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ImmunityBio Receives FDA Expanded Access Authorization for Landmark Treatment of Lymphopenia With ANKTIVA®, the Cancer BioShield™ Platform, in Patients With Solid Tumors

1. ImmunityBio's ANKTIVA® receives FDA Expanded Access for cancer treatment. 2. This authorization allows broader patient access to advanced immunotherapy options.

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FAQ

Why Bullish?

Gaining FDA authorization often boosts investor confidence and stock performance, as shown in similar biotech instances where approvals led to price upticks. Historically, companies like Gilead Sciences saw substantial price increases upon positive FDA news.

How important is it?

The FDA’s Expanded Access authorization is a significant milestone for IBRX, suggesting potential revenue streams and therapeutic advancements. With immunotherapy being a hot market, this news could attract new investments and invigorate the stock.

Why Short Term?

FDA news generally creates immediate investor interest, impacting stock price positively in the short term. Similar announcements in the biotech sector have seen quick spikes in prices, but long-term effects depend heavily on trial outcomes and overall sales.

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CULVER CITY, Calif.--(BUSINESS WIRE)--ImmunityBio, Inc. (NASDAQ: IBRX), a leading immunotherapy company, today announced that the U.S. Food and Drug Administration (FDA) has granted Expanded Access authorization for the use of its Cancer BioShield™ platform, anchored by ANKTIVA® (nogapendekin alfa inbakicept-pmln), to treat lymphopenia in adult patients with refractory or relapsed solid tumors independent of tumor type who have progressed after first-line standard-of-care treatment, chemotherap.

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