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AstraZeneca's Selumetinib Gets Breakthrough Therapy Status

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AstraZeneca Inc. (AZN - Free Report)  announced that the FDA has granted Breakthrough Therapy designation (BTD) to its investigational MEK 1/2 inhibitor, selumetinib for the treatment of neurofibromatosis type 1 (NF1) related plexiform neurofibromas (PN), an incurable genetic condition that affects newborns.

The Breakthrough Therapy designation is granted to speed up the development and review of drugs that target serious or life-threatening conditions. AstraZeneca is developing selumetinib in partnership with Merck & Co. Inc. (MRK - Free Report) . AstraZeneca and Merck entered into a co-development and co-commercialization agreement for selumetinib in 2017.

Shares of AstraZeneca have increased 20.5% year to date compared with the industry’s growth of 20%.

 

The BTD was supported by phase II results from the SPRINT study, testing selumetinib as an oral monotherapy in pediatric patients aged three years or older with inoperable NF1-related PN. Results from the study have shown that selumetinib shrank tumors in children and young adults with NF1 and may improve symptoms such as pain and reduced mobility that result from tumors called, which develop in many people with NF1.

In the study, 36 of the 50 patients (72%) had a partial response to selumetinib, which means the tumor volume shrank at least 20%. Selumetinib was granted Orphan Drug designation for the treatment of NF1 by the FDA in February 2018 and the European Medicines Agency in August 2018. It is being developed as a monotherapy and in combination with other treatments in ongoing studies.

AstraZeneca boasts a strong late-stage oncology pipeline. Other than Selumetinib, the company’s oncology portfolio includes savolitinib (kidney cancer), which is also in late-stage development. An interesting candidate in the company’s immuno-oncology pipeline is Imfinzi (durvalumab), which is being evaluated for multiple cancers, either alone or in combination with other regimens. Imfinzi is presently marketed in the United States for second-line advanced bladder and early-stage lung cancer (NSCLC).

Lynparza, also marketed in partnership with Merck for advanced ovarian and breast cancers, is being evaluated in different studies for a range of tumor types, including prostate and pancreatic cancers, and earlier-line settings for ovarian cancer. Tagrisso is also being evaluated in earlier-line settings for lung cancer.

 

Zacks Rank & Stocks to Consider

AstraZeneca is currently a Zacks Rank #3 (Hold) stock.

Some better-ranked stocks from the same space are Johnson & Johnson (JNJ - Free Report) and Roche Holding AG (RHHBY - Free Report) , each carrying a Zacks Rank #2 (Buy). You can see the complete list of today’s Zacks #1 Rank (Strong Buy) stocks here.

Johnson & Johnson’s earnings per share estimates have increased from $9.20 to $9.21 for 2020 in the past 60 days. The company delivered a positive earnings surprise in all the trailing four quarters, with average of 1.61%.

Roche’s earnings per share estimates have increased from $2.30 to $2.35 for 2019 and from $2.34 to $2.37 for 2020 over the past 90 days.

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