late-stage clinical development.

MetrioPharm firmographics

Firmographics
Name
MetrioPharm
Legal name
MetrioPharm AG
Website
https://metriopharm.com
Company type
Private
Founded year
2007
Operating status
Operating
Headcount range
11–50 employees
Short description
MetrioPharm AG is a Zurich-based, privately held, clinical-stage biopharmaceutical company developing MP1032, a first-in-class oral self-regulating immunomodulator. Its lead indication is Duchenne muscular dystrophy, with a broader pipeline targeting inflammatory conditions including arthritis and psoriasis.
Ownership category
akta.pro rank

MetrioPharm industry classification

Industry
Product category
Clinical-Stage Biopharmaceuticals
NAICS
Pharmaceutical and Medicine Manufacturing (3254), Research and Development in Biotechnology (except Nanobiotechnology) (541714)
SIC
Biological Products, (No Disgnostic Substances) (2836)
akta.pro primary industry
Immunology & Autoimmune Specialty Pharmaceuticals (HLAIACAB)
akta.pro secondary industry
Neurology & CNS Specialty Pharmaceuticals (HLAIACAC)

Keywords

  • Clinical-stage biopharmaceutical
  • Small molecule immunomodulators
  • Corticosteroid-sparing therapy
  • Orphan disease drug development
  • Anti-inflammatory therapeutics

Where MetrioPharm is headquartered

Location

Headquarters

HQ city
Zürich
HQ country
Switzerland
HQ region
Europe

Offices2 records

Markets served

MetrioPharm business model

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

Revenue model

  1. Drug Development and Licensing: As a clinical-stage biopharmaceutical company, MetrioPharm generates no current revenue. The company's business model centers on developing its lead compound MP1032 through clinical stages (Phase I completed, Phase IIa completed in Psoriasis and COVID-19) toward market authorization. Revenue is expected to be generated through out-licensing partnerships with large pharmaceutical companies for commercialization across multiple indications, and through potential co-development arrangements. The company is also exploring Fixed-Dose Combination therapies combining MP1032 with lower doses of generic standard therapies to create novel medications with improved efficacy, fewer side effects, and renewed or extended patent protection.

Go-to-market motion1 record

Distribution channels1 record

Marketing channels9 records

MetrioPharm product offering

Product offering

Core offering

MetrioPharm AG is a clinical-stage biopharmaceutical company developing MP1032, a first-in-class oral small molecule self-regulating immunomodulator (ROS scavenger) that normalizes pathologically reprogrammed mitochondrial energy metabolism in macrophages without causing immunosuppression. The company focuses on advancing MP1032 through clinical development for rare/orphan indications such as Duchenne Muscular Dystrophy (DMD), with the intent to out-license or co-develop the compound with larger pharmaceutical partners for commercialization across multiple indications including psoriasis, COVID-19, rheumatoid arthritis, multiple sclerosis, inflammatory bowel disease, and sepsis.

Product overview

MetrioPharm AG is a clinical-stage biopharmaceutical company developing first-in-class self-regulating immunomodulators for inflammatory and infectious diseases. The company's product portfolio consists of two main offerings: the MP1000 Platform (a proprietary technology platform of oral small molecule immune modulators) and its lead compound MP1032 (the primary drug candidate developed on this platform). MP1032 is a first-in-class ROS scavenger that normalizes pathologically reprogrammed cellular/mitochondrial energy metabolism in inflammatory immune cells without causing immunosuppression. The platform enables corticosteroid-sparing therapies with efficacy comparable to corticosteroids but without serious side effects. The company is currently focused on rare diseases including Duchenne Muscular Dystrophy, with additional development in psoriasis, COVID-19, rheumatoid arthritis, multiple sclerosis, and sepsis.

Differentiator

Problem solved

Functional benefit

Products and services

  • MP1032 MP1032 is MetrioPharm's lead drug candidate — an oral small molecule that acts as a self-regulating reactive oxygen species (ROS) scavenger, normalizing pathologically reprogrammed mitochondrial energy metabolism in inflammatory immune cells (e.g., macrophages) without causing immunosuppression. It is being developed as a corticosteroid-sparing therapy for Duchenne Muscular Dystrophy and other inflammatory/autoimmune and infectious diseases, with demonstrated efficacy in Phase IIa studies in Psoriasis and COVID-19.
  • MP1000 Platform The MP1000 Platform is MetrioPharm's proprietary technology platform of oral small molecule immune modulators that target the pathologically dysregulated (reprogrammed) mitochondrial metabolism in macrophages and other immune cells. The platform enables development of self-regulating immunomodulators without immunosuppressive effects and serves as the foundation for the company's pipeline including MP1032.

Quantifiable outcome

  • Average 2.4 days earlier hospital discharge and 4 days shorter ICU stay for COVID-19 patients treated with MP1032 vs. placebo in Phase IIa study
  • +3 more outcomes

Companies that use MetrioPharm

Customer profile

Segments3 records

Ideal customer profiles3 records

MetrioPharm technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature4 records

MetrioPharm partnerships and signals

Strategic signal

Partnerships

One partnership is on record.

  • iMPact Consortium Partners (ImmunoLogik, Catalyze, MC Toxicology Consulting)coreStrategic or Co-development Partner · 1 January 2021MetrioPharm leads the iMPact project consortium consisting of three additional partners: ImmunoLogik, Catalyze, and MC Toxicology Consulting. The consortium was formed to conduct the international COVID-19 research project including the Phase II clinical trial and preclinical studies on SARS-CoV-2 variants.

Scale indicators7 records

Recent moves7 records

Expansion highlights5 records

MetrioPharm competitors and assessment

Company assessment

Direct peers

  • Sarepta Therapeutics: U.S.-listed commercial-stage biotech focused on Duchenne Muscular Dystrophy with approved gene therapies (Elevidys) and antisense oligonucleotides. Directly comparable DMD franchise with orphan designations and rare disease regulatory pathway; serves as a commercial benchmark for what a successful DMD asset can become.
  • PTC Therapeutics: U.S.-listed rare disease company with multiple DMD assets (Translarna, Emflaza) and a broader pipeline in inflammation and metabolic disorders. Closely comparable business model of orphan drug development, EMA/FDA regulatory navigation, and pipeline diversification from a DMD anchor.
  • Santhera Pharmaceuticals: Swiss-listed rare disease company developing therapies for Duchenne Muscular Dystrophy (e.g., vamorolone) and other neuromuscular disorders. Highly comparable as a small-cap European clinical-stage DMD specialist pursuing similar orphan regulatory pathways and out-licensing economics.
  • BioMarin Pharmaceutical: Established rare disease specialty pharma with multiple approved orphan drugs across neuromuscular and metabolic conditions. Comparable in pursuing small-molecule and biologic therapies for rare inflammatory/genetic diseases via accelerated regulatory pathways.
  • Reata Pharmaceuticals: Clinical-to-commercial rare disease company developing small-molecule therapies targeting inflammation and mitochondrial dysfunction (Skyclarys for Friedreich's ataxia). Highly comparable mechanistic and therapeutic-area overlap with MetrioPharm's ROS/mitochondrial platform.
  • Inflarx NV: European clinical-stage biotech developing first-in-class anti-inflammatory therapeutics (e.g., vilobelimab) targeting the complement system. Comparable as a small-cap inflammation-focused company pursuing novel mechanisms for rare and chronic inflammatory diseases.
  • Galapagos NV: European clinical-stage biotech historically focused on small-molecule immunology (JAK1 inhibitor filgotinib). Comparable as a mid-sized European inflammation-focused drug developer with similar out-licensing and partnership business model.
  • Catabasis Pharmaceuticals: Clinical-stage rare disease company developing small molecules for DMD (edasalonexent) and inflammatory conditions. Direct comparable in targeting inflammatory pathways for Duchenne Muscular Dystrophy with novel mechanisms, and a cautionary tale on clinical execution.

Broad incumbents

  • AbbVie: Large incumbent immunology pharma with Humira, Rinvoq, and Skyrizi dominating anti-inflammatory markets. Represents the competitive standard-of-care and a likely out-licensing/acquisition counterparty for MP1032 in autoimmune indications.
  • Horizon Therapeutics (Amgen): Specialty rare and inflammatory disease pharma (now part of Amgen) with assets in gout, thyroid eye disease, and autoimmune conditions. Comparable as a rare/inflammatory disease-focused commercial-stage player and potential BD partner for orphan-designated assets.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat3 records

Key risks7 records

Key highlights7 records

Customer concentration

MetrioPharm social profiles

Digital presence

MetrioPharm financial estimates

Financial estimate

Revenue estimate

Valuation estimate

MetrioPharm leadership team

Management profile

Number of profiles

Profiles9 records

MetrioPharm subsidiaries and ownership

Company hierarchy

Subsidiaries1 record

MetrioPharm funding detail

Funding detail

Funding overview

Funding rounds2 records

Investors1 record

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

MetrioPharm 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 MetrioPharm

What does MetrioPharm do?

MetrioPharm AG is a clinical-stage biopharmaceutical company developing MP1032, a first-in-class oral small molecule self-regulating immunomodulator (ROS scavenger) that normalizes pathologically reprogrammed mitochondrial energy metabolism in macrophages without causing immunosuppression. The company focuses on advancing MP1032 through clinical development for rare/orphan indications such as Duchenne Muscular Dystrophy (DMD), with the intent to out-license or co-develop the compound with larger pharmaceutical partners for commercialization across multiple indications including psoriasis, COVID-19, rheumatoid arthritis, multiple sclerosis, inflammatory bowel disease, and sepsis.

Is MetrioPharm a public or private company?

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

When was MetrioPharm founded?

MetrioPharm was founded in 2007. It employs 11 to 50 people.

Where is MetrioPharm based?

MetrioPharm is headquartered in Zürich, Switzerland, in the Europe region.

How does MetrioPharm make money?

One revenue line is on record: drug Development and Licensing.

Who are MetrioPharm's main competitors?

Direct peers on record are Sarepta Therapeutics, PTC Therapeutics, Santhera Pharmaceuticals, BioMarin Pharmaceutical, Reata Pharmaceuticals, Inflarx NV, Galapagos NV and Catabasis Pharmaceuticals. Broad incumbents are AbbVie and Horizon Therapeutics (Amgen).

Does MetrioPharm have an API?

No public API is recorded for MetrioPharm.

What industry is MetrioPharm in?

MetrioPharm's product category is Clinical-Stage Biopharmaceuticals. Its primary akta.pro industry code is HLAIACAB, Immunology & Autoimmune Specialty Pharmaceuticals, with a secondary code of HLAIACAC, Neurology & CNS Specialty Pharmaceuticals. Its NAICS code is 3254 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
BioSpaceProf. Dr. med. Jürgen Braun Appointed as New Member of the Scientific Advisory BoardMetrioPharm AG appointed Prof. Dr. med. Jürgen Braun to its Scientific Advisory Board, expanding expertise in inflammatory rheumatic diseases. He has advised the company since December 2025 on the clinical strategy and study design for MP1032 in rheumatological indications.GlobeNewswireDr. Stephan Rietiker elected as new Chairman of the Board of MetrioPharm AGMetrioPharm AG's board unanimously elected Dr. Stephan Rietiker as chairman at its constituent meeting. He brings experience from Roche, Boehringer Mannheim, and other global pharma companies. The company aims to advance its drug MP1032 for inflammatory and infectious diseases.GlobeNewswireMetrioPharm Establishes Scientific Advisory Board of Seasoned Immunology and Pediatric ExpertsMetrioPharm AG announced the establishment of a Scientific Advisory Board with four experts in immunology and pediatric neuromuscular disease. The advisors, including Prof. Dirk Fischer and Prof. Ferdinando Nicoletti, will review R&D activities and support clinical development decisions. The company's lead indication is Duchenne muscular dystrophy.GlobeNewswireMetrioPharm Receives Orphan Drug Designation for the Treatment of Duchenne Muscular DystrophyThe FDA granted orphan drug designation to MetrioPharm's MP1032 for Duchenne muscular dystrophy. The company plans to initiate a Phase II clinical trial in 2024, aiming to improve tolerability and efficacy over existing corticosteroid therapies.MetriopharmPress Release: MetrioPharm Starts Preclinical Experiments in Duchenne Muscular Dystrophy (DMD)MetrioPharm AG announced it has received a €125,000 grant from Duchenne UK to fund preclinical experiments evaluating its lead compound MP1032 for the treatment of Duchenne muscular dystrophy. The company is currently testing the drug's efficacy in an mdx mouse model to determine if it can reduce muscle inflammation and potentially lessen side effects associated with current steroid treatments. This development positions MP1032 for potential clinical trials targeting this orphan disease.GlobeNewswireThomas Christély Joins Management of MetrioPharm AG as CEOThomas Christély will become CEO of MetrioPharm AG on October 1, 2021, taking over business development and financing from co-founder Dr. Wolfgang Brysch. Dr. Brysch will focus on clinical development of the lead compound MP1032, which is in a Phase II trial for COVID-19.GlobeNewswireDGAP-News: MetrioPharm extends drug pipeline to cancer therapyMetrioPharm AG extended its drug pipeline to cancer therapy, focusing on its lead compound Etomoxir. A study from M.D. Anderson and the University of Texas showed Etomoxir inhibits leukaemia cell growth and increases survival by 67% when combined with AraC. The company now plans a development program for oncological indications.GlobeNewswireDGAP-News: MetrioPharm AG announces capital increaseMetrioPharm AG announced a capital increase on March 4, 2010, issuing 3 million new shares to strategic investors for gross proceeds of 750,000 Euros. The shares raised the company's capital from CHF 8 million to CHF 8.6 million, with investors increasing their stake to about 7 percent. Proceeds will fund additional patent applications and pipeline products.GlobeNewswireDGAP-News: Conversion of bearer shares to registered sharesMetrioPharm AG converted its bearer shares to registered shares on 30 September 2009, with trading of the new shares starting 1 December 2009. The conversion is exempt from charges, and the company expects improved investor relations and cost advantages. Shareholders will be recognized only if registered in the share register.