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WKN: A2JRKN | ISIN: KYG0520K1094 | Ticker-Symbol: 2VJ
Stuttgart
08.10.25 | 13:07
1,300 Euro
+11,11 % +0,130
Branche
Biotechnologie
Aktienmarkt
ASIEN
1-Jahres-Chart
ASCLETIS PHARMA INC Chart 1 Jahr
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ASCLETIS PHARMA INC 5-Tage-Chart
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1,2401,31008.10.
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02.10.ASCLETIS-B (01672): NEXT DAY DISCLOSURE RETURN1
02.10.ASCLETIS-B (01672): VOLUNTARY ANNOUNCEMENT - PROPOSED SHARE REPURCHASE UNDER THE REPURCHASE MANDATE2
30.09.ASCLETIS-B (01672): GRANT OF SHARE OPTIONS-
29.09.ASCLETIS-B (01672): INTERIM REPORT 20253
22.09.Ascletis Pharma's ASC47 + Semaglutide Combo Cuts Obesity By 56%2
22.09.Ascletis Pharma Inc.: Ascletis Announces ASC47 in Combination with Semaglutide Demonstrated Up to 56.2% Greater Relative Reduction in Body Weight in Participants with Obesity Compared to Semaglutide Monotherapy104- The gastrointestinal (GI) tolerability of ASC47 in combination with semaglutide was significantly better than placebo in combination with semaglutide...
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22.09.ASCLETIS-B (01672): VOLUNTARY ANNOUNCEMENT - ASCLETIS ANNOUNCES ASC47 IN COMBINATION WITH SEMAGLUTIDE DEMONSTRATED UP TO 56.2% GREATER RELATIVE REDUCTION ...1
ASCLETIS PHARMA Aktie jetzt für 0€ handeln
18.09.ASCLETIS-B (01672): NEXT DAY DISCLOSURE RETURN-
18.09.Ascletis Pharma Inc.: Ascletis Presented Phase III Study Results of First-in-Class FASN Inhibitor Denifanstat (ASC40) for Acne Treatment in the Late Breaking News Sessions of the European Academy of Dermatology and Venereology ...76--Denifanstat (ASC40) met all primary, key secondary and secondary efficacy endpoints (ITT analysis) and significantly improved moderate-to-severe acne compared...
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18.09.ASCLETIS-B (01672): VOLUNTARY ANNOUNCEMENT - ASCLETIS PRESENTED PHASE III STUDY RESULTS OF FIRST-IN-CLASS FASN INHIBITOR DENIFANSTAT (ASC40) FOR ACNE ...4
17.09.Sagimet Biosciences Inc.: Positive Phase 3 Results for Denifanstat for the Treatment of Moderate to Severe Acne to be Presented at the EADV Congress 2025 by Partner Ascletis178Denifanstat met all primary and secondary endpoints versus placebo Denifanstat was generally well tolerated Sagimet initiated first-in-human Phase 1 clinical trial of a second FASN inhibitor, TVB-3567...
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17.09.ASCLETIS-B (01672): VOLUNTARY ANNOUNCEMENT - ASCLETIS PRESENTED RESULTS FROM COHORTS 1 AND 2 OF 28-DAY MULTIPLE ASCENDING DOSE STUDY OF ITS ORAL SMALL ...11
12.09.ASCLETIS-B (01672): VOLUNTARY ANNOUNCEMENT - VOLUNTARY LOCK-UP UNDERTAKING MADE BY CONTROLLING SHAREHOLDERS3
10.09.ASCLETIS-B (01672): NEXT DAY DISCLOSURE RETURN16
09.09.ASCLETIS-B (01672): VOLUNTARY ANNOUNCEMENT - ASCLETIS ANNOUNCES ULTRA-LONG-ACTING SUBCUTANEOUS DEPOT MAINTENANCE FORMULATION OF SMALL MOLECULE GLP-1R ...16
02.09.ASCLETIS-B (01672): VOLUNTARY ANNOUNCEMENT - ASCLETIS TO PRESENT 28-DAY MULTIPLE ASCENDING DOSE STUDY RESULTS OF ORAL SMALL MOLECULE GLP-1R AGONIST ASC30 ...19
28.08.Ascletis Pharma Inc.: Ascletis Announces Favorable and Differentiated Pharmacokinetic Profile of ASC30 Oral Once-Daily Tablet in Its U.S. Phase Ib Multiple Ascending Dose Study149- ASC30 oral once-daily tablet demonstrated approximately 2.3-fold to 3.3-fold greater drug exposure than orforglipron in a cross-trial comparison. - ...
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28.08.ASCLETIS-B (01672): VOLUNTARY ANNOUNCEMENT - ASCLETIS ANNOUNCES FAVORABLE AND DIFFERENTIATED PHARMACOKINETIC PROFILE OF ASC30 ORAL ONCE-DAILY TABLET IN ...4
25.08.ASCLETIS-B (01672): NEXT DAY DISCLOSURE RETURN4
25.08.ASCLETIS-B (01672): COMPLETION OF PLACING OF EXISTING SHARES AND TOP-UP SUBSCRIPTION OF NEW SHARES UNDER THE GENERAL MANDATE-
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