Anktiva Receives Conditional Approval Recommendation in EU
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Feb 14 2026
0mins
Source: stocktwits
- EU Approval Progress: In December 2025, the European Medicines Agency (EMA) recommended a conditional marketing authorization for Anktiva in combination with BCG for treating BCG-unresponsive non-muscle invasive bladder cancer (NMIBC), facilitating early access to a medicine that addresses an unmet medical need.
- FDA Resubmission Plans: ImmunityBio is eyeing the resubmission of its application for Anktiva in BCG-unresponsive NMIBC with papillary tumors, despite a previous refuse to file letter from the FDA, indicating ongoing efforts to advance the drug's market entry.
- Positive Market Reaction: ImmunityBio (IBRX) shares have gained 79% over the past 12 months, and while retail sentiment on Stocktwits remains bearish, investors are showing strong interest in the potential approval of Anktiva, with expectations for a decision as early as next Monday.
- Investor Confidence Boosted: Some investors have increased their holdings in IBRX after seeing a price dip, believing that Anktiva's approval will lead to significant stock price appreciation, reflecting market optimism about the drug's prospects and ImmunityBio's future growth.
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Analyst Views on IBRX
Wall Street analysts forecast IBRX stock price to rise
3 Analyst Rating
3 Buy
0 Hold
0 Sell
Strong Buy
Current: 7.220
Low
5.00
Averages
7.33
High
9.00
Current: 7.220
Low
5.00
Averages
7.33
High
9.00
About IBRX
Immunitybio, Inc. is a vertically integrated, clinical-stage biotechnology company developing therapies and vaccines that bolster the natural immune system to defeat cancers and infectious diseases. Using its applied science and platforms to treat cancers, including the development of potential cancer vaccines, as well as developing immunotherapies and cell therapies to reduce or eliminate the need for standard high-dose chemotherapy. Its platforms and their associated product candidates are designed to attack cancer and infectious pathogens by activating both the innate immune system, including NK cells, dendritic cells, and macrophages, as well as the adaptive immune system comprising B and T cells, in an orchestrated manner. Its platforms for the development of biologic product candidates include antibody-cytokine fusion proteins, vaccine vectors, and cell therapies. Its biologic commercial product candidate, Anktiva, is an IL-15 superagonist antibody-cytokine fusion protein.
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.
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- ImmunityBio Allegations: ImmunityBio, Inc. (NASDAQ:IBRX) is implicated in a class action for the period from January 19, 2026, to March 24, 2026, where executives allegedly overstated Anktiva's capabilities, leading to materially misleading statements about the company's prospects and significant investor losses.
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- Legal Consultation Recommendation: Investors suffering losses in the aforementioned companies are encouraged to contact The Law Offices of Frank R. Cruz to discuss their legal rights and ensure their interests are protected in the class actions.
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- FDA Warning Impact: The FDA issued a warning letter to ImmunityBio, citing misleading claims about Anktiva, which led to a more than 21% drop in share price on March 24, 2026, erasing nearly $2 billion in market capitalization and severely impacting investor confidence.
- Class Action Initiation: Hagens Berman has initiated a class action lawsuit on behalf of investors who purchased ImmunityBio securities between January 19 and March 24, 2026, alleging violations of federal securities laws and urging affected investors to submit their losses to support the investigation.
- Promotional Material Issues: The FDA highlighted that ImmunityBio's TV ads and podcast content were misleading, claiming Anktiva could cure all cancers without supporting data, which poses a potential public health risk and exacerbates legal vulnerabilities for the company.
- Investor Rights Protection: Hagens Berman emphasized its investigation into whether ImmunityBio intentionally misled investors and encouraged whistleblowers to provide information to assist the inquiry, demonstrating a commitment to protecting investor rights.
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- Class Action Notice: Rosen Law Firm reminds investors who purchased ImmunityBio (NASDAQ: IBRX) securities between January 19 and March 24, 2026, to apply as lead plaintiffs by May 26, 2026, to participate in the class action, as those who do not will not be represented.
- Fee Arrangement: Investors joining the class action will incur no out-of-pocket costs, as the law firm operates on a contingency fee basis, which alleviates financial burdens and encourages more victims to seek compensation.
- Lawsuit Background: The lawsuit alleges that ImmunityBio made false and misleading statements during the class period, resulting in investor losses when the truth emerged, potentially impacting the company's reputation and future financing capabilities.
- Law Firm's Credentials: Rosen Law Firm specializes in securities class actions and has achieved the largest settlement against a Chinese company, ranked first by ISS Securities Class Action Services in 2017, demonstrating its expertise and success in this field.
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- Lawsuit Background: ImmunityBio is facing a securities class action lawsuit due to misleading efficacy claims made by its Chief Scientific Officer regarding its lead biologic product, Anktiva, during a podcast, with the class period spanning from January 19 to March 24, 2026, potentially impacting investors significantly.
- FDA Warning Letter: The FDA issued a warning letter to ImmunityBio, stating that promotional materials for Anktiva in a podcast and TV ad were false or misleading, resulting in a 21% drop in share price on March 24, 2026, erasing nearly $2 billion in market capitalization.
- Investor Rights: Hagens Berman is investigating whether ImmunityBio intentionally misled investors and is urging affected investors to submit their losses while also encouraging witnesses to assist in the ongoing investigation, highlighting the firm's commitment to protecting shareholder rights.
- Public Health Impact: The FDA emphasized that ImmunityBio's promotional claims misrepresented Anktiva's benefits and failed to provide complete information regarding its FDA-approved indications, raising serious public health concerns about misleading patients regarding treatment expectations.
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- Class Action Notification: The Schall Law Firm reminds investors of a class action lawsuit against ImmunityBio for violations of §§10(b) and 20(a) of the Securities Exchange Act, concerning securities purchased between January 19 and March 24, 2026.
- False Statement Allegations: The complaint alleges that ImmunityBio made false and misleading statements regarding the capabilities of its Anktiva drug, resulting in investor losses when the truth emerged, highlighting significant deficiencies in the company's disclosure practices.
- Investor Rights Protection: The Schall Law Firm encourages affected investors to contact them before May 26, 2026, to participate in the lawsuit and discuss their rights, demonstrating a commitment to safeguarding investor interests.
- Lawsuit Status Explanation: The class action has not yet been certified, meaning investors are not represented by an attorney during this period, underscoring the importance of participating in the lawsuit to ensure their rights are protected.
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- Class Action Initiated: Bronstein, Gewirtz & Grossman, LLC has announced a class action lawsuit against ImmunityBio, seeking damages for investors who purchased securities between January 19 and March 24, 2026, reflecting strong investor response to potential fraud allegations.
- False Statement Allegations: The complaint alleges that ImmunityBio's executive Soon-Shion materially overstated Anktiva's capabilities, leading to materially false and misleading statements about the company's business and prospects, which could result in significant losses for investors.
- Investor Action Call: Affected investors are encouraged to apply to be lead plaintiffs by May 26, 2026, to share in any potential recovery from the lawsuit, demonstrating the legal team's commitment to protecting investor rights.
- No-Risk Legal Services: Bronstein, Gewirtz & Grossman, LLC offers contingency fee-based legal services, charging only if they successfully recover funds, highlighting the firm's strong focus on investor interests and accountability.
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