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Impact News +++ Masterflex: „Ein echter Meilenstein“ (4investors) +++ MASTERFLEX Aktie +3,75%

IGG Aktie

 >IGG Aktienkurs 
0.461 EUR    (Tradegate)
Ask: 0.5 EUR / 6576 Stück
Bid: 0.422 EUR / 7822 Stück
Tagesumsatz: 0 Stück
Realtime Kurs von 8 bis 22 Uhr!
IGG Aktie über LYNX handeln
>IGG Performance
1 Woche: -9,4%
1 Monat: +13,5%
3 Monate: -8,8%
6 Monate: -5,3%
1 Jahr: +32,8%
laufendes Jahr: -8,1%
>IGG Aktie
Name:  IGG INC. DL-,0000025
Land:  China
Sektor:  Elektronik / Software
ISIN/ Wkn:  KYG6771K1022 / A1W546
Symbol/ Ticker:  I91 (Frankfurt)
Kürzel:  FRA:I91, ETR:I91, I91:GR
Index:  -
Webseite:  https://www.igg.com/
Marktkapitalisierung:  509.61 Mio. EUR
Umsatz:  4969.65 Mio. EUR
EBITDA:  619.29 Mio. EUR
Gewinn je Aktie:  0.052 EUR
Schulden:  72.65 Mio. EUR
Liquide Mittel:  1965.35 Mio. EUR
Umsatz-/ Gewinnwachstum:  8.5% / -42.3%
KGV/ KGV lG:  7.97 / -
KUV/ KBV/ PEG:  0.81 / 1.46 / -
Gewinnm./ Eigenkapitalr.:  10.12% / 19.89%
Dividende je Aktie:  -
Dividendenrendite/ -schätzung:  - / 3.31%
Div. Historie:  18.08.21 - 0.01636€
16.03.21 - 0.05726€
>weitere anzeigen...
Insiderhandel:  -
Suchwörter:  IGG, I GOT GAMES
Letzte Datenerhebung:  24.06.25
>IGG Eigentümer
Aktien: 1140 Mio. St.
f.h. Aktien: 701.5 Mio. St.
Insider Eigner: 36.76%
Instit. Eigner: 5.26%
Leerverk. Aktien: -
>IGG Peer Group

 
14.05.25 - 08:33
Hansa Biopharma data at the 2025 PNS Annual Meeting demonstrates potential of imlifidase in the treatment of GBS (PR Newswire)
 
LUND, Sweden, May 14, 2025 /PRNewswire/ -- Hansa Biopharma AB, "Hansa" (Nasdaq Stockholm: HNSA), will present data from its 15-HMedIdeS-09 Phase 2 single arm study of imlifidase, a first in class IgG cleaving enzyme, in Guillain-Barré Syndrome (GBS) at the Peripheral Nerve Society (PNS)......
14.05.25 - 08:30
Hansa Biopharma data at the 2025 PNS Annual Meeting demonstrates potential of imlifidase in the treatment of GBS (PR Newswire)
 
LUND, Sweden, May 14, 2025 /PRNewswire/ -- Hansa Biopharma AB, "Hansa" (Nasdaq Stockholm: HNSA), will present data from its 15-HMedIdeS-09 Phase 2 single arm study of imlifidase, a first in class IgG cleaving enzyme, in Guillain-Barré Syndrome (GBS) at the Peripheral Nerve Society (PNS)......
30.04.25 - 14:30
Johnson & Johnson receives FDA approval for IMAAVY™ (nipocalimab-aahu), a new FcRn blocker offering long-lasting disease control in the broadest population of people living with generalized myasthenia gravis (gMG) (PR Newswire)
 
First and only FcRn blocker approved in anti-AChR and anti-MuSK antibody positive adults and pediatric gMG patients aged 12 and older IMAAVY delivered rapid and substantial reduction in immunoglobulin G (IgG) levels, one of the root causes of gMG, in both the adult and pediatric pivotal......
10.04.25 - 08:27
Orexo announces positive data for powder-based intranasal vaccine formulated with the AmorphOX technology (PR Newswire)
 
The study was conducted in partnership with Abera Bioscience, a platform and vaccine developer with over 30 years of research in the medical, molecular and microbiological fields. Both formulations tested induced strong systemic antibody response in serum (IgG) as well as locally in the......
10.04.25 - 08:24
Orexo announces positive data for powder-based intranasal vaccine formulated with the AmorphOX technology (PR Newswire)
 
The study was conducted in partnership with Abera Bioscience, a platform and vaccine developer with over 30 years of research in the medical, molecular and microbiological fields. Both formulations tested induced strong systemic antibody response in serum (IgG) as well as locally in the......
03.03.25 - 13:33
Biohaven Reports Positive Degrader Data Achieving > 80% Sustained Reductions in Total IgG with Potential First-in-Class BHV-1300 (PR Newswire)
 
Optimized subcutaneous administration of BHV-1300 achieved rapid, deep and sustained lowering of IgG, differentiating Biohaven's new small molecule class of degraders from the monoclonal antibody FcRn-targeting competition. Up to 84% reduction of total IgG was observed with a median......
27.02.25 - 13:03
Viridian Therapeutics Highlights Recent Progress and Reports Fourth Quarter and Full Year 2024 Financial Results (Business Wire)
 
- Reported positive topline phase 3 data for veligrotug from both THRIVE and THRIVE-2 in patients with active and chronic thyroid eye disease (TED); veligrotug has the potential to transform the standard of care in TED with a differentiated clinical profile achieved with fewer infusions; Biologics License Application (BLA) submission on track for second half of 2025 - - REVEAL-1 and REVEAL-2, phase 3 clinical trials assessing Q4W or Q8W subcutaneous (SC) VRDN-003 in active and chronic TED, progressing as planned and on track for topline data for both trials in the first half of 2026 - - Proof-of-concept IgG reduction clinical data in healthy volunteers anticipated in the third quarter of 2025 for VRDN-006, an Fc fragment inhibitor of the neonatal Fc receptor (FcRn) - - VRDN-008, a bispecific FcRn inhibitor with an extended half-life, expected to have additional preclinical data in 2025 with an Investigational New Drug (IND) submission planned for year-end 2025 - - Viridian appoints Radhika Tripuraneni, M....
22.01.25 - 09:30
Research: CICC Ratings, TPs on CN Dotcoms (Table) (AAStocks)
 
Shares | Ratings | Target prices (HK$)TENCENT(00700.HK) | Outperform | 468 NTES-S(09999.HK) | Outperform | 180 KUAISHOU-W(01024.HK) | Outperform | 66 BILIBILI-W(09626.HK) | Outperform | 188 TME-SW(01698.HK) | Outperform | 52 NETEASE MUSIC(09899.HK) | Outperform | 150 IGG(00799.HK) | Outperform | 4.16 BIDU-SW(09888.HK) | Outperfo......
08.01.25 - 13:06
Viridian Therapeutics Highlights 2025 Corporate Priorities Following Positive Phase 3 Topline Data in Thyroid Eye Disease (Business Wire)
 
- Veligrotug, with recent positive phase 3 topline data in both active and chronic thyroid eye disease (TED), has the potential to transform the standard of care in TED with a differentiated clinical profile achieved with less drug and fewer infusions; Biologics License Application (BLA) submission on track for second half of 2025 - - REVEAL-1 and REVEAL-2, phase 3 clinical trials for subcutaneous (SC) VRDN-003 in active and chronic TED respectively, are currently dosing patients; topline data for both trials, which are evaluating VRDN-003 dosed Q4W or Q8W, is on track for the first half of 2026 - - Investigational New Drug (IND) submitted in December 2024 for VRDN-006, an Fc fragment inhibitor of the neonatal Fc receptor (FcRn); proof-of-concept IgG reduction clinical data in healthy volunteers anticipated in the third quarter of 2025 - - VRDN-008, a bispecific FcRn inhibitor with an extended half-life, progressing with preclinical studies as planned; additional preclinical data expected in 2025 with an ...
17.12.24 - 21:42
Hansa Biopharma announces positive full results from 15-HMedIdeS-09 Phase 2 study and comparative analysis of imlifidase in patients with Guillain-Barré Syndrome (Cision)
 
Lund, Sweden, 17 December 2024. Hansa Biopharma, “Hansa” (Nasdaq Stockholm: HNSA), today announced positive full results from the 15-HMedIdeS-09 single arm Phase 2 study of imlifidase, a first in class IgG cleaving enzyme, in Guillain-Barré Syndrome (GBS) and an indirect treatment comparison of the 15-HMedIdeS-09 study data to the International Guillain-Barré Syndrome Outcome Study (IGOS), a worldwide prospective study by the Inflammatory Neuropathy Consortium on prognosis and biomarkers of GBS. Data from the 15-HMedIdeS-09 study demonstrated that severe GBS patients treated with a...
07.10.24 - 10:02
Hansa Biopharma′s HNSA-5487 Achieved Rapid and Highly Robust IgG Reduction by More Than 95% and Clear Redosing Potential in First-in-Human Trial (Cision)
 
Lund, Sweden, 7 October 2024. Hansa Biopharma AB, (“Hansa” or the “Company”) (Nasdaq Stockholm: HNSA), today announced positive results from a 12-month follow up analysis from the NICE-01 trial of HNSA-5487, the Company's next generation immunoglobulin G (IgG)-cleaving molecule, assessing IgG recovery, immunogenicity and redosing potential. In the NICE-01 trial, HNSA-5487 demonstrated rapid and highly robust reduction of IgG levels by more than 95 percent within a few hours post treatment. In a 12-month follow up analysis IgG levels returned to normal range six months after initial...
08.09.24 - 22:27
XFRA : DIVIDEND/INTEREST INFORMATION - 10.09.2024 - KYG6771K1022 (XETRA)
 
Das Instrument I91 KYG6771K1022 IGG INC. DL-,0000025 EQUITY wird cum Dividende/Zinsen gehandelt am 09.09.2024 und ex Dividende/Zinsen am 10.09.2024 The instrument I91 KYG6771K1022 IGG INC. DL-,0000025 EQUITY has its pre-dividend/interest day on 09.09.2024 and its ex-dividend/interest day on 10.09.2024...
13.08.24 - 05:33
MSCI Hong Kong Small Cap Index Adds 5 Stocks; C-MER MEDICAL, IGG, TEXHONG INTL GP Added to Micro Cap Index (AAStocks)
 
MSCI announced the results of the quarterly index review, and the changes will take place as of the close of market on 30 August. Of which, the MSCI Hong Kong Small Cap Index added DFI Retail Group, ENVISION GREEN (01783.HK), HAO TIAN INTL (01341.HK), SANERGY GROUP (02459.HK) and TIME INTERCON (01729.HK), and deleted C-MER MEDIC......
10.07.24 - 14:09
Twist Bioscience Expands High-Throughput IgG Antibody Portfolio with Launch of CHO Express Antibodies (Business Wire)
 
Um den gesamten Artikel unter morningstar.com zu lesen, klicken Sie bitte auf die Überschrift...
21.05.24 - 07:01
Hansa Biopharma to present data at 2024 American Transplant Congress annual meeting (Cision)
 
Lund, Sweden, 21 May, 2024. Hansa Biopharma, “Hansa” (Nasdaq Stockholm: HNSA), today announced data featuring imlifidase will be presented at the American Transplant Congress (ATC), the joint annual meeting of the American Society of Transplant Surgeons (ASTS) and the American Society of Transplantation (ATS). Imlifidase is Hansa's unique antibody-cleaving enzyme that specifically targets IgG and inhibits IgG-mediated immune response.[1] Søren Tulstrup, CEO and President, Hansa Biopharma, said: “ATC is a valuable opportunity for Hansa to share the latest science and data around...
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