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BioAtla, Inc., a clinical stage biopharmaceutical company, develops specific and selective antibody-based therapeutics for the treatment of solid tumor cancer. Its lead product candidate is BA3011, a conditionally active biologic (CAB) antibody-drug conjugate (ADC) for soft tissue and bone sarcoma tumors, non-small cell lung cancer (NSCLC), and ovarian cancer. It also develops BA3021, a CAB ADC for multiple solid tumor types, including NSCLC, melanoma, and ovarian cancer; and BA3071, which is a CAB anti-cytotoxic T-lymphocyte-associated antigen 4 antibody for renal cell carcinoma, NSCLC, small cell lung cancer, hepatocellular carcinoma, melanoma, bladder cancer, gastric cancer, and cervical cancer. BioAtla, Inc. was founded in 2007 and is based in San Diego, California.

BioAtla, Inc.

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SAN DIEGO, NOV. 21, 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 HAS ENTERED INTO PRE-PAID ADVANCE AGREEMENTS WITH AN AFFILIATE OF YORKVILLE ADVISORS GLOBAL (YORKVILLE) AND FUNDS MANAGED BY OF ANSON ADVISORS INC. TO PROVIDE AN AGGREGATE $7.5 MILLION ADVANCE TO THE COMPANY. BIOATLA ALSO ENTERED INTO A STANDBY EQUITY PURCHASE AGREEMENT IN WHICH YORKVILLE HAS A COMMITMENT TO BUY, IF THE COMPANY EXERCISES ITS OPTION, FOR UP TO A TOTAL OF $15 MILLION OF COMMON STOCK AT A 3% DISCOUNT TO THE THEN CURRENT MARKET PRICES OVER THREE YEARS, SUBJECT TO CERTAIN CONDITIONS.

BIOATLA ENTERS INTO AGREEMENTS FOR UP TO $22.5 MILLION FLEXIBLE FINANCING

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 APPROVAL COMPANY IS IN ADVANCED STAGES TO FINALIZE A STRATEGIC TRANSACTION WITH A POTENTIAL PARTNER AND WE REMAIN ON TRACK TO COMPLETE THE TRANSACTION BY YEAR END BA3182 TRIAL IN ADVANCED ADENOCARCINOMAS IS CURRENTLY ONGOING AND EVALUATING VARIOUS DOSING AND TREATMENT SCHEDULES WITH A READOUT EXPECTED IN THE FIRST HALF OF 2026 ACHIEVED MILESTONE WITH CONTEXT THERAPEUTICS UNDER THE LICENSE AGREEMENT FOR THE CAB-NECTIN4-TCE REFLECTING CONTINUED PROGRESS AND VALIDATION OF BIOATLA'S DIFFERENTIATED CAB T-CELL ENGAGER PLATFORM MANAGEMENT TO HOST A CONFERENCE CALL AND WEBCAST TODAY AT 4:30 P.M. EASTERN TIME SAN DIEGO, NOV. 13, 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 ITS FINANCIAL RESULTS FOR THE THIRD QUARTER ENDED SEPTEMBER 30, 2025 AND PROVIDED HIGHLIGHTS ON ITS CLINICAL PROGRAMS.

BIOATLA REPORTS THIRD QUARTER 2025 FINANCIAL RESULTS AND HIGHLIGHTS RECENT PROGRESS

 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

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

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.

BIOATLA TO ANNOUNCE THIRD QUARTER 2025 FINANCIAL RESULTS AND PROVIDE BUSINESS HIGHLIGHTS ON NOVEMBER 13, 2025

SAN DIEGO, OCT. 23, 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 PRESENTATION OF A POSTER ENTITLED TARGETING HPV E6/E7 UPREGULATION OF THE TRANSMEMBRANE RECEPTOR TYROSINE KINASE ROR2 WITH THE ADC OZURIFTAMAB VEDOTIN IN PATIENTS WITH ADVANCED HPV+ OROPHARYNGEAL SQUAMOUS CELL CARCINOMA WHICH DETAILS CLINICAL DATA FROM ITS INVESTIGATIONAL ANTIBODY-DRUG CONJUGATE (ADC), OZURIFTAMAB VEDOTIN (OZ-V), AT THE INTERNATIONAL PAPILLOMAVIRUS SOCIETY (IPVS) CONFERENCE, TAKING PLACE OCTOBER 2326, 2025, IN BANGKOK, THAILAND.

BIOATLA PRESENTS COMPELLING MECHANISTIC RATIONALE FOR TARGETING ROR2 WITH OZURIFTAMAB VEDOTIN (OZ-V) IN OROPHARYNGEAL SQUAMOUS CELL CARCINOMA (OPSCC) AT THE ANNUAL CONFERENCE OF THE INTERNATIONAL PAPILLOMAVIRUS SOCIETY

ADVERSE EVENTS (AES) GENERALLY TRANSIENT AND READILY MANAGEABLE; ONLY 2 CASES OF CYTOKINE RELEASE SYNDROME (CRS) PROLONGED TUMOR CONTROL WITH INCREASING DOSES OF BA3182; CONFIRMED PARTIAL RESPONSE (CPR) AT 0.6 MG IN A PATIENT WITH INTRAHEPATIC CHOLANGIOCARCINOMA WITHOUT PROGRESSION FOR >6 MONTHS MAXIMALLY TOLERATED DOSE NOT YET DEFINED; DOSE ESCALATION CONTINUES; CURRENTLY TESTING 1.8 MG DOSE LEVEL SAN DIEGO, OCT. 20, 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 PRELIMINARY CLINICAL DATA FROM A PHASE 1 STUDY OF BA3182 DURING A POSTER PRESENTATION TITLED PRELIMINARY RESULTS FROM A FIRST-IN-HUMAN PHASE 1 STUDY OF BA3182, A DUAL-CONDITIONALLY BINDING BIOLOGIC (CAB) EPCAM X CD3 BISPECIFIC T-CELL ENGAGER IN PATIENTS WITH TREATMENT REFRACTORY METASTATIC ADENOCARCINOMA AT THE EUROPEAN SOCIETY FOR MEDICAL ONCOLOGY (ESMO) CONGRESS 2025, HELD IN BERLIN, GERMANY. THE POSTER WAS FEATURED IN THE INVESTIGATIONAL IMMUNOTHERAPY SESSION ON SUNDAY, OCTOBER 19.

BIOATLA PRESENTS PROMISING INTERIM DATA FROM ITS PHASE 1 TRIAL WITH BA3182 IN PATIENTS WITH TREATMENT REFRACTORY METASTATIC ADENOCARCINOMA AT ESMO 2025

SAN DIEGO, OCT. 03, 2025 (GLOBE NEWSWIRE) -- BIOATLA, INC. (NASDAQ: BCAB), A GLOBAL CLINICAL-STAGE BIOTECHNOLOGY COMPANY FOCUSED ON THE DEVELOPMENT OF CONDITIONALLY ACTIVE BIOLOGIC (CAB) ANTIBODY THERAPEUTICS USING ITS PROPRIETARY CAB PLATFORM FOR THE TREATMENT OF SOLID TUMORS, TODAY ANNOUNCED THAT CLINICAL DATA FOR ITS INVESTIGATIONAL AXL-TARGETING ANTIBODY-DRUG CONJUGATE (ADC), MECBOTAMAB VEDOTIN (BA3011), WILL BE PRESENTED AT THE UPCOMING SOCIETY FOR IMMUNOTHERAPY OF CANCER (SITC) 2025 ANNUAL MEETING TO BE HELD AT NATIONAL HARBOR, MD FROM NOVEMBER 5-9, 2025.

BIOATLA TO PRESENT CLINICAL DATA FOR MECBOTAMAB VEDOTIN (BA3011) IN SOFT TISSUE SARCOMA AT SITC 2025

FDA ALIGNMENT ON PHASE 3 OZURIFTAMAB VEDOTIN (OZ-V) TRIAL DESIGN, INCLUDING DOSING REGIMEN AND ENDPOINTS TO SUPPORT POTENTIAL ACCELERATED APPROVAL COMPANY CONTINUES PREPARATIONS FOR ENABLING INITIATION OF THE PHASE 3 STUDY WITH THE GOAL OF ADVANCING THE STUDY WITH A STRATEGIC PARTNER EARLY NEXT YEAR COMPANY MAINTAINS PREVIOUS GUIDANCE FOR COMPLETION OF A STRATEGIC PARTNERSHIP WITH ONE OF OUR ADVANCED CLINICAL ASSETS THIS YEAR SAN DIEGO, SEPT. 08, 2025 (GLOBE NEWSWIRE) -- BIOATLA, INC. (NASDAQ: BCAB), A GLOBAL CLINICAL-STAGE BIOTECHNOLOGY COMPANY FOCUSED ON THE DEVELOPMENT OF CONDITIONALLY ACTIVE BIOLOGIC (CAB) ANTIBODY THERAPEUTICS USING ITS PROPRIETARY CAB PLATFORM FOR THE TREATMENT OF SOLID TUMORS, TODAY ANNOUNCED OUTCOMES FROM ITS TYPE B MEETING WITH THEUNITED STATES FOOD AND DRUG ADMINISTRATION(FDA).

BIOATLA ANNOUNCES REGULATORY UPDATE ON CLINICAL DEVELOPMENT PLAN FOR OZURIFTAMAB VEDOTIN IN OROPHARYNGEAL SQUAMOUS CELL CARCINOMA (OPSCC) FOLLOWING PRODUCTIVE TYPE B (END OF PHASE 2) MEETING WITH FDA

CAB-EPCAM X CAB-CD3 BISPECIFIC T-CELL ENGAGER (TCE) (BA3182) PHASE 1 DOSE-ESCALATION STUDY ONGOING, CURRENTLY DOSING 1.2 MG COHORT; PHASE 1 DATA READOUT

BioAtla, Inc.

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