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WKN: A2JRKN | ISIN: KYG0520K1094 | Ticker-Symbol: 2VJ
Tradegate
15.12.25 | 12:48
1,460 Euro
+2,82 % +0,040
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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1,3801,46015.12.
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MoAscletis Pharma Inc.: Ascletis Announces Positive Topline Results from U.S. Phase I Study of ASC50, a Potential Best-in-Class Oral Small Molecule IL-17 Inhibitor148- The elimination half-life of ASC50 after a single oral dose was 43, 89, 91, 87, 104, and 85 hours for 10 mg, 30 mg, 100 mg, 200 mg, 400 mg, and 600 mg, respectively...
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MoASCLETIS-B (01672): VOLUNTARY ANNOUNCEMENT - ASCLETIS ANNOUNCES POSITIVE TOPLINE RESULTS FROM U.S. PHASE I STUDY OF ASC50, A POTENTIAL BEST-IN-CLASS ORAL ...1
FrASCLETIS-B (01672): NEXT DAY DISCLOSURE RETURN6
ASCLETIS PHARMA Aktie jetzt für 0€ handeln
MiSagimet Biosciences Inc.: Sagimet's License Partner Ascletis Announced Acceptance of New Drug Application for Denifanstat for the Treatment of Moderate to Severe Acne by China's National Medical Products Administration107SAN MATEO, Calif., Dec. 10, 2025 (GLOBE NEWSWIRE) -- Sagimet Biosciences Inc. (Nasdaq: SGMT), a clinical-stage biopharmaceutical company developing novel therapeutics targeting dysfunctional metabolic...
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MiASCLETIS-B (01672): VOLUNTARY ANNOUNCEMENT - ASCLETIS ANNOUNCES CHINA NATIONAL MEDICAL PRODUCTS ADMINISTRATION ACCEPTANCE OF NEW DRUG APPLICATION FOR ...2
09.12.Citi: Ph2a Data of ASCLETIS-B's ASC30 Further Demonstrates Best-in-Class Potential & Superior Tolerability14
09.12.ASCLETIS-B Snowballs 22% as GLP-1 Drug ASC30 Shows Positive Results in Obesity Treatment Study7
08.12.China's Ascletis reports 7.7% weight loss for oral GLP-1 contender in US phase 2 study5
08.12.ASCLETIS-B (01672): VOLUNTARY ANNOUNCEMENT - ASCLETIS' ORAL SMALL MOLECULE GLP-1, ASC30, DEMONSTRATED PLACEBO-ADJUSTED WEIGHT LOSS OF 7.7% WITH BETTER ...2
03.12.ASCLETIS-B (01672): NEXT DAY DISCLOSURE RETURN1
30.11.Ascletis Pharma Inc.: Ascletis Selects Its First Oral GLP-1R/GIPR/GCGR Triple Peptide Agonist, ASC37, for Clinical Development84- Utilizing Ascletis' Peptide Oral Transport ENhancement Technology (POTENT), ASC37 oral tablets achieved average absolute oral bioavailability of 4.2%, approximately...
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13.11.ASCLETIS-B (01672): VOLUNTARY ANNOUNCEMENT - ASCLETIS ANNOUNCES CO-FORMULATION OF ASC36, ONCE-MONTHLY NEXT-GENERATION AMYLIN RECEPTOR AGONIST AND ASC35, ...16
05.11.ASCLETIS-B (01672): NEXT DAY DISCLOSURE RETURN5
05.11.ASCLETIS-B (01672): VOLUNTARY ANNOUNCEMENT - ASCLETIS PRESENTS FULL ANALYSIS OF PHASE IB STUDY OF ASC30 ORAL TABLET, PHASE IB STUDY OF ASC30 INJECTION, ...3
30.10.ASCLETIS-B (01672): VOLUNTARY ANNOUNCEMENT - ASCLETIS SELECTS A BEST-IN-CLASS ONCE-MONTHLY SUBCUTANEOUSLY ADMINISTERED AMYLIN RECEPTOR AGONIST, ASC36, ...4
27.10.ASCLETIS-B (01672): NEXT DAY DISCLOSURE RETURN10
27.10.ASCLETIS-B (01672): VOLUNTARY ANNOUNCEMENT - ASCLETIS TO PRESENT STUDY RESULTS OF ASC30 ORAL TABLET, ASC30 INJECTION, AND COMBINATION OF ASC31 AND ASC47 ...1
20.10.Ascletis Pharma Inc.: Ascletis Completes Enrollment in U.S. Phase IIa Study for Its Once-Monthly Subcutaneous Depot Treatment Formulation of Small Molecule GLP-1R Agonist ASC30 for Obesity191- The 12-week U.S. Phase IIa study is evaluating the efficacy, safety and tolerability of the once-monthly subcutaneous (SQ) depot formulation (treatment...
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20.10.ASCLETIS-B (01672): VOLUNTARY ANNOUNCEMENT - ASCLETIS COMPLETES ENROLLMENT IN U.S. PHASE IIA STUDY FOR ITS ONCE-MONTHLY SUBCUTANEOUS DEPOT TREATMENT FORMULATION ...1
17.10.ASCLETIS-B (01672): NEXT DAY DISCLOSURE RETURN1
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