Biotek-snakken — September 2024
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Jazz, er ret sikker på, at vi sagtens kan se 8-10 SEK på en godkendelse af Tesofensine, hvilket vil give en fast indtjening fremover og her hedmed noget tryghed for investorerne og kommer der 1-2 partneraftaler her i 2024, ja så er vi i min verden forbi 12 SEK og også højere. Deres pipeline er helt fantastisk som du selv skriver.
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Summit's bispecific halves risk of disease progression, death versus Keytruda in lung cancer study https://firstwordpharma.com/story/5893230
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Regeneron's Five-Year Phase 3 Trial Shows Durable Survival Benefit Of Libtayo In PD-L1 High NSCLC https://proinvestor.com/investornyt/1211512/regenerons-five-year-phase-3-trial-shows-durable-survival-benefit-of-libtayo-in-pd-l1-high-nsclc
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AstraZeneca :Dato-DXd Fails To Significantly Improve Overall Survival In Phase III Lung Cancer Trial https://proinvestor.com/investornyt/1211502/astrazeneca-dato-dxd-fails-to-significantly-improve-overall-survival-in-phase-iii-lung-cancer-trial
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ArriVent Announces Positive Phase 1b Data For Firmonertinib In NSCLC With EGFR PACC Mutations https://proinvestor.com/investornyt/1211514/arrivent-announces-positive-phase-1b-data-for-firmonertinib-in-nsclc-with-egfr-pacc-mutations
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2 Biotech Stocks To Watch In September 2024 https://proinvestor.com/investornyt/1211993/2-biotech-stocks-to-watch-in-september-2024
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BridgeBio's BBP-812 Canavan Disease Gene Therapy Receives FDA RMAT Designation https://proinvestor.com/investornyt/1212014/bridgebios-bbp-812-canavan-disease-gene-therapy-receives-fda-rmat-designation
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Godmorgen
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Innovent Biologics : Phase 3 Trial Results Of Mazdutide In Type 2 Diabetes Presented At EASD 2024 https://proinvestor.com/investornyt/1212496/innovent-biologics-phase-3-trial-results-of-mazdutide-in-type-2-diabetes-presented-at-easd-2024
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Ascendis Pharma Gets U.S. Orphan Drug Exclusivity For YORVIPATH In Adult Hypoparathyroidism https://proinvestor.com/investornyt/1212489/ascendis-pharma-gets-us-orphan-drug-exclusivity-for-yorvipath-in-adult-hypoparathyroidism
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J&J's TREMFYA Receives FDA Approval For Moderately To Severely Active Ulcerative Colitis In Adults https://proinvestor.com/investornyt/1212487/jampjs-tremfya-receives-fda-approval-for-moderately-to-severely-active-ulcerative-colitis-in-adults
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Board member purchases shares in Acarix
I dag kl. 14:02 ∙ MFN
Acarix, a leader in advanced acoustic-based cardiac diagnostics, announces that Dr. Tony Daz, Board member of Acarix, purchased 2,000,600 shares in the company between September 9 and September 11 at an average price of USD 0.031 per share. His total ownership amounts to 2,000,600 shares.
"I have great faith in the company and its product. The Acarix system is a disruptive technology to rapidly rule out CAD in a cost-effective way and -
Godmorgen
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