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BioAtla Announces Upcoming Poster Presentation at the IASLC 2024 Hot Topic in Basic & Translational Science Meeting

Key Takeaway: BioAtla, Inc. has announced that it will present a poster on its research regarding the KRAS genotype and clinical outcomes in patients treated with Mecbotamab Vedotin at the IASLC 2024 meeting in Washington, DC. The presentation is scheduled for December 14, 2024, during a designated poster reception session. BioAtla's work focuses on Conditionally Active Biologic therapeutics for solid tumors, with ongoing Phase 2 clinical testing for key candidates.
Price reaction · baseline $81 (2024-12-09 close) · hit after-hours · clean, no other BCAB news in the window
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Market Sentiment Analysis

POSITIVE FACTORS

  • Announcement of a poster presentation at a major scientific meeting demonstrates BioAtla's active engagement in research.
  • The poster focuses on important genetic insights related to advanced NSCLC, which may contribute to better treatment strategies.
  • BioAtla has a strong portfolio of innovative CAB therapies in development, indicating potential commercial success.

BiopharmaWatch Analysis

From our catalyst data and publicly available data · not financial advice
Best trade, last catalyst
+117%
120-day peak, hindsight
Typical move
8.3%
average across 6 past catalysts
Cash runway
~11 mo
Medium dilution risk
Lead asset
CAB-AXL-ADC
Phase 2 · Non-Small-Cell Lung Cancer

Full Press Release Details

SAN DIEGO, Dec. 10, 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 a poster presentation at the upcoming International Association for the Study of Lung Cancer (IASLC) 2024 Hot Topic in Basic & Translational Science Meeting to be held in Washington, DC from December 13–15, 2024.
Presentation Details:
Title: Characterization of Mutated KRAS Genotype and Clinical Outcomes in Patients With Advanced NSCLC Treated With Mecbotamab Vedotin, a CAB-AXL-ADC
Authors: Julia Rotow, Grace K. Dy, Edwin Yau, Elaine Shum, Mariam Alexander, Karen L. Reckamp, Roland Leung, Dariusz M. Kowalski, Jose Fuentes Pradera, Jon Zugazagoitia Fraile, Kyechin Chen, Kartik Aysola, D. Ross Camidge
Poster Number: PP01.03
Session Type: Poster Reception
Session Date and Time: Saturday, December 14, 2024 from 5:40 P.M. – 6:40 P.M. ET
A copy of the presentation materials can be accessed on the “Publication” section of the Company’s website at www.bioatla.com once the presentation has 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 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 780 active patent matters, more than 500 of which are issued patents. 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, a novel conditionally active AXL-targeted antibody-drug conjugate (CAB-AXL-ADC), and ozuriftamab vedotin, a novel conditionally active ROR2-targeted antibody-drug conjugate (CAB-ROR2-ADC). The Phase 2 stage CAB-CTLA-4 antibody, evalstotug, 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 dual CAB 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 www.bioatla.com.

Frequently Asked Questions

What is the focus of BioAtla, Inc.?

BioAtla develops Conditionally Active Biologic (CAB) therapeutics for solid tumors.

When will BioAtla present its poster at IASLC?

The presentation is on December 14, 2024, from 5:40 P.M. to 6:40 P.M. ET.

What is mecbotamab vedotin?

Mecbotamab vedotin is a CAB-AXL-ADC for treating advanced NSCLC.

Where is BioAtla headquartered?

BioAtla is based in San Diego, California, with operations in Beijing.

What are the benefits of CAB technology?

CAB technology offers selective targeting, higher efficacy, lower toxicity, and cost-efficiency.

Last updated: Dec 10, 2024