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Enzyvant Sciences

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uuid000aqg9

Namestring
Enzyvant Sciences
Websiteurl
enzyvant.com
Company typeenum
Private
Founded yearint
2016
Descriptiontext

Enzyvant Sciences is a clinical-stage biotechnology company focused on developing cell and gene therapies for rare diseases. Founded in 2016 and headquartered in Basel, Switzerland, the company operates in the cell and gene therapy (CGT) sector, where approximately 4,099 therapies are reportedly in development industry-wide and 51% of newly initiated gene therapy trials target non-oncology indications. Enzyvant was recognized among 100 Cell and Gene Therapy Leaders to Watch in 2025, an evaluation based on FDA-approved products, clinical pipeline stage, patent activity, strategic partnerships, and funding milestones.

The company's core technology is described as a cell and gene therapy development platform, though specific proprietary features, scientific platform architecture, and pipeline assets are not publicly disclosed in available sources. Enzyvant operates with a lean team of 11-50 employees, consistent with an early-stage development model reliant on specialized scientific talent rather than large-scale operations. No patents, trademark registrations, regulatory designations, or named partnerships are disclosed in the available data.

Enzyvant's business model is pre-commercial: the company has no FDA-approved products, no disclosed revenue, no public pricing structure, and no established distribution channels. Revenue mechanics would only materialize upon regulatory approval of therapeutic candidates. Commercial pricing and distribution would be established post-approval. As a private company founded in 2016 with no disclosed funding rounds, ownership structure, or named investors in the available source material, the firm's capital base and runway are not verifiable from public data.

Short descriptiontext

Enzyvant Sciences is a clinical-stage biotechnology company founded in 2016 and headquartered in Basel, Switzerland, focused on developing cell and gene therapies for rare diseases. The firm operates with 11-50 employees and has no approved products.

Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersBasel, Switzerland
HQ citystring
Basel
HQ countrystring
Switzerland
HQ regionstring
Europe
Markets served

Serves global market

Keyword5 values
rare disease therapies, cell and gene therapy, biopharmaceutical development, clinical stage biotechnology, genetic medicines
Industry1 code
1Gene Therapy for Rare/Monogenic Diseases
CodeHLAAACAEPrimaryYes
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
Cell and Gene Therapy for Rare Diseases
Social media profiles1 record
Cost components3 values
Personnel, Technology or R&D, Operations
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

Enzyvant Sciences is a clinical-stage biopharmaceutical company developing cell and gene therapies for rare diseases. The company operates within the broader cell and gene therapy sector, building a pipeline of therapeutic candidates aimed at addressing unmet medical needs in rare disease populations. Its activities focus on preclinical and clinical development of advanced therapy candidates rather than commercial-stage product sales.

Differentiator
Functional benefit
Problem solved
Product overview1 text field

Enzyvant Sciences is a biopharmaceutical company focused on developing cell and gene therapies for rare diseases. The company operates in the cell and gene therapy (CGT) sector, with a development pipeline targeting unmet medical needs. Based on the source material, Enzyvant Sciences is identified among 100 leading cell and gene therapy organizations to watch in 2025, evaluated on FDA-approved products, clinical pipeline stage, patent activity, strategic partnerships, and funding milestones.

Scale indicator1 record

Each record includes

Type, Value, Description, Source

Recent move2 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight1 record

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Clinical-stage gene therapy company developing treatments for severe genetic and rare diseases. Highly comparable to Enzyvant given shared focus on cell and gene therapies targeting rare/monogenic conditions with similar regulatory and manufacturing challenges.

TypeDirect peer
Description

Commercial-stage gene therapy company specializing in rare neuromuscular diseases. Directly comparable as a CGT-focused rare disease specialist with both approved products and active pipeline development.

TypeDirect peer
Description

Commercial biopharmaceutical company focused on rare diseases, including gene therapy products. Comparable in rare disease specialization, with overlapping therapeutic areas and similar regulatory pathways for orphan drug development.

TypeDirect peer
Description

Clinical and commercial-stage rare disease biopharmaceutical company developing novel therapies including gene therapies. Comparable in rare disease specialization and pipeline approach, with parallel gene therapy development programs.

TypeDirect peer
Description

Gene therapy company (now part of Roche) that pioneered approved AAV-based gene therapies for rare inherited diseases. Highly comparable in CGT modality and rare disease focus, with established commercial gene therapy experience.

TypeBroad incumbent
Description

Gene therapy subsidiary of Novartis focused on rare diseases, including the SMA gene therapy Zolgensma. Comparable in CGT rare disease focus, with greater scale and resources as part of a global pharmaceutical leader.

TypeDirect peer
Description

Gene therapy company developing AAV-based treatments for rare diseases including hemophilia and Huntington's disease. Closely comparable in modality, therapeutic focus, and development stage as a clinical-stage gene therapy specialist.

TypeEmerging player
Description

Clinical-stage gene therapy company developing AAV-based treatments for neurological diseases. Comparable in gene therapy platform approach and rare disease focus, though at smaller scale and earlier development stage.

TypeDirect peer
Description

Clinical-stage gene therapy company developing AAV therapeutics for rare diseases including wet AMD and Duchenne muscular dystrophy. Comparable in gene therapy modality, rare disease focus, and partnership-driven commercialization strategy.

TypeBroad incumbent
Description

Commercial-stage biopharmaceutical company focused on genetic diseases and rare conditions. Comparable in rare disease specialization with broader pipeline diversification across multiple therapeutic areas.

Market position
Strengths4 records

Each record includes

Headline, Details, Source

Weaknesses4 records

Each record includes

Headline, Details, Source

Competitive moat3 records

Each record includes

Type, Details

Key risks5 records

Each record includes

Headline, Details, Source

Key highlights4 records

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
No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds

Each record includes

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

Investors

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 →

Enzyvant Sciences

Cell and Gene Therapy for Rare Diseasesenzyvant.com

Enzyvant Sciences is a clinical-stage biotechnology company founded in 2016 and headquartered in Basel, Switzerland, focused on developing cell and gene therapies for rare diseases. The firm operates with 11-50 employees and has no approved products.

What Enzyvant Sciences does

Enzyvant Sciences is a clinical-stage biotechnology company focused on developing cell and gene therapies for rare diseases. Founded in 2016 and headquartered in Basel, Switzerland, the company operates in the cell and gene therapy (CGT) sector, where approximately 4,099 therapies are reportedly in development industry-wide and 51% of newly initiated gene therapy trials target non-oncology indications. Enzyvant was recognized among 100 Cell and Gene Therapy Leaders to Watch in 2025, an evaluation based on FDA-approved products, clinical pipeline stage, patent activity, strategic partnerships, and funding milestones.

The company's core technology is described as a cell and gene therapy development platform, though specific proprietary features, scientific platform architecture, and pipeline assets are not publicly disclosed in available sources. Enzyvant operates with a lean team of 11-50 employees, consistent with an early-stage development model reliant on specialized scientific talent rather than large-scale operations. No patents, trademark registrations, regulatory designations, or named partnerships are disclosed in the available data.

Enzyvant's business model is pre-commercial: the company has no FDA-approved products, no disclosed revenue, no public pricing structure, and no established distribution channels. Revenue mechanics would only materialize upon regulatory approval of therapeutic candidates. Commercial pricing and distribution would be established post-approval. As a private company founded in 2016 with no disclosed funding rounds, ownership structure, or named investors in the available source material, the firm's capital base and runway are not verifiable from public data.

Enzyvant Sciences firmographics

Firmographics
Name
Enzyvant Sciences
Website
https://enzyvant.com
Company type
Private
Founded year
2016
Headcount range
11–50 employees
Short description
Enzyvant Sciences is a clinical-stage biotechnology company founded in 2016 and headquartered in Basel, Switzerland, focused on developing cell and gene therapies for rare diseases. The firm operates with 11-50 employees and has no approved products.
Ownership category
akta.pro rank

Enzyvant Sciences industry classification

Industry
Product category
Cell and Gene Therapy for Rare Diseases
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
Gene Therapy for Rare/Monogenic Diseases (HLAAACAE)

Keywords

  • Rare disease therapies
  • Cell and gene therapy
  • Biopharmaceutical development
  • Clinical stage biotechnology
  • Genetic medicines

Where Enzyvant Sciences is headquartered

Location

Headquarters

HQ city
Basel
HQ country
Switzerland
HQ region
Europe

Markets served

Enzyvant Sciences business model

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

Enzyvant Sciences product offering

Product offering

Core offering

Enzyvant Sciences is a clinical-stage biopharmaceutical company developing cell and gene therapies for rare diseases. The company operates within the broader cell and gene therapy sector, building a pipeline of therapeutic candidates aimed at addressing unmet medical needs in rare disease populations. Its activities focus on preclinical and clinical development of advanced therapy candidates rather than commercial-stage product sales.

Product overview

Enzyvant Sciences is a biopharmaceutical company focused on developing cell and gene therapies for rare diseases. The company operates in the cell and gene therapy (CGT) sector, with a development pipeline targeting unmet medical needs. Based on the source material, Enzyvant Sciences is identified among 100 leading cell and gene therapy organizations to watch in 2025, evaluated on FDA-approved products, clinical pipeline stage, patent activity, strategic partnerships, and funding milestones.

Differentiator

Problem solved

Functional benefit

Companies that use Enzyvant Sciences

Customer profile

Ideal customer profiles1 record

Enzyvant Sciences technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Enzyvant Sciences partnerships and signals

Strategic signal

Scale indicators1 record

Recent moves2 records

Expansion highlights1 record

Enzyvant Sciences competitors and assessment

Company assessment

Direct peers

  • Bluebird Bio: Clinical-stage gene therapy company developing treatments for severe genetic and rare diseases. Highly comparable to Enzyvant given shared focus on cell and gene therapies targeting rare/monogenic conditions with similar regulatory and manufacturing challenges.
  • Sarepta Therapeutics: Commercial-stage gene therapy company specializing in rare neuromuscular diseases. Directly comparable as a CGT-focused rare disease specialist with both approved products and active pipeline development.
  • BioMarin Pharmaceutical: Commercial biopharmaceutical company focused on rare diseases, including gene therapy products. Comparable in rare disease specialization, with overlapping therapeutic areas and similar regulatory pathways for orphan drug development.
  • Ultragenyx Pharmaceutical: Clinical and commercial-stage rare disease biopharmaceutical company developing novel therapies including gene therapies. Comparable in rare disease specialization and pipeline approach, with parallel gene therapy development programs.
  • Spark Therapeutics (Roche): Gene therapy company (now part of Roche) that pioneered approved AAV-based gene therapies for rare inherited diseases. Highly comparable in CGT modality and rare disease focus, with established commercial gene therapy experience.
  • uniQure: Gene therapy company developing AAV-based treatments for rare diseases including hemophilia and Huntington's disease. Closely comparable in modality, therapeutic focus, and development stage as a clinical-stage gene therapy specialist.
  • Regenxbio: Clinical-stage gene therapy company developing AAV therapeutics for rare diseases including wet AMD and Duchenne muscular dystrophy. Comparable in gene therapy modality, rare disease focus, and partnership-driven commercialization strategy.

Broad incumbents

  • AveXis (Novartis): Gene therapy subsidiary of Novartis focused on rare diseases, including the SMA gene therapy Zolgensma. Comparable in CGT rare disease focus, with greater scale and resources as part of a global pharmaceutical leader.
  • BridgeBio Pharma: Commercial-stage biopharmaceutical company focused on genetic diseases and rare conditions. Comparable in rare disease specialization with broader pipeline diversification across multiple therapeutic areas.

Emerging players

  • Voyager Therapeutics: Clinical-stage gene therapy company developing AAV-based treatments for neurological diseases. Comparable in gene therapy platform approach and rare disease focus, though at smaller scale and earlier development stage.

Market position

Strengths4 records

Weaknesses4 records

Competitive moat3 records

Key risks5 records

Key highlights4 records

Customer concentration

Enzyvant Sciences social profiles

Digital presence

Enzyvant Sciences financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Enzyvant Sciences leadership team

Management profile

Number of profiles

Enzyvant Sciences funding detail

Funding detail

Funding overview

Funding rounds

Investors

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

Enzyvant Sciences 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 Enzyvant Sciences

What does Enzyvant Sciences do?

Enzyvant Sciences is a clinical-stage biopharmaceutical company developing cell and gene therapies for rare diseases. The company operates within the broader cell and gene therapy sector, building a pipeline of therapeutic candidates aimed at addressing unmet medical needs in rare disease populations. Its activities focus on preclinical and clinical development of advanced therapy candidates rather than commercial-stage product sales.

When was Enzyvant Sciences founded?

Enzyvant Sciences was founded in 2016. It employs 11 to 50 people.

Where is Enzyvant Sciences based?

Enzyvant Sciences is headquartered in Basel, Switzerland, in the Europe region.

Who are Enzyvant Sciences's main competitors?

Direct peers on record are Bluebird Bio, Sarepta Therapeutics, BioMarin Pharmaceutical, Ultragenyx Pharmaceutical, Spark Therapeutics (Roche), uniQure and Regenxbio. Broad incumbents are AveXis (Novartis) and BridgeBio Pharma. Voyager Therapeutics is listed as an emerging player.

Does Enzyvant Sciences have an API?

No public API is recorded for Enzyvant Sciences.

What industry is Enzyvant Sciences in?

Enzyvant Sciences's product category is Cell and Gene Therapy for Rare Diseases. Its primary akta.pro industry code is HLAAACAE, Gene Therapy for Rare/Monogenic Diseases. Its NAICS code is 325414 and its SIC code is 2836.

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Live signals
GlobeNewswireEnzyvant Receives 2022 Rare Impact Industry Innovation Award from the National Organization for Rare Disorders (NORD) for Novel, Tissue-Based Therapy to Treat Ultra-Rare, Life-Threatening Pediatric CoEnzyvant received a 2022 NORD Industry Innovation Award for its FDA-approved RETHYMIC therapy for pediatric congenital athymia. The tissue-based treatment is the first and only FDA-approved option for immune reconstitution in this ultra-rare condition, affecting about 17-24 infants annually in the U.S.GlobeNewswireEnzyvant Appoints Johanna Rossell as Chief Commercial OfficerEnzyvant appointed Johanna Rossell as Chief Commercial Officer, bringing experience from Novartis, Merck, Mallinckrodt, and Biogen. The company's FDA-approved RETHYMIC, a tissue-based regenerative therapy for pediatric congenital athymia, was approved in October 2021. Rossell will lead commercialization and pursue growth into new markets and indications.PR NewswireIn-depth Analysis of the 22q11.2 Deletion Syndrome Market, 2017-2030 - If Zygel (ZYN002) Gets Approved, the Market Will Grow as There Will Be No Expected CompetitionResearchAndMarkets.com has published a market research report on 22q11.2 Deletion Syndrome covering epidemiology data and market forecasts for the United States, EU5 countries, and Japan from 2018 to 2030. The report projects the market in the seven major markets to grow at a CAGR of 41.9%, with pipeline drugs including Zygel (ZYN002) from Zynerba Pharmaceuticals and RVT-802 from Enzyvant/Roivant Sciences/Sumitomo Dainippon Pharma. According to the analysis, if Zygel receives regulatory approval, the market is expected to expand further with no anticipated competition.GlobeNewswireEnzyvant Receives FDA Approval for RETHYMIC® (allogeneic processed thymus tissue-agdc), a One-Time Regenerative Tissue-Based Therapy for Pediatric Congenital AthymiaEnzyvant announced FDA approval of RETHYMIC, a one-time regenerative tissue therapy for immune reconstitution in pediatric patients with congenital athymia. The therapy was studied in 105 patients, with survival rates of 77% at one year and 94% long-term among survivors. The company received a Priority Review Voucher under the Rare Pediatric Disease Program.GlobeNewswireEnzyvant Announces Publication of Positive Clinical Data in Pediatric Patients with Congenital Athymia Treated with Investigational RVT-802 (allogeneic processed thymus tissue-agdc)Enzyvant published positive clinical data from RVT-802 trials in 105 pediatric patients with congenital athymia. Kaplan-Meier survival was 77% at one year and 76% at two years, with 93% long-term survival among those alive at one year. The FDA expected action on the BLA on October 8, 2021.Business Wire BlogAceragen Launches with Acquisition of Enzyvant‘s Investigational Therapy for Farber Disease and $35 Million Product Financing with NovaQuestAceragen has acquired Enzyvant's investigational therapy RVT-801, now designated ACG-801, for treating Farber disease, and has secured $35 million in product financing from NovaQuest. The acquisition includes an upfront payment and potential milestone payments totaling up to $226 million for Enzyvant, alongside several regulatory designations facilitating the therapy's development. Aceragen aims to advance ACG-801 towards clinical studies to address the significant unmet needs of Farber disease patients.FierceBiotechAceragen bags Enzyvant drug and $35M, plots fast path to marketAceragen has acquired the preclinical Farber disease therapy RVT-801 (now ACG-801) from Enzyvant for an upfront payment and up to $226 million in milestones. NovaQuest Capital Management is providing $35 million in product financing to support Aceragen's plan to advance the drug into clinical trials.PR NewswireRoivant Provides Corporate Updates in Advance of Second Annual Pipeline DayRoivant Sciences announced a series of corporate updates across its subsidiary companies ahead of its second annual Pipeline Day, including multiple positive clinical trial results and regulatory milestones. Key developments include Enzyvant's FDA acceptance of its BLA submission for RVT-802, positive Phase 3 results from Myovant's LIBERTY 1 study and Urovant's EMPOWUR study, and Datavant's acquisition of Health Data Link. The company noted positive clinical data across multiple Vants along with substantial technology investments over the past year.PR NewswireEnzyvant's Investigational Regenerative Treatment (RVT-802) for Congenital Athymia to be Discussed in Symposium, Platform Presentation and Poster Session at Clinical Immunology Society MeetingEnzyvant announced that its investigational treatment RVT-802 for congenital athymia will be presented at the Clinical Immunology Society 2019 annual meeting. The company is also preparing to submit a rolling Biologics License Application to the FDA in the first half of 2019, following a transition to cGMP manufacturing standards developed in partnership with Duke University.