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BeiGene (BGNE) Gets FDA Nod for Brukinsa Label Expansion
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BeiGene, Ltd. (BGNE - Free Report) announced that the FDA has approved its marketed drug Brukinsa (zanubrutinib) for an additional indication. The drug has been approved for the treatment of adult patients with Waldenström’s macroglobulinemia (“WM”), a rare type of lymphoma. This marks the second FDA approval for Brukinsa in the United States.
The latest FDA nod was based on data from the phase III ASPEN study which compared Brukinsa to Imbruvica (ibrutinib) in adult patients with WM. Data from the same showed that treatment with Brukinsa improved tolerability across a number of clinically important side effects.
Imbruvica, which is an approved medicine for treating cancer, is jointly marketed by AbbVie (ABBV - Free Report) and J&J (JNJ - Free Report) across the world.
Per the company, the new indication for Brukinsa is likely to provide a new treatment option with demonstrated efficacy and safety benefits for patients with WM.
We remind investors that in February 2021, the FDA accepted BeiGene’s supplemental new drug application for Brukinsa for the treatment of adult patients with WM. A decision from the regulatory body was expected on Oct 18, 2021. Hence the above approval came before the scheduled period of time.
Shares of BeiGene have rallied 26.7% so far this year compared with the industry’s rise of 1.2%.
Image Source: Zacks Investment Research
Brukinsa is currently approved in the United States for the treatment of mantle cell lymphoma in adult patients who have received at least one prior therapy. The drug is also approved for other types of lymphoma indications in several other countries across the globe.
In the first six months of 2021, Brukinsa generated worldwide sales worth $64.5 million, reflecting a significant year-over-year increase.
BeiGene is currently evaluating Brukinsa as a monotherapy and in combination with other therapies to treat various B-cell malignancies in a broad clinical program. If successfully developed and upon potential approval in new indications, Brukinsa should boost sales for the company.
Image: Bigstock
BeiGene (BGNE) Gets FDA Nod for Brukinsa Label Expansion
BeiGene, Ltd. (BGNE - Free Report) announced that the FDA has approved its marketed drug Brukinsa (zanubrutinib) for an additional indication. The drug has been approved for the treatment of adult patients with Waldenström’s macroglobulinemia (“WM”), a rare type of lymphoma. This marks the second FDA approval for Brukinsa in the United States.
The latest FDA nod was based on data from the phase III ASPEN study which compared Brukinsa to Imbruvica (ibrutinib) in adult patients with WM. Data from the same showed that treatment with Brukinsa improved tolerability across a number of clinically important side effects.
Imbruvica, which is an approved medicine for treating cancer, is jointly marketed by AbbVie (ABBV - Free Report) and J&J (JNJ - Free Report) across the world.
Per the company, the new indication for Brukinsa is likely to provide a new treatment option with demonstrated efficacy and safety benefits for patients with WM.
We remind investors that in February 2021, the FDA accepted BeiGene’s supplemental new drug application for Brukinsa for the treatment of adult patients with WM. A decision from the regulatory body was expected on Oct 18, 2021. Hence the above approval came before the scheduled period of time.
Shares of BeiGene have rallied 26.7% so far this year compared with the industry’s rise of 1.2%.
Image Source: Zacks Investment Research
Brukinsa is currently approved in the United States for the treatment of mantle cell lymphoma in adult patients who have received at least one prior therapy. The drug is also approved for other types of lymphoma indications in several other countries across the globe.
In the first six months of 2021, Brukinsa generated worldwide sales worth $64.5 million, reflecting a significant year-over-year increase.
BeiGene is currently evaluating Brukinsa as a monotherapy and in combination with other therapies to treat various B-cell malignancies in a broad clinical program. If successfully developed and upon potential approval in new indications, Brukinsa should boost sales for the company.
Zacks Rank & Stock to Consider
BeiGene currently carries a Zacks Rank #4 (Sell).
A better-ranked stock in the biotech sector is Corvus Pharmaceuticals, Inc. (CRVS - Free Report) , which has a Zacks Rank #2 (Buy) at present. You can see the complete list of today’s Zacks #1 Rank (Strong Buy) stocks here.
Corvus Pharmaceuticals’ loss per share estimates have narrowed 24.4% for 2021 and 21.4% for 2022, over the past 60 days.