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Gilead gets US FDA approval for inflammatory liver disease drug

UPDATE 3-Gilead gets US FDA approval for inflammatory liver disease drug Adds pricing in paragraph 4, company comments in paragraphs 6-7, details on common symptom in paragraphs 10-12 By Puyaan Singh and Leroy Leo Aug 14 (Reuters) - The U.S. Food and Drug Administration on Wednesday approved Gilead Sciences' GILD.O liver disease treatment, Livdelzi, which it gained through a $4.3 billion buyout of CymaBay Therapeutics earlier this year.
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EMA Says CHMP Recommended Not Granting Marketing Authorisation For Leqembi (Lecanemab)

BRIEF-EMA Says CHMP Recommended Not Granting Marketing Authorisation For Leqembi (Lecanemab) July 26 (Reuters) - Biogen Inc BIIB.O EMA SAYS CHMP EXTENSIONS OF INDICATION FOR 11 MEDICINES THAT ARE ALREADY AUTHORISED IN THE EU INCLUDING AREXVY EMA SAYS CHMP RECOMMENDED NOT GRANTING MARKETING AUTHORISATION FOR LEQEMBI (LECANEMAB) EMA SAYS CHMP RECOMME
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Ipsen drops on H1 results, as guidance hike already anticipated

BUZZ-Ipsen drops on H1 results, as guidance hike already anticipated ** Shares in Ipsen drop 6.8% after the French biopharma company announced H1 results ** "We expect shares to underperform," says Barclays, adding investors will focus on Sonatuline erosion risk and M&A. ** Broker notes disappointing miss from key growth driver Dysport ** Company also raised guidance to >7% CER growth, but this had already been anticipated by consensus, adds analyst ** Ipsen additionally announced exclusive ex-U
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Ipsen And Day One Enter Into Exclusive Ex-U.S. Licensing Agreement To Commercialize Tovorafenib For The Most Common Childhood Brain Tumor

BRIEF-Ipsen And Day One Enter Into Exclusive Ex-U.S. Licensing Agreement To Commercialize Tovorafenib For The Most Common Childhood Brain Tumor July 25 (Reuters) - Ipsen SA IPN.PA : IPSEN AND DAY ONE ENTER INTO EXCLUSIVE EX-U.S. LICENSING AGREEMENT TO COMMERCIALIZE TOVORAFENIB FOR THE MOST COMMON CHILDHOOD BRAIN TUMOR IPSEN SA - DAY ONE RECEIVES AP
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Ipsen And Day One Enter Into Exclusive Ex-U.S. Licensing Agreement To Commercialize Tovorafenib For The Most Common Childhood Brain Tumor

BRIEF-Ipsen And Day One Enter Into Exclusive Ex-U.S. Licensing Agreement To Commercialize Tovorafenib For The Most Common Childhood Brain Tumor July 25 (Reuters) - Ipsen SA IPN.PA : IPSEN AND DAY ONE ENTER INTO EXCLUSIVE EX-U.S. LICENSING AGREEMENT TO COMMERCIALIZE TOVORAFENIB FOR THE MOST COMMON CHILDHOOD BRAIN TUMOR IPSEN SA - DAY ONE RECEIVES AP
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Ipsen Raises FY 2024 Guidance

BRIEF-Ipsen Raises FY 2024 Guidance July 25 (Reuters) - Ipsen SA IPN.PA : IPSEN DELIVERS STRONG RESULTS IN THE FIRST HALF OF 2024, PROGRESSES ON LAUNCHES AND UPGRADES ITS FULL-YEAR GUIDANCE H1 FREE CASH FLOW EUR 393.5 MILLION OUTLOOK 2024 UPGRADED: TOTAL-SALES GROWTH GREATER THAN 7.0%, AT CONSTANT CURRENCY OUTLOOK 2024 UPGRADED: CORE OPERATING MARG
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Ipsen, Foreseen Biotechnology Enter Licensing Agreement For Antibody-Drug Conjugate

BRIEF-Ipsen, Foreseen Biotechnology Enter Licensing Agreement For Antibody-Drug Conjugate July 11 (Reuters) - Ipsen SA IPN.PA : IPSEN AND FORESEEN BIOTECHNOLOGY ANNOUNCE EXCLUSIVE GLOBAL LICENSING AGREEMENT FOR ANTIBODY-DRUG CONJUGATE WITH FIRST-IN-CLASS POTENTIAL EXCLUSIVE GLOBAL RIGHTS SECURED FOR DEVELOPMENT, MANUFACTURE AND COMMERCIALIZATION OF
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Pearson, Softcat, Trelleborg

EUROPE RESEARCH ROUNDUP- Pearson, Softcat, Trelleborg July 5 (Reuters) - Securities analysts revised their ratings and price targets on several European companies including Pearson, Softcat and Trelleborg, on Friday. HIGHLIGHTS * Aker BP ASA AKRBP.OL : Jefferies cuts target price to NOK 340 from NOK 345 * GSK GSK.L : Citigroup cuts target price to 1900p from 2120p * Pearson PSON.L : Deutsche Bank raises target price to 1052p from 1050p * Softcat Plc SCTS.L : Jefferies cuts target price to 1,490p
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Ipsen To Seek Marketing Authorizations For Cabometyx Outside Of U.S., Japan

BRIEF-Ipsen To Seek Marketing Authorizations For Cabometyx Outside Of U.S., Japan July 2 (Reuters) - Ipsen SA IPN.PA : IPSEN EXPANDS COLLABORATION AND LICENSE AGREEMENT FOR DEVELOPMENT OF CABOMETYX IN ADVANCED NEUROENDOCRINE TUMORS BASED ON POSITIVE CABINET PHASE III TRIAL DECISION ADDS TO EXISTING COLLABORATION AGREEMENT WITH EXELIXIS, PERMITTING IPSEN TO SEEK POTENTIAL MARKETING AUTHORIZATIONS FOR CABOMETYX OUTSIDE OF U.S.
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Ipsen’S Iqirvo® Receives U.S. FDA Accelerated Approval As A First-In-Class Ppar Treatment For Primary Biliary Cholangitis

BRIEF-Ipsen’S Iqirvo® Receives U.S. FDA Accelerated Approval As A First-In-Class Ppar Treatment For Primary Biliary Cholangitis Ipsen SA IPN.PA : IPSEN’S IQIRVO® RECEIVES U.S. FDA ACCELERATED APPROVAL AS A FIRST-IN-CLASS PPAR TREATMENT FOR PRIMARY BILIARY CHOLANGITIS IPSEN SA - IQIRVO MAY BE PRESCRIBED IMMEDIATELY IN U.S. FOR ELIGIBLE PATIENTS.
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US FDA grants accelerated approval to Genfit and Ipsen's liver disease drug

UPDATE 3-US FDA grants accelerated approval to Genfit and Ipsen's liver disease drug Adds details on pricing in paragraph 3, background throughout By Puyaan Singh and Mariam Sunny June 10 (Reuters) - The U.S. Food and Drug Administration granted accelerated approval to French drugmakers Ipsen IPN.PA and Genfit's GNFT.PA drug for a chronic inflammatory liver disease, Iqirvo, the companies said on Monday.
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US FDA approves Genfit and Ipsen's liver disease drug

US FDA approves Genfit and Ipsen's liver disease drug June 10 (Reuters) - The U.S. Food and Drug Administration has approved French drugmakers Ipsen IPN.PA and Genfit's GNFT.PA drug to treat a chronic inflammatory liver disease, Ipsen said on Monday. Reporting by Puyaan Singh in Bengaluru; Editing by Alan Barona
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Ipsen Initiates Share Buy-Back Program

BRIEF-Ipsen Initiates Share Buy-Back Program June 3 (Reuters) - Ipsen SA IPN.PA : IPSEN INITIATES A SHARE BUY-BACK PROGRAM TO COVER ITS FREE EMPLOYEE SHARE-ALLOCATION PLAN IPSEN APPOINTED AN INVESTMENT-SERVICES PROVIDER TO PURCHASE AN AGGREGATE NUMBER OF IPSEN S.A. SHARES UP TO 400,000, OR ABOUT 0.47% OF SHARE CAPITAL HAS APPOINTED AN INVESTMENT-SERVICES PROVIDER TO PURCHASE AN AGGREGATE NUMBER OF IPSEN S.A.
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