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Center for Breakthrough Medicines

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uuid0000lhe

Namestring
Center for Breakthrough Medicines
Legal namestring
SK pharmteco Inc.
Company typeenum
Private
Founded yearint
2020
Descriptiontext

Center for Breakthrough Medicines (CBM) is a cell and gene therapy contract development and manufacturing organization (CDMO) headquartered in King of Prussia, Pennsylvania, now operating as the US cell and gene therapy arm of SK Pharmteco following SK Inc.'s initial $350 million corporate investment in January 2022 and SK Pharmteco's full takeover by 2026. The company provides end-to-end CDMO services to pharmaceutical and biotech drug developers, spanning process development, CGMP manufacturing, analytical testing, plasmid engineering, aseptic fill-finish, and regulatory support from preclinical stages through commercialization. Its manufacturing footprint includes a King of Prussia, PA facility commissioned in 2022 with three independent production suites, two aseptic fill-finish lines, and bioreactor capacity up to 500 L scalable to 1,000 L via multiplexing, complemented by a large-scale facility south of Paris brought online in 2024 with six production suites, dedicated fill-finish, and bioreactor capacity up to 2,000 L.

The company's core technology centers on viral vector manufacturing across three modalities — adeno-associated virus (AAV), lentivirus (LVV), and adenovirus (AdV) — unified under its proprietary SKyvec™ Viral Vector Platform, which is designed to harmonize process development, manufacturing, and scale-up across vector types. Regulatory expertise spanning FDA and EMA interactions is integrated into the service offering, addressing the manufacturing bottlenecks, variable yields, lengthy optimization cycles, and scalability constraints that limit patient access to gene therapies.

CBM operates as a professional services CDMO, generating revenue through direct, enterprise-scale contract manufacturing engagements with biotech and pharmaceutical sponsors. It goes to market via direct enterprise sales targeting drug developers globally across North America and Europe, with marketing activities concentrated in industry conferences (e.g., Cell & Gene Therapy Summit 2026, Advanced Therapies Xchange San Francisco 2026, Meeting on the Mesa), digital and content marketing through technical white papers, case studies, and webinars, and brand presence via LinkedIn and YouTube. As of the latest data, CBM has 101-250 employees against a stated plan to hire 2,000 people over four years to support the stated objective of building the world's largest cell and gene therapy manufacturing facility by 2025.

Short descriptiontext

Center for Breakthrough Medicines is a cell and gene therapy CDMO providing process development, CGMP manufacturing, and regulatory support for AAV, lentiviral, and adenoviral vectors to pharmaceutical and biotech drug developers across US and European facilities, now operating as SK pharmteco Cell & Gene US.

Operating statusenum
Acquired
Ownership categoryenum
Headcount rangeband
101–250
akta.pro rankint
HeadquartersKing Of Prussia, United States
HQ citystring
King Of Prussia
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
cell therapy CDMO, gene therapy manufacturing, viral vector production, plasmid manufacturing, biologics contract development
Industry5 codes
1Gene Therapy (Viral Vector/Plasmid) CDMO
CodeHLAGABAEPrimaryYes
2Gene Therapy Vector Manufacturing & CDMO Services
CodeHLAAACAJPrimaryNo
3Drug Substance–Drug Product Integrated CDMO
CodeHLAGABAGPrimaryNo
4Clinical Trial Material (CTM) Manufacturing & Supply CDMO
CodeHLAGABAKPrimaryNo
5Cell Therapy CDMO
CodeHLAGABADPrimaryNo
NAICS code2 codes
  • Biological Product (except Diagnostic) Manufacturing325414
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
SIC code1 code
  • Biological Products, (No Disgnostic Substances)2836
Product category
Biopharmaceutical CDMO Services
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1Contract Manufacturing Services
TypeProfessional Services
Description

CDMO services for gene and cell therapy manufacturing, providing process development, CGMP manufacturing, analytical testing, and regulatory support to pharmaceutical and biotech clients

koreajoongangdaily.joins.com
Marketing channels3 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

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

Cost components6 values
Personnel, Operations, Infrastructure, Technology or R&D, Supply Chain, Marketing or Sales
GTM typeB2B
B2B
Offering typeServices
Services
Core offering1 text field

Center for Breakthrough Medicines is a contract development and manufacturing organization (CDMO) providing end-to-end services for gene and cell therapy developers. Its core offerings include CGMP viral vector manufacturing (AAV, lentiviral, and adenoviral), process development, plasmid engineering, analytical testing, aseptic fill-finish, and regulatory support, delivered through its proprietary SKyvec™ platform. Services span clinical to commercial scale with bioreactor capacity up to 2,000 L across U.S. and French facilities.

Differentiator
Functional benefit
Problem solved
Product and service6 records
1Viral Vector Contract Manufacturing
CategoryViral Vector Manufacturing
Description

CGMP contract manufacturing of viral vectors—AAV, lentiviral, and adenoviral—for gene therapy developers, scaled from clinical to commercial using single-use bioreactors up to 2,000 L via the SKyvec™ platform. Service is targeted at gene therapy sponsors and biopharmaceutical companies requiring outsourced viral vector supply for clinical trials and commercial launch.

2Process Development Services
CategoryProcess Development
Description

Standalone upstream and downstream process development services for gene and cell therapy products, supporting client programs from early development through technology transfer and scale-up. Offered to biopharmaceutical sponsors that require specialized viral vector, plasmid, or cell therapy process development expertise prior to or alongside CGMP manufacturing.

3Plasmid Engineering and Manufacturing
CategoryPlasmid Manufacturing
Description

Contract plasmid engineering and CGMP manufacturing services, producing plasmid DNA used as raw material for viral vector production and as standalone plasmid products. Service is provided to gene therapy developers, vaccine developers, and biopharmaceutical clients requiring plasmid supply.

4Analytical Testing Services
CategoryAnalytical Testing
Description

CGMP analytical testing, characterization, and release services for gene and cell therapy products, supporting in-process and final product testing requirements. Offered to biopharmaceutical sponsors requiring qualified analytical methods for viral vector, plasmid, and cell therapy products.

5Aseptic Fill-Finish Services
CategoryAseptic Fill-Finish
Description

Aseptic fill-finish services for gene and cell therapy drug substance and drug product, providing final dosage form preparation for advanced therapy products. Service is provided to biopharmaceutical sponsors requiring fill-finish capacity for clinical or commercial gene/cell therapy supply.

6Regulatory Support Services
CategoryRegulatory Support
Description

CMC and regulatory affairs support services for gene and cell therapy clients, including documentation, regulatory submission support, and compliance guidance associated with CGMP manufacturing of advanced therapy products. Service is provided to biopharmaceutical sponsors preparing regulatory filings for gene/cell therapy programs.

Scale indicator2 records

Each record includes

Type, Value, Description, Source

Partnership1 partner
Strategic tierMinorTypeStrategic or Co-development PartnerAnnounced on2026-03-12
Description

CBM (as SK pharmteco Cell & Gene US) is part of a consortium including BioCurie, Caring Cross, St. Jude Children's Research Hospital, and University City Science Center working on an ARPA-H funded project to develop an AI platform for scalable gene therapy manufacturing.

Recent move4 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

Catalent is a large global CDMO with substantial cell and gene therapy (viral vector) and biologics capabilities serving similar pharmaceutical and biotech clients. Comparable as a multi-modality CDMO peer with overlapping viral vector manufacturing services, though Catalent operates at significantly larger scale across many modalities.

TypeBroad incumbent
Description

Lonza is one of the world's largest CDMOs with established cell and gene therapy services, including viral vector manufacturing. Directly comparable as a global CDMO serving gene therapy developers, but Lonza offers a far broader portfolio spanning biologics, small molecules, and cell therapy.

TypeDirect peer
Description

AGC Biologics operates a dedicated Cell and Gene Therapy CDMO business with viral vector and cell therapy manufacturing capabilities across multiple sites. Directly comparable as a gene therapy-focused CDMO offering process development, GMP manufacturing, and analytical services to pharma and biotech clients.

TypeDirect peer
Description

Forge Biologics is a gene therapy CDMO specializing in AAV viral vector manufacturing and process development, operating a large-scale cGMP production facility. Highly comparable as a focused viral vector CDMO targeting the same client base of gene therapy developers requiring scalable AAV manufacturing.

TypeDirect peer
Description

Yposkesi is a European cell and gene therapy CDMO providing viral vector (AAV, lentiviral) and cell therapy manufacturing services from its French facility. Directly comparable as a viral vector-focused CDMO with European operations, overlapping with CBM's France site and similar target customers.

TypeDirect peer
Description

Aldevron (acquired by Danaher) manufactures plasmid DNA, mRNA, and viral vector components serving gene therapy developers. Comparable as a CDMO in the viral vector and genetic medicine supply chain, though Aldevron is more focused on plasmid and nucleic acid inputs while CBM focuses on full viral vector production.

TypeBroad incumbent
Description

Thermo Fisher's viral vector services business (incorporating Brammer Bio) provides viral vector and gene therapy CDMO services globally. Comparable as a major CDMO offering viral vector manufacturing at scale, but as part of Thermo Fisher's broader life sciences tools and pharma services portfolio.

TypeDirect peer
Description

Cobra Biologics, now part of Charles River Laboratories, provides viral vector and plasmid DNA manufacturing CDMO services for gene therapy and vaccine developers. Directly comparable as a viral vector-focused CDMO serving similar biotech and pharma clients with overlapping AAV and lentiviral manufacturing capabilities.

TypeDirect peer
Description

Oxford BioMedica is a clinical and commercial-stage CDMO specializing in lentiviral vector manufacturing for cell and gene therapies. Directly comparable as a viral vector CDMO with proprietary LentiVector platform, serving similar gene therapy developer clients with process development and GMP manufacturing services.

TypeEmerging player
Description

Vigene Biosciences (merged with AavantiBio) provides AAV and lentiviral viral vector manufacturing services for gene therapy developers. Comparable as a smaller viral vector CDMO with overlapping AAV manufacturing capabilities, though at a smaller scale than CBM's planned facility footprint.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat5 records

Each record includes

Type, Details

Key risks5 records

Each record includes

Headline, Details, Source

Key highlights6 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 profile2 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
No
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
Profiles5 records

Each record includes

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

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds1 record

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 →

Center for Breakthrough Medicines

Biopharmaceutical CDMO Servicesbreakthroughmedicines.com

Center for Breakthrough Medicines is a cell and gene therapy CDMO providing process development, CGMP manufacturing, and regulatory support for AAV, lentiviral, and adenoviral vectors to pharmaceutical and biotech drug developers across US and European facilities, now operating as SK pharmteco Cell & Gene US.

What Center for Breakthrough Medicines does

Center for Breakthrough Medicines (CBM) is a cell and gene therapy contract development and manufacturing organization (CDMO) headquartered in King of Prussia, Pennsylvania, now operating as the US cell and gene therapy arm of SK Pharmteco following SK Inc.'s initial $350 million corporate investment in January 2022 and SK Pharmteco's full takeover by 2026. The company provides end-to-end CDMO services to pharmaceutical and biotech drug developers, spanning process development, CGMP manufacturing, analytical testing, plasmid engineering, aseptic fill-finish, and regulatory support from preclinical stages through commercialization. Its manufacturing footprint includes a King of Prussia, PA facility commissioned in 2022 with three independent production suites, two aseptic fill-finish lines, and bioreactor capacity up to 500 L scalable to 1,000 L via multiplexing, complemented by a large-scale facility south of Paris brought online in 2024 with six production suites, dedicated fill-finish, and bioreactor capacity up to 2,000 L.

The company's core technology centers on viral vector manufacturing across three modalities — adeno-associated virus (AAV), lentivirus (LVV), and adenovirus (AdV) — unified under its proprietary SKyvec™ Viral Vector Platform, which is designed to harmonize process development, manufacturing, and scale-up across vector types. Regulatory expertise spanning FDA and EMA interactions is integrated into the service offering, addressing the manufacturing bottlenecks, variable yields, lengthy optimization cycles, and scalability constraints that limit patient access to gene therapies.

CBM operates as a professional services CDMO, generating revenue through direct, enterprise-scale contract manufacturing engagements with biotech and pharmaceutical sponsors. It goes to market via direct enterprise sales targeting drug developers globally across North America and Europe, with marketing activities concentrated in industry conferences (e.g., Cell & Gene Therapy Summit 2026, Advanced Therapies Xchange San Francisco 2026, Meeting on the Mesa), digital and content marketing through technical white papers, case studies, and webinars, and brand presence via LinkedIn and YouTube. As of the latest data, CBM has 101-250 employees against a stated plan to hire 2,000 people over four years to support the stated objective of building the world's largest cell and gene therapy manufacturing facility by 2025.

Center for Breakthrough Medicines firmographics

Firmographics
Name
Center for Breakthrough Medicines
Legal name
SK pharmteco Inc.
Website
https://breakthroughmedicines.com
Company type
Private
Founded year
2020
Operating status
Acquired
Headcount range
101–250 employees
Short description
Center for Breakthrough Medicines is a cell and gene therapy CDMO providing process development, CGMP manufacturing, and regulatory support for AAV, lentiviral, and adenoviral vectors to pharmaceutical and biotech drug developers across US and European facilities, now operating as SK pharmteco Cell & Gene US.
Ownership category
akta.pro rank

Center for Breakthrough Medicines industry classification

Industry
Product category
Biopharmaceutical CDMO Services
NAICS
Biological Product (except Diagnostic) Manufacturing (325414), Research and Development in Biotechnology (except Nanobiotechnology) (541714)
SIC
Biological Products, (No Disgnostic Substances) (2836)
akta.pro primary industry
Gene Therapy (Viral Vector/Plasmid) CDMO (HLAGABAE)
akta.pro secondary industries
Gene Therapy Vector Manufacturing & CDMO Services (HLAAACAJ), Drug Substance–Drug Product Integrated CDMO (HLAGABAG), Clinical Trial Material (CTM) Manufacturing & Supply CDMO (HLAGABAK), Cell Therapy CDMO (HLAGABAD)

Keywords

  • Cell therapy CDMO
  • Gene therapy manufacturing
  • Viral vector production
  • Plasmid manufacturing
  • Biologics contract development

Where Center for Breakthrough Medicines is headquartered

Location

Headquarters

HQ city
King Of Prussia
HQ country
United States
HQ region
North America

Offices2 records

Markets served

Center for Breakthrough Medicines business model

Business model
GTM type
B2B
Offering type
Services
Cost components
Personnel, Operations, Infrastructure, Technology or R&D, Supply Chain, Marketing or Sales

Revenue model

  1. Contract Manufacturing Services: CDMO services for gene and cell therapy manufacturing, providing process development, CGMP manufacturing, analytical testing, and regulatory support to pharmaceutical and biotech clients

Go-to-market motion1 record

Distribution channels1 record

Marketing channels3 records

Center for Breakthrough Medicines product offering

Product offering

Core offering

Center for Breakthrough Medicines is a contract development and manufacturing organization (CDMO) providing end-to-end services for gene and cell therapy developers. Its core offerings include CGMP viral vector manufacturing (AAV, lentiviral, and adenoviral), process development, plasmid engineering, analytical testing, aseptic fill-finish, and regulatory support, delivered through its proprietary SKyvec™ platform. Services span clinical to commercial scale with bioreactor capacity up to 2,000 L across U.S. and French facilities.

Differentiator

Problem solved

Functional benefit

Products and services

  • Viral Vector Contract Manufacturing CGMP contract manufacturing of viral vectors—AAV, lentiviral, and adenoviral—for gene therapy developers, scaled from clinical to commercial using single-use bioreactors up to 2,000 L via the SKyvec™ platform. Service is targeted at gene therapy sponsors and biopharmaceutical companies requiring outsourced viral vector supply for clinical trials and commercial launch.
  • Process Development Services Standalone upstream and downstream process development services for gene and cell therapy products, supporting client programs from early development through technology transfer and scale-up. Offered to biopharmaceutical sponsors that require specialized viral vector, plasmid, or cell therapy process development expertise prior to or alongside CGMP manufacturing.
  • Plasmid Engineering and Manufacturing Contract plasmid engineering and CGMP manufacturing services, producing plasmid DNA used as raw material for viral vector production and as standalone plasmid products. Service is provided to gene therapy developers, vaccine developers, and biopharmaceutical clients requiring plasmid supply.
  • Analytical Testing Services CGMP analytical testing, characterization, and release services for gene and cell therapy products, supporting in-process and final product testing requirements. Offered to biopharmaceutical sponsors requiring qualified analytical methods for viral vector, plasmid, and cell therapy products.
  • Aseptic Fill-Finish Services Aseptic fill-finish services for gene and cell therapy drug substance and drug product, providing final dosage form preparation for advanced therapy products. Service is provided to biopharmaceutical sponsors requiring fill-finish capacity for clinical or commercial gene/cell therapy supply.
  • Regulatory Support Services CMC and regulatory affairs support services for gene and cell therapy clients, including documentation, regulatory submission support, and compliance guidance associated with CGMP manufacturing of advanced therapy products. Service is provided to biopharmaceutical sponsors preparing regulatory filings for gene/cell therapy programs.

Companies that use Center for Breakthrough Medicines

Customer profile

Segments1 record

Ideal customer profiles2 records

Center for Breakthrough Medicines technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature4 records

Center for Breakthrough Medicines partnerships and signals

Strategic signal

Partnerships

One partnership is on record.

  • BioCurieminorStrategic or Co-development Partner · 12 March 2026CBM (as SK pharmteco Cell & Gene US) is part of a consortium including BioCurie, Caring Cross, St. Jude Children's Research Hospital, and University City Science Center working on an ARPA-H funded project to develop an AI platform for scalable gene therapy manufacturing.

Scale indicators2 records

Recent moves4 records

Expansion highlights5 records

Center for Breakthrough Medicines competitors and assessment

Company assessment

Broad incumbents

  • Catalent: Catalent is a large global CDMO with substantial cell and gene therapy (viral vector) and biologics capabilities serving similar pharmaceutical and biotech clients. Comparable as a multi-modality CDMO peer with overlapping viral vector manufacturing services, though Catalent operates at significantly larger scale across many modalities.
  • Lonza: Lonza is one of the world's largest CDMOs with established cell and gene therapy services, including viral vector manufacturing. Directly comparable as a global CDMO serving gene therapy developers, but Lonza offers a far broader portfolio spanning biologics, small molecules, and cell therapy.
  • Thermo Fisher Scientific (Viral Vector Services / Brammer Bio): Thermo Fisher's viral vector services business (incorporating Brammer Bio) provides viral vector and gene therapy CDMO services globally. Comparable as a major CDMO offering viral vector manufacturing at scale, but as part of Thermo Fisher's broader life sciences tools and pharma services portfolio.

Direct peers

  • AGC Biologics: AGC Biologics operates a dedicated Cell and Gene Therapy CDMO business with viral vector and cell therapy manufacturing capabilities across multiple sites. Directly comparable as a gene therapy-focused CDMO offering process development, GMP manufacturing, and analytical services to pharma and biotech clients.
  • Forge Biologics: Forge Biologics is a gene therapy CDMO specializing in AAV viral vector manufacturing and process development, operating a large-scale cGMP production facility. Highly comparable as a focused viral vector CDMO targeting the same client base of gene therapy developers requiring scalable AAV manufacturing.
  • Yposkesi: Yposkesi is a European cell and gene therapy CDMO providing viral vector (AAV, lentiviral) and cell therapy manufacturing services from its French facility. Directly comparable as a viral vector-focused CDMO with European operations, overlapping with CBM's France site and similar target customers.
  • Aldevron: Aldevron (acquired by Danaher) manufactures plasmid DNA, mRNA, and viral vector components serving gene therapy developers. Comparable as a CDMO in the viral vector and genetic medicine supply chain, though Aldevron is more focused on plasmid and nucleic acid inputs while CBM focuses on full viral vector production.
  • Cobra Biologics (Charles River Laboratories): Cobra Biologics, now part of Charles River Laboratories, provides viral vector and plasmid DNA manufacturing CDMO services for gene therapy and vaccine developers. Directly comparable as a viral vector-focused CDMO serving similar biotech and pharma clients with overlapping AAV and lentiviral manufacturing capabilities.
  • Oxford BioMedica: Oxford BioMedica is a clinical and commercial-stage CDMO specializing in lentiviral vector manufacturing for cell and gene therapies. Directly comparable as a viral vector CDMO with proprietary LentiVector platform, serving similar gene therapy developer clients with process development and GMP manufacturing services.

Emerging players

  • Vigene Biosciences (AavantiBio): Vigene Biosciences (merged with AavantiBio) provides AAV and lentiviral viral vector manufacturing services for gene therapy developers. Comparable as a smaller viral vector CDMO with overlapping AAV manufacturing capabilities, though at a smaller scale than CBM's planned facility footprint.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat5 records

Key risks5 records

Key highlights6 records

Customer concentration

Center for Breakthrough Medicines social profiles

Digital presence

Center for Breakthrough Medicines financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Center for Breakthrough Medicines leadership team

Management profile

Number of profiles

Profiles5 records

Center for Breakthrough Medicines funding detail

Funding detail

Funding overview

Funding rounds1 record

Investors1 record

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

Center for Breakthrough Medicines 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 Center for Breakthrough Medicines

What does Center for Breakthrough Medicines do?

Center for Breakthrough Medicines is a contract development and manufacturing organization (CDMO) providing end-to-end services for gene and cell therapy developers. Its core offerings include CGMP viral vector manufacturing (AAV, lentiviral, and adenoviral), process development, plasmid engineering, analytical testing, aseptic fill-finish, and regulatory support, delivered through its proprietary SKyvec™ platform. Services span clinical to commercial scale with bioreactor capacity up to 2,000 L across U.S. and French facilities.

Is Center for Breakthrough Medicines a public or private company?

Center for Breakthrough Medicines is a private company. It is classified as corporate owned and is currently acquired.

When was Center for Breakthrough Medicines founded?

Center for Breakthrough Medicines was founded in 2020. It employs 101 to 250 people.

Where is Center for Breakthrough Medicines based?

Center for Breakthrough Medicines is headquartered in King Of Prussia, United States, in the North America region.

How does Center for Breakthrough Medicines make money?

One revenue line is on record: contract Manufacturing Services.

Who are Center for Breakthrough Medicines's main competitors?

Broad incumbents on record are Catalent, Lonza and Thermo Fisher Scientific (Viral Vector Services / Brammer Bio). Direct peers are AGC Biologics, Forge Biologics, Yposkesi, Aldevron, Cobra Biologics (Charles River Laboratories) and Oxford BioMedica. Vigene Biosciences (AavantiBio) is listed as an emerging player.

Does Center for Breakthrough Medicines have an API?

No public API is recorded for Center for Breakthrough Medicines.

What industry is Center for Breakthrough Medicines in?

Center for Breakthrough Medicines's product category is Biopharmaceutical CDMO Services. Its primary akta.pro industry code is HLAGABAE, Gene Therapy (Viral Vector/Plasmid) CDMO, with a secondary code of HLAAACAJ, Gene Therapy Vector Manufacturing & CDMO Services. Its NAICS code is 325414 and its SIC code is 2836.

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Live signals
GlobeNewswireWhy the Radiopharmaceutical CDMO Market is a Smart Investment: USD 8.50 Bn by 2035The global radiopharmaceutical CDMO market is projected to grow from USD 3.24 billion in 2025 to USD 8.50 billion by 2035, representing a compound annual growth rate of 10.12%, driven by rising nuclear medicine adoption, increasing outsourcing trends, and growing demand for targeted cancer therapies. North America currently leads the market with approximately 49% revenue share, while Asia-Pacific is expected to be the fastest-growing region through 2035. The industry is experiencing significant consolidation, with companies like Lantheus acquiring Evergreen Theragnostics for up to $1 billion, PharmaLogic acquiring a majority stake in Norway-based Agilera Pharma, and SK Pharmteco taking control of the Center for Breakthrough Medicines to expand multi-modality and radiopharmaceutical manufacturing capabilities.PR NewswireCenter for Breakthrough Medicines and Virion Therapeutics Announce Strategic Partnership to Manufacture Virion's Proprietary CD8+ T cell-based Clinical Development Programs for Infectious Diseases andCenter for Breakthrough Medicines (CBM) and Virion Therapeutics announced a strategic collaboration agreement wherein CBM will manufacture Virion's checkpoint modifier clinical development programs, including the First-in-Human VRON-0200 immunotherapy for patients with chronic Hepatitis B Virus infection. The partnership also covers the VRON-2000, a pan-genotypic therapeutic immunotherapy for chronic HBV, which affects over 295 million people worldwide. Virion CEO Andrew Luber stated the collaboration will assist in advancing programs from early- to later-stage clinical trials.PR NewswireAsimov and Center for Breakthrough Medicines Form Strategic Partnership for Viral Vector ProductionAsimov, a synthetic biology company, announced a strategic partnership with Center for Breakthrough Medicines (CBM), a contract development and manufacturing organization, to license Asimov's clonal GMP HEK293 suspension cell line for viral vector production in cell and gene therapies. CBM will now offer its clients immediate access to this high-performance cell line to accelerate development and manufacturing timelines while reducing costs for advanced therapies. The partnership validates Asimov's viral vector platform and supports broader research in host cell optimization, genetic system engineering, and bioreactor process development.PR NewswireAsimov and Center for Breakthrough Medicines Form Strategic Partnership for Viral Vector ProductionAsimov, a synthetic biology company, has formed a strategic partnership with Center for Breakthrough Medicines (CBM) to license its clonal GMP HEK293 suspension cell line for pre-clinical and clinical production of viral vectors used in gene therapies. CBM, a contract development and manufacturing organization, will now offer this high-performance cell line to its clients as part of its end-to-end vector manufacturing capabilities designed to reduce costs and accelerate development timelines. The partnership validates Asimov's viral vector production platform and supports broader accessibility of rare disease therapies globally.PR NewswireCenter for Breakthrough Medicines Amplifies Viral Vector Manufacturing Capabilities by Licensing Asimov's High-Performance GMP Suspension HEK293 PlatformCenter for Breakthrough Medicines (CBM) announced a licensing agreement with Boston-based Asimov to adopt their clonal HEK293 suspension cell line for viral vector manufacturing, immediately making the platform available for GMP manufacturing up to 1000L scale and non-GMP productions up to 500L. The cell line, already GMP-banked and qualified, complements CBM's Genesis Vector Manufacturing Solutions™ and is expected to accelerate development timelines while reducing costs for vector-based advanced therapies. The partnership aims to remove a key barrier for therapy developers and increase patient access to rare disease treatments globally.PR NewswireAutolomous fournira des solutions numériques au Center for Breakthrough Medicines pour rationaliser et automatiser la fabrication des thérapies cellulaires et géniquesAutolomous has entered into an agreement to provide its AutoloMATE® digital platform to the Center for Breakthrough Medicines (CBM) to streamline and automate the manufacturing of cell and gene therapies. This partnership aims to digitize CBM's supply chain, centralize data visibility, and reduce costs to improve patient access to life-saving treatments.PR NewswireAutolomous to Provide Digital Solutions to Center for Breakthrough Medicines to Streamline and Automate Manufacturing of Cell & Gene TherapiesAutolomous LTD, a London-based developer of manufacturing management systems for cell and gene therapies, announced a license agreement with U.S.-based Center for Breakthrough Medicines (CBM) to deploy its AutoloMATE® digital platform across CBM's manufacturing operations. The platform will digitize batch record reviews, integrate facility systems, and provide centralized data visibility to streamline compliance and reduce costs of goods. The partnership aims to enhance manufacturing scalability and improve patient access to cell and gene therapies.PR NewswireCenter for Breakthrough Medicines Launches Genesis Vector Manufacturing Solutions™ with New State-of-the-Art Vector Suites to Accelerate the Commercialization of Advanced TherapiesThe Center for Breakthrough Medicines (CBM), a cell and gene therapy contract development and manufacturing organization, has launched Genesis Vector Manufacturing Solutions, an end-to-end offering that includes plasmid manufacturing, process development, and high-throughput GMP vector manufacturing suites at its Pennsylvania facility. The new manufacturing suites support batch output two to five times greater than traditional designs while integrating testing, supply chain, and regulatory services at a single site, reducing analytical batch release from 22 weeks to 6 weeks. The company states this addresses the needs of the 200 million patients worldwide with rare and ultra-rare genetic diseases by aiming to drive down costs and accelerate access to advanced therapies.PR NewswireCenter for Breakthrough Medicines (CBM) Expands Contract Testing Services with the launch of the Analytical Accelerator™ for AAV Testing to Serve Growing Pipeline of Gene TherapiesThe Center for Breakthrough Medicines (CBM), a contract development and manufacturing organization based in King of Prussia, Pennsylvania, has launched its Analytical Accelerator™ for AAV Testing platform, offering 40+ GMP AAV platform assays to serve the growing gene therapy pipeline.PR NewswireCenter for Breakthrough Medicine Appoints Joseph Lingle as Chief People OfficerThe Center for Breakthrough Medicines appointed Joseph Lingle as Chief People Officer effective June 1, 2022. Lingle brings over 30 years of experience in operations and human resources, having previously worked at Bristol Myers Squibb and other large pharmaceutical organizations. He will oversee HR activities to support the company's mission of accelerating the development of advanced therapies.