Regeneron, a big biotech company, has made a medicine called Ordspono. This medicine helps people with certain types of cancer (lymphoma). The big people who make rules for medicines in Europe said it's okay to use this medicine, so now it's available there for patients who need it. This is good news for the company and people who are sick with lymphoma. Read from source...
"The article “Regeneron Pharmaceuticals Receives EU Approval for Odronextamab for Lymphomas” by John F. Kennedy on October 24, 2024 on Benzinga.com is an example of how critics can use storytelling to spread their ideas and influence the public.
Firstly, the article starts off by stating that Regeneron Pharmaceuticals has received EU approval for Odronextamab for treating adult patients with relapsed or refractory follicular lymphoma or relapsed or refractory diffuse large B-cell lymphoma after two or more lines of systemic therapy. The article then goes on to discuss the positive results from the phase I ELM-1 and pivotal phase II ELM-2 trials, and how these results have led to the approval in the EU.
However, the article then discusses how the company's efforts to get odronextamab approved in the United States suffered a setback when the regulatory body issued complete response letters (CRLs) for its BLA for odronextamab in March 2024. The article states that the CRLs (one for R/R FL and one for R/R DLBCL) did not identify any issue with the clinical efficacy or safety, trial design, labeling or manufacturing. The CRLs only identified an issue related to the enrollment status of the confirmatory trials.
The article then discusses how the successful development of these oncology drugs should be a great boost for REGN and how the firm is looking to strengthen its oncology franchise. The article also discusses the regulatory setbacks that REGN has experienced with odronextamab and other pipeline candidates.
In terms of inconsistencies, the article discusses the positive results from the phase I ELM-1 and pivotal phase II ELM-2 trials, but then highlights the setback that REGN experienced with the regulatory body issuing CRLs for its BLA for odronextamab. This creates confusion and inconsistency in the story.
In terms of biases, the article seems to be biased towards Regeneron Pharmaceuticals, as it highlights the positive results from the clinical trials and the potential benefits of odronextamab. The article also seems to downplay the regulatory setbacks that REGN has experienced, by only discussing the issue related to the enrollment status of the confirmatory trials.
In terms of emotional behavior, the article seems to be written in a way that is designed to evoke emotions from the reader. For example, the article uses words like "setback" and "suffered" to describe REGN's regulatory set
Neutral
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