Incyte Announces European Commission Approval of Jakavi® (ruxolitinib) as the First Post-Steroid Treatment for Acute and Chronic Graft-Versus-Host Disease
Incyte Corporation (INCY)
Last incyte corporation earnings: 2/13 07:00 am
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Source: Business Wire
Jakavi® (ruxolitinib) is the first JAK1/2 inhibitor available for patients in Europe who previously had no approved therapies for the treatment of steroid-refractory graft-versus-host disease (GVHD)1,2In clinical trials, Jakavi demonstrated superiority versus best available therapy in patients with steroid-refractory/dependent acute and chronic GVHD, with overall response rates of 62% vs. 39%, and 50% vs. 26% respectively2,3GVHD is a common and potentially life-threatening complication that arises in approximately half of patients following allogeneic stem cell transplants4 WILMINGTON, Del.--(BUSINESS WIRE)--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.“With the approval
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News
- 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
- Incyte Co. (NASDAQ: INCY) is now covered by analysts at Cantor Fitzgerald. They set a "neutral" rating on the stock.MarketBeat
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