Berotralstat
Names | |
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Trade names | Orladeyo |
Other names | BCX7353, BCX-7353 |
IUPAC name
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Clinical data | |
Drug class | Plasma kallikrein inhibitor |
Main uses | Hereditary angioedema (HAE)[1] |
Side effects | Abdominal pain, vomiting, diarrhea, back pain, heartburn[1] |
WHO AWaRe | UnlinkedWikibase error: ⧼unlinkedwikibase-error-statements-entity-not-set⧽ |
Routes of use | By mouth |
Typical dose | 150 mg OD[1] |
External links | |
AHFS/Drugs.com | Monograph |
Legal | |
License data |
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Legal status | |
Chemical and physical data | |
Formula | C30H26F4N6O |
Molar mass | 562.573 g·mol−1 |
3D model (JSmol) | |
SMILES
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InChI
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Berotralstat, sold under the brand name Orladeyo, is a medication used to prevent attacks of hereditary angioedema (HAE).[1] It is used in people aged twelve years and older.[1] It is taken by mouth.[1]
Common side effects include abdominal pain, vomiting, diarrhea, back pain, and heartburn.[1] Other side effects may include QT prolongation.[1] While there is no evidence of harm in pregnancy, such use has not been well studied.[1] It is a plasma kallikrein inhibitor.[1]
Berotralstat was approved for medical use in the United States in 2020 and Europe in 2021.[1][4] In the United Kingdom 4 weeks costs the NHS about £10,200 as of 2022.[5] This amount in the United States costs about 40,500 USD.[6]
Medical uses
It is used to prevent attacks of hereditary angioedema (HAE).[1] It decreases the rate of attacks from about 2.4 per month on placebo to 1.3 with treatment.[4]
Dosage
It is generally taken at a dose of 150 mg once per day.[1]
History
Berotralstat was approved based on evidence from one clinical trial (Trial 1 /NCT03485911) of 120 participants with hereditary angioedema.[3] The trial was conducted at 40 sites in the United States, the European Union, and Canada.[3] Trial investigators evaluated participants 12 years and older[7] with hereditary angioedema for eight weeks to determine the number of attacks for each participant.[3] The trial enrolled only participants who had at least two attacks during the eight-week period.[3] Participants were assigned to receive one of two doses of berotralstat or placebo once every day for 24 weeks.[3] Neither the participants nor the investigators knew which treatment was being given until after the trial was completed.[3] All participants could use other medications for treatment of attacks.[3]
References
- 1 2 3 4 5 6 7 8 9 10 11 12 13 14 "Orladeyo- berotralstat hydrochloride capsule". DailyMed. Archived from the original on 1 November 2022. Retrieved 25 December 2020.
- ↑ https://pdf.hres.ca/dpd_pm/00066149.PDF Archived 1 October 2022 at the Wayback Machine
- 1 2 3 4 5 6 7 8 "Drug Trials Snapshot: Orladeyo". U.S. Food and Drug Administration. 3 December 2020. Archived from the original on 24 October 2021. Retrieved 25 December 2020. This article incorporates text from this source, which is in the public domain.
- 1 2 3 "Orladeyo EPAR". European Medicines Agency (EMA). 24 February 2021. Archived from the original on 12 July 2021. Retrieved 12 July 2021.
- ↑ "Berotralstat". SPS - Specialist Pharmacy Service. 21 July 2018. Archived from the original on 12 December 2021. Retrieved 3 November 2022.
- ↑ "Orladeyo Prices, Coupons, Copay & Patient Assistance". Drugs.com. Archived from the original on 21 May 2022. Retrieved 3 November 2022.
- ↑ "Berotralstat (Oral Route) Side Effects - Mayo Clinic". www.mayoclinic.org. Archived from the original on 17 April 2021. Retrieved 3 March 2021.
External links
External sites: |
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Identifiers: |
- Clinical trial number NCT03485911 for "Efficacy and Safety Study of BCX7353 as an Oral Treatment for the Prevention of Attacks in HAE (APeX-2)" at ClinicalTrials.gov