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IBRXImmunityBio, Inc.
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  • 10.14After-hours26.10.15 06:19
    8-KKey event#●●●#●●●

    ImmunityBio, Inc.Bullish

    On October 14, 2026, ImmunityBio announced that the U.S. FDA expanded the approved indication for ANKTIVA in combination with BCG to include patients with BCG-unresponsive NMIBC with papillary-only tumors. This approval broadens the eligible patient population beyond those with carcinoma in situ (CIS), marking the first FDA-approved therapy for both CIS and papillary-only disease in this setting.…more

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  • 10.6After-hours26.10.07 07:06
    4Ownership

    ImmunityBio, Inc.

    Insider Barry J. Simon of ImmunityBio, Inc. filed a Form 4 report on October 6, 2026, regarding changes in beneficial ownership of securities as of October 5, 2026. This filing serves as a standard disclosure of insider equity transactions.…more

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  • 10.6After-hours26.10.07 07:05
    4Ownership

    ImmunityBio, Inc.

    Insider Cheryl Cohen of ImmunityBio, Inc. reported a change in beneficial ownership of securities as of October 2, 2026. This filing serves as a standard disclosure of insider equity movement and does not involve material corporate events such as capital raising or delisting.…more

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  • 4d agoPre-market26.10.21 20:38
    #●●●#●●●

    ImmunityBio Sets November 2026 for ANKTIVA Bladder Cancer Trial Results…more

    ImmunityBio expects to report topline results for its ANKTIVA combination therapy in BCG-naïve NMIBC patients by November 2026. The company remains on track to submit a supplemental Biologics License Application to the FDA in the fourth quarter of 2026.…more

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  • 4d agoPre-market26.10.21 20:37

    ●●●●●●●● ●●●●● ●●●●●●

    ImmunityBio has completed the database lock for its Phase 3 trial of ANKTIVA in bladder cancer patients and has begun final data analysis. The company expects to report topline results in November 2026 and remains on track to submit a supplemental BLA to the FDA by the end of 2026.…more

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  • 5d agoRegular26.10.20 00:52

    ●●●●●●●● ●●●●● ●●●●●●

    ImmunityBio's bladder cancer treatment, ANKTIVA, demonstrated a 71% complete response rate and strong survival metrics in recent long-term clinical studies. These findings reinforce the clinical evidence for the FDA-approved therapy and support its potential for continued market adoption.…more

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