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We've announced that the U.S. Food and Drug Administration (FDA) has granted Expanded Access authorization for the use of our Cancer BioShield™ platform, anchored by ANKTIVA®, to treat lymphopenia in adult patients with refractory or relapsed solid tumors who have progressed after first-line standard-of-care treatment, chemotherapy, radiation, or immunotherapy. Learn more: https://immunitybio.com/immunitybio-receives-fda-expanded-access-authorization-for-landmark-treatment-of-lymphopenia-with-an
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Health | Wellness | Longevity on Instagram: "Dr. Patrick Soon-Shiong is revolutionizing cancer treatment with a paradigm-shifting approach that protects rather than destroys your immune system. His FDA-approved therapy Anktiva activates natural killer cells NewsNation—your body’s innate cancer-fighting defenders—using an IL-15 superagonist. Unlike traditional chemotherapy and radiation that destroy the very immune cells patients need to cure cancer ImmunityBio, Soon-Shiong’s method strengthens t
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Thank you to everyone on X who helped push the FDA to approve my husband for the ANKTIVA Bioshield trial. We just received the news—he’s approved. We believe God has guided every step of this journey, and that this therapy has the potential to save lives. Our mission is not only to cure Andrew of this devastating disease, but to ensure others can access treatments that have been withheld from the general public for far too long. We are hopeful he will begin therapy by the end of next week. To ev
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