XOMA Royalty Corporation (XOMA)
(Delayed Data from NSDQ)
$30.97 USD
+0.77 (2.55%)
Updated Nov 8, 2024 04:00 PM ET
After-Market: $30.89 -0.08 (-0.26%) 7:58 PM ET
2-Buy of 5 2
F Value C Growth A Momentum D VGM
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$30.97 USD
+0.77 (2.55%)
Updated Nov 8, 2024 04:00 PM ET
After-Market: $30.89 -0.08 (-0.26%) 7:58 PM ET
2-Buy of 5 2
F Value C Growth A Momentum D VGM
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Alkermes (ALKS) Beats Q4 Earnings, Revenue Estimates
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Alkermes (ALKS) tops earnings and sales estimates in the fourth quarter of 2017 on the back of strong growth of Vivitrol and Aristada. The company provided a decent outlook for 2018.
Zoetis (ZTS) Beats on Q4 Earnings & Sales, Gives 2018 View
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Zoetis' (ZTS) results exceed both earnings and sales expectations in the fourth quarter of 2017, making it the first animal health company to deliver more than $5 billion in revenues.
Agios (AGIO) Q4 Loss Wider Than Expected, Revenues Slump Y/Y
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Agios (AGIO) reports wider-than-expected loss in the fourth quarter of 2017. Revenues fall short of expectations. The top line also declines year over year.
Prothena's (PRTA) Loss Narrows in Q4, Pipeline Progresses
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Prothena (PRTA) reported a narrower-than-expected loss in the fourth quarter as the company continued with its pipeline progress.
Shire (SHPG) Q4 Earnings Beat, Immunology Franchise Strong
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Shire (SHPG) reported better-than-expected fourth-quarter earnings and also registered strong growth in immunology franchise and newly launched products.
AVEO (AVEO) to Get $2 Million from EUSA Pharma for Fotivda
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AVEO Oncology (AVEO) is due to receive $2 million from its partner EUSA Pharma as the latter has been granted positive NICE recommendation for Fotivda (tivozanib).
Catalyst Gets Positive FDA Advise on Firdapse NDA Refiling
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Catalyst (CPRX) posts positive results from a recent Type C meeting with the FDA on resubmitting the new drug application for Firdapse in treating Lambert-Eaton myasthenic syndrome.
Vertex's Third Cystic Fibrosis Treatment Gets FDA Approval
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ImmunoGen (IMGN) Q4 Loss Wider Than Expected, Revenues Grow
by Zacks Equity Research
ImmunoGen (IMGN) reports wider-than-expected loss in Q4. However, higher license and milestone fees drive substantial revenue rise year over year.
FDA Okays J&J's Prostate Cancer Drug in First-Line Setting
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The FDA lends a nod to the label expansion of Johnson & Johnson's (JNJ) Zytiga in combination with prednisone for metastatic high-risk castration-sensitive prostate cancer.
Theravance, J&J Ink Deal for Inflammatory Intestinal Drug
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Theravance (TBPH) signs a global collaboration agreement with Johnson & Johnson to jointly develop and commercialize TD-1473 for inflammatory intestinal diseases.
Alexion's (ALXN) Earnings and Sales Beat Estimates in Q4
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Alexion (ALXN) surpass earnings and sales estimates in the fourth quarter of 2017. The company received FDA approval for label expansion of Soliris in the United States.
Keryx (KERX) Loss Wider Than Expected in Q4, Stock Down
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Keryx (KERX) reports wider-than-expected loss in Q4. However, sales surpassed estimates.
Pfizer Files for Xtandi in Early Stage Prostate Cancer
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Pfizer (PFE) announces detailed results from a late-stage study which can expand the label of Xtandi to include early-stage patients. It also files for approval in U.S. and EU.
Allergan's Anti-Infective Drug Avycaz Receives Third FDA Nod
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The FDA's label expansion approval for Allergan's (AGN) Avycaz marks its third therapeutic indication nod for the anti-infective drug in the United States.
Puma, CANbridge Team Up to Commercialize Nerlynx in China
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Puma (PBYI) enters an exclusive agreement with CANbridge under which the latter will seek regulatory approval for Nerlynx in China and develop and commercialize it in the region.
Alnylam's (ALNY) RNAi Candidate's NDA Gets Priority Review
by Zacks Equity Research
Alnylam's NDA for lead candidate patisiran is accepted by the FDA and granted priority review. The FDA also set an action date of Aug 11, 2018.
Novo Nordisk (NVO) Misses Q4 Earnings Estimates, Sales Beat
by Zacks Equity Research
Novo Nordisk's (NVO) top-line growth was backed by growth in new-generation insulin, Victoza, Saxenda, and haemophilia products.
Amgen Gets CHMP Nod to Add ENDEAVOR Data on Kyprolis Label
by Zacks Equity Research
Amgen (AMGN) gains consent from the Committee for Medicinal Products for Human Use to add overall survival data from a phase III study on the label of its cancer drug, Kyprolis.
Puma & Medison Team Up to Commercialize Nerlynx in Israel
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Puma (PBYI) and Medison enters into a licensing deal to commercialize Puma's breast cancer treatment drug Nerlynx in Israel.
Theravance's NDA for COPD Candidate Gets FDA Acceptance
by Debapriya Chakraborty
The FDA accepts the new drug application for Theravance (TBPH) and partner Mylan's COPD candidate, revefenacin. A response on the same is expected on Nov 13, 2018.
Glaxo's Shingles Vaccine Shingrix Gets Positive CHMP Opinion
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The Committee for Medicinal Products for Human Use passes a positive viewpoint on Glaxo's (GSK) shingles vaccine, Shingrix. A final decision from the EU is awaited in April 2018.
Dr. Reddy's (RDY) Q3 Earnings Fall, Revenues Improve Y/Y
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Dr. Reddy's (RDY) earnings per American Depositary Share were down 27.3% in third-quarter fiscal 2018 from the year-ago quarter while the top line beat the prior-year figure.