Healthcare entity

ImmunityBio

Company IBRX

All 1 tracked stories fall under one category: regulation. FDA is the most frequent co-covered peer, appearing in 1 of the 1 tracked story. The 7 average consequence score is above the beat benchmark of 5.8 in the same window.

Last mentioned: Mar 24, 2026

Entity pulse

Recent coverage · ImmunityBio

1 story
7 avg impact
0% positive
100% negative

Coverage balance Negative coverage leads. Negative coverage exceeds positive coverage by 100 percentage points.

  • 100% negative

Figures are computed live from our source-verified story record — see our methodology for how impact and sentiment are derived.

What the coverage shows about ImmunityBio

All 1 tracked stories fall under one category: regulation. FDA is the most frequent co-covered peer, appearing in 1 of the 1 tracked story. The 7 average consequence score is above the beat benchmark of 5.8 in the same window. They are less corroborated than the beat average, carrying 2 original sources each against 2.4 for the same window. We currently track 1 Healthcare story that mention ImmunityBio, all published on March 24, 2026.

Stories tracked
1
Sources per story
2

Computed from the 1 stories linked to this entity, with beat comparisons drawn from all 29 Healthcare stories published in the same date window. Shares are omitted below five stories and comparisons below a twenty-story baseline.

Coverage cohort

Appears alongside

Other entities that clear the same relevance threshold in stories also covering ImmunityBio. Shared-story counts are live from our verified record — not editorial picks.

Timeline

  1. FDA Warning Issued

    The FDA flags the podcast statements as misleading and issues an Untitled Letter to ImmunityBio.

  2. Podcast Appearance

    Patrick Soon-Shiong discusses the drug's potential on a high-profile industry podcast.

  3. Initial FDA Approval

    Anktiva (N-803) receives FDA approval for BCG-unresponsive NMIBC.

Stories mentioning ImmunityBio 1

Health Policy Negative

FDA Issues Warning to ImmunityBio Over Soon-Shiong’s Cancer Drug Claims

The FDA has issued a formal warning to ImmunityBio and its founder, Patrick Soon-Shiong, regarding misleading public statements about the company's bladder cancer drug. The regulator cited claims made during a podcast that suggested broader efficacy than currently approved, raising concerns about off-label promotion.

2 sources

ImmunityBio is linked from 1 story on this site, each scored at or above our 35% relevance threshold — see how these pages are built.

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