ImmunityBio's Immunotherapy ANKTIVA Sparks Revenue Surge as Global Expansion Accelerates (IBRX, NNVC)

Dr. Diwan advised that NV-387 has completed Phase I clinical trial in healthy subjects with no reported adverse events. He further stated that a Phase II clinical trial to test NV-387 for efficacy against Mpox (Monkeypox) virus is ready to begin soon. The ACOREP regulatory agency of the Democratic Republic of Congo (DRC) has already given permission for the clinical trial. The clinical trial application process has been completed.
ImmunityBio (NASDAQ: IBRX) is rapidly transforming into a commercial powerhouse, fueled by the explosive growth of its lead immunotherapy, ANKTIVA. Following a year of breakthrough regulatory wins and clinical milestones, the company has reported a staggering 700% year-over-year increase in preliminary net product revenue, reaching approximately $113 million for 2025.

Commercial Momentum and Global Reach

The company's financial trajectory has caught the attention of Wall Street, with Piper Sandler recently raising its price target to $7.00. Analysts now project 2026 revenues could climb as high as $256 million as the drug penetrates deeper into the bladder cancer market.

Beyond the U.S., ANKTIVA is gaining significant international traction:

Middle East Expansion: The Saudi Food and Drug Authority recently granted accelerated approval for ANKTIVA in both non-muscle invasive bladder cancer (NMIBC) and metastatic non-small cell lung cancer (NSCLC).

European Footprint: Along with existing approvals in the United Kingdom, the drug has received a positive opinion for conditional marketing authorization in the European Union.

Clinical Frontiers: Advancing "Chemo-Free" Treatments

ImmunityBio continues to advance its clinical pipeline. On February 2, 2026, the company initiated ResQ215B, a Phase 2 study for a chemotherapy-free combination in indolent B-cell non-Hodgkin lymphoma. Updated Phase 2 results from the glioblastoma (GBM) program also show promise, with median overall survival not yet reached in a challenging patient group. Dr. Patrick Soon-Shiong, Founder and Executive Chairman, highlighted the potential of the BioShield platform as "Immunotherapy 2.0," aiming for anti-tumor activity without traditional treatment toxicities.

Investor Outlook

Despite ongoing net losses and a new securities investigation by Pomerantz Law Firm following a stock dip in January, major brokerages maintain a positive outlook. Brokerage ratings and price targets include D. Boral Capital (Buy, $24.00), HC Wainwright (Buy, $10.00), BTIG Research (Buy, $9.00), Jefferies (Buy, $9.00), and Piper Sandler (Overweight, $7.00). More details on commercial progress and pipeline updates are available via the ImmunityBio Investor Relations portal.

Another biotech stock that needs attention is NanoViricides, Inc. (NYSE: NNVC), a clinical stage leader developing revolutionary broad-spectrum antiviral drugs that the virus cannot escape, recently today that President Dr. Anil R. Diwan was interviewed on the Mission Matters Podcast by Mr. Adam Torres. The interview video is available at https://youtu.be/nU_2dgd-u1g.

Dr. Diwan explained that NV-387 had shown excellent effectiveness in lethal animal models of infections of viruses including Influenza, RSV, Coronaviruses, MPox, Smallpox as well as Measles. In fact NV-387 treatment led to complete cure of RSV infection in lethally infected animals. Additionally, NV-387 was found to be substantially superior to existing influenza therapeutics, namely Tamiflu (oselatmivir) and Xofluza (baloxavir) in a lethal infection animal model. There is no approved therapy for MPox. Two drugs approved under the US FDA "Animal Rule" process, namely tecovirimat and brincidofovir were put into clinical trials for treatment of MPox. Tecovirimat failed to show improvement over the standard of care. Brincidofovir was dosed in an initial cohort in January, 2025 but no data can be found about its effects, and the clinical trial does not appear to have advanced further. Previously, in three MPox cases treated in the UK under emergency use protocols, brincidofovir led to significant elevation of liver enzymes and the drug was discontinued. No efficacy signal was found in these three cases.

There is no approved therapy for treatment of RSV infection, other than the toxic ribavirin as a last resort. Three antibodies have been approved for treatment of newborns so that they would not come down with RSV infection. A vaccine has been approved for treatment of expectant mothers despite risk of early/preterm births. These approvals indicate the severity of the problem and the need for an actual treatment of RSV infection.

Dr. Diwan advised that NV-387 has completed Phase I clinical trial in healthy subjects with no reported adverse events. He further stated that a Phase II clinical trial to test NV-387 for efficacy against Mpox (Monkeypox) virus is ready to begin soon. The ACOREP regulatory agency of the Democratic Republic of Congo (DRC) has already given permission for the clinical trial. The clinical trial application process has been completed. The trial is expected to begin with dosing of the first cohort of patients once the clinical site preparations are completed. NV-387 is estimated to address a market potential of over $17 Billion by 2030 if approved, based on its broad spectrum and multiple indications. Trading at less than a dollar with a 52-week high of over $2.00, NNVC has significant upside potential. As always, conduct your own due diligence and exercise trader vigilance

Source:

https://ir.immunitybio.com/node/11061/pdf

https://finance.yahoo.com/news/nanoviricides-president-dr-diwan-interviewed-133000134.html

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