U.S. Stocks Mixed; Day One Biopharmaceuticals Shares Surge 20%
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Jan 12 2026
0mins
Should l Buy ATRA?
Source: Benzinga
- Mixed Market Performance: U.S. stocks exhibited mixed results on Monday, with the Nasdaq Composite gaining over 50 points and rising 0.29%, while the Dow Jones fell 0.19% to 49,411.94, indicating market volatility and investor caution.
- Biopharma Surge: Day One Biopharmaceuticals Inc (NASDAQ:DAWN) shares surged 20% to $10.77 after reporting a projected 2025 OJEMDA net product revenue of $155.4 million, a 172% year-over-year increase, highlighting strong market demand and growth potential.
- FDA Response Impact: Atara Biotherapeutics Inc (NASDAQ:ATRA) shares plummeted 53% to $6.41 following a Complete Response Letter from the FDA citing concerns over clinical trial adequacy, raising investor worries about the company's future prospects.
- Sector Sentiment Fluctuations: Financial stocks dipped by 1.1% while consumer staples rose by 1%, reflecting differing investor confidence across sectors, which may influence future investment strategies and market trends.
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Analyst Views on ATRA
Wall Street analysts forecast ATRA stock price to rise
2 Analyst Rating
2 Buy
0 Hold
0 Sell
Moderate Buy
Current: 4.320
Low
18.00
Averages
21.50
High
25.00
Current: 4.320
Low
18.00
Averages
21.50
High
25.00
About ATRA
Atara Biotherapeutics, Inc. is an allogeneic T-cell immunotherapy company. The Company is a developer of T-cell immunotherapy, leveraging its novel allogeneic Epstein-Barr virus (EBV) T-cell platform to develop transformative therapies for patients with serious diseases. Its pipeline products include Ebvallo (Tab-cel), ATA3219, and ATA3431. The Company’s T-cell immunotherapy, tab-cel (tabelecleucel), is in Phase III development for patients with EBV-driven post-transplant lymphoproliferative disease (EBV+ PTLD) who have failed rituximab or rituximab plus chemotherapy, as well as other EBV-driven diseases. Its ATA3219 allogeneic CD19 CAR T immunotherapy, targeting B-cell malignancies and autoimmune diseases, is based on a next-generation 1XX CAR co-stimulatory domain and EBV T-cell platform and does not require TCR or HLA gene editing. ATA3431 is an allogeneic, bispecific CAR directed against CD19 and CD20 for B-cell malignancies and autoimmune disease.
About the author

Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
- Class Action Filed: Pomerantz LLP has initiated a class action lawsuit against Atara Biotherapeutics in the Central District of California on behalf of investors who purchased Atara securities between May 20, 2024, and January 9, 2026, seeking damages for violations of federal securities laws, indicating significant investor concerns about the company's future prospects.
- FDA Regulatory Risks: Atara's Biologics License Application for tabelecleucel received a Complete Response Letter (CRL) from the FDA, citing good manufacturing practice (GMP) compliance issues at a third-party facility, which heightens regulatory scrutiny and jeopardizes ongoing clinical trials, potentially delaying product approval.
- Stock Price Volatility: Following the CRL announcement on January 16, 2025, Atara's stock plummeted by 40.5% to $7.83 per share, reflecting a severe lack of market confidence in the company's regulatory compliance capabilities and exacerbating investor anxiety.
- Deteriorating Financial Condition: With the FDA placing a clinical hold on tabelecleucel trials, Atara's stock fell by 56.99% to $5.88 per share on January 12, 2026, highlighting increasing financial pressures that may hinder future funding and operational capabilities.
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- Class Action Initiation: Rosen Law Firm announces a class action lawsuit on behalf of Atara Biotherapeutics (NASDAQ: ATRA) securities purchasers from May 20, 2024, to January 9, 2026, indicating potential investor losses due to misleading statements.
- Compensation Structure: Participants may receive compensation through a contingency fee arrangement without upfront costs, reducing financial barriers for affected investors and encouraging broader participation in the lawsuit.
- Law Firm Credentials: Rosen Law Firm is renowned for its successful track record in securities class actions, having recovered over $438 million for investors in 2019 alone, showcasing its strength and expertise in handling similar cases.
- Case Details Unveiled: The lawsuit alleges that Atara failed to disclose manufacturing issues and clinical trial risks during the class period, leading to investor misunderstandings about its financial health, which could significantly impact the company's future market performance.
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- Atara Biotherapeutics Lawsuit: A class action lawsuit against Atara Biotherapeutics, Inc. alleges that from May 20, 2024, to January 9, 2026, the company failed to disclose critical facts regarding its manufacturing and tabelecleucel's regulatory prospects, leading to significant investor losses, with a deadline of May 22, 2026, to apply as lead plaintiff.
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- Vital Farms ERP Implementation Dispute: The class action lawsuit against Vital Farms, Inc. claims that from May 8, 2025, to February 26, 2026, the company did not disclose important facts regarding the implementation of its new enterprise resource planning system, with a lead plaintiff application deadline of May 26, 2026.
- Super Micro Compliance Issues: Super Micro Computer, Inc. is involved in a class action lawsuit alleging non-compliance with export control laws from April 30, 2024, to March 19, 2026, with investors needing to apply for lead plaintiff status by May 26, 2026, if they suffered losses during this period.
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- Class Action Reminder: The Schall Law Firm alerts investors of a class action lawsuit against Atara Biotherapeutics for violations of §§10(b) and 20(a) of the Securities Exchange Act, concerning securities purchased between May 20, 2024, and January 9, 2026, with a deadline to contact the firm by May 22, 2026, to participate.
- False Statements Allegation: The complaint alleges that Atara faced manufacturing issues and deficiencies in its ALLELE study, making FDA approval of its BLA for tabelecleucel unlikely, while the company overstated the drug's prospects, leading to investor losses.
- Increased Regulatory Risk: Atara's manufacturing defects have heightened the risk of regulatory action, rendering its public statements false and materially misleading, which further undermines investor confidence and impacts the company's stock price.
- Legal Consultation Opportunity: The Schall Law Firm offers free consultations, encouraging affected investors to reach out to discuss their rights, showcasing the firm's expertise in representing investors in securities class action lawsuits globally.
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- Class Action Initiation: Rosen Law Firm has announced a class action lawsuit on behalf of investors who purchased Atara Biotherapeutics (NASDAQ:ATRA) securities between May 20, 2024, and January 9, 2026, alleging that the company made false and misleading statements during this period, potentially leading to investor losses.
- Compensation Mechanism: Investors participating in the class action will not incur any out-of-pocket expenses, as the law firm will operate on a contingency fee basis, ensuring that investors do not bear additional financial burdens during the legal process.
- Legal Representation Advisory: The Rosen Law Firm emphasizes the importance of selecting qualified counsel with a proven track record, noting that many firms issuing notices may lack the necessary experience and resources, urging investors to be cautious in their choice of legal representation.
- Impact Analysis: The lawsuit claims that Atara faced manufacturing and clinical trial issues that could jeopardize FDA approval of its biologics license application, likely resulting in significant negative impacts on the company's financial condition, prompting investors to monitor developments closely to assess potential losses.
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- Legal Investigation Launched: Faruq & Faruqi, LLP is investigating Atara Biotherapeutics, Inc. for potential claims related to investor losses incurred from May 20, 2024, to January 9, 2026, indicating significant legal risks for the company.
- Investor Rights Reminder: The firm reminds investors that May 22, 2026, is the deadline to seek lead plaintiff status in a federal securities class action, emphasizing the importance of timely legal action to protect their rights.
- Direct Contact Channels: Securities Litigation Partner Josh Wilson encourages affected investors to reach out directly, providing multiple contact options, which demonstrates the firm's commitment to supporting victims.
- Potential Litigation Impact: Should the investigation reveal wrongdoing by Atara, the company may face substantial financial liabilities, potentially affecting its stock price and market confidence, prompting investors to closely monitor developments.
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