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argenx SE (ARGX.OQ)

ARGX.OQ on NASDAQ Stock Exchange Global Select Market

100.04USD
10 Dec 2018
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Latest Key Developments (Source: Significant Developments)

Argenx 9-Mth IAS 18 Operating Loss Widens To EUR ‍​49.1 Million
Thursday, 25 Oct 2018 01:00am EDT 

Oct 25 (Reuters) - ARGENX SE ::9-MONTH IAS 18 OPERATING LOSS EUR ‍​49.1 MILLION VERSUS LOSS OF EUR 13.5 MILLION YEAR AGO.CASH AND CASH EQUIVALENTS AT END PERIOD EUR 582.3‍​ MILLION VERSUS EUR 161.7 MILLION YEAR AGO.9-MONTH TOTAL COMPREHENSIVE LOSS IAS 18 EUR 38.3 MILLION VERSUS LOSS OF EUR 16.5 MILLION YEAR AGO.9-MONTH IAS 18 REVENUE EUR ‍​17.9 MILLION VERSUS EUR 28.4 MILLION YEAR AGO.  Full Article

Argenx Raises About $300.6 Millionin U.S. Public Offering
Friday, 21 Sep 2018 04:00pm EDT 

Sept 21 (Reuters) - ARGENX SE ::REG-ARGENX ANNOUNCES CLOSING OF U.S. PUBLIC OFFERING FOR GROSS PROCEEDS OF APPROXIMATELY $300.6 MILLION.REG-ARGENX ANNOUNCES CLOSING OF U.S. PUBLIC OFFERING FOR GROSS PROCEEDS OF APPROXIMATELY $300.6 MILLION.PRICE TO PUBLIC OF $86.50 PER ADS.GRANTED UNDERWRITERS AN OPTION TO PURCHASE UP TO AN ADDITIONAL 521,250 ADSS, REPRESENTING 15% OF ADSS SOLD.OPTION CAN BE EXERCISED DURING 30-DAY PERIOD COMMENCING SEPTEMBER 18, 2018..  Full Article

ArgenX Reports Positive Topline Results From Phase 2 Proof-Of-Concept Trial Of Efgartigimod In Primary Immune Thrombocytopenia
Monday, 17 Sep 2018 01:00am EDT 

Sept 17 (Reuters) - ARGENX SE ::REG-ARGENX REPORTS POSITIVE TOPLINE RESULTS FROM PHASE 2 PROOF-OF-CONCEPT TRIAL OF EFGARTIGIMOD IN PRIMARY IMMUNE THROMBOCYTOPENIA.FAVORABLE SAFETY AND TOLERABILITY CONSISTENT WITH EFGARTIGIMOD CLINICAL TRIALS TO DATE.CLINICALLY MEANINGFUL PLATELET COUNT IMPROVEMENTS SHOWED CLEAR SEPARATION FROM PLACEBO AT INCREASING RESPONSE THRESHOLDS.PLAN TO ADVANCE ITP PROGRAM INTO PHASE 3 DEVELOPMENT.CIDP ANNOUNCED AS FOURTH INDICATION FOR EFGARTIGIMOD.ALSO EXPECTS TO INITIATE A PHASE 2 TRIAL IN ITP USING A SUBCUTANEOUS FORMULATION OF EFGARTIGIMOD.ANNOUNCED PLANS TO INITIATE A PHASE 2 PROOF-OF-CONCEPT TRIAL OF EFGARTIGIMOD (IV) IN CHRONIC INFLAMMATORY DEMYELINATING POLYNEUROPATHY (CIDP) H1 2019.  Full Article

Argenx Receives Feedback From Japan's PMDA On Phase 3 Clinical Trial
Wednesday, 29 Aug 2018 01:00am EDT 

Aug 29 (Reuters) - ARGENX SE ::REG-ARGENX RECEIVES FEEDBACK FROM JAPAN'S PMDA ON PHASE 3 CLINICAL TRIAL AND REGULATORY PATHWAY FOR EFGARTIGIMOD IN GENERALIZED MYASTHENIA GRAVIS.DATA FROM PLANNED GLOBAL PHASE 3 REGISTRATION TRIAL, IF POSITIVE, TO SERVE AS BASIS TO SUBMIT FOR MARKETING AUTHORIZATION IN JAPAN.PLANS TO INITIATE GLOBAL PHASE 3 REGISTRATION TRIAL OF EFGARTIGIMOD IN GMG BEFORE END OF 2018.EXPECTS DATA FROM PLANNED GLOBAL PHASE 3 REGISTRATION TRIAL, IF POSITIVE, WILL SERVE AS BASIS TO SUBMIT FOR MARKETING AUTHORIZATION IN JAPAN..GLOBAL PHASE 3 TRIAL EXPECTS TO ENROLL APPROXIMATELY 150 PATIENTS WITH GMG, INCLUDING PATIENTS FROM JAPAN AS WELL AS NORTH AMERICA AND EUROPE.DATA, IF POSITIVE, MAY SERVE AS BASIS FOR BIOLOGICS LICENSE APPLICATION IN U.S. BASED ON FEEDBACK FROM FDA.PATIENTS CAN ROLL OVER INTO AN OPEN-LABEL EXTENSION STUDY FOR A PERIOD OF ONE YEAR.  Full Article

Argenx Receives Milestone Payment From Strategic Collaboration With Shire
Tuesday, 17 Jul 2018 01:00am EDT 

July 17 (Reuters) - ARGENX SE ::REG-ARGENX RECEIVES MILESTONE PAYMENT FROM STRATEGIC COLLABORATION WITH SHIRE.HAS REACHED A PRECLINICAL MILESTONE IN ITS STRATEGIC COLLABORATION WITH SHIRE PLC.MILESTONE TRIGGERED BY SHIRE EXERCISING OPTION TO IN-LICENSE AN ANTIBODY DISCOVERED AND DEVELOPED USING CO'S SIMPLE ANTIBODY PLATFORM AND FC ENGINEERING TECHNOLOGIES.  Full Article

Argenx SE Says Euronext Has Selected Argenx SE For Inclusion In BEL 20 Index On Euronext Brussels
Tuesday, 5 Jun 2018 04:00pm EDT 

June 5 (Reuters) - argenx SE ::ARGENX SE SAYS EURONEXT HAS SELECTED ARGENX SE FOR INCLUSION IN BEL 20 INDEX ON EURONEXT BRUSSELS, EFFECTIVE JUNE 18, 2018.  Full Article

Argenx SE Files For Potential Mixed Shelf Offering
Friday, 1 Jun 2018 05:43pm EDT 

June 1 (Reuters) - argenx SE ::ARGENX SE FILES FOR POTENTIAL MIXED SHELF OFFERING; SIZE NOT DISCLOSED - SEC FILING.  Full Article

Argenx Q1 Operating Income Down At 6.9 Million Euros
Wednesday, 9 May 2018 01:01am EDT 

May 9 (Reuters) - ARGENX NV ::ARGENX REPORTS FIRST QUARTER 2018 FINANCIAL RESULTS AND PROVIDES BUSINESS UPDATE.Q1 OPERATING INCOME OF EUR 6.9 MILLION (MARCH 31, 2017: EUR 7.2 MILLION)..Q1 TOTAL COMPREHENSIVE LOSS OF EUR 17.7 MILLION (MARCH 31, 2017: EUR 8.4 MILLION).CASH POSITION OF EUR 346.6 MILLION (MARCH 31, 2017: EUR 85.0 MILLION).EXPECTED MILESTONE: PROGRESS ARGX-113 INTO PHASE 3 CLINICAL DEVELOPMENT IN GENERALIZED MG BEFORE END OF YEAR.  Full Article

Argenx To Present Complete Data From Phase 2 Proof-Of-Concept Trial Of Efgartigimod (Argx-113)
Tuesday, 24 Apr 2018 01:00am EDT 

April 24 (Reuters) - ARGENX NV ::REG-ARGENX TO PRESENT COMPLETE DATA FROM PHASE 2 PROOF-OF-CONCEPT TRIAL OF EFGARTIGIMOD (ARGX-113) IN GENERALIZED MYASTHENIA GRAVIS AT AMERICAN ACADEMY OF NEUROLOGY (AAN) ANNUAL MEETING.EIGHT-WEEK FOLLOW-UP DATA SHOW SEPARATION OF CLINICAL EFFICACY SCORES BETWEEN TREATMENT GROUP AND PLACEBO GROUP THROUGH DURATION OF STUDY.TOTAL AND PATHOGENIC IGG REDUCTION CORRELATES WITH DISEASE SCORE IMPROVEMENTS.  Full Article

Argenx To Receive Third Preclinical Milestone Payment From Collaboration With Leo Pharma
Thursday, 12 Apr 2018 01:00am EDT 

April 12 (Reuters) - ARGENX ::TO RECEIVE THIRD PRECLINICAL MILESTONE PAYMENT FROM COLLABORATION WITH LEO PHARMA - MILESTONE ASSOCIATED WITH CTA APPROVAL FOR ARGX .AS PART OF AGREEMENT, ARGENX HAS GRANTED LEO PHARMA AN EXCLUSIVE OPTION TO OBTAIN A WORLDWIDE, EXCLUSIVE LICENSE TO ARGX-112 PROGRAM,.ARGX-112 PROGRAM AIMS TO DEVELOP AND COMMERCIALIZE LICENSED PRODUCTS FOR INFLAMMATORY SKIN DISORDERS.MAY RECEIVE FURTHER REGULATORY AND CLINICAL MILESTONE PAYMENTS UP TO APPROX. EUR 100MM AS WELL AS ROYALTIES ON NET SALES OF ANY PRODUCT.  Full Article

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AbbVie doubles down on cancer project with biotech group Argenx

BRUSSELS Biotech group Argenx said on Wednesday U.S. pharma group AbbVie had exercised an exclusive option to develop and commercialize one of its experimental drugs which could lead to payments of up to $625 million.