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The Kevzara Resubmission Journey: From FDA CRL to Approval 

By learning from the Vyleesi resubmission experience, current drug developers can better navigate the regulatory landscape, avoid common pitfalls, and increase the likelihood of a successful first review cycle approval. Stay diligent and strategic, CERES Regulatory Services

Hello Regulatory Scientists,  Today, let’s dive into the journey of Kevzara (sarilumab) from receiving an FDA Complete Response Letter (CRL) to achieving approval. This case study provides valuable insights and lessons that can guide companies developing new drugs today.  Regulatory History and Initial Submission  Drug: Kevzara (sarilumab) Mechanism of Action: IL-6 receptor antagonist, which helps reduce […]

The Addyi Resubmission Journey: From FDA CRL to Approval

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Hello Regulatory Scientists, Today, let’s delve into the journey of Addyi (flibanserin) from receiving an FDA Complete Response Letter (CRL) to achieving approval. This case study provides valuable insights and lessons that can guide companies developing new drugs today. Regulatory History and Initial Submission Drug: Addyi (flibanserin) Mechanism of Action: Serotonin 1A receptor agonist and […]