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Immune to Cancer: The CRI Blog

  • FDA Approves Expanded Use of Nivolumab for Lung Cancer

    Nivolumab, a PD-1 immunotherapy, is now approved as second-line therapy for the most common type of lung…

    October 9, 2015| Matthew Tontonoz
  • FDA Approves PD-1 Immunotherapy for Most Common Type of Lung Cancer

    Patients with non-small cell lung cancer may now receive a PD-1 immunotherapy as second-line treatment after chemotherapy.

    October 2, 2015| Matthew Tontonoz
  • In a First, FDA Approves Immunotherapy Combination for Advanced Melanoma

    The approval of a combination of two immunotherapy drugs for melanoma represents a treatment milestone.

    October 1, 2015| Matthew Tontonoz
  • European Regulators Approve Pembrolizumab (Keytruda) as First-line Treatment of Advanced Melanoma

    The decision makes pembrolizumab the second PD-1-blocking drug to receive approval in Europe.

    July 22, 2015| Matthew Tontonoz
  • What Cancer Patients Need to Know About the Opdivo Approval

    Now that Opdivo (nivolumab) has been FDA approved for two cancer types, many patients are wondering: what’s…

    March 13, 2015| Emily Helck
  • Big News: FDA Approves Opdivo (Nivolumab) for Lung Cancer

    The PD-1 checkpoint inhibitor Opdivo® (nivolumab) is a new treatment option for patients with non-small cell lung…

    March 4, 2015| Matthew Tontonoz
  • New Cancer Immunotherapy Opdivo Approved by FDA

    Just hours ago, the FDA approved Bristol-Myers Squibb's PD-1 drug for melanoma.

    December 22, 2014| Jill O'Donnell-Tormey, PhD
  • FDA Approves New Immunotherapy for Leukemia

    Amgen’s Blincyto was approved by the FDA, making it the first approved bispecific T cell engaging (BiTE)…

    December 8, 2014| Alexandra Mulvey
  • FDA Approves New Cancer Immunotherapy

    Merck's new immunotherapy, Keytruda (pembrolizumab), was approved today by the FDA, making it the first PD-1 inhibitor…

    September 4, 2014| Jill O'Donnell-Tormey, PhD
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  • About
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  • What is Immunotherapy?
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    • Connect with ImmunoAdvocates
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