BioCryst Pharmaceuticals, Inc. @BioCrystPharma
We develop oral small-molecule and protein therapeutics to target complement-mediated & other rare diseases. Community guidelines: https://t.co/HJsf9ax79K BioCryst.com Durham, North Carolina Joined July 2012-
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We will be presenting at The American Academy of Allergy, Asthma & Immunology's (@AAAAI_org) 2024 Annual Meeting taking place at Walter E. Washington Convention Center in Washington, D.C., from February 23-26 #AAAAI24 bit.ly/3wk7man
We’re looking forward to connecting with the #HAE community and those in the allergy and immunology field in Washington, D.C. at #AAAAI24. bit.ly/3uw4WVw @AAAAI_org
Happening now: BioCryst CEO, Jon Stonehouse, is presenting at #JPM2024. Webcast: bit.ly/3tSnZJl #JPMHC24
BioCryst to present at the 42nd Annual J.P. Morgan Healthcare Conference on Tuesday, January 9th at 6:00PM ET bit.ly/3H1RUC2 #JPMHC24
#DYK... There are more than 6,000 identified rare diseases. Learn more about our commitment to advancing novel therapeutics for patients with complement-mediated and other rare diseases. biocryst.com
We’re excited to attend the @ASH_hematology Annual Meeting to discuss the latest research and scientific advancements with the hematology community. #ASH23
We’re looking forward to connecting with the #HAE community and those in the allergy and immunology field at @ACAAI 23. bit.ly/46oiIqt #ACAAI23
We’re looking forward to connecting with the #HAE community at the @ACAAI 2023 Annual Scientific Meeting. Stop by our poster sessions to learn more. #ACAAI23 bit.ly/46MvGiE
IgA Nephropathy (IgAN) is an autoimmune disease that attacks the kidneys. IgAN occurs when abnormal antibody immunoglobulin A’s (IgA) are produced. For further information visit igan.org
Today we announced updates to our drug discovery process and additional therapies from our pipeline that will be highlighted at our R&D Day at 1pm ET. bit.ly/47f6WiT
Today we announced a partnership with @clearsidebio to develop an investigational ocular plasma kallikrein inhibitor for patients with diabetic macular edema (#DME) with Clearside’s suprachoroidal injection platform. bit.ly/3QJP2zq
We are excited to attend @ASNKidney Week 2023, joining our peers to discuss the latest scientific and medical advances in the field. #KidneyWk
We will be presenting at The American College of Allergy, Asthma & Immunology's (@ACAAI) 2023 Annual Scientific Meeting taking place at the Anaheim Convention Center November 9-13. #ACAAI23 bit.ly/46MvGiE
We announced the enrollment of the first patient with paroxysmal nocturnal hemoglobinuria, #PNH, in a proof-of-concept clinical trial. bit.ly/46K1d4N
We enjoyed attending the Canadian Society of Allergy and Clinical Immunology Annual Scientific Meeting last week and connecting with the allergy, asthma, and immunology community. @CSACI_ca
It was great to connect with the Alabama biotech community and share more about the experience of patients living with complement-mediated and rare diseases at the 2023 @BioAlabama Conference. #BioAlabama #ALBioTech
BioCryst was founded in Birmingham, Alabama in 1986. We are grateful to have our history rooted in the life sciences industry of Alabama and excited to hear about plans for future innovation this week at the 2023 @BioAlabama Conference. #BioAlabama #ALBioTech
We enjoyed attending the 2023 @NCBIO Annual Meeting where we learned about the latest updates in North Carolina’s bioscience industry. #ncbio
In a recent interview, Luke Robinson, General Manager, UK, Ireland, and Nordics explains how collaboration in the rare disease community can lead to improved outcomes for patients. Read more: bit.ly/457CqGf
#DYK…There are over 300 million people around the world living with a rare disease. Learn more: globalgenes.org
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Today is #HereditaryAngioedemaDay. On #RareDiseaseDay in February, we released our spotlight edition focusing on #HereditaryAngioedema (#HAE), in partnership with @BioCrystPharma. Read our HAE RDD edition for FREE here: bit.ly/RDD2023-HAE
The Rt Hon Sir Iain Duncan Smith MP and Angela Metcalfe CEO of HAE UK supporting Rare Disease Day 2023 #RareDiseaseDay2023 #SupportingPatients #HAEUK
Spoke with @UnityHealthTO's Dr. Stephen Betschel to learn about #hereditaryangioedema, a condition that involves recurrent attacks of severe swelling. He explains how each type of HAE presents and how patients can optimize their mental and physical health. patientvoice.io/rarevoices-qa/…
In 2018, Kim was diagnosed with hereditary angioedema (#HAE), a #raredisease often mistaken for more common conditions. Now, she advocates for disease awareness and improved 💊 access for all 🇨🇦 patients. Story below. In collaboration with @HAE_Canada. patientvoice.io/rarevoices/kim
Yesterday, Innovate Alabama partners and CEO Cynthia Crutchfield were welcomed by the @CityofHoover and @58_inc to tour a few of @ShelbyCoAl’s innovation assets. We are proud leaders like @McLeodSoftware, @BioCrystPharma and @NCFI_Official call Alabama home. #InnovateAlabama
@BioCrystPharma @GlobalGenes Such an important topic! #GGSummit22
@PatientWorthy @BioCrystPharma @GlobalGenes Yes! Looking forward to speaking with & learning from Dakota during this session!
Thank you for Bronze Level Support to these sponsors: @ApellisPharma @BioCrystPharma @TaihoOncology @Novartis
The IFOPA turns 34 today 🎂 🥳 💚 💙 🌍 34 years of coming together. 34 years of learning and growing. 34 years of support during times of grief and celebration. 34 years of commitment to treatments and a cure. 34 years of hope. 34 years as a global family. 1/2 #cureFOP
Happy hae day 2022 Please share to help us raise awareness of Hereditary Angioedema on hae day :-) #happyhaeday2022 #haeukpatientsupport
Happy hae day :-) we made it 1 trip around the world - congrats! So far, you've generated >55,875,000 steps in 39 countries for our activity challenge :-) Today, 16 May events & activities held around the world create awareness of HAE: buff.ly/2KXiwqH #active4hae #haeday
We are so excited to partner with @BioCrystPharma to light up businesses in Birmingham in #rarediseaseday colors on Monday February 28! Learn more at alabamarare.org/light-up-for-r…
Help us shine a light on rare conditions by watching and retweeting our trailer for our @ITNProductions news programme coverage launching on #RareDiseaseDay - 28 February 2022! #LightOnRare
In latest @elonuniversity poll, Cooper gains lead over McCrory in NC governor’s race #ncpol bit.ly/1qCXAbS
This doesn't suck. What a day!
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