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Google Keyword Rankings for : kallikrein inhibitor hereditary angioedema
1
Specific Targeting of Plasma Kallikrein for ... - PubMed
https://pubmed.ncbi.nlm.nih.gov/34838707/
Hereditary angioedema nl-C1INH is caused by either a known or unknown genetic mutation. The underlying mechanism of HAE-nl-C1INH is less well understood but is ...
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https://pubmed.ncbi.nlm.nih.gov/34838707/
Hereditary angioedema nl-C1INH is caused by either a known or unknown genetic mutation. The underlying mechanism of HAE-nl-C1INH is less well understood but is ...
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2
A new oral kallikrein inhibitor for long‐term prophylaxis of ...
https://onlinelibrary.wiley.com/doi/10.1111/all.14798
Hereditary angioedema (HAE) is a rare inherited chronic disease characterized by unpredictable recurrent attacks of cutaneous and submucosal ...
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https://onlinelibrary.wiley.com/doi/10.1111/all.14798
Hereditary angioedema (HAE) is a rare inherited chronic disease characterized by unpredictable recurrent attacks of cutaneous and submucosal ...
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3
A review of kallikrein inhibitor lanadelumab ... - Future Medicine
https://www.futuremedicine.com/doi/10.2217/imt-2018-0197
Hereditary angioedema (HAE) is a rare autosomal dominant genetic disorder caused by mutations in the SERPING1 gene that trigger severe swelling ...
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https://www.futuremedicine.com/doi/10.2217/imt-2018-0197
Hereditary angioedema (HAE) is a rare autosomal dominant genetic disorder caused by mutations in the SERPING1 gene that trigger severe swelling ...
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4
How Do Kallikrein Inhibitors Work? - Uses, Side Effects, Drug ...
https://www.rxlist.com/how_do_kallikrein_inhibitors_work/drug-class.htm
Kallikrein inhibitors are a class of drugs used to prevent and treat attacks due to an inherited immune disease “hereditary angioedema” ...
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https://www.rxlist.com/how_do_kallikrein_inhibitors_work/drug-class.htm
Kallikrein inhibitors are a class of drugs used to prevent and treat attacks due to an inherited immune disease “hereditary angioedema” ...
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5
Specific Targeting of Plasma Kallikrein for Treatment of ...
https://www.jaci-inpractice.org/article/S2213-2198(21)01289-7/fulltext
Hereditary angioedema nl-C1INH is caused by either a known or unknown genetic mutation. The underlying mechanism of HAE-nl-C1INH is less well ...
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https://www.jaci-inpractice.org/article/S2213-2198(21)01289-7/fulltext
Hereditary angioedema nl-C1INH is caused by either a known or unknown genetic mutation. The underlying mechanism of HAE-nl-C1INH is less well ...
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6
What Causes Hereditary Angioedema (HAE)?
https://www.discoverhae.com/hereditary-angioedema-causes
When there is not enough functioning C1 esterase inhibitor, the activity of plasma kallikrein increases. Too much plasma kallikrein activity triggers the ...
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https://www.discoverhae.com/hereditary-angioedema-causes
When there is not enough functioning C1 esterase inhibitor, the activity of plasma kallikrein increases. Too much plasma kallikrein activity triggers the ...
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7
Berotralstat (BCX7353): Structure-Guided Design of a Potent ...
https://pubs.acs.org/doi/10.1021/acs.jmedchem.1c00511
Background : Avoralstat is a potent small-mol. oral plasma kallikrein inhibitor under development for treatment of hereditary angioedema (HAE).
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https://pubs.acs.org/doi/10.1021/acs.jmedchem.1c00511
Background : Avoralstat is a potent small-mol. oral plasma kallikrein inhibitor under development for treatment of hereditary angioedema (HAE).
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8
Hereditary Angioedema Medication - Medscape Reference
https://emedicine.medscape.com/article/135604-medication
A human plasma kallikrein inhibitor, ecallantide binds to plasma kallikrein and blocks its binding site. It reduces conversion of kininogen to ...
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https://emedicine.medscape.com/article/135604-medication
A human plasma kallikrein inhibitor, ecallantide binds to plasma kallikrein and blocks its binding site. It reduces conversion of kininogen to ...
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9
Preclinical Characterization of BCX7353, an Oral Plasma ...
https://www.jacionline.org/article/S0091-6749(16)32259-X/abstract
Preclinical Characterization of BCX7353, an Oral Plasma Kallikrein Inhibitor, for the Treatment of Hereditary Angioedema (HAE) ; Conclusions. These data suggest ...
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https://www.jacionline.org/article/S0091-6749(16)32259-X/abstract
Preclinical Characterization of BCX7353, an Oral Plasma Kallikrein Inhibitor, for the Treatment of Hereditary Angioedema (HAE) ; Conclusions. These data suggest ...
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10
Hereditary Angioedema Therapy: Kallikrein Inhibition and ...
https://waojournal.biomedcentral.com/articles/10.1186/1939-4551-3-S3-S34
Current strategies for the treatment of hereditary angioedema (HAE) include targeted inhibition or antagonism of the contact system, ...
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https://waojournal.biomedcentral.com/articles/10.1186/1939-4551-3-S3-S34
Current strategies for the treatment of hereditary angioedema (HAE) include targeted inhibition or antagonism of the contact system, ...
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11
Full article: Hereditary angioedema: examining the landscape ...
https://www.tandfonline.com/doi/full/10.1080/14728222.2019.1608949
Plasma kallikrein cleaves high-molecular-weight kininogen releasing bradykinin. Bradykinin binds to the B2 receptor to release NO, prostacyclin, ...
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https://www.tandfonline.com/doi/full/10.1080/14728222.2019.1608949
Plasma kallikrein cleaves high-molecular-weight kininogen releasing bradykinin. Bradykinin binds to the B2 receptor to release NO, prostacyclin, ...
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12
Hereditary angioedema (due to C1 inhibitor deficiency)
https://www.uptodate.com/contents/hereditary-angioedema-due-to-c1-inhibitor-deficiency-general-care-and-long-term-prophylaxis
Hereditary angioedema (HAE) with C1 inhibitor deficiency is a rare genetic disorder in which mutations in theSERPING1gene result in ...
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https://www.uptodate.com/contents/hereditary-angioedema-due-to-c1-inhibitor-deficiency-general-care-and-long-term-prophylaxis
Hereditary angioedema (HAE) with C1 inhibitor deficiency is a rare genetic disorder in which mutations in theSERPING1gene result in ...
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13
Kallikrein Inhibitors | DrugBank Online
https://go.drugbank.com/categories/DBCAT004400
Kallikrein Inhibitors ; Berotralstat, An inhibitor of plasma kallikrein used for prophylaxis of angioedema attacks in patients with hereditary angioedema.
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https://go.drugbank.com/categories/DBCAT004400
Kallikrein Inhibitors ; Berotralstat, An inhibitor of plasma kallikrein used for prophylaxis of angioedema attacks in patients with hereditary angioedema.
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14
A novel murine in vivo model for acute hereditary angioedema ...
https://www.nature.com/articles/s41598-021-95125-0.pdf?proof=t
The plasma kallikrein inhibitor ecallantide inhibits SiNP‑induced blood pressure decrease. We used ecallantide (Kalbitor), an FDA-approved HAE therapy, ...
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https://www.nature.com/articles/s41598-021-95125-0.pdf?proof=t
The plasma kallikrein inhibitor ecallantide inhibits SiNP‑induced blood pressure decrease. We used ecallantide (Kalbitor), an FDA-approved HAE therapy, ...
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15
Evaluation of avoralstat, an oral kallikrein inhibitor, in a Phase ...
https://profiles.wustl.edu/en/publications/evaluation-of-avoralstat-an-oral-kallikrein-inhibitor-in-a-phase-
Background: Effective inhibition of plasma kallikrein may have significant benefits for patients with hereditary angioedema due to deficiency of C1 inhibitor ( ...
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https://profiles.wustl.edu/en/publications/evaluation-of-avoralstat-an-oral-kallikrein-inhibitor-in-a-phase-
Background: Effective inhibition of plasma kallikrein may have significant benefits for patients with hereditary angioedema due to deficiency of C1 inhibitor ( ...
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16
Publications | KalVista Pharmaceuticals, Inc
https://www.kalvista.com/healthcare-providers/publications
KVD900 as a Single Dose, Rapid, Oral Plasma Kallikrein Inhibitor for the On-Demand Treatment of Hereditary Angioedema Attacks: Pharmacokinetic and ...
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https://www.kalvista.com/healthcare-providers/publications
KVD900 as a Single Dose, Rapid, Oral Plasma Kallikrein Inhibitor for the On-Demand Treatment of Hereditary Angioedema Attacks: Pharmacokinetic and ...
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17
ACAAI 2021: Investigational Plasma Kallikrein Inhibitor STAR ...
https://www.practiceupdate.com/content/acaai-2021-investigational-plasma-kallikrein-inhibitor-star-215-shows-promise-in-hereditary-angioedema/127036
News · November 16, 2021. ACAAI 2021: Investigational Plasma Kallikrein Inhibitor STAR-215 Shows Promise in Hereditary Angioedema.
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https://www.practiceupdate.com/content/acaai-2021-investigational-plasma-kallikrein-inhibitor-star-215-shows-promise-in-hereditary-angioedema/127036
News · November 16, 2021. ACAAI 2021: Investigational Plasma Kallikrein Inhibitor STAR-215 Shows Promise in Hereditary Angioedema.
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18
Hereditary Angioedema - Medical Clinical Policy Bulletins
https://www.aetna.com/cpb/medical/data/700_799/0782.html
Ruconest (recombinant C1 esterase inhibitor) is available as 2100 U lyophilized powder for reconstitution for injection in a single use vial. For intravenous ...
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https://www.aetna.com/cpb/medical/data/700_799/0782.html
Ruconest (recombinant C1 esterase inhibitor) is available as 2100 U lyophilized powder for reconstitution for injection in a single use vial. For intravenous ...
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19
PRO7 A NETWORK META-ANALYSIS COMPARING C1 AND ...
https://www.valueinhealthjournal.com/article/S1098-3015(19)31833-9/fulltext
Hereditary angioedema (HAE) is a rare autosomal dominant genetic disorder caused mostly due to deficient (Type-1) or dysfunctional (Type-2) C1 esterase ...
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https://www.valueinhealthjournal.com/article/S1098-3015(19)31833-9/fulltext
Hereditary angioedema (HAE) is a rare autosomal dominant genetic disorder caused mostly due to deficient (Type-1) or dysfunctional (Type-2) C1 esterase ...
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20
A review of oral kallikrein inhibitor berotralstat for hereditary ...
https://pennstate.pure.elsevier.com/en/publications/a-review-of-oral-kallikrein-inhibitor-berotralstat-for-hereditary
Preclinical and phase I studies showed promising efficacy and safety, and several multicenter international Angioedema Prophylaxis (APeX) phase ...
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https://pennstate.pure.elsevier.com/en/publications/a-review-of-oral-kallikrein-inhibitor-berotralstat-for-hereditary
Preclinical and phase I studies showed promising efficacy and safety, and several multicenter international Angioedema Prophylaxis (APeX) phase ...
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21
Prices for popular plasma kallikrein inhibitors - GoodRx
https://www.goodrx.com/classes/plasma-kallikrein-inhibitors
Plasma Kallikrein Inhibitors. Plasma kallikrein inhibitors are used to treat hereditary angioedema. They work by preventing attacks and reducing swelling.
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https://www.goodrx.com/classes/plasma-kallikrein-inhibitors
Plasma Kallikrein Inhibitors. Plasma kallikrein inhibitors are used to treat hereditary angioedema. They work by preventing attacks and reducing swelling.
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22
Hereditary Angioedema (HAE), Treatment and Prophylaxis
https://www.uhcprovider.com/content/dam/provider/docs/public/policies/comm-medical-drug/hereditary-angioedema-treatment-prophylaxis.pdf
Suppression of contact system activation by C1 inhibitor through the inactivation of plasma kallikrein and factor XIIa is thought to modulate ...
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https://www.uhcprovider.com/content/dam/provider/docs/public/policies/comm-medical-drug/hereditary-angioedema-treatment-prophylaxis.pdf
Suppression of contact system activation by C1 inhibitor through the inactivation of plasma kallikrein and factor XIIa is thought to modulate ...
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23
Hereditary Angioedema Agents | AmeriHealth
https://www.amerihealth.com/pdfs/providers/pharmacy_information/pharmacy_policies/hereditary-angioedema-agents.pdf
Orladeyo™ (berotralstat) is a plasma kallikrein inhibitor indicated for prophylaxis to prevent attacks of hereditary angioedema (HAE) in adults and ...
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https://www.amerihealth.com/pdfs/providers/pharmacy_information/pharmacy_policies/hereditary-angioedema-agents.pdf
Orladeyo™ (berotralstat) is a plasma kallikrein inhibitor indicated for prophylaxis to prevent attacks of hereditary angioedema (HAE) in adults and ...
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24
Prophylaxis with anti-activated factor XII for hereditary ...
https://www.thelancet.com/journals/lancet/article/PIIS0140-6736(21)02436-3/fulltext
FXIIa inhibition with garadacimab is a promising prophylactic strategy for patients with hereditary angioedema and is once again broadening the ...
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https://www.thelancet.com/journals/lancet/article/PIIS0140-6736(21)02436-3/fulltext
FXIIa inhibition with garadacimab is a promising prophylactic strategy for patients with hereditary angioedema and is once again broadening the ...
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25
Hereditary angioedema Information | Mount Sinai - New York
https://www.mountsinai.org/health-library/diseases-conditions/hereditary-angioedema
Hereditary angioedema (HAE) is caused by a low level or improper function of a protein called the C1 inhibitor. It affects the blood vessels. An HAE attack can ...
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https://www.mountsinai.org/health-library/diseases-conditions/hereditary-angioedema
Hereditary angioedema (HAE) is caused by a low level or improper function of a protein called the C1 inhibitor. It affects the blood vessels. An HAE attack can ...
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26
STAR-0215, a Kallikrein Inhibitor for HAE, Has Lasting Effect ...
https://angioedemanews.com/news/star-0215-kallikrein-inhibitor-hae-has-lasting-effect-monkeys/
STAR-0215, an investigational therapy to prevent swelling attacks in people with hereditary angioedema (HAE), rapidly and durably suppressed ...
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https://angioedemanews.com/news/star-0215-kallikrein-inhibitor-hae-has-lasting-effect-monkeys/
STAR-0215, an investigational therapy to prevent swelling attacks in people with hereditary angioedema (HAE), rapidly and durably suppressed ...
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27
Mechanism of Action | ORLADEYO® (berotralstat) HCP
https://orladeyohcp.com/clinical-info/mechanism-of-action/
Targeted inhibition of plasma kallikrein has long been known to help prevent hereditary angioedema (HAE) attacks ... HAE is primarily caused by uncontrolled ...
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https://orladeyohcp.com/clinical-info/mechanism-of-action/
Targeted inhibition of plasma kallikrein has long been known to help prevent hereditary angioedema (HAE) attacks ... HAE is primarily caused by uncontrolled ...
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28
A case of normal C1 esterase inhibitor hereditary angioedema ...
https://www.annallergy.org/article/S1081-1206(22)00016-3/fulltext
During this time, we were able to offer the patient oral treatment with berotralstat, a plasma kallikrein inhibitor that was approved as a once- ...
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https://www.annallergy.org/article/S1081-1206(22)00016-3/fulltext
During this time, we were able to offer the patient oral treatment with berotralstat, a plasma kallikrein inhibitor that was approved as a once- ...
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29
Oral Plasma Kallikrein Inhibitor Significantly Reduces Attacks ...
https://www.hcplive.com/view/oral-plasma-kallikrein-inhibitor-significantly-reduces-attacks-of-hereditary-angioedema
Hereditary angioedema (HAE) can be treated with a new drug called BCX7353, according to a paper published in The New England Journal of ...
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https://www.hcplive.com/view/oral-plasma-kallikrein-inhibitor-significantly-reduces-attacks-of-hereditary-angioedema
Hereditary angioedema (HAE) can be treated with a new drug called BCX7353, according to a paper published in The New England Journal of ...
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30
Oral Plasma Kallikrein Inhibitor for Prophylaxis in Hereditary ...
https://www.zora.uzh.ch/id/eprint/168172/
BACKGROUND: Hereditary angioedema is a life-threatening illness caused by mutations in the gene encoding C1 inhibitor (also called C1 esterase inhibitor) that ...
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https://www.zora.uzh.ch/id/eprint/168172/
BACKGROUND: Hereditary angioedema is a life-threatening illness caused by mutations in the gene encoding C1 inhibitor (also called C1 esterase inhibitor) that ...
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31
A Phase II, Cross-over Clinical Trial Evaluating the Efficacy ...
https://clinicaltrials.gov/ct2/show/NCT04208412
... an Oral Plasma Kallikrein Inhibitor, in the On-demand Treatment of Angioedema Attacks in Adult Subjects With Hereditary Angioedema Type I or II.
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https://clinicaltrials.gov/ct2/show/NCT04208412
... an Oral Plasma Kallikrein Inhibitor, in the On-demand Treatment of Angioedema Attacks in Adult Subjects With Hereditary Angioedema Type I or II.
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32
5.01.587 Hereditary Angioedema - Premera Blue Cross
https://www.premera.com/medicalpolicies/5.01.587.pdf
Suppression of contact system activation by C1 esterase inhibitor is primarily mediated through inactivation of plasma kallikrein and factor ...
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https://www.premera.com/medicalpolicies/5.01.587.pdf
Suppression of contact system activation by C1 esterase inhibitor is primarily mediated through inactivation of plasma kallikrein and factor ...
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33
Hereditary Angioedema: A Broad Review for Clinicians
https://jamanetwork.com/journals/jamainternalmedicine/fullarticle/649449
Kallikrein in turn cleaves high-molecular-weight plasma kininogens, resulting in excessive release of various kinins, especially bradykinin and ...
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https://jamanetwork.com/journals/jamainternalmedicine/fullarticle/649449
Kallikrein in turn cleaves high-molecular-weight plasma kininogens, resulting in excessive release of various kinins, especially bradykinin and ...
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34
Use of recombinant plasma kallikrein inhibitor in hereditary ...
https://www.joms.org/article/S0278-2391(04)01173-5/fulltext
Hereditary angioedema (HAE) is a disease characterized by a rapid onset of nonpitting edema affecting the face, extremities, and mucosal surfaces of the ...
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https://www.joms.org/article/S0278-2391(04)01173-5/fulltext
Hereditary angioedema (HAE) is a disease characterized by a rapid onset of nonpitting edema affecting the face, extremities, and mucosal surfaces of the ...
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35
Hereditary Angioedema Therapies - Rare Disease Advisor
https://www.rarediseaseadvisor.com/disease-info-pages/hereditary-angioedema-therapies/
Kallikrein inhibitors are therefore used in HAE to bind plasma kallikrein and prevent the cleavage of high-molecular-weight kininogen (HMWK) to ...
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https://www.rarediseaseadvisor.com/disease-info-pages/hereditary-angioedema-therapies/
Kallikrein inhibitors are therefore used in HAE to bind plasma kallikrein and prevent the cleavage of high-molecular-weight kininogen (HMWK) to ...
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36
Inhibiting Plasma Kallikrein for Hereditary Angioedema ...
https://www.medscape.org/medline/abstract/28225674
BACKGROUND: Hereditary angioedema with C1 inhibitor deficiency is characterized by recurrent, unpredictable swelling episodes caused by uncontrolled plasma ...
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https://www.medscape.org/medline/abstract/28225674
BACKGROUND: Hereditary angioedema with C1 inhibitor deficiency is characterized by recurrent, unpredictable swelling episodes caused by uncontrolled plasma ...
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37
Recognition and Management of Hereditary Angioedema
https://link.springer.com/article/10.1007/s13555-021-00593-x
Patients with HAE have either deficiency or dysfunction of the C1 inhibitor (C1INH) protein that inhibits proteases in the contact, complement, ...
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https://link.springer.com/article/10.1007/s13555-021-00593-x
Patients with HAE have either deficiency or dysfunction of the C1 inhibitor (C1INH) protein that inhibits proteases in the contact, complement, ...
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38
Oral Plasma Kallikrein Inhibitor Prevents HAE Attacks in ...
https://www.empr.com/home/news/drugs-in-the-pipeline/oral-plasma-kallikrein-inhibitor-prevents-hae-attacks-in-phase-3-trial/
Results from a phase 3 trial evaluating BCX7353 (BioCryst), an investigational therapy for hereditary angioedema (HAE), showed that it ...
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https://www.empr.com/home/news/drugs-in-the-pipeline/oral-plasma-kallikrein-inhibitor-prevents-hae-attacks-in-phase-3-trial/
Results from a phase 3 trial evaluating BCX7353 (BioCryst), an investigational therapy for hereditary angioedema (HAE), showed that it ...
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39
Genetic Variation of Kallikrein-Kinin System and Related ...
https://www.frontiersin.org/articles/10.3389/fmed.2019.00028/full
Hereditary angioedema (HAE) is an autosomal dominant disease caused by C1-INH deficiency due to mutations in SERPING1 (C1-INH-HAE) in most ...
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https://www.frontiersin.org/articles/10.3389/fmed.2019.00028/full
Hereditary angioedema (HAE) is an autosomal dominant disease caused by C1-INH deficiency due to mutations in SERPING1 (C1-INH-HAE) in most ...
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40
plasma kallikrein inhibitors and uses thereof for treating ...
https://patentscope.wipo.int/search/en/detail.jsf?docId=WO2020047352
Provided herein are methods of treating and preventing hereditary angioedema attack in certain human patient subpopulations using antibodies ...
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https://patentscope.wipo.int/search/en/detail.jsf?docId=WO2020047352
Provided herein are methods of treating and preventing hereditary angioedema attack in certain human patient subpopulations using antibodies ...
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41
Hereditary Angioedema (HAE) Therapy - Cigna
https://static.cigna.com/assets/chcp/pdf/coveragePolicies/pharmacy/ph_1019_coveragepositioncriteria_hereditary_angioedema.pdf
TAKHZYRO is a plasma kallikrein inhibitor (monoclonal antibody) indicated for prophylaxis to prevent attacks of hereditary angioedema (HAE) in patients.
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https://static.cigna.com/assets/chcp/pdf/coveragePolicies/pharmacy/ph_1019_coveragepositioncriteria_hereditary_angioedema.pdf
TAKHZYRO is a plasma kallikrein inhibitor (monoclonal antibody) indicated for prophylaxis to prevent attacks of hereditary angioedema (HAE) in patients.
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42
Oral Plasma Kallikrein Inhibitor BCX7353 is Safe and Effective ...
https://ir.biocryst.com/static-files/2b3e13b9-ad24-432c-9ac5-15711d954d88
Hereditary Angioedema (HAE) Patients: Results of the ZENITH-1 Trial ... HAE attacks. ▫ BCX7353 is an investigational oral kallikrein inhibitor in Phase 3.
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https://ir.biocryst.com/static-files/2b3e13b9-ad24-432c-9ac5-15711d954d88
Hereditary Angioedema (HAE) Patients: Results of the ZENITH-1 Trial ... HAE attacks. ▫ BCX7353 is an investigational oral kallikrein inhibitor in Phase 3.
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43
Inhibiting Plasma Kallikrein for Hereditary ... - YouTube
https://www.youtube.com/watch?v=JtVeZk1hiUM
in this video
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https://www.youtube.com/watch?v=JtVeZk1hiUM
in this video
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44
Angioedema Latest Advances - MediFind
https://www.medifind.com/conditions/angioedema/269/treatment-advance/312126976
Berotralstat (BCX7353): Structure-Guided Design of a Potent, Selective, and Oral Plasma Kallikrein Inhibitor to Prevent Attacks of Hereditary ...
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https://www.medifind.com/conditions/angioedema/269/treatment-advance/312126976
Berotralstat (BCX7353): Structure-Guided Design of a Potent, Selective, and Oral Plasma Kallikrein Inhibitor to Prevent Attacks of Hereditary ...
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45
Bradykinin's Role In HAE Attacks - Firazyr
https://www.firazyr.com/hcp/what-is-firazyr/bradykinin
Most patients with HAE have an underlying deficiency of functional C1 esterase inhibitor that leads to an increase in plasma kallikrein activity, ...
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https://www.firazyr.com/hcp/what-is-firazyr/bradykinin
Most patients with HAE have an underlying deficiency of functional C1 esterase inhibitor that leads to an increase in plasma kallikrein activity, ...
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46
Advances in Hereditary Angioedema: The Prevention of ...
https://journals.lww.com/journalofinfusionnursing/Fulltext/2020/05000/Advances_in_Hereditary_Angioedema__The_Prevention.4.aspx
Hereditary angioedema (HAE) is a debilitating condition caused by a functional C1-inhibitor (C1-INH) deficiency and characterized clinically by episodes of ...
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https://journals.lww.com/journalofinfusionnursing/Fulltext/2020/05000/Advances_in_Hereditary_Angioedema__The_Prevention.4.aspx
Hereditary angioedema (HAE) is a debilitating condition caused by a functional C1-inhibitor (C1-INH) deficiency and characterized clinically by episodes of ...
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47
A new oral kallikrein inhibitor for long-term prophylaxis of ...
https://europepmc.org/article/med/33641193
Lanadelumab for the treatment of hereditary angioedema. Wu MA · Expert Opin Biol Ther, 19(12):1233-1245, 04 Nov 2019. Cited by: 0 articles | PMID ...
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https://europepmc.org/article/med/33641193
Lanadelumab for the treatment of hereditary angioedema. Wu MA · Expert Opin Biol Ther, 19(12):1233-1245, 04 Nov 2019. Cited by: 0 articles | PMID ...
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48
Ecallantide for the treatment of acute attacks of hereditary ...
https://www.openaccessjournals.com/articles/ecallantide-for-the-treatment-of-acute-attacks-of-hereditary-angioedema-due-to-c1inhibitor-deficiency.pdf
inhibitor approved for the treatment of acute attacks of HAE-C1INH. In ... Keywords: angioedema • clinical trials • ecallantide • plasma kallikrein.
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https://www.openaccessjournals.com/articles/ecallantide-for-the-treatment-of-acute-attacks-of-hereditary-angioedema-due-to-c1inhibitor-deficiency.pdf
inhibitor approved for the treatment of acute attacks of HAE-C1INH. In ... Keywords: angioedema • clinical trials • ecallantide • plasma kallikrein.
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49
an inhibitory regulatory role for the factor XII heavy chain | Blood
https://ashpublications.org/blood/article-abstract/133/10/1152/272753/A-mechanism-for-hereditary-angioedema-with-normal
Kallikrein cleaves high-molecular-weight kininogen (HK), releasing the vasoactive peptide bradykinin. Patients with hereditary angioedema (HAE) experience ...
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https://ashpublications.org/blood/article-abstract/133/10/1152/272753/A-mechanism-for-hereditary-angioedema-with-normal
Kallikrein cleaves high-molecular-weight kininogen (HK), releasing the vasoactive peptide bradykinin. Patients with hereditary angioedema (HAE) experience ...
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50
Treatment of Hereditary Angioedema | AAAAI
https://www.aaaai.org/Tools-for-the-Public/Drug-Guide/Immunomodulator-Medications
Kallikrein inhibitor- human ; Lanadelumab. Takhzyro Takhzyro Website. 12 years and above Type I and II hereditary angioedema 300 mg subcutaneous every 2 weeks; ...
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https://www.aaaai.org/Tools-for-the-Public/Drug-Guide/Immunomodulator-Medications
Kallikrein inhibitor- human ; Lanadelumab. Takhzyro Takhzyro Website. 12 years and above Type I and II hereditary angioedema 300 mg subcutaneous every 2 weeks; ...
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51
A review of kallikrein inhibitor lanadelumab in ... - ProQuest
https://search.proquest.com/openview/babbf33e45f990dd7359734518dd7cc8/1?pq-origsite=gscholar&cbl=55027
Hereditary angioedema with C1 esterase inhibitor deficiency is a rare disorder characterized by unpredictable swelling of the face, larynx and gastrointestinal ...
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https://search.proquest.com/openview/babbf33e45f990dd7359734518dd7cc8/1?pq-origsite=gscholar&cbl=55027
Hereditary angioedema with C1 esterase inhibitor deficiency is a rare disorder characterized by unpredictable swelling of the face, larynx and gastrointestinal ...
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52
Hereditary Angioedema and Gastrointestinal Complications
https://www.hindawi.com/journals/crii/2015/925861/
Hereditary Angioedema (HAE) is a rare autosomal dominant (AD) disease characterized by deficient (type 1) or nonfunctional (type 2) C1 inhibitor protein.
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https://www.hindawi.com/journals/crii/2015/925861/
Hereditary Angioedema (HAE) is a rare autosomal dominant (AD) disease characterized by deficient (type 1) or nonfunctional (type 2) C1 inhibitor protein.
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53
Kallikrein Inhibitor Lanadelumab Prevents Hereditary ...
https://rheumnow.com/content/kallikrein-inhibitor-lanadelumab-prevents-hereditary-angioedema-attacks
Hereditary angioedema is a rare autosomal dominant disorder due to C1 inhibitor deficiency (type I) or dysfunction (type II) that leads to ...
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https://rheumnow.com/content/kallikrein-inhibitor-lanadelumab-prevents-hereditary-angioedema-attacks
Hereditary angioedema is a rare autosomal dominant disorder due to C1 inhibitor deficiency (type I) or dysfunction (type II) that leads to ...
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54
hereditary angioedema | The Medical Letter Inc.
https://secure.medicalletter.org/taxonomy/term/15348
The FDA has approved lanadelumab-flyo (Takhzyro – Takeda), a subcutaneously-administered plasma kallikrein inhibitor, for prevention of hereditary ...
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https://secure.medicalletter.org/taxonomy/term/15348
The FDA has approved lanadelumab-flyo (Takhzyro – Takeda), a subcutaneously-administered plasma kallikrein inhibitor, for prevention of hereditary ...
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55
Current and Emerging Therapies to Prevent Hereditary ...
https://www.ajmc.com/view/current-and-emerging-therapies-to-prevent-hae-attacks
Ecallantide is an SC administered fixed-dose potent and selective inhibitor of plasma kallikrein that is FDA approved for the treatment of ...
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https://www.ajmc.com/view/current-and-emerging-therapies-to-prevent-hae-attacks
Ecallantide is an SC administered fixed-dose potent and selective inhibitor of plasma kallikrein that is FDA approved for the treatment of ...
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56
Hereditary Angioedema - Texas Health and Human Services
https://www.hhs.texas.gov/sites/default/files/documents/apr-2022-durb-agenda-item5v.pdf
C1-INH = C1 esterase inhibitor; HAE = hereditary angioedema ... (Ruconest), subcutaneous plasma kallikrein inhibitor ecallantide (Kalbitor), ...
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https://www.hhs.texas.gov/sites/default/files/documents/apr-2022-durb-agenda-item5v.pdf
C1-INH = C1 esterase inhibitor; HAE = hereditary angioedema ... (Ruconest), subcutaneous plasma kallikrein inhibitor ecallantide (Kalbitor), ...
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57
Oral Plasma Kallikrein Inhibitor for Prophylaxis in Hereditary ...
https://www.semanticscholar.org/paper/Oral-Plasma-Kallikrein-Inhibitor-for-Prophylaxis-in-Ayg%C3%B6ren%E2%80%90P%C3%BCrs%C3%BCn-Bygum/ca21fcf37a827025f36d803579f18f0bcab0016c
Oral Plasma Kallikrein Inhibitor for Prophylaxis in Hereditary Angioedema · E. Aygören‐Pürsün, A. Bygum, +30 authors. M. Cicardi · Published 26 ...
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https://www.semanticscholar.org/paper/Oral-Plasma-Kallikrein-Inhibitor-for-Prophylaxis-in-Ayg%C3%B6ren%E2%80%90P%C3%BCrs%C3%BCn-Bygum/ca21fcf37a827025f36d803579f18f0bcab0016c
Oral Plasma Kallikrein Inhibitor for Prophylaxis in Hereditary Angioedema · E. Aygören‐Pürsün, A. Bygum, +30 authors. M. Cicardi · Published 26 ...
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58
Hereditary angioedema: an update on causes, manifestations ...
https://www.magonlinelibrary.com/doi/10.12968/hmed.2019.80.7.391
Hereditary angioedema is a rare genetic disorder caused by deficiency of C1 esterase inhibitor (C1-INH) and characterized by recurrent ...
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https://www.magonlinelibrary.com/doi/10.12968/hmed.2019.80.7.391
Hereditary angioedema is a rare genetic disorder caused by deficiency of C1 esterase inhibitor (C1-INH) and characterized by recurrent ...
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59
Antisense Drug Slashed Hereditary Angioedema Attacks in ...
https://www.medpagetoday.com/allergyimmunology/allergy/97702
Donidalorsen acts by degrading the mRNA of plasma prekallikrein, a precursor to kallikrein. By the end of the 17-week study period, ...
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https://www.medpagetoday.com/allergyimmunology/allergy/97702
Donidalorsen acts by degrading the mRNA of plasma prekallikrein, a precursor to kallikrein. By the end of the 17-week study period, ...
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60
Hereditary angioedema: what the gastroenterologist needs to ...
https://www.dovepress.com/hereditary-angioedema-what-the-gastroenterologist-needs-to-know-peer-reviewed-fulltext-article-CEG
Because elevated levels of bradykinin are essential for the development of symptoms of HAE, inhibition of bradykinin release is an important ...
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https://www.dovepress.com/hereditary-angioedema-what-the-gastroenterologist-needs-to-know-peer-reviewed-fulltext-article-CEG
Because elevated levels of bradykinin are essential for the development of symptoms of HAE, inhibition of bradykinin release is an important ...
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61
Hereditary angioedema | DermNet
https://dermnetnz.org/topics/hereditary-angioedema
The most common type of hereditary angioedema is associated with a deficiency of functional C1-esterase inhibitor (C1-INH), a serine protease inhibitor that ...
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https://dermnetnz.org/topics/hereditary-angioedema
The most common type of hereditary angioedema is associated with a deficiency of functional C1-esterase inhibitor (C1-INH), a serine protease inhibitor that ...
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62
Hereditary angioedema: MedlinePlus Medical Encyclopedia
https://medlineplus.gov/ency/article/001456.htm
Hereditary angioedema (HAE) is caused by a low level or improper function of a protein called the C1 inhibitor. It affects the blood vessels ...
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https://medlineplus.gov/ency/article/001456.htm
Hereditary angioedema (HAE) is caused by a low level or improper function of a protein called the C1 inhibitor. It affects the blood vessels ...
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63
Oral Plasma Kallikrein Inhibitor for Prophylaxis in ... - sonar.ch
https://sonar.ch/global/documents/48427
Hereditary angioedema is a life-threatening illness caused by mutations in the gene encoding C1 inhibitor (also called C1 esterase inhibitor) that lead to ...
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https://sonar.ch/global/documents/48427
Hereditary angioedema is a life-threatening illness caused by mutations in the gene encoding C1 inhibitor (also called C1 esterase inhibitor) that lead to ...
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64
Hereditary and Acquired Angioedema - Merck Manuals
https://www.merckmanuals.com/professional/immunology-allergic-disorders/allergic,-autoimmune,-and-other-hypersensitivity-disorders/hereditary-and-acquired-angioedema
C1 inhibitor ; C1 inhibitor obtained from the milk of transgenic rabbits ; Ecallantide (a recombinant protein that acts as a reversible inhibitor of kallikrein).
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https://www.merckmanuals.com/professional/immunology-allergic-disorders/allergic,-autoimmune,-and-other-hypersensitivity-disorders/hereditary-and-acquired-angioedema
C1 inhibitor ; C1 inhibitor obtained from the milk of transgenic rabbits ; Ecallantide (a recombinant protein that acts as a reversible inhibitor of kallikrein).
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65
Overview of hereditary angioedema caused by C1-inhibitor ...
http://www.eurannallergyimm.com/cont/journals-articles/54/volume-overview-hereditary-angioedema-caused-cinhibitor-138allasp1.pdf
antagonists, and kallikrein-inhibitors, have become available for both treatment and pre- vention of angioedema attacks. This article reviews the clinical ...
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http://www.eurannallergyimm.com/cont/journals-articles/54/volume-overview-hereditary-angioedema-caused-cinhibitor-138allasp1.pdf
antagonists, and kallikrein-inhibitors, have become available for both treatment and pre- vention of angioedema attacks. This article reviews the clinical ...
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66
Hereditary Angioedema - Immunology - Medbullets Step 1
https://step1.medbullets.com/immunology/105011/hereditary-angioedema
C1 esterase inhibitor deficiency. C1 esterase inhibitor inhibits kallikrein-kinin pathway. remember kallikrein activates bradykinin; bradykinin.
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https://step1.medbullets.com/immunology/105011/hereditary-angioedema
C1 esterase inhibitor deficiency. C1 esterase inhibitor inhibits kallikrein-kinin pathway. remember kallikrein activates bradykinin; bradykinin.
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67
The Genetics of Hereditary Angioedema: A Review - MDPI
https://www.mdpi.com/2077-0383/10/9/2023/htm
C1 esterase inhibitor (C1-INH) is a major regulator of critical enzymes that are implicated in the cascades of bradykinin generation, which increases the ...
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https://www.mdpi.com/2077-0383/10/9/2023/htm
C1 esterase inhibitor (C1-INH) is a major regulator of critical enzymes that are implicated in the cascades of bradykinin generation, which increases the ...
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68
Oral plasma kallikrein inhibitor for prophylaxis in hereditary ...
https://portal.findresearcher.sdu.dk/en/publications/oral-plasma-kallikrein-inhibitor-for-prophylaxis-in-hereditary-an
BACKGROUND Hereditary angioedema is a life-threatening illness caused by mutations in the gene encoding C1 inhibitor (also called C1 esterase ...
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https://portal.findresearcher.sdu.dk/en/publications/oral-plasma-kallikrein-inhibitor-for-prophylaxis-in-hereditary-an
BACKGROUND Hereditary angioedema is a life-threatening illness caused by mutations in the gene encoding C1 inhibitor (also called C1 esterase ...
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69
Hereditary Angioedema (C1 Esterase Inhibitor Deficiency)
https://www.lecturio.com/concepts/hereditary-angioedema-c1-esterase-inhibitor-deficiency/
Hereditary angioedema (HAE), also known as C1 esterase inhibitor deficiency, is an autosomal dominant disorder characterized by recurrent ...
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https://www.lecturio.com/concepts/hereditary-angioedema-c1-esterase-inhibitor-deficiency/
Hereditary angioedema (HAE), also known as C1 esterase inhibitor deficiency, is an autosomal dominant disorder characterized by recurrent ...
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70
Hereditary Angioedema - BINASSS
https://www.binasss.sa.cr/feb22/31.pdf
Targeted treatment for acute HAE attacks focuses on decreasing the production of bra- dykinin through inhibition of kallikrein, and replacement of C1-INH, ...
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https://www.binasss.sa.cr/feb22/31.pdf
Targeted treatment for acute HAE attacks focuses on decreasing the production of bra- dykinin through inhibition of kallikrein, and replacement of C1-INH, ...
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71
Hereditary angioedema - A.D.A.M. Inc.
http://thnm.adam.com/content.aspx?productid=617&pid=1&gid=001456
Hereditary angioedema (HAE) is caused by a low level or improper function of a protein called the C1 inhibitor. It affects the blood vessels. An ...
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http://thnm.adam.com/content.aspx?productid=617&pid=1&gid=001456
Hereditary angioedema (HAE) is caused by a low level or improper function of a protein called the C1 inhibitor. It affects the blood vessels. An ...
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72
Astria Therapeutics Announces Initiation of Phase 1a Trial of ...
https://www.yahoo.com/now/astria-therapeutics-announces-initiation-phase-120000093.html
STAR-0215 is a monoclonal antibody inhibitor of plasma kallikrein designed to provide long-acting, effective attack prevention for hereditary ...
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https://www.yahoo.com/now/astria-therapeutics-announces-initiation-phase-120000093.html
STAR-0215 is a monoclonal antibody inhibitor of plasma kallikrein designed to provide long-acting, effective attack prevention for hereditary ...
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73
HAE Treatments - US Hereditary Angioedema Association
https://www.haea.org/pages/p/treatments
ORLADEYO® is a plasma kallikrein inhibitor indicated for routine prevention of HAE attacks in adults and pediatric patients 12 years and older. ORLADEYO is ...
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https://www.haea.org/pages/p/treatments
ORLADEYO® is a plasma kallikrein inhibitor indicated for routine prevention of HAE attacks in adults and pediatric patients 12 years and older. ORLADEYO is ...
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74
Hereditary Angioedema
https://www.clevelandclinicmeded.com/medicalpubs/diseasemanagement/allergy/hereditary-angioedema/
These factors are both inhibited by C1 inhibitor. Active plasma kallikrein induces production of bradykinin. In 2009, ecallantide (Kalbitor), a kallikrein– ...
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https://www.clevelandclinicmeded.com/medicalpubs/diseasemanagement/allergy/hereditary-angioedema/
These factors are both inhibited by C1 inhibitor. Active plasma kallikrein induces production of bradykinin. In 2009, ecallantide (Kalbitor), a kallikrein– ...
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75
Oral Plasma Kallikrein Inhibitor for Prophylaxis in ... - AIR Unimi
https://air.unimi.it/bitstream/2434/667175/2/NEJMoa1716995.pdf
Hereditary angioedema is a life-threatening illness caused by mutations in the gene encoding C1 inhibitor (also called C1 esterase inhibitor) ...
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https://air.unimi.it/bitstream/2434/667175/2/NEJMoa1716995.pdf
Hereditary angioedema is a life-threatening illness caused by mutations in the gene encoding C1 inhibitor (also called C1 esterase inhibitor) ...
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76
The Voice of the Patient - Hereditary Angioedema - FDA
https://www.fda.gov/files/about%20fda/published/The-Voice-of-the-Patient---Hereditary-Angioedema.pdf
by the FDA for the treatment or prophylaxis of HAE attacks. ... about by the treatments targeting C1-Esterase Inhibitor and kallikrein-bradykinin pathway.
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https://www.fda.gov/files/about%20fda/published/The-Voice-of-the-Patient---Hereditary-Angioedema.pdf
by the FDA for the treatment or prophylaxis of HAE attacks. ... about by the treatments targeting C1-Esterase Inhibitor and kallikrein-bradykinin pathway.
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77
Hereditary angioedema | British Society for Immunology
https://www.immunology.org/public-information/bitesized-immunology/immune-dysfunction/hereditary-angioedema
The vast majority of cases result from mutations affecting SERPING1 which encodes C1 esterase inhibitor (C1INH). Mutations can result in either low levels of ...
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https://www.immunology.org/public-information/bitesized-immunology/immune-dysfunction/hereditary-angioedema
The vast majority of cases result from mutations affecting SERPING1 which encodes C1 esterase inhibitor (C1INH). Mutations can result in either low levels of ...
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78
Hereditary Angioedema Market Snapshot: Room For Pills And ...
https://scrip.pharmaintelligence.informa.com/SC146260/Hereditary-Angioedema-Market-Snapshot-Room-For-Pills-And-Injections-As-Prophylaxis-Makes-Gains
The hereditary angioedema (HAE) market was shaken up last year by the launch of BioCryst Pharmaceuticals, Inc.'s plasma kallikrein inhibitor ...
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https://scrip.pharmaintelligence.informa.com/SC146260/Hereditary-Angioedema-Market-Snapshot-Room-For-Pills-And-Injections-As-Prophylaxis-Makes-Gains
The hereditary angioedema (HAE) market was shaken up last year by the launch of BioCryst Pharmaceuticals, Inc.'s plasma kallikrein inhibitor ...
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79
Hereditary angioedema | Lima Memorial Health System
https://www.limamemorial.org/health-library/HIE%20Multimedia-TextOnly/1/001456
Hereditary angioedema (HAE) is caused by a low level or improper function of a protein called the C1 inhibitor. It affects the blood vessels. An ...
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https://www.limamemorial.org/health-library/HIE%20Multimedia-TextOnly/1/001456
Hereditary angioedema (HAE) is caused by a low level or improper function of a protein called the C1 inhibitor. It affects the blood vessels. An ...
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80
Kallikrein Inhibition and Bradykinin Receptor Antagonism
https://www.worldallergyorganizationjournal.org/article/S1939-4551(19)30498-3/abstract
Hereditary angioedema (HAE) is a rare genetic condition caused by C1 esterase inhibitor (C1INH) deficiency and marked by episodic cutaneous, ...
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https://www.worldallergyorganizationjournal.org/article/S1939-4551(19)30498-3/abstract
Hereditary angioedema (HAE) is a rare genetic condition caused by C1 esterase inhibitor (C1INH) deficiency and marked by episodic cutaneous, ...
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81
Diagnosis and Treatment of Bradykinin-Mediated Angioedema
https://www.karger.com/Article/Fulltext/368404
Several treatments exist for HAE types I/II, including C1-INH, the β2 bradykinin receptor antagonist icatibant, and the kallikrein inhibitor ...
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https://www.karger.com/Article/Fulltext/368404
Several treatments exist for HAE types I/II, including C1-INH, the β2 bradykinin receptor antagonist icatibant, and the kallikrein inhibitor ...
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82
Ongoing Contact Activation in Patients with Hereditary ... - PLOS
https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0074043
Hereditary angioedema (HAE) is predominantly caused by a deficiency in C1 esterase inhibitor (C1INH) (HAE-C1INH).
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https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0074043
Hereditary angioedema (HAE) is predominantly caused by a deficiency in C1 esterase inhibitor (C1INH) (HAE-C1INH).
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83
(PDF) Inhibiting Plasma Kallikrein for Hereditary Angioedema ...
https://www.researchgate.net/publication/313902749_Inhibiting_Plasma_Kallikrein_for_Hereditary_Angioedema_Prophylaxis
Background: Hereditary angioedema with C1 inhibitor deficiency is characterized by recurrent, unpredictable swelling episodes caused by ...
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https://www.researchgate.net/publication/313902749_Inhibiting_Plasma_Kallikrein_for_Hereditary_Angioedema_Prophylaxis
Background: Hereditary angioedema with C1 inhibitor deficiency is characterized by recurrent, unpredictable swelling episodes caused by ...
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84
Recognizing and managing hereditary angioedema
https://www.ccjm.org/content/ccjom/80/5/297.full.pdf
kallikrein and activated factor XII. Without enough C1 inhibitor, the contact system is . Hereditary angioedema and its treatment.
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https://www.ccjm.org/content/ccjom/80/5/297.full.pdf
kallikrein and activated factor XII. Without enough C1 inhibitor, the contact system is . Hereditary angioedema and its treatment.
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85
The Interplay of COVID-19 and Hereditary Angioedema - Cureus
https://www.cureus.com/articles/109951-the-interplay-of-covid-19-and-hereditary-angioedema-preventing-an-acute-attack
Hereditary angioedema (HAE) is a rare inherited disease that is caused by the inactivation of the C1 esterase inhibitor.
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https://www.cureus.com/articles/109951-the-interplay-of-covid-19-and-hereditary-angioedema-preventing-an-acute-attack
Hereditary angioedema (HAE) is a rare inherited disease that is caused by the inactivation of the C1 esterase inhibitor.
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86
A Primer on Hereditary Angioedema - tl;dr pharmacy
https://www.tldrpharmacy.com/content/a-primer-on-hereditary-angioedema
Bradykinin-mediated angioedema is further divided into three subtypes: hereditary (Types I, II, III), acquired, and ACE inhibitor-associated.
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https://www.tldrpharmacy.com/content/a-primer-on-hereditary-angioedema
Bradykinin-mediated angioedema is further divided into three subtypes: hereditary (Types I, II, III), acquired, and ACE inhibitor-associated.
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87
Hereditary angioedema - Healthing.ca
https://www.healthing.ca/other/hereditary-angioedema
Hereditary angioedema (HAE) is caused by a low level or improper function of a protein called the C1 inhibitor. With HAE, the blood vessels ...
→ Check Latest Keyword Rankings ←
https://www.healthing.ca/other/hereditary-angioedema
Hereditary angioedema (HAE) is caused by a low level or improper function of a protein called the C1 inhibitor. With HAE, the blood vessels ...
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88
Hereditary angioedema: An update
https://ijdvl.com/hereditary-angioedema-an-update/
Hereditary angioedema (HAE) is a rare, autosomal dominant disorder of C1 inhibitor (C1-INH) deficiency manifested with any combination of cutaneous ...
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https://ijdvl.com/hereditary-angioedema-an-update/
Hereditary angioedema (HAE) is a rare, autosomal dominant disorder of C1 inhibitor (C1-INH) deficiency manifested with any combination of cutaneous ...
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89
Advances in the Pharmacotherapy of Hereditary Angioedema
https://www.uspharmacist.com/article/advances-in-the-pharmacotherapy-of-hereditary-angioedema
Ecallantide (Kalbitor): The kallikrein inhibitor ecallantide is supplied as three 10 mg SC injections to be administered consecutively as one ...
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https://www.uspharmacist.com/article/advances-in-the-pharmacotherapy-of-hereditary-angioedema
Ecallantide (Kalbitor): The kallikrein inhibitor ecallantide is supplied as three 10 mg SC injections to be administered consecutively as one ...
→ Check Latest Keyword Rankings ←
90
Hereditary angioedema - Read by QxMD
https://read.qxmd.com/read/16217168/hereditary-angioedema
PURPOSE OF REVIEW: Hereditary angioedema is an autosomal-dominant deficiency of C1 inhibitor--a serpin inhibitor of kallikrein, C1r, C1s, factor XII, ...
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https://read.qxmd.com/read/16217168/hereditary-angioedema
PURPOSE OF REVIEW: Hereditary angioedema is an autosomal-dominant deficiency of C1 inhibitor--a serpin inhibitor of kallikrein, C1r, C1s, factor XII, ...
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91
What Is the Best Management of Hereditary Angioedema?
https://www.the-hospitalist.org/hospitalist/article/125801/what-best-management-hereditary-angioedema
Hereditary angioedema (HAE) is an autosomal dominant condition characterized by intermittent mucocutaneous swelling episodes. · HAE is generally ...
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https://www.the-hospitalist.org/hospitalist/article/125801/what-best-management-hereditary-angioedema
Hereditary angioedema (HAE) is an autosomal dominant condition characterized by intermittent mucocutaneous swelling episodes. · HAE is generally ...
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92
Hereditary Angioedema: Causes, Symptoms, and Treatment
https://www.ankitparakh.com/hereditary-angioedema-causes-symptoms-and-treatment/
Hereditary angioedema (HAE) is caused by a low level or improper function of a protein called the C1 inhibitor. There are three types of ...
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https://www.ankitparakh.com/hereditary-angioedema-causes-symptoms-and-treatment/
Hereditary angioedema (HAE) is caused by a low level or improper function of a protein called the C1 inhibitor. There are three types of ...
→ Check Latest Keyword Rankings ←
93
Dr. Wim Souverijns, Pharvaris: Developing Novel Treatments ...
https://www.docwirenews.com/docwire-pick/dr-wim-souverijns-pharvaris-developing-novel-treatments-for-hereditary-angioedema/
Pharvaris is a clinical-stage company which develops novel therapies oral bradykinin B2-receptor antagonists to treat hereditary angioedema, ...
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https://www.docwirenews.com/docwire-pick/dr-wim-souverijns-pharvaris-developing-novel-treatments-for-hereditary-angioedema/
Pharvaris is a clinical-stage company which develops novel therapies oral bradykinin B2-receptor antagonists to treat hereditary angioedema, ...
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