Crizanlizumab: Difference between revisions

From Wikipedia, the free encyclopedia
Browse history interactively
← Previous edit
Content deleted Content added
VisualWikitext
update infobox
 
(33 intermediate revisions by 16 users not shown)
Line 1: Line 1:
{{Short description|Monoclonal antibody}}
{{Use dmy dates|date=November 2019}}
{{Use dmy dates|date=November 2019}}
{{Infobox drug
{{Infobox drug
⚫
| image =
⚫
| width =
⚫
| alt =
⚫
| caption =
| type = mab
| type = mab
⚫
| image =
⚫
| width =
⚫
| alt =
⚫
| caption =

<!-- Monoclonal antibody data -->
| mab_type = mab
| mab_type = mab
| source = zu
| source = zu
| target = [[selectin P]]
| target = [[selectin P]]

<!-- Clinical data -->
<!-- Clinical data -->
| pronounce =
| pronounce =
Line 16: Line 20:
| licence_CA = <!-- Health Canada may use generic or brand name (generic name preferred) -->
| licence_CA = <!-- Health Canada may use generic or brand name (generic name preferred) -->
| licence_EU = <!-- EMA uses INN (or special INN_EMA) -->
| licence_EU = <!-- EMA uses INN (or special INN_EMA) -->
| DailyMedID = Crizanlizumab
| DailyMedID = Crizanlizumab
| licence_US = Adakveo
| licence_US =
| pregnancy_AU = <!-- A/B1/B2/B3/C/D/X -->
| pregnancy_AU = B1
| pregnancy_AU_comment =
| pregnancy_AU_comment = <ref name="AusPAR: Crizanlizumab" /><ref name="Adakveo APM summary" />
⚫
| pregnancy_category=
⚫
| pregnancy_US = N
⚫
| routes_of_administration = [[Intravenous therapy|Intravenous]]
| pregnancy_US_comment = <ref name="Drugs.com pregnancy">{{cite web | title=Crizanlizumab (Adakveo) Use During Pregnancy | website=Drugs.com | date=4 December 2019 | url=https://www.drugs.com/pregnancy/crizanlizumab.html | access-date=23 January 2020}}</ref>
⚫
| class =
⚫
| pregnancy_category=
⚫
| ATCvet =
| dependency_liability =
| addiction_liability =
⚫
| routes_of_administration = IV
⚫
| class =
⚫
| ATCvet =
| ATC_prefix = B06
| ATC_prefix = B06
| ATC_suffix = AX01
| ATC_suffix = AX01
| ATC_supplemental =
| ATC_supplemental =
⚫
| biosimilars =

<!-- Legal status -->
<!-- Legal status -->
| legal_AU = <!-- S2, S3, S4, S5, S6, S7, S8, S9 or Unscheduled-->
| legal_AU = S4
| legal_AU_comment = <ref name="AusPAR: Crizanlizumab">{{cite web | title=AusPAR: Crizanlizumab | website=Therapeutic Goods Administration (TGA) | date=24 August 2021 | url=https://www.tga.gov.au/auspar/auspar-crizanlizumab | access-date=4 September 2021}}</ref><ref name="Adakveo APM summary">{{cite web | title=Adakveo | website=Therapeutic Goods Administration (TGA) | date=16 April 2021 | url=https://www.tga.gov.au/apm-summary/adakveo | access-date=6 September 2021}}</ref>
| legal_AU_comment =
| legal_BR = <!-- OTC, A1, A2, A3, B1, B2, C1, C2, C3, C4, C5, D1, D2, E, F-->
| legal_BR = <!-- OTC, A1, A2, A3, B1, B2, C1, C2, C3, C4, C5, D1, D2, E, F-->
| legal_BR_comment =
| legal_BR_comment =
| legal_CA = <!-- OTC, Rx-only, Schedule I, II, III, IV, V, VI, VII, VIII -->
| legal_CA = <!-- OTC, Rx-only, Schedule I, II, III, IV, V, VI, VII, VIII -->
| legal_CA_comment =
| legal_CA_comment =
| legal_DE = <!-- Anlage I, II, III or Unscheduled-->
| legal_DE = <!-- Anlage I, II, III or Unscheduled-->
| legal_DE_comment =
| legal_DE_comment =
| legal_NZ = <!-- Class A, B, C -->
| legal_NZ = <!-- Class A, B, C -->
| legal_NZ_comment =
| legal_NZ_comment =
| legal_UK = <!-- GSL, P, POM, CD, CD Lic, CD POM, CD No Reg POM, CD (Benz) POM, CD (Anab) POM or CD Inv POM / Class A, B, C -->
| legal_UK = <!-- GSL, P, POM, CD, CD Lic, CD POM, CD No Reg POM, CD (Benz) POM, CD (Anab) POM or CD Inv POM / Class A, B, C -->
| legal_UK_comment =
| legal_UK_comment =
| legal_US = Rx-only
| legal_US = Rx-only
| legal_US_comment = <ref name="Adakveo FDA label">{{cite web | title=Adakveo- crizanlizumab injection | website=DailyMed | date=8 September 2022 | url=https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b2b7f8b4-fe9a-4a86-8129-9e43f99a20c6 | access-date=4 March 2023}}</ref>
| legal_US_comment =
| legal_EU = Rx-only
| legal_EU_comment = <ref name="Adakveo EPAR">{{cite web | title=Adakveo EPAR | website=European Medicines Agency | date=20 July 2020 | url=https://www.ema.europa.eu/en/medicines/human/EPAR/adakveo | access-date=5 March 2023}} Text was copied from this source which is copyright European Medicines Agency. Reproduction is authorized provided the source is acknowledged.</ref><ref>{{cite web | title=Adakveo Product information | website=Union Register of medicinal products | url=https://ec.europa.eu/health/documents/community-register/html/h1476.htm | access-date=3 March 2023}}</ref>
| legal_UN = <!-- N I, II, III, IV / P I, II, III, IV-->
| legal_UN = <!-- N I, II, III, IV / P I, II, III, IV-->
| legal_UN_comment =
| legal_UN_comment =
| legal_status = <!--For countries not listed above-->
| legal_status = <!--For countries not listed above-->

<!-- Pharmacokinetic data -->
<!-- Pharmacokinetic data -->
| bioavailability =
| bioavailability =
| protein_bound =
| protein_bound =
| metabolism =
| metabolism =
| metabolites =
| metabolites =
| onset =
| onset =
| elimination_half-life =
| elimination_half-life =
| duration_of_action =
| duration_of_action =
| excretion =
| excretion =

<!-- Identifiers -->
<!-- Identifiers -->
| CAS_number = 1690318-25-2
| CAS_number = 1690318-25-2
| CAS_supplemental =
| CAS_supplemental =
| PubChem =
| PubChem =
⚫
| IUPHAR_ligand =
| PubChemSubstance = 384585456
⚫
| IUPHAR_ligand =
| DrugBank = DB15271
| DrugBank = DB15271
| ChemSpiderID = none
| ChemSpiderID = none
| UNII = L7451S9126
| UNII = L7451S9126
| KEGG = D11480
| KEGG = D11480
| ChEBI =
| ChEBI =
| ChEMBL =
| ChEMBL =
| NIAID_ChemDB =
| NIAID_ChemDB =
| PDB_ligand =
| PDB_ligand =
| synonyms = SEG101, SelG1, crizanlizumab-tmca
| synonyms = SEG101, SelG1, crizanlizumab-tmca

<!-- Chemical and physical data -->
<!-- Chemical and physical data -->
| IUPAC_name =
| IUPAC_name =
| C=6458 | H=9948 | N=1712 | O=2050 | S=58
| C=6458 | H=9948 | N=1712 | O=2050 | S=58
| SMILES =
| SMILES =
| StdInChI =
| StdInChI =
| StdInChI_comment =
| StdInChI_comment =
| StdInChIKey =
| StdInChIKey =
| density =
| density =
| density_notes =
| density_notes =
| melting_point =
| melting_point =
| melting_high =
| melting_high =
| melting_notes =
| melting_notes =
| boiling_point =
| boiling_point =
| boiling_notes =
| boiling_notes =
| solubility =
| solubility =
| sol_units =
| sol_units =
| specific_rotation =
| specific_rotation =
}}
}}


'''Crizanlizumab''', (brand name '''Adakveo'''), is a [[monoclonal antibody]] developed by [[Novartis]] targeted towards [[P-selectin]]. It was announced by the company as an effective drug to prevent [[vaso-occlusive crisis]] in patients with [[sickle cell anemia]]. The result of the Phase II SUSTAIN clinical trial was published in December 2016.<ref name=NEJM001>{{cite journal |vauthors=Ataga KI, Kutlar A, Kanter J, Liles D, Cancado R, Friedrisch J, Guthrie TH, Knight-Madden J, Alvarez OA, Gordeuk VR, Gualandro S, Colella MP, Smith WR, Rollins SA, Stocker JW, Rother RP |title=Crizanlizumab for the Prevention of Pain Crises in Sickle Cell Disease |journal=N. Engl. J. Med. |volume=376 |issue=5 |pages=429–439 |date=February 2017 |pmid=27959701 |pmc=5481200 |doi=10.1056/NEJMoa1611770 }}</ref>
'''Crizanlizumab''', sold under the brand name '''Adakveo''' among others, is a [[monoclonal antibody]] medication that binds to [[P-selectin]].<ref name="Adakveo FDA label" /> It is a medication used to reduce the frequency of [[vaso-occlusive crisis]] in people aged 16 years and older who have [[sickle cell anemia]].<ref name="Adakveo FDA label" /><ref name="Adakveo EPAR" /><ref name="FDA PR" /> It is given by injection into a vein.<ref name="Adakveo FDA label" /><ref name="Adakveo EPAR" />


The most common side effects include joint pain, nausea, back pain, fever and abdominal (belly) pain.<ref name="Adakveo EPAR" />
Crizanlizumab is a treatment to reduce the frequency of vaso-occlusive crisis – a common and painful complication of sickle cell disease that occurs when blood circulation is obstructed by sickled red blood cells – for those 16 years and older.<ref name="FDA PR" />


In November 2019, crizanlizumab-tmca was approved in the United States.<ref name="FDA PR">{{cite web | title=FDA approves first targeted therapy to treat patients with painful complication of sickle cell disease | website=U.S. [[Food and Drug Administration]] (FDA) | date=15 November 2019 | url=https://www.fda.gov/news-events/press-announcements/fda-approves-first-targeted-therapy-treat-patients-painful-complication-sickle-cell-disease | archive-url=https://web.archive.org/web/20191121062636/https://www.fda.gov/news-events/press-announcements/fda-approves-first-targeted-therapy-treat-patients-painful-complication-sickle-cell-disease | archive-date=21 November 2019 | url-status=live | access-date=20 November 2019}}{{PD-notice}}</ref><ref>{{cite web | title=Drug Approval Package: Adakveo (crizanlizumab-tmca) | website=U.S. [[Food and Drug Administration]] (FDA) | date=17 December 2019 | url=https://www.accessdata.fda.gov/drugsatfda_docs/nda/2019/761128Orig1s000TOC.cfm | access-date=22 January 2020}}</ref><ref name="FDA Snapshot">{{cite web | title=Drug Trials Snapshots Adakveo | website=U.S. [[Food and Drug Administration]] (FDA) | date=15 November 2019 | url=http://www.fda.gov/drugs/drug-approvals-and-databases/drug-trials-snapshots-adakveo | access-date=26 January 2020 | archive-url=https://web.archive.org/web/20200124193905/https://www.fda.gov/drugs/drug-approvals-and-databases/drug-trials-snapshots-adakveo | archive-date= 24 January 2020}} {{PD-notice}}</ref>
Crizanlizumab was approved for medical use in the United States in November 2019.<ref name="FDA PR">{{cite press release | title=FDA approves first targeted therapy to treat patients with painful complication of sickle cell disease | website=U.S. [[Food and Drug Administration]] (FDA) | date=15 November 2019 | url=https://www.fda.gov/news-events/press-announcements/fda-approves-first-targeted-therapy-treat-patients-painful-complication-sickle-cell-disease | archive-url=https://web.archive.org/web/20191121062636/https://www.fda.gov/news-events/press-announcements/fda-approves-first-targeted-therapy-treat-patients-painful-complication-sickle-cell-disease | archive-date=21 November 2019 | url-status=live | access-date=20 November 2019}}{{PD-notice}}</ref><ref>{{cite web | title=Drug Approval Package: Adakveo (crizanlizumab-tmca) | website=U.S. [[Food and Drug Administration]] (FDA) | date=17 December 2019 | url=https://www.accessdata.fda.gov/drugsatfda_docs/nda/2019/761128Orig1s000TOC.cfm | access-date=22 January 2020}}</ref><ref name="FDA Snapshot">{{cite web | title=Drug Trials Snapshots Adakveo | website=U.S. [[Food and Drug Administration]] (FDA) | date=15 November 2019 | url=http://www.fda.gov/drugs/drug-approvals-and-databases/drug-trials-snapshots-adakveo | access-date=26 January 2020 | archive-url=https://web.archive.org/web/20200124193905/https://www.fda.gov/drugs/drug-approvals-and-databases/drug-trials-snapshots-adakveo | archive-date= 24 January 2020}} {{PD-notice}}</ref> The EU's EMA withdrew authorization in May 2023 based on no significant effects from a phase 3 trial.<ref>{{Cite web |title=Novartis sickle cell drug's approval formally revoked by EU regulators |url=https://www.biopharmadive.com/news/novartis-adakveo-europe-revoke-withdraw-sickle-cell/690000/ |access-date=2023-08-19 |website=BioPharma Dive |language=en-US}}</ref> The U.S. [[Food and Drug Administration]] (FDA) considers it to be a [[first-in-class medication]].<ref>{{cite web | title=New Drug Therapy Approvals 2019 | website=U.S. Food and Drug Administration | date=31 December 2019 | url=https://www.fda.gov/drugs/new-drugs-fda-cders-new-molecular-entities-and-new-therapeutic-biological-products/new-drug-therapy-approvals-2019 | access-date=15 September 2020}}</ref>

== Medical uses ==
Crizanlizumab is [[indicated]] for the prevention of recurrent vaso occlusive crises in sickle cell disease patients aged 16 years and older.<ref name="Adakveo EPAR" /> It can be given as an add on therapy to hydroxyurea/hydroxycarbamide (HU/HC) or as monotherapy in patients for whom HU/HC is inappropriate or inadequate.<ref name="Adakveo FDA label" /><ref name="Adakveo EPAR" />

Vaso-occlusive crisis is a common and painful complication of sickle cell disease that occurs when blood circulation is obstructed by sickled red blood cells (red cells are usually round and flexible, but sometimes many red cells in a person with sickle cell anemia will become rigid and crescent-shaped due to [[polymerization]] of hemoglobin).<ref>{{cite journal | vauthors = Darbari DS, Sheehan VA, Ballas SK | title = The vaso-occlusive pain crisis in sickle cell disease: Definition, pathophysiology, and management | journal = European Journal of Haematology | volume = 105 | issue = 3 | pages = 237–246 | date = September 2020 | pmid = 32301178 | doi = 10.1111/ejh.13430 | s2cid = 215801719 | doi-access = free }}</ref>


==Pathophysiology==
==Pathophysiology==
[[P-selectin]] molecules are present on the surface of vascular [[endothelial cell]]s and have been linked to sickle cell vaso-occlusive crises.<ref>{{cite journal |vauthors=Manwani D, Frenette PS |title=Vaso-occlusion in sickle cell disease: pathophysiology and novel targeted therapies |journal=Blood |volume=122 |issue=24 |pages=3892–8 |date=December 2013 |pmid=24052549 |pmc=3854110 |doi=10.1182/blood-2013-05-498311 }}</ref><ref>{{cite journal |vauthors=Manwani D, Frenette PS |title=Vaso-occlusion in sickle cell disease: pathophysiology and novel targeted therapies |journal=Hematology Am Soc Hematol Educ Program |volume=2013 |issue= |pages=362–9 |date=December 2013 |pmid=24319205 |doi=10.1182/asheducation-2013.1.362 |pmc=3854110 }}</ref><ref>{{cite journal |vauthors=Riley TR, Boss A, McClain D, Riley TT |title=Review of Medication Therapy for the Prevention of Sickle Cell Crisis |journal=P T |volume=43 |issue=7 |pages=417–437 |date=July 2018 |pmid=30013299 |pmc=6027858 |doi= }}</ref>
[[P-selectin]] molecules are present on the surface of activated platelets and vascular [[endothelial cell]]s and have been linked to sickle cell vaso-occlusive crises.<ref>{{cite journal | vauthors = Manwani D, Frenette PS | title = Vaso-occlusion in sickle cell disease: pathophysiology and novel targeted therapies | journal = Blood | volume = 122 | issue = 24 | pages = 3892–3898 | date = December 2013 | pmid = 24052549 | pmc = 3854110 | doi = 10.1182/blood-2013-05-498311 }}</ref><ref>{{cite journal | vauthors = Manwani D, Frenette PS | title = Vaso-occlusion in sickle cell disease: pathophysiology and novel targeted therapies | journal = Hematology. American Society of Hematology. Education Program | volume = 2013 | pages = 362–369 | date = December 2013 | pmid = 24319205 | pmc = 3854110 | doi = 10.1182/asheducation-2013.1.362 }}</ref><ref>{{cite journal | vauthors = Riley TR, Boss A, McClain D, Riley TT | title = Review of Medication Therapy for the Prevention of Sickle Cell Crisis | journal = P & T | volume = 43 | issue = 7 | pages = 417–437 | date = July 2018 | pmid = 30013299 | pmc = 6027858 }}</ref>


==History==
==History==
The U.S. [[Food and Drug Administration]] (FDA) approved crizanlizumab based on evidence from one clinical trial (Trial 1/NCT01895361) of 132 patients with sickle cell diseases who had a history of vaso-occlusive crisis.<ref name="FDA Snapshot" /> The trial was conducted at 60 sites in the United States, Brazil and Jamaica.<ref name="FDA Snapshot" />
The US [[Food and Drug Administration]] (FDA) approved crizanlizumab based on evidence from one clinical trial (Trial 1/NCT01895361) of 132 participants with sickle cell diseases who had a history of vaso-occlusive crisis.<ref name="FDA Snapshot" /> The trial was conducted at 60 sites in the United States, Brazil and Jamaica.<ref name="FDA Snapshot" />


The FDA granted the application for crizanlizumab-tmca [[priority review]], [[breakthrough therapy]] designation, and [[orphan drug]] designation.<ref name="FDA PR" /> The FDA granted approval of Adakveo to Novartis.<ref name="FDA PR" /><ref name="FDA Snapshot" />
The FDA granted the application for crizanlizumab [[priority review]], [[breakthrough therapy]] designation, and [[orphan drug]] designation.<ref name="FDA PR" /> The FDA granted approval of Adakveo to [[Novartis]].<ref name="FDA PR" /><ref name="FDA Snapshot" />


The European Medicines Agency's human medicines committee (CHMP) has recommended the withdrawal of Adakveo (crizanlizumab), a medicine for preventing vaso-occlusive crises in patients with sickle cell disease, due to the lack of sufficient benefits outweighing the risks.<ref>{{Cite press release |last=EMA |date=2023-05-26 |title=EMA recommends revocation of authorisation for sickle cell disease medicine Adakveo |url=https://www.ema.europa.eu/en/news/ema-recommends-revocation-authorisation-sickle-cell-disease-medicine-adakveo |access-date=2023-05-26 |website=European Medicines Agency }}</ref> The STAND phase III study showed that Adakveo does not effectively reduce the number of painful crises requiring healthcare visits or treatment at home compared to a placebo, and it exhibits a higher rate of severe side effects.<ref>{{Cite press release |title=Novartis provides update on Phase III STAND trial assessing crizanlizumab |url=https://www.novartis.com/news/novartis-provides-update-phase-iii-stand-trial-assessing-crizanlizumab |access-date=2023-05-26 |website=Novartis }}</ref><ref>{{Cite press release |date=2023-05-26 |title=EMA recommends revocation of authorisation for sickle cell disease medicine Adakveo |url=https://www.ema.europa.eu/en/news/ema-recommends-revocation-authorisation-sickle-cell-disease-medicine-adakveo |access-date=2023-05-26 |website=European Medicines Agency }}</ref>
⚫
==References==

⚫
== References ==
{{Reflist}}
{{Reflist}}


==External links==
== External links ==
* {{ClinicalTrialsGov|NCT01895361|Study to Assess Safety and Impact of SelG1 With or Without Hydroxyurea Therapy in Sickle Cell Disease Patients With Pain Crises (SUSTAIN)}}
* {{cite web| url = https://druginfo.nlm.nih.gov/drugportal/name/crizanlizumab | publisher = U.S. National Library of Medicine| work = Drug Information Portal| title = Crizanlizumab }}


{{monoclonals for immune system}}
{{Monoclonals for immune system}}
{{Portal bar | Medicine}}
{{Portal bar | Medicine}}


[[Category:Breakthrough therapy]]
[[Category:Hematology]]
[[Category:Hematology]]
[[Category:Monoclonal antibodies]]
[[Category:Monoclonal antibodies]]
[[Category:Orphan drugs]]
[[Category:Orphan drugs]]
[[Category:Sickle-cell disease]]
[[Category:Sickle-cell disease]]



{{blood-drug-stub}}
{{blood-drug-stub}}

Latest revision as of 11:43, 12 December 2023

Crizanlizumab
Monoclonal antibody
TypeWhole antibody
SourceHumanized
Targetselectin P
Clinical data
Trade namesAdakveo
Other namesSEG101, SelG1, crizanlizumab-tmca
AHFS/Drugs.comMonograph
MedlinePlusa620010
License data
Pregnancy
category
Routes of
administration		Intravenous
ATC code
Legal status
Legal status
Identifiers
CAS Number
DrugBank
ChemSpider
  • none
UNII
KEGG
Chemical and physical data
FormulaC6458H9948N1712O2050S58
Molar mass146232.04 g·mol−1

Crizanlizumab, sold under the brand name Adakveo among others, is a monoclonal antibody medication that binds to P-selectin.[3] It is a medication used to reduce the frequency of vaso-occlusive crisis in people aged 16 years and older who have sickle cell anemia.[3][4][6] It is given by injection into a vein.[3][4]

The most common side effects include joint pain, nausea, back pain, fever and abdominal (belly) pain.[4]

Crizanlizumab was approved for medical use in the United States in November 2019.[6][7][8] The EU's EMA withdrew authorization in May 2023 based on no significant effects from a phase 3 trial.[9] The U.S. Food and Drug Administration (FDA) considers it to be a first-in-class medication.[10]

Medical uses[edit]

Crizanlizumab is indicated for the prevention of recurrent vaso occlusive crises in sickle cell disease patients aged 16 years and older.[4] It can be given as an add on therapy to hydroxyurea/hydroxycarbamide (HU/HC) or as monotherapy in patients for whom HU/HC is inappropriate or inadequate.[3][4]

Vaso-occlusive crisis is a common and painful complication of sickle cell disease that occurs when blood circulation is obstructed by sickled red blood cells (red cells are usually round and flexible, but sometimes many red cells in a person with sickle cell anemia will become rigid and crescent-shaped due to polymerization of hemoglobin).[11]

Pathophysiology[edit]

P-selectin molecules are present on the surface of activated platelets and vascular endothelial cells and have been linked to sickle cell vaso-occlusive crises.[12][13][14]

History[edit]

The US Food and Drug Administration (FDA) approved crizanlizumab based on evidence from one clinical trial (Trial 1/NCT01895361) of 132 participants with sickle cell diseases who had a history of vaso-occlusive crisis.[8] The trial was conducted at 60 sites in the United States, Brazil and Jamaica.[8]

The FDA granted the application for crizanlizumab priority review, breakthrough therapy designation, and orphan drug designation.[6] The FDA granted approval of Adakveo to Novartis.[6][8]

The European Medicines Agency's human medicines committee (CHMP) has recommended the withdrawal of Adakveo (crizanlizumab), a medicine for preventing vaso-occlusive crises in patients with sickle cell disease, due to the lack of sufficient benefits outweighing the risks.[15] The STAND phase III study showed that Adakveo does not effectively reduce the number of painful crises requiring healthcare visits or treatment at home compared to a placebo, and it exhibits a higher rate of severe side effects.[16][17]

References[edit]

  1. ^ a b "AusPAR: Crizanlizumab". Therapeutic Goods Administration (TGA). 24 August 2021. Retrieved 4 September 2021.
  2. ^ a b "Adakveo". Therapeutic Goods Administration (TGA). 16 April 2021. Retrieved 6 September 2021.
  3. ^ a b c d e "Adakveo- crizanlizumab injection". DailyMed. 8 September 2022. Retrieved 4 March 2023.
  4. ^ a b c d e f "Adakveo EPAR". European Medicines Agency. 20 July 2020. Retrieved 5 March 2023. Text was copied from this source which is copyright European Medicines Agency. Reproduction is authorized provided the source is acknowledged.
  5. ^ "Adakveo Product information". Union Register of medicinal products. Retrieved 3 March 2023.
  6. ^ a b c d "FDA approves first targeted therapy to treat patients with painful complication of sickle cell disease". U.S. Food and Drug Administration (FDA) (Press release). 15 November 2019. Archived from the original on 21 November 2019. Retrieved 20 November 2019.Public Domain This article incorporates text from this source, which is in the public domain.
  7. ^ "Drug Approval Package: Adakveo (crizanlizumab-tmca)". U.S. Food and Drug Administration (FDA). 17 December 2019. Retrieved 22 January 2020.
  8. ^ a b c d "Drug Trials Snapshots Adakveo". U.S. Food and Drug Administration (FDA). 15 November 2019. Archived from the original on 24 January 2020. Retrieved 26 January 2020. Public Domain This article incorporates text from this source, which is in the public domain.
  9. ^ "Novartis sickle cell drug's approval formally revoked by EU regulators". BioPharma Dive. Retrieved 19 August 2023.
  10. ^ "New Drug Therapy Approvals 2019". U.S. Food and Drug Administration. 31 December 2019. Retrieved 15 September 2020.
  11. ^ Darbari DS, Sheehan VA, Ballas SK (September 2020). "The vaso-occlusive pain crisis in sickle cell disease: Definition, pathophysiology, and management". European Journal of Haematology. 105 (3): 237–246. doi:10.1111/ejh.13430. PMID 32301178. S2CID 215801719.
  12. ^ Manwani D, Frenette PS (December 2013). "Vaso-occlusion in sickle cell disease: pathophysiology and novel targeted therapies". Blood. 122 (24): 3892–3898. doi:10.1182/blood-2013-05-498311. PMC 3854110. PMID 24052549.
  13. ^ Manwani D, Frenette PS (December 2013). "Vaso-occlusion in sickle cell disease: pathophysiology and novel targeted therapies". Hematology. American Society of Hematology. Education Program. 2013: 362–369. doi:10.1182/asheducation-2013.1.362. PMC 3854110. PMID 24319205.
  14. ^ Riley TR, Boss A, McClain D, Riley TT (July 2018). "Review of Medication Therapy for the Prevention of Sickle Cell Crisis". P & T. 43 (7): 417–437. PMC 6027858. PMID 30013299.
  15. ^ EMA (26 May 2023). "EMA recommends revocation of authorisation for sickle cell disease medicine Adakveo". European Medicines Agency (Press release). Retrieved 26 May 2023.
  16. ^ "Novartis provides update on Phase III STAND trial assessing crizanlizumab". Novartis (Press release). Retrieved 26 May 2023.
  17. ^ "EMA recommends revocation of authorisation for sickle cell disease medicine Adakveo". European Medicines Agency (Press release). 26 May 2023. Retrieved 26 May 2023.

External links[edit]

  • Clinical trial number NCT01895361 for "Study to Assess Safety and Impact of SelG1 With or Without Hydroxyurea Therapy in Sickle Cell Disease Patients With Pain Crises (SUSTAIN)" at ClinicalTrials.gov
Stub icon

This drug article relating to the blood and blood forming organs is a stub. You can help Wikipedia by expanding it.

Retrieved from "https://en.wikipedia.org/w/index.php?title=Crizanlizumab&oldid=1189528359"