BCAB BIOATLA INC

BioAtla Announces Poster Presentations at the 2024 American Association for Cancer Research (AACR) Annual Meeting

BioAtla Announces Poster Presentations at the 2024 American Association for Cancer Research (AACR) Annual Meeting

  • Five abstracts accepted for poster presentation highlight Company’s proprietary Conditionally Active Biologic (CAB) technology
  • Differentiated preclinical activity for CAB anti-Nectin4-antibody drug conjugate (ADC) with superior efficacy to enfortumab vedotin analogue in a patient derived pancreatic cancer model
  • No clinical and histopathologic signs of toxicities in non-human primates with conditionally active tetravalent B7-H3 x CD3 T-cell engager (BA3142)

SAN DIEGO, March 07, 2024 (GLOBE NEWSWIRE) -- BioAtla, Inc. (Nasdaq: BCAB), a global clinical-stage biotechnology company focused on the development of Conditionally Active Biologic (CAB) antibody therapeutics for the treatment of solid tumors, today announced preclinical poster presentations at the upcoming 2024 American Association for Cancer Research (AACR) Annual Meeting to be held at the San Diego Convention Center in San Diego, California from April 5–10, 2024. 

Presentation Details:

Poster Title: Using a novel NextGen linker system to generate a Conditionally Active Biologic (CAB) anti-Nectin4-ADC demonstrates improved efficacy in pancreatic PDX cancer models and improved tolerability and toxicity profile in non-human primates
Authors:

 Jing Wang, Jian Chen, Gerhard Frey, Haizhen Liu, Charles Xing, Kathryn Woodard, Cathy Chang, William J. Boyle, and Jay M. Short
Poster Number:

 743 / 29
Session:

 PO.ET02.06 - Tumor Microenvironment
Date / Time:

 Sunday, April 7, 2024 / 1:30 – 5:00 PM PT
Location:

 Section 29

         

Poster Title: 

 Novel Conditionally Active Tetravalent B7-H3 x CD3 T-cell Engagers Targeting Solid Tumors
Authors: 

 Ana Paula Cugnetti, Haizhen Liu, Patricia McNeeley, Charles Xing, Kathryn Woodard, Cathy Chang, Gerhard Frey, William J. Boyle, and Jay M. Short
Poster Number: 

 6340 / 1
Session: 

 PO.CL06.08 - Antibodies 2
Date / Time:

 Tuesday, April 9, 2024 / 1:30 – 5:00 PM PT
Location:

 Section 41



Poster Title: 

 Novel Conditionally Active Biologic (CAB) tetravalent T-cell engagers targeting solid tumors
Authors: 

 Ana Paula Cugnetti, Haizhen Liu, Patricia McNeeley, Charles Xing, Kathryn Woodard, Cathy Chang, Gerhard Frey, William J. Boyle, and Jay M. Short
Poster Number:

 744 / 30
Session:

 PO.ET02.06 - Tumor Microenvironment
Date / Time:

 Sunday, April 7, 2024 / 1:30 – 5:00 PM PT
Location: 

 Section 29



Poster Title:

 Targeting novel senescence markers by Conditionally Active Biologics eliminates senescence-associated secretory phenotype in in vitro and in vivo models
Authors:  

 Jian Chen, Jing Wang, Haizhen Liu, Cathy Chang, William J. Boyle and Jay M. Short
Poster Number: 

 2969 / 16
Session: 

 PO.MCB04.02 - Cellular Stress Responses 2
Date / Time: 

 Monday, April 8, 2024 / 1:30 – 5:00 PM PT
Location:

 Section 15



Poster Title:

 Development of a humanized anti-IL-22 antibody for cancer and inflammation therapy
Authors: 

 Jian Chen, Cathy Chang, Gerhard Frey, Haizhen Liu, Jing Wang, William J. Boyle and Jay M. Short
Poster Number:

 1405 / 3
Session: 

 PO.IM01.05 - Inflammation, Host Factors, and Epigenetic Influences on Cancer Development and Treatment
Date / Time:

 Monday, April 8, 2024 / 9:00 AM – 12:30 PM PT
Location: 

 Section 5
   

A copy of the presentation materials can be accessed on the “” section of the Company’s website at once the presentations have concluded.

About BioAtla®, Inc. 

BioAtla is a global clinical-stage biotechnology company with operations in San Diego, California, and in Beijing, China through our contractual relationship with BioDuro-Sundia, a provider of preclinical development services. Utilizing its proprietary Conditionally Active Biologics (CAB) technology, BioAtla develops novel, reversibly active monoclonal and bispecific antibodies and other protein therapeutic product candidates. CAB product candidates are designed to have more selective targeting, greater efficacy with lower toxicity, and more cost-efficient and predictable manufacturing than traditional antibodies. BioAtla has extensive and worldwide patent coverage for its CAB technology and products with greater than 750 patents filed, more than 475 of which have been issued. Broad patent coverage in all major markets include methods of making, screening and manufacturing CAB product candidates in a wide range of formats and composition of matter coverage for specific products. BioAtla has two first-in-class CAB programs currently in Phase 2 clinical testing, mecbotamab vedotin, BA3011, a novel conditionally active AXL-targeted antibody-drug conjugate (CAB-AXL-ADC), and ozuriftamab vedotin, BA3021, a novel conditionally active ROR2-targeted antibody-drug conjugate (CAB-ROR2-ADC). The Phase 2 stage CAB-CTLA-4 antibody, BA3071, is a novel CTLA-4 inhibitor designed to reduce systemic toxicity and potentially enable safer combination therapies with checkpoint inhibitors such as anti-PD-1 antibody. The company’s first bispecific T-cell engager antibody, BA3182, is currently in Phase 1 development. BA3182 targets EpCAM, which is highly and frequently expressed on many adenocarcinomas while engaging human CD3 expressing T cells. To learn more about BioAtla, Inc. visit . 

Internal Contact: 

Richard Waldron 

Chief Financial Officer 

BioAtla, Inc. 

  

858.356.8945 

External Contact: 

Bruce Mackle

LifeSci Advisors, LLC 

 

 



EN
07/03/2024

Underlying

To request access to management, click here to engage with our
partner Phoenix-IR's CorporateAccessNetwork.com

Reports on BIOATLA INC

 PRESS RELEASE

BioAtla and GATC Health Announce a $40 Million Special Purpose Vehicle...

BioAtla and GATC Health Announce a $40 Million Special Purpose Vehicle (SPV) Transaction to Advance Ozuriftamab Vedotin (Oz-V) into a Registrational Trial for 2L+ Oropharyngeal Squamous Cell Carcinoma (OPSCC) BioAtla will receive an initial $5 million for general operating and Phase 3 clinical trial expenses to advance Oz-V in 2L+ OPSCC with the remaining $35 million anticipated to close in Q1 2026.BioAtla to retain 65% ownership of Oz-V across all solid tumor indications after completion of the SPV transaction.BioAtla will lead Phase 3 trial execution for Oz-V in OPSCC through data readout...

 PRESS RELEASE

BioAtla Enters into Agreements for up to $22.5 Million Flexible Financ...

BioAtla Enters into Agreements for up to $22.5 Million Flexible Financing These agreements are designed to be a flexible financing solution to support operations while finalizing a strategic partnershipCompany is in advanced stages to finalize a strategic transaction with a potential partner, and it remains on track to complete the transaction by year endThese agreements ensure BioAtla can maintain operational momentum while completing that process SAN DIEGO, Nov. 21, 2025 (GLOBE NEWSWIRE) -- BioAtla, Inc. (Nasdaq: BCAB), a global clinical-stage biotechnology company focused on the devel...

 PRESS RELEASE

BioAtla Reports Third Quarter 2025 Financial Results and Highlights Re...

BioAtla Reports Third Quarter 2025 Financial Results and Highlights Recent Progress Company achieved FDA alignment on Phase 3 Oz-V trial for the treatment of 2L+ OPSCC, which will evaluate dual primary endpoints with potential of achieving accelerated approval followed by full approvalCompany is in advanced stages to finalize a strategic transaction with a potential partner and we remain on track to complete the transaction by year endBA3182 trial in advanced adenocarcinomas is currently ongoing and evaluating various dosing and treatment schedules with a readout expected in the first half ...

 PRESS RELEASE

BioAtla’s Mecbotamab Vedotin (Mec-V), an AXL-targeting ADC, Demonstrat...

BioAtla’s Mecbotamab Vedotin (Mec-V), an AXL-targeting ADC, Demonstrates a Median Overall Survival (OS) of 21.5 months in Subtypes of Refractory Soft Tissue Sarcomas — Mec-V demonstrates median OS of 21.5 months in patients with treatment-refractory leiomyosarcoma, liposarcoma, and undifferentiated pleomorphic sarcoma compared with approximately 12 months with approved agents — Mec-V safety profile as monotherapy, and in combination with anti-PD-1 antibody, was manageable and consistent with conditional binding of the AXL target restricted to the tumor microenvironment SAN DIEGO, Nov. 07...

 PRESS RELEASE

BioAtla to Announce Third Quarter 2025 Financial Results and Provide B...

BioAtla to Announce Third Quarter 2025 Financial Results and Provide Business Highlights on November 13, 2025 SAN DIEGO, Nov. 05, 2025 (GLOBE NEWSWIRE) -- BioAtla, Inc. (Nasdaq: BCAB), a global clinical-stage biotechnology company focused on the development of Conditionally Active Biologic (CAB) antibody therapeutics for the treatment of solid tumors, today announced that it plans to host a conference call and webcast on Thursday, November 13, 2025 at 4:30 p.m. ET to discuss its financial results for the third quarter ended September 30, 2025 and provide business highlights. Conference C...

ResearchPool Subscriptions

Get the most out of your insights

Get in touch