Incyte Announces European Commission Approval Of Jakavi® (ruxolitinib) As The First Post-Steroid Treatment For Acute And Chronic Graft-Versus-Host Disease [TheStreet.com]
Incyte Corporation (INCY)
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Source: TheStreet.com
Incyte (Nasdaq:INCY) today announced the European Commission (EC) has approved Jakavi ® (ruxolitinib) for the treatment of patients aged 12 years and older with acute or chronic GVHD who have inadequate response to corticosteroids or other systemic therapies. Ruxolitinib is marketed as Jakavi by Novartis in Europe and as Jakafi ® by Incyte in the United States. div widget "With the approval of this new indication for Jakavi, patients in Europe with acute or chronic GVHD who do respond to first-line steroid therapies have a new option that could redefine treatment for their condition," said Peter Langmuir, M.D., Group Vice President, Oncology Targeted Therapies, Incyte. "Unfortunately, many people who receive allogenic stem cell transplants experience GVHD, and it is our hope that this Incyte-discovered medicine will make a significant impact for this patient population." The approval of Jakavi follows the positive opinion granted in March 2022 by the Committee for Medicinal Product
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News
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- Incyte Co. (NASDAQ: INCY) had its price target lowered by analysts at Oppenheimer Holdings Inc. from $92.00 to $84.00. They now have an "outperform" rating on the stock.MarketBeat
- Incyte (INCY) to Report Q1 Earnings: What's in the Cards? [Yahoo! Finance]Yahoo! Finance
- Incyte to acquire immune-focused drug developer Escient [Seeking Alpha]Seeking Alpha
- Incyte Announces Acquisition of Escient Pharmaceuticals and its Pipeline of First-in-Class Oral MRGPR Antagonists [Yahoo! Finance]Yahoo! Finance
INCY
Earnings
- 2/13/24 - Beat
INCY
Sec Filings
- 4/2/24 - Form 4
- 4/2/24 - Form 4
- 4/1/24 - Form 4
- INCY's page on the SEC website