Last Updated: September 27, 2026

Aphelion Company Profile


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What is the competitive landscape for APHELION

APHELION has one approved drug.

There are six US patents protecting APHELION drugs.

Summary for Aphelion
US Patents:6
Tradenames:1
Ingredients:1
NDAs:1

Drugs and US Patents for Aphelion

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Aphelion PYLARIFY TRUVU piflufolastat f-18 SOLUTION;INTRAVENOUS 220089-001 Mar 6, 2026 RX Yes Yes 11,851,407 ⤷  Start Trial Y Y ⤷  Start Trial
Aphelion PYLARIFY TRUVU piflufolastat f-18 SOLUTION;INTRAVENOUS 220089-001 Mar 6, 2026 RX Yes Yes 8,487,129 ⤷  Start Trial Y Y ⤷  Start Trial
Aphelion PYLARIFY TRUVU piflufolastat f-18 SOLUTION;INTRAVENOUS 220089-001 Mar 6, 2026 RX Yes Yes 12,070,513 ⤷  Start Trial Y Y ⤷  Start Trial
Aphelion PYLARIFY TRUVU piflufolastat f-18 SOLUTION;INTRAVENOUS 220089-001 Mar 6, 2026 RX Yes Yes 8,778,305 ⤷  Start Trial Y Y ⤷  Start Trial
Aphelion PYLARIFY TRUVU piflufolastat f-18 SOLUTION;INTRAVENOUS 220089-001 Mar 6, 2026 RX Yes Yes 9,861,713 ⤷  Start Trial Y Y ⤷  Start Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration

Supplementary Protection Certificates for Aphelion Drugs

Patent Number Supplementary Protection Certificate SPC Country SPC Expiration SPC Description
2318366 CR 2023 00032 Denmark ⤷  Start Trial PRODUCT NAME: PIFLUFOLASTAT (18F) ELLER ET FARMACEUTISK ACCEPTABELT SALT DERAF; REG. NO/DATE: EU/1/23/1746 20230725
2318366 PA2023534,C2318366 Lithuania ⤷  Start Trial PRODUCT NAME: PIFLUFOLASTATAS (18F) ARBA JO FARMACINIU POZIURIU PRIIMTINA DRUSKA; REGISTRATION NO/DATE: EU/1/23/1746 20230724
2318366 37/2023 Austria ⤷  Start Trial PRODUCT NAME: PIFLUFOLASTAT (18F) ODER EIN PHARMAZEUTISCH ANNEHMBARES SALZ DAVON; REGISTRATION NO/DATE: EU/1/23/1746 (MITTEILUNG) 20230725
2318366 202340025 Slovenia ⤷  Start Trial PRODUCT NAME: PIFLUFOLASTAT (18F) OR ITS PHARMACEUTICALLY ACCEPTABLE SALT; NATIONAL AUTHORISATION NUMBER: EU/1/23/1746; DATE OF NATIONAL AUTHORISATION: 20230724; AUTHORITY FOR NATIONAL AUTHORISATION: EU
2318366 301250 Netherlands ⤷  Start Trial PRODUCT NAME: PIFLUFOLASTAT (18F) OF EEN FARMACEUTISCH AANVAARDBAAR ZOUT DAARVAN; REGISTRATION NO/DATE: EU/1/23/1746 20230725
>Patent Number >Supplementary Protection Certificate >SPC Country >SPC Expiration >SPC Description
Similar Applicant Names
Applicants may be listed under multiple names.
Here is a list of applicants with similar names.

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Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.