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27.02.25 - 13:03
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Viridian Therapeutics Highlights Recent Progress and Reports Fourth Quarter and Full Year 2024 Financial Results (Business Wire)
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- 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....
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22.01.25 - 09:30
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Research: CICC Ratings, TPs on CN Dotcoms (Table) (AAStocks)
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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......
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08.01.25 - 13:06
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Viridian Therapeutics Highlights 2025 Corporate Priorities Following Positive Phase 3 Topline Data in Thyroid Eye Disease (Business Wire)
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- 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 ...
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08.09.24 - 22:27
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XFRA : DIVIDEND/INTEREST INFORMATION - 10.09.2024 - KYG6771K1022 (XETRA)
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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...
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21.05.24 - 07:01
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Hansa Biopharma to present data at 2024 American Transplant Congress annual meeting (Cision)
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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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