Welcome to our dedicated page for Bioatla news (Ticker: BCAB), a resource for investors and traders seeking the latest updates and insights on Bioatla stock.
BioAtla, Inc. (BCAB) is a clinical-stage biopharmaceutical innovator advancing conditionally active biologic therapies for cancer treatment. This news hub provides investors and industry professionals with essential updates on the company’s proprietary CAB technology platform, clinical trial progress, and strategic developments.
Access timely press releases covering key milestones including regulatory filings, partnership announcements, and financial results. Our curated collection features updates on antibody-drug conjugate trials, intellectual property expansions, and operational developments across BioAtla’s global facilities.
This resource serves as your primary source for tracking BCAB’s progress in developing tumor-selective therapies. Bookmark this page for direct access to verified corporate communications and objective reporting on clinical advancements. Check regularly for updates on pipeline candidates and business strategy execution.
BioAtla, Inc. (Nasdaq: BCAB), a global clinical-stage biotechnology company focused on developing Conditionally Active Biologic (CAB) antibody therapeutics for solid tumor treatment, has announced a poster presentation at the 39th Society for Immunotherapy of Cancer (SITC) Annual Meeting. The event will take place from November 8–10, 2024, at the George R. Brown Convention Center in Houston, TX.
The presentation, titled 'Updated results from a phase 1 study of evalstotug (BA3071), an anti-CTLA-4 conditionally active biologic, with or without nivolumab, in advanced solid tumors', is scheduled for Friday, November 8, 2024, at 9:00a CDT in Exhibit Halls AB. The presentation materials will be available on the 'Publication' section of BioAtla's website after the presentation concludes.
BioAtla, Inc. (Nasdaq: BCAB), a global clinical-stage biotechnology company focused on developing Conditionally Active Biologic (CAB) antibody therapeutics for solid tumors, has announced an upcoming oral presentation at the Society for Melanoma Research 21st International Congress (SMR) in New Orleans, LA, from October 10–13, 2024.
The presentation details are as follows:
- Title: Evalstotug (BA3071): a potent conditionally active biologic (CAB) anti-CTLA-4 antibody designed to enable high exposures, extended dosing, and reduced immune-mediated toxicity
- Presenting Author: William Boyle, Ph.D.
- Session Category: Developmental Immunotherapy
- Date & Time: Friday, October 11th, 2024 from 8:00am–10:20am CDT
The abstract will be published in the 2024 SMR Abstract book and online in the PCMR journal. Presentation materials will be available on BioAtla's website after the presentation concludes.
BioAtla and Context Therapeutics have entered into an exclusive worldwide license agreement for the development and commercialization of BA3362, a Nectin-4 x CD3 T Cell Engaging Antibody. Key points include:
1. Context obtains exclusive rights to BA3362
2. BioAtla to receive $15.0 million in upfront and near-term milestones
3. Potential for up to $118.5 million in additional clinical, regulatory, and commercial milestones, plus royalties on net sales
4. Context anticipates IND filing for BA3362 in mid-2026
This agreement allows BioAtla to focus on its lead clinical CAB programs while potentially advancing BA3362 under Context's leadership. The transaction aligns with Context's strategy of building a pipeline of TCE assets through strategic in-licensing or acquisition.
BioAtla (NASDAQ: BCAB) presented promising Phase 2 trial data for ozuriftamab vedotin, a conditionally active ROR2-ADC, in treating squamous cell carcinoma of the head and neck (SCCHN) at the 2024 ESMO Annual Meeting. The trial showed an overall response rate of 32% across two dosing regimens, including an ongoing complete response. The drug demonstrated meaningful antitumor activity with manageable tolerability in heavily pretreated patients.
Key highlights include:
- 77% disease control rate
- 10 responses (1 CR, 9 PRs) among 31 evaluable patients
- Well-tolerated treatment with mostly low-grade adverse events
- FDA Fast Track Designation for R/M SCCHN treatment
BioAtla, Inc. (Nasdaq: BCAB), a global clinical-stage biotechnology company, has announced a poster presentation at the upcoming 2024 European Society for Medical Oncology (ESMO) Annual Meeting in Barcelona, Spain. The presentation, titled 'Phase 2 trial of ozuriftamab vedotin (BA3021), a conditionally active biologic (CAB)-ROR2-ADC, in patients with recurrent or metastatic squamous cell carcinoma of the head and neck (R/M SCCHN),' will be presented on September 14, 2024. The poster (Number: 868P) will showcase BioAtla's research on Conditionally Active Biologic antibody therapeutics for solid tumor treatment. Presentation materials will be available on the company's website after the event.
BioAtla (Nasdaq: BCAB), a global clinical-stage biotechnology company, has announced its participation in the H.C. Wainwright 26th Annual Global Investment Conference. The event is scheduled for September 9-11, 2024. BioAtla's management will provide a corporate update in a pre-recorded fireside chat format, which will be available on-demand starting Monday, September 9, at 7:00 a.m. ET.
BioAtla specializes in developing Conditionally Active Biologic (CAB) antibody therapeutics for the treatment of solid tumors. This conference participation offers an opportunity for investors and industry professionals to gain insights into BioAtla's latest developments and strategic direction in the field of oncology therapeutics.
BioAtla (NASDAQ: BCAB) reported Q2 2024 financial results and clinical progress. Key highlights include:
1. Ozuriftamab vedotin granted Fast Track Designation by FDA for head and neck cancer; FDA meeting anticipated in 2H 2024.
2. Evalstotug showed low incidence of immune-related adverse events; Phase 2 combination study with pembrolizumab on track for initial data in 2H 2024.
3. Mecbotamab vedotin Phase 2 trial in NSCLC showed improved overall survival in patients with KRAS mutations.
4. Cash balance projected to fund operations through Q3 2025.
5. Q2 2024 financial results: R&D expenses $16.2M (down from $31.0M in Q2 2023), G&A expenses $5.8M, net loss $21.1M, cash and equivalents $61.7M as of June 30, 2024.
BioAtla (Nasdaq: BCAB), a global clinical-stage biotechnology company specializing in Conditionally Active Biologic (CAB) antibody therapeutics for solid tumors, has announced its upcoming second quarter 2024 financial results and business highlights conference call. The event is scheduled for Thursday, August 8, 2024, at 4:30 p.m. ET.
Investors and interested parties can access the webcast through the provided link or join via phone using the dial-in numbers. The financial results press release will be available on the company's website prior to the call. A replay of the conference call will also be accessible through the Investors section of BioAtla's website.
BioAtla (Nasdaq: BCAB) hosted a virtual R&D Day highlighting updates on its clinical programs. Key findings include:
1. Mecbotamab vedotin (CAB-AXL-ADC): Showed clinical benefit in NSCLC patients with mutant KRAS variants. AXL expression ≥1% correlated with clinical benefit in heavily pretreated patients.
2. Evalstotug (CAB-CTLA-4 antibody): Demonstrated promising anti-tumor activity as monotherapy and in combination with PD-1, with a differentiated safety profile and low incidence of immune-related adverse events.
The event featured insights from key opinion leaders Dr. Edwin Yau, Dr. Omid Hamid, and Dr. Ankit Mangla, who shared positive observations on the clinical benefits and safety profiles of BioAtla's therapies.
BioAtla (Nasdaq: BCAB) has received FDA Fast Track Designation for ozuriftamab vedotin (CAB-ROR2-ADC) to treat recurrent or metastatic squamous cell carcinoma of the head and neck (SCCHN). This conditionally active antibody drug conjugate has shown promising clinical activity and a manageable safety profile in treatment-refractory SCCHN patients during its Phase 2 trial. The company plans to meet with the FDA in the second half of 2024 to discuss a potential registrational trial. Fast Track Designation could expedite development and review, potentially leading to priority review if supported by clinical data at BLA submission.
