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Intellia Therapeutics

@intelliatx • 12,248 subscribers

We're a #GeneEditing company, developing novel, potentially curative therapeutics leveraging #CRISPR-based technologies. Guidelines: https://t.co/u2gHl9Tmgr

Shorts

📢 $NTLA News: And so the countdown begins... We are proud to share the FDA has accepted Intellia's Biologics License Application (BLA) with Priority Review for our potential one-time #hereditaryangioedema treatment. The PDUFA target action date is March 10, 2027. Read the full announcement:

📢 $NTLA News: And so the countdown begins... We are proud to share the FDA has accepted Intellia's Biologics License Application (BLA) with Priority Review for our potential one-time #hereditaryangioedema treatment. The PDUFA target action date is March 10, 2027. Read the full announcement:

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#ATTR News: Intellia doses the first patient in its Phase 3 MAGNITUDE study of NTLA-2001 for the potential treatment of #transthyretinamyloidosis with cardiomyopathy: #GeneEditing #CRISPR

#ATTR News: Intellia doses the first patient in its Phase 3 MAGNITUDE study of NTLA-2001 for the potential treatment of #transthyretinamyloidosis with cardiomyopathy: #GeneEditing #CRISPR

26,660 次观看

#ATTR News: $NTLA announces positive new clinical data from the ongoing Phase 1 trial of nexiguran ziclumeran (nex-z) in patients with #ATTR amyloidosis with cardiomyopathy. Full details here: Join us at 12 p.m. ET for a webcast discussing the data, as well as an update from the ongoing Phase 1 polyneuropathy cohort. #CRISPR #GeneEditing

#ATTR News: $NTLA announces positive new clinical data from the ongoing Phase 1 trial of nexiguran ziclumeran (nex-z) in patients with #ATTR amyloidosis with cardiomyopathy. Full details here: Join us at 12 p.m. ET for a webcast discussing the data, as well as an update from the ongoing Phase 1 polyneuropathy cohort. #CRISPR #GeneEditing

19,292 次观看

NEWS: $NTLA receives authorization by the MHRAgovuk to initiate a Phase 1/2 of NTLA-3001 for the treatment of #alpha1 antitrypsin deficiency-associated lung disease. This is Intellia's first wholly owned in vivo gene insertion program. #CRISPR #AATD

NEWS: $NTLA receives authorization by the MHRAgovuk to initiate a Phase 1/2 of NTLA-3001 for the treatment of #alpha1 antitrypsin deficiency-associated lung disease. This is Intellia's first wholly owned in vivo gene insertion program. #CRISPR #AATD

19,072 次观看

$NTLA News: We are pleased to announce that the FDA has granted Regenerative Medicine Advanced Therapy (RMAT) designation to nexiguran ziclumeran (nex-z, also known as NTLA-2001) for the treatment of #ATTR #amyloidosis with polyneuropathy: #CRISPR #GeneEditing

$NTLA News: We are pleased to announce that the FDA has granted Regenerative Medicine Advanced Therapy (RMAT) designation to nexiguran ziclumeran (nex-z, also known as NTLA-2001) for the treatment of #ATTR #amyloidosis with polyneuropathy: #CRISPR #GeneEditing

14,242 次观看

Congratulations to Vertex Pharmaceuticals and CRISPR Therapeutics for achieving the first-ever MHRAgovuk approval of a #CRISPR therapy. This historic milestone is paving the way for the future of #geneediting.

Congratulations to Vertex Pharmaceuticals and CRISPR Therapeutics for achieving the first-ever MHRAgovuk approval of a #CRISPR therapy. This historic milestone is paving the way for the future of #geneediting.

16,935 次观看

Intellia announces positive long-term data from its ongoing Phase 1 study of NTLA-2002 for #hereditaryangioedema at EAACI 2024 Congress. Full details here: #HAE #CRISPR #geneediting

Intellia announces positive long-term data from its ongoing Phase 1 study of NTLA-2002 for #hereditaryangioedema at EAACI 2024 Congress. Full details here: #HAE #CRISPR #geneediting

13,400 次观看

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