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Cellares

Full company profile

uuid00002sz

Namestring
Cellares
Legal namestring
Cellares Corporation
Websiteurl
cellares.com
Company typeenum
Private
Founded yearint
2017
Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
101–250
akta.pro rankint
HeadquartersSouth San Francisco, United States
HQ citystring
South San Francisco
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices4 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
cell therapy manufacturing, automated bioprocessing platforms, CDMO services, GMP cell therapy production, cell therapy automation
Industry3 codes
1Cell Therapy CDMO
CodeHLAGABADPrimaryYes
2Drug Substance–Drug Product Integrated CDMO
CodeHLAGABAGPrimaryNo
3Sample Logistics, Biorepository & IVD Kit Management (Trial Support)
CodeHLAGAEAIPrimaryNo
NAICS code3 codes
  • Industrial and Commercial Fan and Blower and Air Purification Equipment Manufacturing333413
  • Ventilation, Heating, Air-Conditioning, and Commercial Refrigeration Equipment Manufacturing3334
  • Food Product Machinery Manufacturing333241
SIC code3 codes
  • Laboratory Apparatus & Furniture3821
  • General Industrial Machinery & Equipment3560
  • Industrial Process Furnaces & Ovens3567
Product category
Cell Therapy Contract Manufacturing
Social media profiles1 record
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model3 records
1Manufacturing Capacity Reservation & Supply Agreements
TypeManaged Services
Description

Long-term, multi-year, multi-hundred-million-dollar capacity reservation and supply agreements with biopharma partners (e.g., $380M global agreement with Bristol Myers Squibb reserving commercial-scale capacity in the US, Europe, and Japan; 10-year commercial supply agreement with Cabaletta Bio for rese-cel). Functions as a forward-purchased manufacturing services commitment, anchoring capacity utilization across Smart Factories.

cellares.com
2CDMO / IDMO Manufacturing Services
TypeProfessional Services
Description

Fee-for-service clinical and commercial cGMP manufacturing, process development, analytical development, QA/QC, and regulatory support delivered via the IDMO model. Predictable per-batch pricing (transparent, no hidden fees) for partners across preclinical through commercial stages. Currently active in autologous CAR-T, TCR-T, progenitor T-cell, HSC, and gene-edited programs.

cellares.com
3Technology Adoption / Feasibility Evaluation Programs
TypeProfessional Services
Description

Paid technology adoption and feasibility evaluation engagements with biotech and pharma partners (e.g., TScan for TSC-101, Autolus for AUCATZYL/obe-cel, Kite, Lyell, Poseida). These programs assess automated process translation on Cell Shuttle as a step toward commercial supply agreements and generate near-term service revenue plus option value on long-term contracts.

cellares.com
Marketing channels8 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels2 records

Each record includes

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

Cost components6 values
Personnel, Infrastructure, Technology or R&D, Operations, Supply Chain, Marketing or Sales
Pricing details1 tier
1Quote-based, multi-year manufacturing and capacity reservation agreements; transparent per-batch pricing with no hidden fees.
ModelOtherBilling cadenceMulti-year contract
Notes

Specific price points are not publicly disclosed. Contracts are structured as multi-year capacity reservations and supply agreements (e.g., $380M BMS global capacity reservation; 10-year Cabaletta commercial supply agreement). The model emphasizes predictable per-batch economics and long-term cost visibility vs traditional CDMOs.

cellares.com
GTM typeB2B
B2B
Offering typeServices
Services
Brand1 of 3 records shown
1Cell Shuttle
Description

The company's flagship automated, end-to-end, cGMP cell therapy manufacturing platform; first cell therapy manufacturing platform to receive the FDA's Advanced Manufacturing Technology (AMT) designation.

cellares.com
+2 more records
Core offering1 text field

Cellares is the first Integrated Development and Manufacturing Organization (IDMO) providing automated, large-scale cGMP manufacturing of cell therapies. The company operates its proprietary Cell Shuttle® manufacturing platform and Cell Q™ automated quality control workcell inside a global network of IDMO Smart Factories, delivering clinical and commercial manufacturing services, process development, analytical development, QA/QC, and regulatory support to biopharma partners.

Differentiator
Functional benefit
Problem solved
Product overview1 text field

Cellares offers a platform-plus-modules architecture unified under the world's first Integrated Development and Manufacturing Organization (IDMO) model. The core manufacturing platform is the Cell Shuttle®, a high-throughput, end-to-end, cGMP, closed-system automated cell therapy manufacturing platform and the first recipient of the FDA's Advanced Manufacturing Technology (AMT) designation. Complementing it is Cell Q™, the world's first automated cGMP QC workcell that automates in-process and release quality control testing. Both are deployed across Cellares' global network of IDMO Smart Factories, and together with Process Translation & Automation, Analytical Bridging & Automation, and Global Quality & Regulatory Consultation services, they constitute the company's IDMO offering for cell therapy developers — spanning preclinical development through commercial-scale manufacturing.

Product and service4 records
1Cell Shuttle®
CategoryAutomated Manufacturing Platform
2Cell Q™
CategoryAutomated Quality Control Platform
3IDMO Services
CategoryIntegrated Development and Manufacturing Services
4IDMO Smart Factory Network
CategoryGlobal Manufacturing Infrastructure
Scale indicator13 records

Each record includes

Type, Value, Description, Source

Partnership19 partners
Strategic tierPolicy / Industry Coalition MemberTypeStrategic or Co-development PartnerAnnounced on2026-06-10
Description

Cellares joined NAIA, a multi-sector trade association with 1,000+ decision-makers representing $1T+ in investable capital, dedicated to rebuilding America's strategic industrial base and domestic manufacturing leadership.

Strategic tierCore Commercial PartnerTypeStrategic or Co-development PartnerAnnounced on2026-06-03
Description

Agreement to evaluate automated clinical manufacturing of lead TCR-T candidate TSC-101 for AML/MDS using Cell Shuttle and Cell Q. TScan advances TSC-101 toward a pivotal trial expected to begin Q2 2026, with Cellares as a candidate commercial manufacturing partner.

Strategic tierCore Development PartnerTypeStrategic or Co-development PartnerAnnounced on2026-05-13
Description

Partnership to automate manufacturing and quality control of ProT-096, ProTgen's personalized progenitor T-cell therapy for refractory leukemia and hematologic malignancies, including regulatory expertise toward IND submission.

Strategic tierFlagship Commercial Partner And Clinical ValidatorTypeStrategic or Co-development PartnerAnnounced on2026-04-28
Description

Original technology adoption partnership began November 2023; expanded through 2024–2026 with successful completion of the Manufacturing Technology Adoption Program (March 2025), FDA IND Amendment clearance (January 2026), first two GMP patient doses (April 14, 2026), and a 10-year commercial supply agreement (April 28, 2026) to scale rese-cel for autoimmune diseases.

Strategic tierCore Academic PartnerTypeStrategic or Co-development PartnerAnnounced on2026-02-18
Description

Expanded partnership to support clinical manufacturing and regulatory process for CRISPR-edited GD2 CAR-T therapy for solid tumors; Cellares provides Cell Shuttle and Cell Q platforms plus regulatory expertise for IND application with the FDA. UW retains full ownership and leadership of the IND filing.

Strategic tierCore Academic PartnerTypeStrategic or Co-development PartnerAnnounced on2026-02-03
Description

Collaboration to automate manufacturing and release testing for gene-edited hematopoietic stem cell (HSC) therapies targeting HIV and inherited diseases.

Strategic tierEuropean Real Estate PartnerTypeOthersAnnounced on2026-01-12
Description

Real estate developer partner for Cellares' European Smart Factory at Leiden Bio Science Park in the Netherlands (~9,741 m² facility in the Nexus building).

Strategic tierCore Academic PartnerTypeStrategic or Co-development PartnerAnnounced on2026-01-09
Description

Collaboration to evaluate automated manufacturing of a CAR T-cell therapy targeting glioblastoma using Cellares' automation platforms.

Strategic tierCore Commercial PartnerTypeStrategic or Co-development PartnerAnnounced on2026-01-06
Description

Autolus to evaluate Cell Shuttle for commercial manufacturing of AUCATZYL (obe-cel) for relapsed/refractory B-ALL and potential expansion into pediatric B-ALL, lupus, and multiple sclerosis.

Strategic tierFlagship Asia Pacific PartnerTypeStrategic or Co-development PartnerAnnounced on2025-11-01
Description

Partnership for first IDMO Smart Factory in Japan at Kashiwanoha Smart City, Chiba (groundbreaking November 2025); four-storey facility targeting up to 75,000 patients/year with 30+ Cell Shuttle units, operations scheduled to begin 2027.

Strategic tierCore Technology PartnerTypeTechnology or IntegrationAnnounced on2025-10-29
Description

Strategic collaboration to integrate Slingshot's TruCytes biomarker controls into Cellares' Cell Q automated quality control platform, improving data integrity, reducing failure rates, and enabling faster production scaling.

Strategic tierCore Technology Partners (Cell Q Ecosystem)TypeTechnology or IntegrationAnnounced on2025-09-17
Description

Cellares selected five best-in-class technology providers — Tecan, Advanced Instruments, Cytek Biosciences, Slingshot Biosciences, and AltemisLab — to expand Cell Q's capabilities in meeting demands for commercial-scale cell therapy quality control.

Strategic tierFlagship Technology PartnerTypeTechnology or IntegrationAnnounced on2024-09-12
Description

Joint development collaboration to integrate Sony's flow cytometry-based sorting and online analysis into Cellares' automated, high-throughput cell therapy manufacturing platform.

Strategic tierCore Commercial PartnerTypeStrategic or Co-development PartnerAnnounced on2024-06-27
Description

Agreement for Kite to evaluate Cellares' Cell Shuttle automated manufacturing platform as a potential complement to Kite's commercial operations.

Strategic tierFlagship / Anchor Commercial PartnerTypeStrategic or Co-development PartnerAnnounced on2024-04-22
Description

$380M worldwide capacity reservation and supply agreement signed April 2024 reserving commercial-scale capacity in the US, Europe, and Japan for CAR-T programs including Breyanzi and Abecma. Partnership expanded October 2023 to include a second CAR-T program in Cellares' Technology Adoption Partnership Program. BMS participated in Cellares' Series D financing.

Strategic tierDevelopment PartnerTypeStrategic or Co-development PartnerAnnounced on2023-09-11
Description

Partnership to evaluate automated manufacturing of Lyell's CAR T-cell therapy on the Cell Shuttle platform.

Strategic tierDevelopment PartnerTypeStrategic or Co-development PartnerAnnounced on2021-07-14
Description

Early Access Partnership Program engagement to accelerate cell therapy manufacturing on the Cell Shuttle.

Strategic tierDevelopment PartnerTypeStrategic or Co-development PartnerAnnounced on2021-01-08
Description

Joined Cellares' Early Access Partnership Program (January 2021) to evaluate Cell Shuttle for cell therapy manufacturing.

Strategic tierAcademic PartnerTypeStrategic or Co-development PartnerAnnounced on2020-10-29
Description

Joined Cellares' Early Access Partnership Program in October 2020.

Recent move16 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Closest direct peer in automated cell therapy manufacturing. Ori Biotech's IRO platform is the only other cell therapy manufacturing platform with an FDA Advanced Manufacturing Technology designation (September 2025), targeting similar autologous CAR-T and gene-edited programs and competing for the same IDMO/capacity-reservation contracts.

TypeBroad incumbent
Description

Global CDMO incumbent with a large cell and gene therapy services franchise across autologous and allogeneic modalities. Comparable as a multi-modality manufacturing services competitor, though Lonza operates at much broader scale and lacks a single end-to-end automated cell-therapy-only platform like Cellares' IDMO.

TypeBroad incumbent
Description

Diversified life-sciences tools and CDMO player with cell therapy services through Patheon and Brammer Bio. Competes for clinical and commercial cell therapy manufacturing engagements and brings vertically integrated bioprocessing tools and analytical instruments.

TypeBroad incumbent
Description

Major global CDMO offering cell therapy manufacturing services including viral vector and cell therapy capacity. A relevant comparator for commercial-scale cell therapy CDMO engagements, though Catalent's portfolio spans many therapeutic modalities beyond cell therapy.

TypeEmerging player
Description

Cell engineering technology provider whose electroporation platform underpins many clinical-stage cell therapy programs. Comparable as a cell therapy manufacturing technology enabler; Cellares' new CCO previously led commercial efforts at MaxCyte, illustrating personnel overlap and ecosystem ties.

TypeBroad incumbent
Description

Bioprocessing equipment and consumables supplier whose cell therapy workflow tools (Xuri, Sepax) compete in adjacent automation slots. Comparable as a supplier of automation that CDMOs use, and an indirect competitor to Cellares' vertically integrated IDMO model.

TypeEmerging player
Description

Technology-focused biomanufacturing company building automated, distributed manufacturing capacity for advanced therapies including cell and gene therapies. Shares Cellares' thesis of replacing manual CDMO operations with automated, networked manufacturing.

TypeBroad incumbent
Description

Global CDMO with cell and gene therapy services (including the former Novartis Stein facility and a gene therapy center of excellence). Competes for clinical and commercial cell therapy manufacturing contracts at comparable scale to Lonza and Catalent.

TypeBroad incumbent
Description

Large Asia- and US-based CDMO with cell and gene therapy manufacturing services. Relevant comparator for global multi-region cell therapy manufacturing capacity, particularly given Cellares' Asia expansion into Kashiwa, Japan.

TypeBroad incumbent
Description

Contract development and manufacturing organization with cell therapy services (via its HemaCare and CDMO businesses). Competes for early- and clinical-stage cell therapy manufacturing engagements and provides related discovery and safety assessment services.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat7 records

Each record includes

Type, Details

Key risks5 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers14 records

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment4 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

Integration6 records

Each record includes

Title, Type, Description, Source

AI maturity
App detail

Has app

Feature6 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles7 records

Each record includes

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

No data
Compliance4 records

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds4 records

Each record includes

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

Investors19 records

Each record includes

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

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

M&A

Each record includes

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

Investment

Each record includes

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

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

Cellares

Cell Therapy Contract Manufacturingcellares.com

Cellares firmographics

Firmographics
Name
Cellares
Legal name
Cellares Corporation
Website
https://cellares.com
Company type
Private
Founded year
2017
Operating status
Operating
Headcount range
101–250 employees
Ownership category
akta.pro rank

Cellares industry classification

Industry
Product category
Cell Therapy Contract Manufacturing
NAICS
Industrial and Commercial Fan and Blower and Air Purification Equipment Manufacturing (333413), Ventilation, Heating, Air-Conditioning, and Commercial Refrigeration Equipment Manufacturing (3334), Food Product Machinery Manufacturing (333241)
SIC
Laboratory Apparatus & Furniture (3821), General Industrial Machinery & Equipment (3560), Industrial Process Furnaces & Ovens (3567)
akta.pro primary industry
Cell Therapy CDMO (HLAGABAD)
akta.pro secondary industries
Drug Substance–Drug Product Integrated CDMO (HLAGABAG), Sample Logistics, Biorepository & IVD Kit Management (Trial Support) (HLAGAEAI)

Keywords

  • Cell therapy manufacturing
  • Automated bioprocessing platforms
  • CDMO services
  • GMP cell therapy production
  • Cell therapy automation

Where Cellares is headquartered

Location

Headquarters

HQ city
South San Francisco
HQ country
United States
HQ region
North America

Offices4 records

Markets served

Cellares business model

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

Revenue model

  1. Manufacturing Capacity Reservation & Supply Agreements: Long-term, multi-year, multi-hundred-million-dollar capacity reservation and supply agreements with biopharma partners (e.g., $380M global agreement with Bristol Myers Squibb reserving commercial-scale capacity in the US, Europe, and Japan; 10-year commercial supply agreement with Cabaletta Bio for rese-cel). Functions as a forward-purchased manufacturing services commitment, anchoring capacity utilization across Smart Factories.
  2. CDMO / IDMO Manufacturing Services: Fee-for-service clinical and commercial cGMP manufacturing, process development, analytical development, QA/QC, and regulatory support delivered via the IDMO model. Predictable per-batch pricing (transparent, no hidden fees) for partners across preclinical through commercial stages. Currently active in autologous CAR-T, TCR-T, progenitor T-cell, HSC, and gene-edited programs.
  3. Technology Adoption / Feasibility Evaluation Programs: Paid technology adoption and feasibility evaluation engagements with biotech and pharma partners (e.g., TScan for TSC-101, Autolus for AUCATZYL/obe-cel, Kite, Lyell, Poseida). These programs assess automated process translation on Cell Shuttle as a step toward commercial supply agreements and generate near-term service revenue plus option value on long-term contracts.

Pricing tiers

ModelBillingPrice
OtherMulti-year contractQuote-based, multi-year manufacturing and capacity reservation agreements; transparent per-batch pricing with no hidden fees.

Go-to-market motion1 record

Distribution channels2 records

Marketing channels8 records

Cellares product offering

Product offering

Core offering

Cellares is the first Integrated Development and Manufacturing Organization (IDMO) providing automated, large-scale cGMP manufacturing of cell therapies. The company operates its proprietary Cell Shuttle® manufacturing platform and Cell Q™ automated quality control workcell inside a global network of IDMO Smart Factories, delivering clinical and commercial manufacturing services, process development, analytical development, QA/QC, and regulatory support to biopharma partners.

Product overview

Cellares offers a platform-plus-modules architecture unified under the world's first Integrated Development and Manufacturing Organization (IDMO) model. The core manufacturing platform is the Cell Shuttle®, a high-throughput, end-to-end, cGMP, closed-system automated cell therapy manufacturing platform and the first recipient of the FDA's Advanced Manufacturing Technology (AMT) designation. Complementing it is Cell Q™, the world's first automated cGMP QC workcell that automates in-process and release quality control testing. Both are deployed across Cellares' global network of IDMO Smart Factories, and together with Process Translation & Automation, Analytical Bridging & Automation, and Global Quality & Regulatory Consultation services, they constitute the company's IDMO offering for cell therapy developers — spanning preclinical development through commercial-scale manufacturing.

Differentiator

Problem solved

Functional benefit

Brands

  • Cell Shuttle: The company's flagship automated, end-to-end, cGMP cell therapy manufacturing platform; first cell therapy manufacturing platform to receive the FDA's Advanced Manufacturing Technology (AMT) designation.
  • Cell Q
  • IDMO Smart Factories

Products and services

  • Cell Shuttle®
  • Cell Q™
  • IDMO Services
  • IDMO Smart Factory Network

Companies that use Cellares

Customer profile

Named customers14 records

Segments4 records

Ideal customer profiles3 records

Cellares technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Integration6 records

Feature6 records

Cellares partnerships and signals

Strategic signal

Partnerships

19 partnerships are on record, tiered policy / industry coalition member, core commercial partner, core development partner, flagship commercial partner and clinical validator, core academic partner, european real estate partner, flagship asia pacific partner, core technology partner, core technology partners (cell q ecosystem), flagship technology partner, flagship / anchor commercial partner, development partner and academic partner.

  • New American Industrial Alliance (NAIA)policy / industry coalition memberStrategic or Co-development Partner · 10 June 2026Cellares joined NAIA, a multi-sector trade association with 1,000+ decision-makers representing $1T+ in investable capital, dedicated to rebuilding America's strategic industrial base and domestic manufacturing leadership.
  • TScan Therapeuticscore commercial partnerStrategic or Co-development Partner · 3 June 2026Agreement to evaluate automated clinical manufacturing of lead TCR-T candidate TSC-101 for AML/MDS using Cell Shuttle and Cell Q. TScan advances TSC-101 toward a pivotal trial expected to begin Q2 2026, with Cellares as a candidate commercial manufacturing partner.
  • ProTgencore development partnerStrategic or Co-development Partner · 13 May 2026Partnership to automate manufacturing and quality control of ProT-096, ProTgen's personalized progenitor T-cell therapy for refractory leukemia and hematologic malignancies, including regulatory expertise toward IND submission.
  • Cabaletta Bioflagship commercial partner and clinical validatorStrategic or Co-development Partner · 28 April 2026Original technology adoption partnership began November 2023; expanded through 2024–2026 with successful completion of the Manufacturing Technology Adoption Program (March 2025), FDA IND Amendment clearance (January 2026), first two GMP patient doses (April 14, 2026), and a 10-year commercial supply agreement (April 28, 2026) to scale rese-cel for autoimmune diseases.
  • University of Wisconsin School of Medicine and Public Healthcore academic partnerStrategic or Co-development Partner · 18 February 2026Expanded partnership to support clinical manufacturing and regulatory process for CRISPR-edited GD2 CAR-T therapy for solid tumors; Cellares provides Cell Shuttle and Cell Q platforms plus regulatory expertise for IND application with the FDA. UW retains full ownership and leadership of the IND filing.
  • Stanford Medicine (Stanford Center for Definitive and Curative Medicine; Stanford Innovative Medicines Accelerator)core academic partnerStrategic or Co-development Partner · 3 February 2026Collaboration to automate manufacturing and release testing for gene-edited hematopoietic stem cell (HSC) therapies targeting HIV and inherited diseases.
  • Dura Vermeer Commercieel Vastgoedeuropean real estate partnerOthers · 12 January 2026Real estate developer partner for Cellares' European Smart Factory at Leiden Bio Science Park in the Netherlands (~9,741 m² facility in the Nexus building).
  • City of Hopecore academic partnerStrategic or Co-development Partner · 9 January 2026Collaboration to evaluate automated manufacturing of a CAR T-cell therapy targeting glioblastoma using Cellares' automation platforms.
  • Autolus Therapeuticscore commercial partnerStrategic or Co-development Partner · 6 January 2026Autolus to evaluate Cell Shuttle for commercial manufacturing of AUCATZYL (obe-cel) for relapsed/refractory B-ALL and potential expansion into pediatric B-ALL, lupus, and multiple sclerosis.
  • Mitsui Fudosanflagship asia pacific partnerStrategic or Co-development Partner · 1 November 2025Partnership for first IDMO Smart Factory in Japan at Kashiwanoha Smart City, Chiba (groundbreaking November 2025); four-storey facility targeting up to 75,000 patients/year with 30+ Cell Shuttle units, operations scheduled to begin 2027.
  • Slingshot Biosciencescore technology partnerTechnology or Integration · 29 October 2025Strategic collaboration to integrate Slingshot's TruCytes biomarker controls into Cellares' Cell Q automated quality control platform, improving data integrity, reducing failure rates, and enabling faster production scaling.
  • Tecan, Advanced Instruments, Cytek Biosciences, AltemisLabcore technology partners (cell q ecosystem)Technology or Integration · 17 September 2025Cellares selected five best-in-class technology providers — Tecan, Advanced Instruments, Cytek Biosciences, Slingshot Biosciences, and AltemisLab — to expand Cell Q's capabilities in meeting demands for commercial-scale cell therapy quality control.
  • Sonyflagship technology partnerTechnology or Integration · 12 September 2024Joint development collaboration to integrate Sony's flow cytometry-based sorting and online analysis into Cellares' automated, high-throughput cell therapy manufacturing platform.
  • Kite (Gilead)core commercial partnerStrategic or Co-development Partner · 27 June 2024Agreement for Kite to evaluate Cellares' Cell Shuttle automated manufacturing platform as a potential complement to Kite's commercial operations.
  • Bristol Myers Squibbflagship / anchor commercial partnerStrategic or Co-development Partner · 22 April 2024$380M worldwide capacity reservation and supply agreement signed April 2024 reserving commercial-scale capacity in the US, Europe, and Japan for CAR-T programs including Breyanzi and Abecma. Partnership expanded October 2023 to include a second CAR-T program in Cellares' Technology Adoption Partnership Program. BMS participated in Cellares' Series D financing.
  • Lyell Immunopharmadevelopment partnerStrategic or Co-development Partner · 11 September 2023Partnership to evaluate automated manufacturing of Lyell's CAR T-cell therapy on the Cell Shuttle platform.
  • Poseida Therapeuticsdevelopment partnerStrategic or Co-development Partner · 14 July 2021Early Access Partnership Program engagement to accelerate cell therapy manufacturing on the Cell Shuttle.
  • PACT Pharmadevelopment partnerStrategic or Co-development Partner · 8 January 2021Joined Cellares' Early Access Partnership Program (January 2021) to evaluate Cell Shuttle for cell therapy manufacturing.
  • Fred Hutchinson Cancer Research Centeracademic partnerStrategic or Co-development Partner · 29 October 2020Joined Cellares' Early Access Partnership Program in October 2020.

Scale indicators13 records

Recent moves16 records

Expansion highlights6 records

Cellares competitors and assessment

Company assessment

Direct peers

  • Ori Biotech: Closest direct peer in automated cell therapy manufacturing. Ori Biotech's IRO platform is the only other cell therapy manufacturing platform with an FDA Advanced Manufacturing Technology designation (September 2025), targeting similar autologous CAR-T and gene-edited programs and competing for the same IDMO/capacity-reservation contracts.

Broad incumbents

  • Lonza Group: Global CDMO incumbent with a large cell and gene therapy services franchise across autologous and allogeneic modalities. Comparable as a multi-modality manufacturing services competitor, though Lonza operates at much broader scale and lacks a single end-to-end automated cell-therapy-only platform like Cellares' IDMO.
  • Thermo Fisher Scientific (Patheon / Brammer Bio): Diversified life-sciences tools and CDMO player with cell therapy services through Patheon and Brammer Bio. Competes for clinical and commercial cell therapy manufacturing engagements and brings vertically integrated bioprocessing tools and analytical instruments.
  • Catalent: Major global CDMO offering cell therapy manufacturing services including viral vector and cell therapy capacity. A relevant comparator for commercial-scale cell therapy CDMO engagements, though Catalent's portfolio spans many therapeutic modalities beyond cell therapy.
  • Cytiva (Danaher): Bioprocessing equipment and consumables supplier whose cell therapy workflow tools (Xuri, Sepax) compete in adjacent automation slots. Comparable as a supplier of automation that CDMOs use, and an indirect competitor to Cellares' vertically integrated IDMO model.
  • AGC Biologics: Global CDMO with cell and gene therapy services (including the former Novartis Stein facility and a gene therapy center of excellence). Competes for clinical and commercial cell therapy manufacturing contracts at comparable scale to Lonza and Catalent.
  • WuXi Advanced Therapies (WuXi AppTec): Large Asia- and US-based CDMO with cell and gene therapy manufacturing services. Relevant comparator for global multi-region cell therapy manufacturing capacity, particularly given Cellares' Asia expansion into Kashiwa, Japan.
  • Charles River Laboratories: Contract development and manufacturing organization with cell therapy services (via its HemaCare and CDMO businesses). Competes for early- and clinical-stage cell therapy manufacturing engagements and provides related discovery and safety assessment services.

Emerging players

  • MaxCyte: Cell engineering technology provider whose electroporation platform underpins many clinical-stage cell therapy programs. Comparable as a cell therapy manufacturing technology enabler; Cellares' new CCO previously led commercial efforts at MaxCyte, illustrating personnel overlap and ecosystem ties.
  • National Resilience: Technology-focused biomanufacturing company building automated, distributed manufacturing capacity for advanced therapies including cell and gene therapies. Shares Cellares' thesis of replacing manual CDMO operations with automated, networked manufacturing.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat7 records

Key risks5 records

Key highlights7 records

Customer concentration

Cellares social profiles

Digital presence

Cellares compliance and trust

Trust signal

Compliance4 records

Cellares financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Cellares leadership team

Management profile

Number of profiles

Profiles7 records

Cellares funding detail

Funding detail

Funding overview

Funding rounds4 records

Investors19 records

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

Cellares 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 Cellares

What does Cellares do?

Cellares is the first Integrated Development and Manufacturing Organization (IDMO) providing automated, large-scale cGMP manufacturing of cell therapies. The company operates its proprietary Cell Shuttle® manufacturing platform and Cell Q™ automated quality control workcell inside a global network of IDMO Smart Factories, delivering clinical and commercial manufacturing services, process development, analytical development, QA/QC, and regulatory support to biopharma partners.

Is Cellares a public or private company?

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

When was Cellares founded?

Cellares was founded in 2017. It employs 101 to 250 people.

Where is Cellares based?

Cellares is headquartered in South San Francisco, United States, in the North America region.

How does Cellares make money?

Three revenue lines are on record. Manufacturing Capacity Reservation & Supply Agreements are the primary driver. The others are CDMO / IDMO Manufacturing Services and technology Adoption / Feasibility Evaluation Programs.

Who are Cellares's main competitors?

Ori Biotech is listed as a direct peer. Broad incumbents are Lonza Group, Thermo Fisher Scientific (Patheon / Brammer Bio), Catalent, Cytiva (Danaher), AGC Biologics, WuXi Advanced Therapies (WuXi AppTec) and Charles River Laboratories. Emerging players are MaxCyte and National Resilience.

Does Cellares have an API?

No public API is recorded for Cellares.

What industry is Cellares in?

Cellares's product category is Cell Therapy Contract Manufacturing. Its primary akta.pro industry code is HLAGABAD, Cell Therapy CDMO, with a secondary code of HLAGABAG, Drug Substance–Drug Product Integrated CDMO. Its NAICS code is 333413 and its SIC code is 3821.

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Seeking AlphaCabaletta Bio: 40% Sell-Off Creates an Opportunity Despite Cash ConcernsCabaletta Bio's stock trades 40% below its $2.41 pipeline value, with a single-asset risk profile. Its lead CAR T asset, rese-cel, has pivotal Phase 1/2 data expected mid-2027 and a BLA submission planned for late 2027. A 10-year manufacturing deal with Cellares lowers future COGS, supporting margin expansion if approved.FiercePharmaCellares pens 2nd automation test with Asia-based cell therapy partner in 2 weeksCellares signed a second agreement with Seoul National University Hospital in South Korea to test its Cell Shuttle platform on the hospital's gene-modified stem cell manufacturing process. The trial will assess automation for a PNH investigational therapy, aiming to establish a production strategy for future U.S. clinical development.Business Wire BlogCellares and Seoul National University Hospital Launch Proof-of-Concept for Automated Manufacturing of Gene-Modified HSPC Therapy on the Cell Shuttle® PlatformCellares and Seoul National University Hospital announced a partnership to evaluate automated manufacturing of a gene-modified HSPC therapy for paroxysmal nocturnal hemoglobinuria on Cellares' Cell Shuttle platform. The collaboration aims to support SNUH's PNH program toward clinical development in the United States, marking Cellares' second Asia collaboration.Pharmaceutical TechnologyCellares, GenomeFrontier to assess automated GF-CART01 productionCellares and GenomeFrontier Therapeutics announced a collaboration to assess automated manufacturing for GenomeFrontier's investigational CAR-T cell therapy GF-CART01 on the Cell Shuttle platform. The evaluation focuses on adapting GenomeFrontier's virus-free process to the Cell Shuttle system, aiming to enhance reliability and reduce costs. GF-CART01 targets B-cell malignancies, with ongoing Phase I trial recruitment in the US.GenengnewsCellares and GenomeFrontier Therapeutics Partner to Advance Automated Manufacturing of GF-CART01Cellares and GenomeFrontier Therapeutics partnered to evaluate automated manufacturing of GF-CART01 on Cellares' Cell Shuttle platform. The collaboration focuses on translating GenomeFrontier's process, including electroporation, and supports GenomeFrontier's U.S. Phase I clinical trial for B-cell malignancies.FiercePharmaCellares links with GenomeFrontier to test automation approach for virus-free CAR-TsCellares partnered with GenomeFrontier Therapeutics to test its Cell Shuttle platform for producing virus-free CAR-T therapies, focusing on GF-CART01. The virus-free approach aims to reduce manufacturing costs and complexities, and the collaboration is Cellares' first development deal in Asia.BioSpaceCellares and GenomeFrontier Therapeutics Partner to Evaluate Automated Manufacturing for GF-CART01 on the Cell Shuttle® PlatformCellares and GenomeFrontier Therapeutics announced a partnership to evaluate automated manufacturing of GF-CART01, a virus-free CAR-T therapy, on Cellares' Cell Shuttle platform. The collaboration marks Cellares' first development collaboration in Asia and aims to support GenomeFrontier's U.S. clinical initiative. The companies seek to improve manufacturing reliability and reduce costs for future scale.Business Wire BlogCellares and GenomeFrontier Therapeutics Partner to Evaluate Automated Manufacturing for GF-CART01 on the Cell Shuttle® PlatformCellares and GenomeFrontier Therapeutics announced a partnership to evaluate automated manufacturing for GF-CART01, a virus-free CAR-T therapy, on Cellares' Cell Shuttle platform. The collaboration aims to support GenomeFrontier's U.S. Phase 1 clinical trial for B-cell malignancies. The companies seek to improve manufacturing reliability and reduce costs.NJBIZCellares plans 68 layoffs in Bridgewater (updated)Cellares plans to eliminate 68 jobs at its Bridgewater production site by mid-November, part of a broader restructuring. The layoffs follow the loss of a $380 million partnership with Bristol Myers Squibb, and the company expects to cut 100 jobs at headquarters this fall.FiercePharmaCellares downsizes New Jersey operations after losing BMS cell therapy contractCellares announced 68 layoffs in its New Jersey smart factory, following a loss of a large pharmaceutical customer. The company said the cuts are to concentrate resources on growing customer programs, and no further reductions are anticipated. The affected teams are associated with near-term global expansion efforts.