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Tag: Serious Adverse Drug Reactions (ADR’s)

New Treatment Modality: Nivolumab (Opdivo) has been approved for the treatment of patients with previously treated metastatic squamous non-small cell lung cancer (NSCLC)

By Joseph Gut - thasso Posted on June 17, 2015 Posted in New Drug Approval, Thasso Post, Theragenomic Medicine Tagged with Advanced Melanoma, American Food & Drug Administration (FDA), Clinical Trial, Lungevity Foundation, Nivolumab (Opdivo), Programmed Death Receptor-1 (PD-1, Serious Adverse Drug Reactions (ADR's)
New Treatment Modality: Nivolumab (Opdivo) has been approved for the treatment of patients with previously treated metastatic squamous non-small cell lung cancer (NSCLC)

June 17, 2015 – Bristol Myers Squipp recently announced that the U.S. Food and Drug Administration (FDA) has approved Nivolumab (Opdivo) injection, for intravenous use, for the treatment of patients with metastatic squamous non-small cell lung cancer (NSCLC) with progression on …

New Treatment Modality: Nivolumab (Opdivo) has been approved for the treatment of patients with previously treated metastatic squamous non-small cell lung cancer (NSCLC) Read more »

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