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WKN: A2JRKN | ISIN: KYG0520K1094 | Ticker-Symbol: 2VJ
Tradegate
29.01.26 | 10:18
1,370 Euro
-3,52 % -0,050
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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MoAscletis Pharma Inc.: Ascletis Announces First Participants Dosed in a 13-week U.S. Phase II Study with ASC30, an Oral Small Molecule GLP-1R Agonist for the Treatment of Diabetes72- Topline data from the Phase II study for the treatment of diabetes are expected in the third quarter of 2026. -ASC30 demonstrated placebo-adjusted weight loss...
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MoASCLETIS-B (01672): VOLUNTARY ANNOUNCEMENT - ASCLETIS ANNOUNCES FIRST PARTICIPANTS DOSED IN A 13-WEEK U.S. PHASE II STUDY WITH ASC30, AN ORAL SMALL MOLECULE ...3
20.01.ASCLETIS-B (01672): VOLUNTARY ANNOUNCEMENT - ASCLETIS SELECTS A NEXT-GENERATION ONCE-MONTHLY SUBCUTANEOUSLY ADMINISTERED GLP-1R/GIPR/GCGR TRIPLE PEPTIDE ...-
20.01.Ascletis Pharma Inc.: Ascletis Selects a Next-Generation Once-Monthly Subcutaneously Administered GLP-1R/GIPR/GCGR Triple Peptide Agonist, ASC37, for Clinical Development157- In head-to-head non-human primate (NHP) studies, average observed half-life of ASC37 was approximately 17 days, 7-fold longer than retatrutide, which supports...
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05.01.Ascletis Pharma Inc.: Ascletis Announces U.S. FDA IND Clearance for 13-Week Phase II Study of Its Oral Small Molecule GLP-1, ASC30, in Participants with Diabetes148-The Phase II study for diabetes is a 13-week, randomized, double-blind, placebo-controlled and multi-center study to evaluate the efficacy, safety, and tolerability...
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05.01.ASCLETIS-B (01672): VOLUNTARY ANNOUNCEMENT - ASCLETIS ANNOUNCES U.S. FDA IND CLEARANCE FOR 13-WEEK PHASE II STUDY OF ITS ORAL SMALL MOLECULE GLP-1, ASC30, ...1
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29.12.25ASCLETIS-B (01672): NEXT DAY DISCLOSURE RETURN1
19.12.25ASCLETIS-B (01672): NEXT DAY DISCLOSURE RETURN-
16.12.25ASCLETIS-B (01672): VOLUNTARY ANNOUNCEMENT - UPSIZING OF PROPOSED SHARE REPURCHASE UNDER THE REPURCHASE MANDATE-
15.12.25Ascletis 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 Inhibitor319- 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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15.12.25ASCLETIS-B (01672): VOLUNTARY ANNOUNCEMENT - ASCLETIS ANNOUNCES POSITIVE TOPLINE RESULTS FROM U.S. PHASE I STUDY OF ASC50, A POTENTIAL BEST-IN-CLASS ORAL ...1
12.12.25ASCLETIS-B (01672): NEXT DAY DISCLOSURE RETURN6
10.12.25Sagimet 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 Administration182SAN 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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10.12.25ASCLETIS-B (01672): VOLUNTARY ANNOUNCEMENT - ASCLETIS ANNOUNCES CHINA NATIONAL MEDICAL PRODUCTS ADMINISTRATION ACCEPTANCE OF NEW DRUG APPLICATION FOR ...2
08.12.25China's Ascletis reports 7.7% weight loss for oral GLP-1 contender in US phase 2 study5
08.12.25ASCLETIS-B (01672): VOLUNTARY ANNOUNCEMENT - ASCLETIS' ORAL SMALL MOLECULE GLP-1, ASC30, DEMONSTRATED PLACEBO-ADJUSTED WEIGHT LOSS OF 7.7% WITH BETTER ...2
03.12.25ASCLETIS-B (01672): NEXT DAY DISCLOSURE RETURN1
30.11.25Ascletis Pharma Inc.: Ascletis Selects Its First Oral GLP-1R/GIPR/GCGR Triple Peptide Agonist, ASC37, for Clinical Development128- Utilizing Ascletis' Peptide Oral Transport ENhancement Technology (POTENT), ASC37 oral tablets achieved average absolute oral bioavailability of 4.2%, approximately...
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13.11.25ASCLETIS-B (01672): VOLUNTARY ANNOUNCEMENT - ASCLETIS ANNOUNCES CO-FORMULATION OF ASC36, ONCE-MONTHLY NEXT-GENERATION AMYLIN RECEPTOR AGONIST AND ASC35, ...16
05.11.25ASCLETIS-B (01672): NEXT DAY DISCLOSURE RETURN5
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