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The Zacks Analyst Blog AbbVie's, Rinvoq and AstraZeneca's and Novartis

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For Immediate Releases

Chicago, IL – April 14, 2025 – Zacks.com announces the list of stocks featured in the Analyst Blog. Every day the Zacks Equity Research analysts discuss the latest news and events impacting stocks and the financial markets. Stocks recently featured in the blog include AbbVie’s ABBV, Rinvoq and AstraZeneca’s AZN and Novartis NVS.

Here are highlights from Monday’s Analyst Blog:

Pharma Stock Roundup: EU Gives Nod to Expanded Use for ABBV, AZN Drugs & More

This week, the European Commission granted marketing authorization to the expanded use of AbbVie’s  Rinvoq and AstraZeneca’s blockbuster cancer drugs, Imfinzi and Daiichi-Sankyo partnered, Enhertu. Novartis announced plans to invest $23 billion over the next five years to boost manufacturing, R&D and technology in the United States amid the tariff threats.

Here's a recap of the week’s most important stories.

European Commission Approves AbbVie’s Rinvoq for 8th Indication

The European Commission (“EC”) granted marketing approval to AbbVie’s Rinvoq for treating giant cell arteritis (“GCA”), an autoimmune disease that causes inflammation of the large arteries. Rinvoq is the first JAK inhibitor approved in the European Union (“EU”) for this indication, based on data from the phase III SELECT-GCA study. An application seeking approval of Rinvoq for GCA is also under review in the United States.

GCA marks the eighth approved indication for Rinvoq, which is already approved for seven immune-mediated inflammatory diseases in several countries, including the United States and the EU. It is being studied in late-stage studies for some others like systemic lupus erythematosus, hidradenitis suppurativa vitiligo and Takayasu arteritis.

EU Approval for the Expanded Use of AZN’s Key Cancer Drugs

AstraZeneca announced that the EC has approved the expanded use of Imfinzi in combination with chemotherapy for treating adults with resectable non-small cell lung cancer (NSCLC) with no known EGFR mutations or ALK rearrangements. In this regimen, Imfinzi, in combination with neoadjuvant chemotherapy, is administered before surgery and as adjuvant monotherapy after surgery.

The approval in the EU was expected as the Committee for Medicinal Products for Human Use had recommended the approval of Imfinzi for the given indication last month. This approval was based on data from the phase III AEGEAN study. Imfinzi was approved for a similar indication in the United States in August last year.