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Patients Now Have the Option to Undergo Immunotherapy Less Frequently – Curetoday.com

Patients Now Have the Option to Undergo Immunotherapy Less Frequently
Curetoday.com
The Food and Drug Administration (FDA) has approved a supplemental biologics license application adding a four-week dosing schedule for Opdivo (nivolumab) across several of the PD-1 inhibitor's indications. PUBLISHED March 06, 2018. The Food and Drug

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2018-03-06 NEWS
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