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BioAtla

Full company profile

uuid00008bv

Namestring
BioAtla
Legal namestring
BioAtla, Inc.
Websiteurl
bioatla.com
Company typeenum
Public
Founded yearint
2005
Descriptiontext

BioAtla is a San Diego-based clinical-stage biopharmaceutical company founded in 2005 that develops novel antibody therapeutics for cancer using two proprietary platforms: the Conditionally Active Biologics (CAB) platform, which generates antibodies and ADCs that activate selectively in the acidic tumor microenvironment via a Protein-associated Chemical Switches (PaCS) mechanism, and the Comprehensive Integrated Antibody Optimization (CIAO!) platform, which selects antibody candidates in the same host used for final manufacturing to reduce downstream process risk. Its clinical pipeline comprises mecbotamab vedotin (BA3011, AXL-targeting CAB-ADC), ozuriftamab vedotin (BA3021, ROR2-targeting CAB-ADC with FDA Fast Track Designation for SCCHN), evalstotug (BA3071, CAB anti-CTLA-4), BA3182 (bispecific EpCAM x CD3 T-cell engager), and BA3361 (next-generation Nectin-4 CAB-ADC with a glycosidase-cleavable linker).

BioAtla does not sell approved products; instead it monetizes through licensing and co-development partnerships. Himalaya Therapeutics holds an exclusive license for the Greater China market (PRC, Hong Kong, Macau, Taiwan) covering two Phase 1/2 assets and worldwide rights to two preclinical candidates. A $40 million special purpose vehicle, Inversagen AI, was formed in December 2025 with GATC Health Corp to fund Phase 3 development of ozuriftamab vedotin and a senolytic program, with BioAtla retaining 65% ownership of ozuriftamab vedotin across all solid tumor indications. The company has additionally raised capital through a $75M private placement (September 2021), a $65M underwritten offering (November 2022), a $9.2M registered direct offering (December 2024), and $22.5M in flexible financing (November 2025), supplemented by an FDA Fast Track Designation granted in July 2024.

As of early 2026, BioAtla is in significant financial distress: cash reserves stood at $7.1M as of December 31, 2025, the workforce has been cut by a cumulative ~79% (30% in March 2025, then 70% in March 2026), the board has initiated a formal strategic review for asset sales and licensing, and Nasdaq has issued a delisting determination that is currently stayed; a 50-for-1 reverse stock split took effect April 6, 2026 to address listing-compliance deficiencies.

Short descriptiontext

BioAtla is a San Diego-based clinical-stage biopharmaceutical company developing conditionally active antibody therapeutics for cancer via its proprietary CAB platform, generating value through licensing and co-development partnerships rather than commercial product sales.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
51–100
akta.pro rankint
HeadquartersSan Diego, United States
HQ citystring
San Diego
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
conditionally active biologics, antibody drug conjugates, cancer immunotherapy, tumor microenvironment targeting, oncology therapeutics development
Industry4 codes
1Antibody-Drug Conjugates (ADCs) & Antibody Conjugates
CodeHLAAAAAEPrimaryYes
2Bispecific & Multispecific Antibodies
CodeHLAAAAAFPrimaryNo
3Monoclonal Antibody Therapeutics (mAbs)
CodeHLAAAAAAPrimaryNo
4Antibody Discovery & Engineering Platforms (display tech, bispecifics, Fc engineering)
CodeHLAAAIABPrimaryNo
NAICS code2 codes
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
  • Biological Product (except Diagnostic) Manufacturing325414
SIC code1 code
  • Biological Products, (No Disgnostic Substances)2836
Product category
Clinical-stage Oncology Biopharmaceuticals
Social media profiles2 records
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model3 records
1Clinical Development Partnerships
TypeLicensing Royalties
Description

BioAtla generates value through strategic partnerships and licensing agreements. The company retains 65% ownership of ozuriftamab vedotin across all solid tumor indications while Inversagen AI receives 35% stake. Partnerships include upfront payments, milestone payments, and potential royalties.

in.investing.com
2Regional Licensing - Greater China
TypeLicensing Royalties
Description

Himalaya Therapeutics holds exclusive license from BioAtla to develop and commercialize CAB candidates for Greater China market, including two Phase 1/2 clinical stage assets and worldwide rights to two preclinical candidates.

bioatla.com
3Strategic Financing
TypeTransaction Fee
Description

The company has secured financing including $7.5 million pre-paid advance and $15 million standby equity purchase commitment to support operations during strategic partnership finalization.

globenewswire.com
Marketing channels3 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels3 records

Each record includes

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

Cost components4 values
Technology or R&D, Personnel, Operations, Marketing or Sales
Pricing details1 tier
1No public pricing available - biopharmaceutical development company
ModelOtherBilling cadenceMulti-year contract
Notes

No consumer-facing pricing as products are in clinical development stage

globenewswire.com
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

BioAtla develops conditionally active antibody therapeutics for the treatment of solid tumor cancers using its proprietary Conditionally Active Biologics (CAB) and Comprehensive Integrated Antibody Optimization (CIAO!) platforms. The company advances a portfolio of clinical-stage drug candidates including CAB antibody-drug conjugates, immune checkpoint inhibitors, and bispecific T-cell engagers, generating value through strategic licensing partnerships and co-development arrangements with pharmaceutical companies.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 3 values shown
  • Median OS of 21.5 months among 44 patients with treatment-refractory leiomyosarcoma, liposarcoma, and undifferentiated pleomorphic sarcoma treated with mecbotamab vedotin
+2 more records
Product overview1 text field

BioAtla is a clinical-stage biopharmaceutical company developing novel therapeutics using its proprietary Conditionally Active Biologics™ (CAB) platform and Comprehensive Integrated Antibody Optimization (CIAO!™) platform. The CAB platform generates antibodies and biologics that are conditionally active in the tumor microenvironment, enabling more selective targeting of cancer tissue. The company's product portfolio includes multiple CAB-based drug candidates in various stages of development: Mecbotamab Vedotin (BA3011) and Ozuriftamab Vedotin (BA3021) are CAB antibody-drug conjugates (ADCs); Evalstotug (BA3071) is a CAB immune checkpoint inhibitor; BA3182 is a bispecific T-cell engager; and BA3361 is a next-generation CAB-ADC. These programs target various solid tumor indications including sarcoma, lung cancer, head and neck cancer, melanoma, and adenocarcinoma.

Product and service7 records
1Conditionally Active Biologics (CAB) Platform
Categorycore_platform
Description

BioAtla's proprietary technology platform for developing antibodies and biologics that can be activated or inactivated under defined physiological conditions, such as the acidic tumor microenvironment, enabling more selective targeting of cancer tissue.

2Mecbotamab Vedotin (BA3011)
Categorydrug_candidate
Description

A CAB Antibody Drug Conjugate targeting AXL receptor tyrosine kinase, being evaluated for the treatment of undifferentiated pleomorphic sarcoma (UPS), non-small cell lung cancer (NSCLC), and ovarian cancer.

3Ozuriftamab Vedotin (BA3021)
Categorydrug_candidate
Description

A CAB Antibody Drug Conjugate targeting ROR2 receptor, being evaluated for melanoma and squamous cell carcinoma of the head and neck (SCCHN). FDA has granted Fast Track Designation for recurrent or metastatic SCCHN.

4Evalstotug (BA3071)
Categorydrug_candidate
Description

A CAB immune checkpoint inhibitor targeting CTLA-4, designed to enable high exposures, extended dosing, and reduced immune-mediated toxicity for treatment of various carcinomas.

5BA3182
Categorydrug_candidate
Description

A bispecific T-cell engager targeting EpCAM and CD3 for treatment of treatment-refractory metastatic adenocarcinoma; Phase 1 data presented at ESMO 2025 showed manageable safety profile and antitumor activity.

6BA3361 (Next-Gen CAB-ADC)
Categorydrug_candidate
Description

A next-generation CAB-ADC targeting Nectin-4 with an ultra-stable glycosidase-cleavable linker, designed for improved efficacy in pancreatic cancer and other tumor types.

7Comprehensive Integrated Antibody Optimization (CIAO!) Platform
Categorycore_platform
Description

BioAtla's proprietary platform that integrates manufacturing and process development features into antibody discovery, selecting molecules in the same host used for final manufacturing to reduce downstream development risks.

Scale indicator8 records

Each record includes

Type, Value, Description, Source

Partnership3 partners
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-12-31
Description

Formed Inversagen AI, LLC as a $40 million special purpose vehicle with GATC Health to advance Phase III trials of ozuriftamab vedotin for oropharyngeal squamous cell carcinoma and develop conditionally active biologic senolytic therapies. BioAtla and GATC Health are equal partners. Initial $5 million deployed immediately with remaining $35 million expected Q1 2026.

2Inversagen AI, LLC
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-12-31
Description

$40 million special purpose vehicle formed with GATC Health to advance BioAtla's cancer drug ozuriftamab vedotin into Phase 3 clinical trials. Inversagen AI receives 35% stake in Oz-V across all solid tumor indications while BioAtla retains 65% ownership.

genengnews.com
Strategic tierCoreTypeChannel Partner/ Reseller/ Distributor
Description

Clinical stage therapeutic company with exclusive license from BioAtla to develop and commercialize several CAB candidates for Greater China market (PRC, Hong Kong, Macau, Taiwan), including two Phase 1/2 clinical stage assets and worldwide rights to two additional preclinical candidates.

Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Clinical-stage biopharmaceutical company developing a pipeline of antibody-drug conjugates (ADCs) for oncology, using proprietary platforms (Dolasynthen, Immunosynthen). Directly comparable to BioAtla as a similarly-sized clinical-stage ADC developer targeting solid tumors with novel linker and payload chemistry.

TypeDirect peer
Description

Clinical-stage oncology company developing immune-stimulating antibody conjugates (ISACs) that combine tumor-targeting antibodies with immune activators. Comparable to BioAtla as a small-cap clinical-stage antibody-conjugate company working on novel targeted oncology biologics.

TypeDirect peer
Description

Clinical-stage oncology company developing antibody-drug conjugates and immunotherapies. Directly comparable to BioAtla as a similarly-sized public biotech building a pipeline of ADCs targeting solid tumor indications.

TypeBroad incumbent
Description

Pioneer in ADC technology with approved products (Elahere) now operating as a wholly owned subsidiary of AbbVie. Comparable to BioAtla as an ADC-focused oncology developer, though operating at far greater scale with commercial-stage assets.

TypeBroad incumbent
Description

Global pharmaceutical company and ADC market leader, developer of Enhertu (with AstraZeneca) and Datroway. Comparable to BioAtla as a major ADC innovator, though at vastly greater scale and with multiple approved/commercialized ADC products.

TypeBroad incumbent
Description

Pfizer acquired Seagen in 2023 for $43B, making it one of the largest ADC-focused oncology platforms globally with multiple approved products (Adcetris, Padcev, Tukysa, Tivdak). Comparable to BioAtla as a major player in the ADC space, though operating at a fundamentally different scale with commercial revenue.

TypeBroad incumbent
Description

International biotechnology company developing differentiated antibody therapeutics including bispecific antibodies (e.g., bispecifics partnered with AbbVie and others). Comparable to BioAtla in developing novel antibody formats for oncology, though Genmab has multiple approved products and broader partnerships.

TypeEmerging player
Description

Clinical-stage biotechnology company developing ADCs engineered with novel antibody-based protein therapeutics for cancer treatment. Comparable to BioAtla as a similarly-sized private/emerging ADC-focused oncology biotech working on next-generation antibody formats.

TypeEmerging player
Description

Chinese clinical-stage biopharmaceutical company developing a broad oncology pipeline including novel bispecific antibodies and ADCs. Comparable to BioAtla in developing novel antibody-based oncology therapeutics, including bispecifics (similar to BioAtla's BA3182).

TypeEmerging player
Description

Chinese biopharmaceutical company developing innovative biologics including antibody-drug conjugates and bispecific antibodies. Comparable to BioAtla as a clinical-stage developer of antibody-based oncology therapeutics using novel conjugation and targeting approaches.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat4 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights6 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers3 records

Each record includes

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

Segment3 records

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
Yes
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature6 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles11 records

Each record includes

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

Subsidiaries2 records

Each record includes

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

No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds8 records

Each record includes

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

Investors20 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

Investment1 record

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 →

BioAtla

Clinical-stage Oncology Biopharmaceuticalsbioatla.com

BioAtla is a San Diego-based clinical-stage biopharmaceutical company developing conditionally active antibody therapeutics for cancer via its proprietary CAB platform, generating value through licensing and co-development partnerships rather than commercial product sales.

What BioAtla does

BioAtla is a San Diego-based clinical-stage biopharmaceutical company founded in 2005 that develops novel antibody therapeutics for cancer using two proprietary platforms: the Conditionally Active Biologics (CAB) platform, which generates antibodies and ADCs that activate selectively in the acidic tumor microenvironment via a Protein-associated Chemical Switches (PaCS) mechanism, and the Comprehensive Integrated Antibody Optimization (CIAO!) platform, which selects antibody candidates in the same host used for final manufacturing to reduce downstream process risk. Its clinical pipeline comprises mecbotamab vedotin (BA3011, AXL-targeting CAB-ADC), ozuriftamab vedotin (BA3021, ROR2-targeting CAB-ADC with FDA Fast Track Designation for SCCHN), evalstotug (BA3071, CAB anti-CTLA-4), BA3182 (bispecific EpCAM x CD3 T-cell engager), and BA3361 (next-generation Nectin-4 CAB-ADC with a glycosidase-cleavable linker).

BioAtla does not sell approved products; instead it monetizes through licensing and co-development partnerships. Himalaya Therapeutics holds an exclusive license for the Greater China market (PRC, Hong Kong, Macau, Taiwan) covering two Phase 1/2 assets and worldwide rights to two preclinical candidates. A $40 million special purpose vehicle, Inversagen AI, was formed in December 2025 with GATC Health Corp to fund Phase 3 development of ozuriftamab vedotin and a senolytic program, with BioAtla retaining 65% ownership of ozuriftamab vedotin across all solid tumor indications. The company has additionally raised capital through a $75M private placement (September 2021), a $65M underwritten offering (November 2022), a $9.2M registered direct offering (December 2024), and $22.5M in flexible financing (November 2025), supplemented by an FDA Fast Track Designation granted in July 2024.

As of early 2026, BioAtla is in significant financial distress: cash reserves stood at $7.1M as of December 31, 2025, the workforce has been cut by a cumulative ~79% (30% in March 2025, then 70% in March 2026), the board has initiated a formal strategic review for asset sales and licensing, and Nasdaq has issued a delisting determination that is currently stayed; a 50-for-1 reverse stock split took effect April 6, 2026 to address listing-compliance deficiencies.

BioAtla firmographics

Firmographics
Name
BioAtla
Legal name
BioAtla, Inc.
Website
https://bioatla.com
Company type
Public
Founded year
2005
Operating status
Operating
Headcount range
51–100 employees
Short description
BioAtla is a San Diego-based clinical-stage biopharmaceutical company developing conditionally active antibody therapeutics for cancer via its proprietary CAB platform, generating value through licensing and co-development partnerships rather than commercial product sales.
Ownership category
akta.pro rank

BioAtla industry classification

Industry
Product category
Clinical-stage Oncology Biopharmaceuticals
NAICS
Research and Development in Biotechnology (except Nanobiotechnology) (541714), Biological Product (except Diagnostic) Manufacturing (325414)
SIC
Biological Products, (No Disgnostic Substances) (2836)
akta.pro primary industry
Antibody-Drug Conjugates (ADCs) & Antibody Conjugates (HLAAAAAE)
akta.pro secondary industries
Bispecific & Multispecific Antibodies (HLAAAAAF), Monoclonal Antibody Therapeutics (mAbs) (HLAAAAAA), Antibody Discovery & Engineering Platforms (display tech, bispecifics, Fc engineering) (HLAAAIAB)

Keywords

  • Conditionally active biologics
  • Antibody drug conjugates
  • Cancer immunotherapy
  • Tumor microenvironment targeting
  • Oncology therapeutics development

Where BioAtla is headquartered

Location

Headquarters

HQ city
San Diego
HQ country
United States
HQ region
North America

Offices2 records

Markets served

BioAtla business model

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

Revenue model

  1. Clinical Development Partnerships: BioAtla generates value through strategic partnerships and licensing agreements. The company retains 65% ownership of ozuriftamab vedotin across all solid tumor indications while Inversagen AI receives 35% stake. Partnerships include upfront payments, milestone payments, and potential royalties.
  2. Regional Licensing - Greater China: Himalaya Therapeutics holds exclusive license from BioAtla to develop and commercialize CAB candidates for Greater China market, including two Phase 1/2 clinical stage assets and worldwide rights to two preclinical candidates.
  3. Strategic Financing: The company has secured financing including $7.5 million pre-paid advance and $15 million standby equity purchase commitment to support operations during strategic partnership finalization.

Pricing tiers

ModelBillingPrice
OtherMulti-year contractNo public pricing available - biopharmaceutical development company

Go-to-market motion2 records

Distribution channels3 records

Marketing channels3 records

BioAtla product offering

Product offering

Core offering

BioAtla develops conditionally active antibody therapeutics for the treatment of solid tumor cancers using its proprietary Conditionally Active Biologics (CAB) and Comprehensive Integrated Antibody Optimization (CIAO!) platforms. The company advances a portfolio of clinical-stage drug candidates including CAB antibody-drug conjugates, immune checkpoint inhibitors, and bispecific T-cell engagers, generating value through strategic licensing partnerships and co-development arrangements with pharmaceutical companies.

Product overview

BioAtla is a clinical-stage biopharmaceutical company developing novel therapeutics using its proprietary Conditionally Active Biologics™ (CAB) platform and Comprehensive Integrated Antibody Optimization (CIAO!™) platform. The CAB platform generates antibodies and biologics that are conditionally active in the tumor microenvironment, enabling more selective targeting of cancer tissue. The company's product portfolio includes multiple CAB-based drug candidates in various stages of development: Mecbotamab Vedotin (BA3011) and Ozuriftamab Vedotin (BA3021) are CAB antibody-drug conjugates (ADCs); Evalstotug (BA3071) is a CAB immune checkpoint inhibitor; BA3182 is a bispecific T-cell engager; and BA3361 is a next-generation CAB-ADC. These programs target various solid tumor indications including sarcoma, lung cancer, head and neck cancer, melanoma, and adenocarcinoma.

Differentiator

Problem solved

Functional benefit

Products and services

  • Conditionally Active Biologics (CAB) Platform BioAtla's proprietary technology platform for developing antibodies and biologics that can be activated or inactivated under defined physiological conditions, such as the acidic tumor microenvironment, enabling more selective targeting of cancer tissue.
  • Mecbotamab Vedotin (BA3011) A CAB Antibody Drug Conjugate targeting AXL receptor tyrosine kinase, being evaluated for the treatment of undifferentiated pleomorphic sarcoma (UPS), non-small cell lung cancer (NSCLC), and ovarian cancer.
  • Ozuriftamab Vedotin (BA3021) A CAB Antibody Drug Conjugate targeting ROR2 receptor, being evaluated for melanoma and squamous cell carcinoma of the head and neck (SCCHN). FDA has granted Fast Track Designation for recurrent or metastatic SCCHN.
  • Evalstotug (BA3071) A CAB immune checkpoint inhibitor targeting CTLA-4, designed to enable high exposures, extended dosing, and reduced immune-mediated toxicity for treatment of various carcinomas.
  • BA3182 A bispecific T-cell engager targeting EpCAM and CD3 for treatment of treatment-refractory metastatic adenocarcinoma; Phase 1 data presented at ESMO 2025 showed manageable safety profile and antitumor activity.
  • BA3361 (Next-Gen CAB-ADC) A next-generation CAB-ADC targeting Nectin-4 with an ultra-stable glycosidase-cleavable linker, designed for improved efficacy in pancreatic cancer and other tumor types.
  • Comprehensive Integrated Antibody Optimization (CIAO!) Platform BioAtla's proprietary platform that integrates manufacturing and process development features into antibody discovery, selecting molecules in the same host used for final manufacturing to reduce downstream development risks.

Quantifiable outcome

  • Median OS of 21.5 months among 44 patients with treatment-refractory leiomyosarcoma, liposarcoma, and undifferentiated pleomorphic sarcoma treated with mecbotamab vedotin
  • +2 more outcomes

Companies that use BioAtla

Customer profile

Named customers3 records

Segments3 records

Ideal customer profiles2 records

BioAtla technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature6 records

BioAtla partnerships and signals

Strategic signal

Partnerships

Three partnerships are on record, tiered core.

  • GATC Health CorpcoreStrategic or Co-development Partner · 31 December 2025Formed Inversagen AI, LLC as a $40 million special purpose vehicle with GATC Health to advance Phase III trials of ozuriftamab vedotin for oropharyngeal squamous cell carcinoma and develop conditionally active biologic senolytic therapies. BioAtla and GATC Health are equal partners. Initial $5 million deployed immediately with remaining $35 million expected Q1 2026.
  • Inversagen AI, LLCcoreStrategic or Co-development Partner · 31 December 2025$40 million special purpose vehicle formed with GATC Health to advance BioAtla's cancer drug ozuriftamab vedotin into Phase 3 clinical trials. Inversagen AI receives 35% stake in Oz-V across all solid tumor indications while BioAtla retains 65% ownership.
  • Himalaya TherapeuticscoreChannel Partner/ Reseller/ DistributorClinical stage therapeutic company with exclusive license from BioAtla to develop and commercialize several CAB candidates for Greater China market (PRC, Hong Kong, Macau, Taiwan), including two Phase 1/2 clinical stage assets and worldwide rights to two additional preclinical candidates.

Scale indicators8 records

Recent moves7 records

Expansion highlights5 records

BioAtla competitors and assessment

Company assessment

Direct peers

  • Mersana Therapeutics: Clinical-stage biopharmaceutical company developing a pipeline of antibody-drug conjugates (ADCs) for oncology, using proprietary platforms (Dolasynthen, Immunosynthen). Directly comparable to BioAtla as a similarly-sized clinical-stage ADC developer targeting solid tumors with novel linker and payload chemistry.
  • Bolt Biotherapeutics: Clinical-stage oncology company developing immune-stimulating antibody conjugates (ISACs) that combine tumor-targeting antibodies with immune activators. Comparable to BioAtla as a small-cap clinical-stage antibody-conjugate company working on novel targeted oncology biologics.
  • Pyxis Oncology: Clinical-stage oncology company developing antibody-drug conjugates and immunotherapies. Directly comparable to BioAtla as a similarly-sized public biotech building a pipeline of ADCs targeting solid tumor indications.

Broad incumbents

  • ImmunoGen (AbbVie): Pioneer in ADC technology with approved products (Elahere) now operating as a wholly owned subsidiary of AbbVie. Comparable to BioAtla as an ADC-focused oncology developer, though operating at far greater scale with commercial-stage assets.
  • Daiichi Sankyo: Global pharmaceutical company and ADC market leader, developer of Enhertu (with AstraZeneca) and Datroway. Comparable to BioAtla as a major ADC innovator, though at vastly greater scale and with multiple approved/commercialized ADC products.
  • Pfizer (Seagen): Pfizer acquired Seagen in 2023 for $43B, making it one of the largest ADC-focused oncology platforms globally with multiple approved products (Adcetris, Padcev, Tukysa, Tivdak). Comparable to BioAtla as a major player in the ADC space, though operating at a fundamentally different scale with commercial revenue.
  • Genmab: International biotechnology company developing differentiated antibody therapeutics including bispecific antibodies (e.g., bispecifics partnered with AbbVie and others). Comparable to BioAtla in developing novel antibody formats for oncology, though Genmab has multiple approved products and broader partnerships.

Emerging players

  • Mythic Therapeutics: Clinical-stage biotechnology company developing ADCs engineered with novel antibody-based protein therapeutics for cancer treatment. Comparable to BioAtla as a similarly-sized private/emerging ADC-focused oncology biotech working on next-generation antibody formats.
  • Akeso: Chinese clinical-stage biopharmaceutical company developing a broad oncology pipeline including novel bispecific antibodies and ADCs. Comparable to BioAtla in developing novel antibody-based oncology therapeutics, including bispecifics (similar to BioAtla's BA3182).
  • RemeGen: Chinese biopharmaceutical company developing innovative biologics including antibody-drug conjugates and bispecific antibodies. Comparable to BioAtla as a clinical-stage developer of antibody-based oncology therapeutics using novel conjugation and targeting approaches.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Key risks6 records

Key highlights6 records

Customer concentration

BioAtla social profiles

Digital presence

BioAtla financial estimates

Financial estimate

Revenue estimate

Valuation estimate

BioAtla leadership team

Management profile

Number of profiles

Profiles11 records

BioAtla subsidiaries and ownership

Company hierarchy

Subsidiaries2 records

BioAtla funding detail

Funding detail

Funding overview

Funding rounds8 records

Investors20 records

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

BioAtla M&A and investment

M&A and investment

M&A

Investments1 record

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

Frequently asked questions about BioAtla

What does BioAtla do?

BioAtla develops conditionally active antibody therapeutics for the treatment of solid tumor cancers using its proprietary Conditionally Active Biologics (CAB) and Comprehensive Integrated Antibody Optimization (CIAO!) platforms. The company advances a portfolio of clinical-stage drug candidates including CAB antibody-drug conjugates, immune checkpoint inhibitors, and bispecific T-cell engagers, generating value through strategic licensing partnerships and co-development arrangements with pharmaceutical companies.

Is BioAtla a public or private company?

BioAtla is a public company. It is classified as public and is currently operating.

When was BioAtla founded?

BioAtla was founded in 2005. It employs 51 to 100 people.

Where is BioAtla based?

BioAtla is headquartered in San Diego, United States, in the North America region.

How does BioAtla make money?

Three revenue lines are on record. Clinical Development Partnerships are the primary driver. The others are regional Licensing - Greater China and strategic Financing.

Who are BioAtla's main competitors?

Direct peers on record are Mersana Therapeutics, Bolt Biotherapeutics and Pyxis Oncology. Broad incumbents are ImmunoGen (AbbVie), Daiichi Sankyo, Pfizer (Seagen) and Genmab. Emerging players are Mythic Therapeutics, Akeso and RemeGen.

Does BioAtla have an API?

No public API is recorded for BioAtla.

What industry is BioAtla in?

BioAtla's product category is Clinical-stage Oncology Biopharmaceuticals. Its primary akta.pro industry code is HLAAAAAE, Antibody-Drug Conjugates (ADCs) & Antibody Conjugates, with a secondary code of HLAAAAAF, Bispecific & Multispecific Antibodies. Its NAICS code is 541714 and its SIC code is 2836.

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Live signals
American Banking and Market NewsBioAtla (NASDAQ:BCAB) and Exicure (NASDAQ:XCUR) Head-To-Head ReviewBioAtla and Exicure are compared on profitability, valuation, and analyst ratings. BioAtla beats Exicure on 7 of 13 factors, with a consensus target price of $200 and a potential upside of 15,167.18%. BioAtla is considered more favorable by analysts.Defense WorldContrasting Emergent Biosolutions (NYSE:EBS) and BioAtla (NASDAQ:BCAB)A comparison of BioAtla and Emergent Biosolutions shows Emergent Biosolutions beats on 10 of 14 factors, including higher revenue and earnings. BioAtla has a higher potential upside from analyst target prices, while Emergent Biosolutions is more affordable. The analysis also notes differences in profitability and volatility.GenengnewsAI In Silico Multi-Omics Technique Cuts Therapeutic Development CostsGATC Health, an AI-driven therapeutic discovery company based in Irvine, California, uses its proprietary Operon™ platform to apply multi-omics analysis and in silico modeling to drug discovery, claiming it can deliver three to five optimized compounds within six months compared to the up to 48 months required by traditional high-throughput screening methods. The company has partnered with BioAtla to form Inversagen AI, LLC—a $40 million special purpose vehicle—to advance Phase III trials of ozuriftamab vedotin for oropharyngeal squamous cell carcinoma and develop conditionally active biologic senolytic therapies, with GATC and BioAtla as equal partners. GATC also offers a clinical trial insurance product underwritten by Medical and Commercial International (MCI) through Lloyd's of London, which reimburses trial costs if safety or efficacy endpoints are not met.Investing.comBioAtla announces 50-for-1 reverse stock split effective April 6 By Investing.comBioAtla, Inc. will implement a 50-for-1 reverse stock split effective April 6, 2026, to increase its per-share trading price and comply with Nasdaq's $1.00 minimum bid price requirement for continued listing on The Nasdaq Capital Market. The reverse split comes as the stock trades near its 52-week low of $0.16, down approximately 78% over the past six months, with a market capitalization of $13.5 million. The company is also undergoing significant restructuring, including reducing its workforce by approximately 70% and is under review by Nasdaq's Listing and Hearing Review Council, which has temporarily stayed suspension and delisting proceedings.Stock TitanBioAtla 50-for-1 share consolidation starts April 6BioAtla, Inc. announced a 50-for-1 share consolidation effective April 6, 2026, designed to increase its per-share trading price to regain compliance with Nasdaq's $1.00 minimum bid price requirement for continued listing on The Nasdaq Capital Market. Stockholders approved the consolidation along with a merger agreement with BA Merger Sub, Inc., BioAtla's wholly-owned subsidiary, at a special meeting held March 23, 2026. No fractional shares will be issued; instead, stockholders entitled to fractional shares will receive cash payments based on the closing price on the effective date.Defense WorldAnalyzing BioAtla (NASDAQ:BCAB) and WAVE Life Sciences (NASDAQ:WVE)This article presents a comparative analysis of two clinical-stage biotechnology companies, WAVE Life Sciences and BioAtla, examining 14 financial and market metrics. WAVE Life Sciences outperforms BioAtla on 8 of the 14 factors compared, including analyst recommendations, with a rating score of 2.86 versus 2.00. Both companies are unprofitable with significant negative net margins, though BioAtla shows a higher potential upside according to consensus price targets.GlobeNewswireBioAtla Announces Formal Process to Evaluate Strategic Options to Monetize AssetsBioAtla announced that its board is evaluating strategic options, including asset sales and partnerships, while implementing a significant restructuring plan with workforce reduction. The company is also actively developing a pipeline of antibody therapeutics targeting solid tumors. It has engaged Tungsten Advisors as a financial advisor in this process.Stock TitanBioAtla starts strategic review, plans 70% job cutsBioAtla, Inc. announced that its Board of Directors has initiated a formal strategic review process to explore options including the sale of preclinical and clinical assets, licensing transactions, and strategic partnerships or other corporate transactions, with no assurance of a successful outcome. Concurrently, the company is implementing a restructuring plan that includes an approximately 70% workforce reduction as part of cost-containment measures. BioAtla has engaged Tungsten Advisors as its exclusive strategic financial advisor to support the process.FierceBiotechBioAtla lays off 70% of workforce, searches for buyers for antibody pipelineBioAtla is reducing its workforce by 70% while exploring strategic options, including potential sale or licensing of its assets. The company, which has faced financial difficulties, is also reviewing its pipeline of biologic antibodies and clinical programs.BioSpaceBioAtla Axes 70% of Staff, Explores Strategic OptionsSan Diego-based biotech BioAtla announced it is cutting approximately 70% of its workforce as part of a strategic review that may include selling assets, licensing transactions, and strategic partnerships. The company, which had previously cut 30% of staff in March 2025, terminated CFO Richard Waldon effective March 2 and appointed Chris Vasquez as his successor, while reporting cash reserves of only $7.1 million as of December 31. BioAtla's clinical-stage pipeline includes ozuriftamab vedotin (Oz-V), a conditionally active antibody drug conjugate, for which the company had a $40 million deal with GATC Health to advance a Phase 3 study in oropharyngeal squamous cell carcinoma.