Chiesi Company Profile
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What is the competitive landscape for CHIESI
CHIESI has fifteen approved drugs.
There are fifty-three US patents protecting CHIESI drugs.
Summary for Chiesi
| US Patents: | 53 |
| Tradenames: | 16 |
| Ingredients: | 10 |
| NDAs: | 15 |
| Patent Litigation for Chiesi: | See patent lawsuits for Chiesi |
Drugs and US Patents for Chiesi
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Chiesi | CARDENE IN 5.0% DEXTROSE IN PLASTIC CONTAINER | nicardipine hydrochloride | INJECTABLE;INTRAVENOUS | 019734-005 | Nov 7, 2008 | DISCN | Yes | No | 8,455,524 | ⤷ Start Trial | ⤷ Start Trial | ||||
| Chiesi | MYCAPSSA | octreotide acetate | CAPSULE, DELAYED RELEASE;ORAL | 208232-001 | Jun 26, 2020 | RX | Yes | Yes | 8,329,198 | ⤷ Start Trial | Y | ⤷ Start Trial | |||
| Chiesi | FERRIPROX | deferiprone | TABLET;ORAL | 212269-001 | May 19, 2020 | RX | Yes | Yes | 10,940,116 | ⤷ Start Trial | Y | ⤷ Start Trial | |||
| Chiesi | CARDENE SR | nicardipine hydrochloride | CAPSULE, EXTENDED RELEASE;ORAL | 020005-002 | Feb 21, 1992 | DISCN | Yes | No | ⤷ Start Trial | ⤷ Start Trial | |||||
| Chiesi | CARDENE | nicardipine hydrochloride | INJECTABLE;INJECTION | 019734-001 | Jan 30, 1992 | AP | RX | Yes | No | ⤷ Start Trial | ⤷ Start Trial | ||||
| Chiesi | JUXTAPID | lomitapide mesylate | CAPSULE;ORAL | 203858-004 | Apr 23, 2015 | RX | Yes | Yes | 7,932,268 | ⤷ Start Trial | ⤷ Start Trial | ||||
| >Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >TE | >Type | >RLD | >RS | >Patent No. | >Patent Expiration | >Product | >Substance | >Delist Req. | >Exclusivity Expiration |
Expired US Patents for Chiesi
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | Patent No. | Patent Expiration |
|---|---|---|---|---|---|---|---|
| Chiesi | JUXTAPID | lomitapide mesylate | CAPSULE;ORAL | 203858-006 | Apr 23, 2015 | 10,555,938 | ⤷ Start Trial |
| Chiesi | ZYFLO CR | zileuton | TABLET, EXTENDED RELEASE;ORAL | 022052-001 | May 30, 2007 | 5,422,123 | ⤷ Start Trial |
| Chiesi | JUXTAPID | lomitapide mesylate | CAPSULE;ORAL | 203858-001 | Dec 21, 2012 | 10,555,938 | ⤷ Start Trial |
| Chiesi | JUXTAPID | lomitapide mesylate | CAPSULE;ORAL | 203858-002 | Dec 21, 2012 | 9,433,617 | ⤷ Start Trial |
| Chiesi | JUXTAPID | lomitapide mesylate | CAPSULE;ORAL | 203858-002 | Dec 21, 2012 | 9,265,758 | ⤷ Start Trial |
| Chiesi | JUXTAPID | lomitapide mesylate | CAPSULE;ORAL | 203858-003 | Dec 21, 2012 | 10,016,404 | ⤷ Start Trial |
| >Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >Patent No. | >Patent Expiration |
Paragraph IV (Patent) Challenges for CHIESI drugs
| Drugname | Dosage | Strength | Tradename | Submissiondate |
|---|---|---|---|---|
| ➤ Subscribe | Injection | 2.5 mg/mL, 10 mL Ampoules | ➤ Subscribe | 2006-12-27 |
| ➤ Subscribe | Inhalation Solution | 300 mg/4 mL | ➤ Subscribe | 2017-08-31 |
| ➤ Subscribe | Injection | 0.1 mg/mL, 200 mL and0.2mg/mL, 200 mL | ➤ Subscribe | 2013-06-20 |
| ➤ Subscribe | Tablets | 500 mg | ➤ Subscribe | 2016-01-29 |
International Patents for Chiesi Drugs
| Country | Patent Number | Estimated Expiration |
|---|---|---|
| Denmark | 2504012 | ⤷ Start Trial |
| New Zealand | 734894 | ⤷ Start Trial |
| Croatia | P20200445 | ⤷ Start Trial |
| Eurasian Patent Organization | 033227 | ⤷ Start Trial |
| Mexico | 2008013407 | ⤷ Start Trial |
| Russian Federation | 2015112963 | ⤷ Start Trial |
| >Country | >Patent Number | >Estimated Expiration |
Supplementary Protection Certificates for Chiesi Drugs
| Patent Number | Supplementary Protection Certificate | SPC Country | SPC Expiration | SPC Description |
|---|---|---|---|---|
| 1725234 | 2014C/002 | Belgium | ⤷ Start Trial | PRODUCT NAME: LOMITAPIDE ET TOUTE FORME THERAPEUTIQUEMENT EQUIVALENTE TELLE QUE PROTEGEE PAR LE BREVET DE BASE; AUTHORISATION NUMBER AND DATE: EU/1/13/851/001 20130805 |
| 1725234 | C 2014 003 | Romania | ⤷ Start Trial | PRODUCT NAME: LOMITAPIDA SAU O SARE ACCEPTABILA FARMACEUTIC SAU PIPERIDIN-N-OXIDUL ACESTEIA; NATIONAL AUTHORISATION NUMBER: EU/1/13/851/001-003; DATE OF NATIONAL AUTHORISATION: 20130731; NUMBER OF FIRST AUTHORISATION IN EUROPEAN ECONOMIC AREA (EEA): EU/1/13/851/001-003; DATE OF FIRST AUTHORISATION IN EEA: 20130731 |
| 3089735 | C03089735/01 | Switzerland | ⤷ Start Trial | PRODUCT NAME: GLYCOPYRRONIUMBROMID, FORMOTEROLFUMARAT-DIHYDRAT UND BECLOMETASONDIPROPIONAT; REGISTRATION NO/DATE: SWISSMEDIC-ZULASSUNG 67223 06.05.2020 |
| 1758555 | 641 | Finland | ⤷ Start Trial | |
| 2515855 | 314 50020-2017 | Slovakia | ⤷ Start Trial | PRODUCT NAME: GLYKOPYRONIUMBROMID/FORMOTEROL VO VSETKYCH FORMACH CHRANENYCH ZAKLADNYM PATENTOM/- BEKLOMETAZONDIPROPIONAT; REGISTRATION NO/DATE: EU/1/17/1208 20170717 |
| 2515855 | 2018/002 | Ireland | ⤷ Start Trial | PRODUCT NAME: A COMBINATION OF GLYCOPYRRONIUM BROMIDE, FORMOTEROL OR A SALT THEREOF AND BECLOMETASONE DIPROPIONATE.; REGISTRATION NO/DATE: EU/1/17/1208 20170717 |
| >Patent Number | >Supplementary Protection Certificate | >SPC Country | >SPC Expiration | >SPC Description |
Similar Applicant Names
Here is a list of applicants with similar names.

