We use cookies to understand how you use our site and to improve your experience. This includes personalizing content and advertising. To learn more, click here. By continuing to use our site, you accept our use of cookies, revised Privacy Policy and Terms of Service.
You are being directed to ZacksTrade, a division of LBMZ Securities and licensed broker-dealer. ZacksTrade and Zacks.com are separate companies. The web link between the two companies is not a solicitation or offer to invest in a particular security or type of security. ZacksTrade does not endorse or adopt any particular investment strategy, any analyst opinion/rating/report or any approach to evaluating individual securities.
If you wish to go to ZacksTrade, click OK. If you do not, click Cancel.
AstraZeneca's Farxiga Gets Fast Track Tag for New Indication
Read MoreHide Full Article
AstraZeneca PLC (AZN - Free Report) announced that the FDA has granted a Fast Track designation to its SGLT2 inhibitor Farxiga (dapagliflozin) for reducing the risk of hospitalization for heart failure (hHF) or cardiovascular (“CV”) death in adult patients, following an acute myocardial infarction (“MI”) or heart attack.
The blockbuster drug, approved to treat type II diabetes (T2D), will be evaluated in a phase III study, namely DAPA-MI to see its effect in adults who have suffered an acute MI. The designation is granted by the FDA based on the study’s design.
The FDA provides a Fast Track designation to help development and faster review of drugs, which treat serious and unmet medical conditions.
The drug also enjoys Fast Track designation for chronic kidney disease (“CKD”). In March, AstraZeneca stopped a phase III DAPA-CKD study evaluating Farxiga for effect on renal outcomes and CV mortality in patients suffering CKD with or without T2D earlier than expected. The decision was taken following a recommendation from an independent Data Monitoring Committee based on overwhelming efficacy. The company expects to file a regulatory application seeking a label expansion for Farxiga to include CKD patients in the second half of 2020.
Meanwhile, several label expansion studies are also ongoing on Farxiga for heart failure indications. In May, the FDA approved the label expansion of the drug as a treatment to reduce the risk of CV death and hHF in adults with HF with reduced ejection fraction (HFrEF) with and without T2D.
Shares of AstraZeneca have rallied 17.1% so far this year compared with the industry’s increase of 1.3%.
Farxiga/Forxiga, a key top-line driver of AstraZeneca, generated sales of $407 million in the first quarter of 2020, representing 19% growth at constant exchange rates. Farxiga enjoys global leadership with significant market share.
Other SGLT2 inhibitors available in the market are Johnson & Johnson’s (JNJ - Free Report) Invokana and Lilly’s (LLY - Free Report) Jardiance, Synjardy (a) and Glyxambi). Apart from SGLT2 inhibitors, there are several other drugs being developed for similar indications which use different mechanisms. We note that a label expansion application seeking approval for Merck’s (MRK - Free Report) vericiguat to reduce the risk of CV death in adults with HFrEF was granted priority review by the FDA earlier this week.
Be among the early investors in the new type of device that experts say could impact society as much as the discovery of electricity. Current technology will soon be outdated and replaced by these new devices. In the process, it’s expected to create 22 million jobs and generate $12.3 trillion in activity.
A select few stocks could skyrocket the most as rollout accelerates for this new tech. Early investors could see gains similar to buying Microsoft in the 1990s. Zacks’ just-released special report reveals 8 stocks to watch. The report is only available for a limited time.
Image: Bigstock
AstraZeneca's Farxiga Gets Fast Track Tag for New Indication
AstraZeneca PLC (AZN - Free Report) announced that the FDA has granted a Fast Track designation to its SGLT2 inhibitor Farxiga (dapagliflozin) for reducing the risk of hospitalization for heart failure (hHF) or cardiovascular (“CV”) death in adult patients, following an acute myocardial infarction (“MI”) or heart attack.
The blockbuster drug, approved to treat type II diabetes (T2D), will be evaluated in a phase III study, namely DAPA-MI to see its effect in adults who have suffered an acute MI. The designation is granted by the FDA based on the study’s design.
The FDA provides a Fast Track designation to help development and faster review of drugs, which treat serious and unmet medical conditions.
The drug also enjoys Fast Track designation for chronic kidney disease (“CKD”). In March, AstraZeneca stopped a phase III DAPA-CKD study evaluating Farxiga for effect on renal outcomes and CV mortality in patients suffering CKD with or without T2D earlier than expected. The decision was taken following a recommendation from an independent Data Monitoring Committee based on overwhelming efficacy. The company expects to file a regulatory application seeking a label expansion for Farxiga to include CKD patients in the second half of 2020.
Meanwhile, several label expansion studies are also ongoing on Farxiga for heart failure indications. In May, the FDA approved the label expansion of the drug as a treatment to reduce the risk of CV death and hHF in adults with HF with reduced ejection fraction (HFrEF) with and without T2D.
Shares of AstraZeneca have rallied 17.1% so far this year compared with the industry’s increase of 1.3%.
Farxiga/Forxiga, a key top-line driver of AstraZeneca, generated sales of $407 million in the first quarter of 2020, representing 19% growth at constant exchange rates. Farxiga enjoys global leadership with significant market share.
Other SGLT2 inhibitors available in the market are Johnson & Johnson’s (JNJ - Free Report) Invokana and Lilly’s (LLY - Free Report) Jardiance, Synjardy (a) and Glyxambi). Apart from SGLT2 inhibitors, there are several other drugs being developed for similar indications which use different mechanisms. We note that a label expansion application seeking approval for Merck’s (MRK - Free Report) vericiguat to reduce the risk of CV death in adults with HFrEF was granted priority review by the FDA earlier this week.
Zacks Rank
AstraZeneca currently carries a Zacks Rank #2 (Buy). You can see the complete list of today’s Zacks #1 Rank (Strong Buy) stocks here.
Biggest Tech Breakthrough in a Generation
Be among the early investors in the new type of device that experts say could impact society as much as the discovery of electricity. Current technology will soon be outdated and replaced by these new devices. In the process, it’s expected to create 22 million jobs and generate $12.3 trillion in activity.
A select few stocks could skyrocket the most as rollout accelerates for this new tech. Early investors could see gains similar to buying Microsoft in the 1990s. Zacks’ just-released special report reveals 8 stocks to watch. The report is only available for a limited time.
See 8 breakthrough stocks now>>