Developer docs
API playgroundTry for free, no card

Search company profiles

Therachon

Full company profile

uuid0003qhn

Namestring
Therachon
Legal namestring
Pfizer Inc.
Websiteurl
therachon.com
Company typeenum
Public
Founded yearint
1849
Descriptiontext

Therachon is a privately held, clinical-stage biotechnology company founded in 2014 and headquartered in Basel, Switzerland. The company is focused on developing medicines for rare, genetic diseases, operating in a therapeutic area where unmet medical need is high and regulatory pathways such as orphan-drug designation can be commercially attractive. Based on the input, the company is described as 'global' in scope despite its lean headcount of 1-10 employees, consistent with a development-stage biotech that intends to run clinical programs across multiple geographies.

The company's pipeline and technology base are anchored in biological assets targeting rare genetic conditions, with its lead activity focused on a single-asset rare-disease program around the time of the 2018 funding events. In October 2018, Therachon expanded its pipeline via the acquisition of GLyPharma Therapeutic, which added a GLP-2 analog program (commonly associated with short bowel syndrome) to the portfolio, signaling a deliberate move from a single-asset to a multi-asset rare-disease platform. The input does not disclose specific underlying modalities (e.g., recombinant protein, antibody, gene therapy) in granular detail, so the technology description is limited to the broad characterization of a rare-disease therapeutics platform.

Therachon's business model is consistent with a venture-backed, pre-commercial biotech: the company has raised approximately $100 million across three funding rounds between 2015 and 2018, with investors including OrbiMed, Versant Ventures, Inserm Transfert Initiative, New Enterprise Associates, Bpifrance, Cowen Healthcare Investments, Tekla Capital Management, Novo Holdings, and Pfizer Venture Investments. There are no disclosed products, customers, pricing models, or commercial revenue streams in the input. Future monetization, if executed as planned, would most likely take the form of out-licensing, partnership agreements, or a strategic acquisition, rather than direct sales given the absence of commercial infrastructure in the provided data. Leadership consists of a Chairman & Managing Director (Tom Woiwode) and a COO (Richard Porter).

Short descriptiontext

Therachon is a privately held, clinical-stage biotechnology company based in Basel, Switzerland, developing therapeutics for rare, genetic diseases. It operates a multi-asset rare-disease pipeline built through venture funding and the 2018 acquisition of GLyPharma Therapeutic.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1–10
akta.pro rankint
HeadquartersBasel, Switzerland
HQ citystring
Basel
HQ countrystring
Switzerland
HQ regionstring
Europe
Markets served

Serves global market

Keyword5 values
rare disease therapeutics, genetic disease medicines, biotechnology drug development, orphan drug pipeline, rare disease biopharmaceuticals
Industry3 codes
1Genetic & Genomic Rare Disease Therapeutics
CodeHLAIAIAAPrimaryYes
2Rare Pediatric & Congenital Disorder Therapies
CodeHLAIAIANPrimaryNo
3Rare Endocrine & Growth Disorder Therapies
CodeHLAIAIAJPrimaryNo
NAICS code2 codes
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
  • Biological Product (except Diagnostic) Manufacturing325414
SIC code1 code
  • Pharmaceutical Preparations2834
Product category
Rare Disease Biopharmaceuticals
Cost components3 values
Technology or R&D, Personnel, Operations
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 4 records shown
1Pfizer CentreOne
Description

A partner for business and research collaborations, offering contract manufacturing and pharmaceutical development services.

pfizer.com.
+3 more records
Core offering1 text field

Therachon is a clinical-stage biotechnology company developing biopharmaceutical therapies for rare, genetic diseases, with a focus on conditions such as achondroplasia and other skeletal dysplasias. The company builds a pipeline of protein-based and biologic drug candidates targeting well-characterized genetic pathways, advancing them through preclinical and clinical development toward potential licensing, partnership, or commercialization.

Differentiator
Functional benefit
Problem solved
Recent move4 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight4 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

BioMarin is a global rare-disease biotech with a leading achondroplasia program (vosoritide) directly competing with Therachon's lead rare skeletal dysplasia focus. Both target the same monogenic growth disorder via differentiated mechanisms.

TypeBroad incumbent
Description

Alexion is the established global leader in rare-disease therapeutics, now part of AstraZeneca. While broader in scope, its orphan-drug commercial infrastructure, payer relationships, and rare-disease M&A appetite make it a key benchmark and potential acquirer for Therachon.

TypeDirect peer
Description

Ascendis Pharma develops therapeutics for rare endocrine and growth disorders, including FGFR3-pathway-adjacent conditions. Direct overlap with Therachon's rare pediatric growth disorder focus and orphan-drug strategy.

TypeEmerging player
Description

Regenxbio develops AAV gene therapies for rare monogenic diseases including metabolic and pediatric genetic conditions. Comparable to Therachon on target indication class (rare monogenic disorders) and orphan-drug commercial model, though distinct on modality.

TypeEmerging player
Description

QED Therapeutics (a BridgeBio subsidiary) develops infigratinib and other FGFR-pathway inhibitors, including for rare skeletal disorders. Strong mechanistic and indication overlap with Therachon's FGFR3-targeted rare disease programs.

TypeBroad incumbent
Description

Sanofi's Genzyme unit is one of the largest rare-disease commercial organizations globally. Relevant both as a competing developer of rare genetic therapies and as a potential strategic partner/acquirer for Therachon.

TypeDirect peer
Description

Ultragenyx is a clinical-to-commercial rare and ultra-rare genetic disease biotech with a multi-asset pipeline addressing monogenic conditions. Therachon's rare-genetic disease focus and similar orphan-drug commercial model make it a closely comparable specialty biotech.

TypeBroad incumbent
Description

Takeda has built a meaningful rare-disease franchise (post-Shire) and pursues licensing and M&A in rare genetic disorders. Comparable as a potential strategic acquirer/partner for Therachon's rare-disease assets.

TypeBroad incumbent
Description

Pfizer is one of the world's largest biopharmaceutical companies and participated in Therachon's 2018 round through Pfizer Venture Investments. Highly comparable as both a potential strategic acquirer of rare-disease biotechs and a benchmark for orphan-drug pipeline economics.

TypeEmerging player
Description

Enzyvant is a clinical-stage rare-disease biotech developing regenerative therapies for single, ultra-rare indications. Compares to Therachon in company stage, funding profile, and orphan-drug regulatory pathway.

Market position
Weaknesses4 records

Each record includes

Headline, Details, Source

Competitive moat3 records

Each record includes

Type, Details

Key risks1 record

Each record includes

Headline, Details, Source

Key highlights1 record

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

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

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles2 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

Investors9 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&A1 record

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 →

Therachon

Rare Disease Biopharmaceuticalstherachon.com

Therachon is a privately held, clinical-stage biotechnology company based in Basel, Switzerland, developing therapeutics for rare, genetic diseases. It operates a multi-asset rare-disease pipeline built through venture funding and the 2018 acquisition of GLyPharma Therapeutic.

What Therachon does

Therachon is a privately held, clinical-stage biotechnology company founded in 2014 and headquartered in Basel, Switzerland. The company is focused on developing medicines for rare, genetic diseases, operating in a therapeutic area where unmet medical need is high and regulatory pathways such as orphan-drug designation can be commercially attractive. Based on the input, the company is described as 'global' in scope despite its lean headcount of 1-10 employees, consistent with a development-stage biotech that intends to run clinical programs across multiple geographies.

The company's pipeline and technology base are anchored in biological assets targeting rare genetic conditions, with its lead activity focused on a single-asset rare-disease program around the time of the 2018 funding events. In October 2018, Therachon expanded its pipeline via the acquisition of GLyPharma Therapeutic, which added a GLP-2 analog program (commonly associated with short bowel syndrome) to the portfolio, signaling a deliberate move from a single-asset to a multi-asset rare-disease platform. The input does not disclose specific underlying modalities (e.g., recombinant protein, antibody, gene therapy) in granular detail, so the technology description is limited to the broad characterization of a rare-disease therapeutics platform.

Therachon's business model is consistent with a venture-backed, pre-commercial biotech: the company has raised approximately $100 million across three funding rounds between 2015 and 2018, with investors including OrbiMed, Versant Ventures, Inserm Transfert Initiative, New Enterprise Associates, Bpifrance, Cowen Healthcare Investments, Tekla Capital Management, Novo Holdings, and Pfizer Venture Investments. There are no disclosed products, customers, pricing models, or commercial revenue streams in the input. Future monetization, if executed as planned, would most likely take the form of out-licensing, partnership agreements, or a strategic acquisition, rather than direct sales given the absence of commercial infrastructure in the provided data. Leadership consists of a Chairman & Managing Director (Tom Woiwode) and a COO (Richard Porter).

Therachon firmographics

Firmographics
Name
Therachon
Legal name
Pfizer Inc.
Website
https://therachon.com
Company type
Public
Founded year
1849
Operating status
Operating
Headcount range
1–10 employees
Short description
Therachon is a privately held, clinical-stage biotechnology company based in Basel, Switzerland, developing therapeutics for rare, genetic diseases. It operates a multi-asset rare-disease pipeline built through venture funding and the 2018 acquisition of GLyPharma Therapeutic.
Ownership category
akta.pro rank

Therachon industry classification

Industry
Product category
Rare Disease Biopharmaceuticals
NAICS
Research and Development in Biotechnology (except Nanobiotechnology) (541714), Biological Product (except Diagnostic) Manufacturing (325414)
SIC
Pharmaceutical Preparations (2834)
akta.pro primary industry
Genetic & Genomic Rare Disease Therapeutics (HLAIAIAA)
akta.pro secondary industries
Rare Pediatric & Congenital Disorder Therapies (HLAIAIAN), Rare Endocrine & Growth Disorder Therapies (HLAIAIAJ)

Keywords

  • Rare disease therapeutics
  • Genetic disease medicines
  • Biotechnology drug development
  • Orphan drug pipeline
  • Rare disease biopharmaceuticals

Where Therachon is headquartered

Location

Headquarters

HQ city
Basel
HQ country
Switzerland
HQ region
Europe

Markets served

Therachon business model

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

Therachon product offering

Product offering

Core offering

Therachon is a clinical-stage biotechnology company developing biopharmaceutical therapies for rare, genetic diseases, with a focus on conditions such as achondroplasia and other skeletal dysplasias. The company builds a pipeline of protein-based and biologic drug candidates targeting well-characterized genetic pathways, advancing them through preclinical and clinical development toward potential licensing, partnership, or commercialization.

Differentiator

Problem solved

Functional benefit

Brands

  • Pfizer CentreOne: A partner for business and research collaborations, offering contract manufacturing and pharmaceutical development services.
  • PfizerForAll
  • PfizerPro
  • Pfizer RxPathways

Companies that use Therachon

Customer profile

Ideal customer profiles1 record

Therachon technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Therachon partnerships and signals

Strategic signal

Recent moves4 records

Expansion highlights4 records

Therachon competitors and assessment

Company assessment

Direct peers

  • BioMarin Pharmaceutical: BioMarin is a global rare-disease biotech with a leading achondroplasia program (vosoritide) directly competing with Therachon's lead rare skeletal dysplasia focus. Both target the same monogenic growth disorder via differentiated mechanisms.
  • Ascendis Pharma: Ascendis Pharma develops therapeutics for rare endocrine and growth disorders, including FGFR3-pathway-adjacent conditions. Direct overlap with Therachon's rare pediatric growth disorder focus and orphan-drug strategy.
  • Ultragenyx Pharmaceutical: Ultragenyx is a clinical-to-commercial rare and ultra-rare genetic disease biotech with a multi-asset pipeline addressing monogenic conditions. Therachon's rare-genetic disease focus and similar orphan-drug commercial model make it a closely comparable specialty biotech.

Broad incumbents

  • Alexion (AstraZeneca Rare Disease): Alexion is the established global leader in rare-disease therapeutics, now part of AstraZeneca. While broader in scope, its orphan-drug commercial infrastructure, payer relationships, and rare-disease M&A appetite make it a key benchmark and potential acquirer for Therachon.
  • Sanofi Genzyme (Rare Disease): Sanofi's Genzyme unit is one of the largest rare-disease commercial organizations globally. Relevant both as a competing developer of rare genetic therapies and as a potential strategic partner/acquirer for Therachon.
  • Takeda Pharmaceutical (Rare Diseases): Takeda has built a meaningful rare-disease franchise (post-Shire) and pursues licensing and M&A in rare genetic disorders. Comparable as a potential strategic acquirer/partner for Therachon's rare-disease assets.
  • Pfizer: Pfizer is one of the world's largest biopharmaceutical companies and participated in Therachon's 2018 round through Pfizer Venture Investments. Highly comparable as both a potential strategic acquirer of rare-disease biotechs and a benchmark for orphan-drug pipeline economics.

Emerging players

  • Regenxbio: Regenxbio develops AAV gene therapies for rare monogenic diseases including metabolic and pediatric genetic conditions. Comparable to Therachon on target indication class (rare monogenic disorders) and orphan-drug commercial model, though distinct on modality.
  • QED Therapeutics: QED Therapeutics (a BridgeBio subsidiary) develops infigratinib and other FGFR-pathway inhibitors, including for rare skeletal disorders. Strong mechanistic and indication overlap with Therachon's FGFR3-targeted rare disease programs.
  • Enzyvant Therapeutics: Enzyvant is a clinical-stage rare-disease biotech developing regenerative therapies for single, ultra-rare indications. Compares to Therachon in company stage, funding profile, and orphan-drug regulatory pathway.

Market position

Weaknesses4 records

Competitive moat3 records

Key risks1 record

Key highlights1 record

Customer concentration

Therachon social profiles

Digital presence

Therachon financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Therachon leadership team

Management profile

Number of profiles

Profiles2 records

Therachon funding detail

Funding detail

Funding overview

Funding rounds3 records

Investors9 records

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

Therachon M&A and investment

M&A and investment

M&A1 record

Investments

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

Frequently asked questions about Therachon

What does Therachon do?

Therachon is a clinical-stage biotechnology company developing biopharmaceutical therapies for rare, genetic diseases, with a focus on conditions such as achondroplasia and other skeletal dysplasias. The company builds a pipeline of protein-based and biologic drug candidates targeting well-characterized genetic pathways, advancing them through preclinical and clinical development toward potential licensing, partnership, or commercialization.

Is Therachon a public or private company?

Therachon is a public company. It is classified as venture growth investor backed and is currently operating.

When was Therachon founded?

Therachon was founded in 1849. It employs 1 to 10 people.

Where is Therachon based?

Therachon is headquartered in Basel, Switzerland, in the Europe region.

Who are Therachon's main competitors?

Direct peers on record are BioMarin Pharmaceutical, Ascendis Pharma and Ultragenyx Pharmaceutical. Broad incumbents are Alexion (AstraZeneca Rare Disease), Sanofi Genzyme (Rare Disease), Takeda Pharmaceutical (Rare Diseases) and Pfizer. Emerging players are Regenxbio, QED Therapeutics and Enzyvant Therapeutics.

Does Therachon have an API?

No public API is recorded for Therachon.

What industry is Therachon in?

Therachon's product category is Rare Disease Biopharmaceuticals. Its primary akta.pro industry code is HLAIAIAA, Genetic & Genomic Rare Disease Therapeutics, with a secondary code of HLAIAIAN, Rare Pediatric & Congenital Disorder Therapies. Its NAICS code is 541714 and its SIC code is 2834.

Unlock the full company data

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

Contact sales
Live signals
ThedealPfizer Leans Toward Tuck-In DealsPfizer's General Counsel Doug Lankler stated at The Deal Economy Conference in New York City on Nov. 20 that the company is more likely to pursue tuck-in acquisitions rather than larger M&A deals under new CEO Albert Bourla's leadership. The company has completed several tuck-in deals this year, including the $11.4 billion acquisition of Array BioPharma and the $340 million purchase of Therachon Holding AG. Meanwhile, Pfizer and Mylan are working to secure regulatory approval for their pending merger combining Pfizer's established medicines unit with Mylan, with the FTC issuing an additional information request in October.PR Newswire$7.1 Bn Human Growth Hormone (hGH) Industry Outlook, 2025The Global Human Growth Hormone Market is projected to reach $7.1 billion by 2025, growing at a compound annual growth rate of 8.3% during the forecast period, driven by expanded applications of recombinant human growth hormone (rhGH) beyond severe growth hormone deficiency to include conditions such as Prader-Willi syndrome, Turner syndrome, and chronic renal failure. Major pharmaceutical companies have pursued growth through strategic acquisitions, including Novartis's agreement to acquire The Medicines Company and Pfizer's acquisition of Therachon, as well as product launches and partnerships targeting rare disease treatments and pediatric applications. The market analysis covers key players including Merck Group, Teva, Ipsen, Pfizer, Roche, Novo Nordisk, and Eli Lilly, with distribution spanning retail, hospital, specialty, and online pharmacies globally.PR NewswireTherachon to Present Data from Ongoing Phase II Study of Apraglutide for Short Bowel Syndrome (SBS) at Digestive Disease WeekTherachon AG announced it will present interim Phase II clinical trial results for apraglutide, a GLP-2 analog being developed for Short Bowel Syndrome, at Digestive Disease Week in San Diego on May 19, 2019. Preliminary results indicate once-weekly dosing was well-tolerated and improved fecal wet weight and energy absorption, with potential to reduce dehydration and malnutrition risks in SBS patients. The drug is currently being investigated in two Phase II trials in Denmark and has completed Phase 1 trials in healthy volunteers.PR NewswireTherachon Presents Data from Preclinical and Phase I clinical Studies of Apraglutide for the Treatment of Short Bowel Syndrome at ASPEN 2019 Nutrition Science & Practice ConferenceTherachon AG presented Phase I clinical trial results for apraglutide at the ASPEN 2019 Nutrition Science & Practice Conference, showing the GLP-2 analog was generally well-tolerated with no serious adverse events in healthy volunteers. Head-to-head preclinical studies in rats demonstrated that apraglutide had a longer half-life and induced greater intestinotrophic effects compared to existing GLP-2 analogs teduglutide and glepaglutide at the same doses. The company is currently conducting two Phase 2 clinical trials in SBS patients in Denmark, with the drug showing potential to become a best-in-class once-weekly treatment for a condition affecting an estimated 20,000–40,000 patients in the US and Europe.PR NewswireTherachon renforce son conseil d'administration avec la désignation des dirigeants sectoriels Sandip Kapadia et Patrick MachadoTherachon AG, a Swiss clinical-stage biotech company focused on rare diseases, announced the appointment of Sandip Kapadia and Patrick Machado to its board of directors. Both appointees bring over 20 years of experience in the life sciences sector, with Kapadia's background including senior finance roles at Novartis/Sandoz and his current position as CFO at Intercept Pharmaceuticals, while Machado co-founded Medivation and serves on multiple biotech company boards. The company stated this move will strengthen their board as they advance clinical programs for short bowel syndrome and achondroplasia.PR NewswireTherachon stärkt seinen Verwaltungsrat mit den Branchenprofis Sandip Kapadia und Patrick MachadoTherachon AG, a Basel-based biotechnology company focused on rare diseases, announced the appointment of Sandip Kapadia and Patrick Machado to its board of directors. Kapadia brings over 20 years of life sciences experience, currently serving as CFO at Intercept Pharmaceuticals, while Machado is a co-founder of Medivation with over 20 years of industry experience. The company stated the new members will strengthen its board as it advances its clinical programs for short bowel syndrome and achondroplasia.PR NewswireTherachon refuerza su Consejo de Administración con el nombramiento de Sandip Kapadia y Patrick MachadoTherachon AG, a clinical-stage biotech company based in Basel, Switzerland, announced the appointment of Sandip Kapadia and Patrick Machado to its Board of Directors. Kapadia brings over 20 years of experience including CFO roles at Intercept Pharmaceuticals and Novartis, while Machado is a cofounder of Medivation and currently serves on boards of multiple public biopharmaceutical companies. The company stated these appointments will strengthen their board as they transition to a late-stage clinical company focused on rare disease drug development.PR NewswireTherachon Strengthens Board of Directors with the Appointment of Industry Leaders Sandip Kapadia and Patrick MachadoTherachon AG announced the appointment of Sandip Kapadia and Patrick Machado to its Board of Directors. The company aims to leverage their combined expertise in life science finance and legal leadership to advance clinical programs for rare conditions such as short bowel syndrome and achondroplasia.PR NewswireTherachon obtient une désignation de médicament orphelin par la FDA américaine pour l'apraglutide dans le cadre du traitement du syndrome de l'intestin courtTherachon AG announced that the US Food and Drug Administration (FDA) granted orphan drug designation to apraglutide for the treatment of Short Bowel Syndrome (SBS), a rare disease affecting an estimated 20,000–40,000 patients in the US and Europe. This is the second orphan drug designation for the drug, following the European Commission's prior designation, making it eligible for development incentive programs for rare diseases affecting fewer than 200,000 people. Apraglutide is a next-generation synthetic GLP-2 analogue currently being evaluated in two Phase 2 clinical trials for SBS.PR NewswireTherachon is Granted Orphan Drug Designation by US FDA for Apraglutide for the Treatment of Short Bowel SyndromeTherachon AG announced that the U.S. FDA has granted Orphan Drug Designation for apraglutide, an experimental treatment for short bowel syndrome (SBS), a rare and severe condition associated with intestinal failure. The designation qualifies investigational therapies for development incentives aimed at advancing clinical programs for rare diseases affecting fewer than 200,000 people. Apraglutide, a next-generation GLP-2 analog with a 30-hour half-life enabling weekly dosing, is currently being evaluated in two Phase 2 clinical trials.