Chiesi Company Profile
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 0.86% SODIUM CHLORIDE IN PLASTIC CONTAINER | nicardipine hydrochloride | INJECTABLE;INTRAVENOUS | 019734-003 | Jul 31, 2008 | AP | RX | Yes | Yes | 8,455,524 | ⤷ Start Trial | ⤷ Start Trial | |||
| Chiesi | CARDENE SR | nicardipine hydrochloride | CAPSULE, EXTENDED RELEASE;ORAL | 020005-001 | Feb 21, 1992 | DISCN | Yes | No | ⤷ Start Trial | ⤷ Start Trial | |||||
| Chiesi | FILSUVEZ | birch triterpenes | GEL;TOPICAL | 215064-001 | Dec 18, 2023 | RX | Yes | Yes | ⤷ Start Trial | ⤷ Start Trial | |||||
| Chiesi | ZYFLO CR | zileuton | TABLET, EXTENDED RELEASE;ORAL | 022052-001 | May 30, 2007 | DISCN | Yes | No | ⤷ 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 | CARDENE | nicardipine hydrochloride | CAPSULE;ORAL | 019488-001 | Dec 21, 1988 | 3,985,758 | ⤷ Start Trial |
| Chiesi | JUXTAPID | lomitapide mesylate | CAPSULE;ORAL | 203858-006 | Apr 23, 2015 | 10,016,404 | ⤷ Start Trial |
| Chiesi | JUXTAPID | lomitapide mesylate | CAPSULE;ORAL | 203858-003 | Dec 21, 2012 | 10,555,938 | ⤷ Start Trial |
| Chiesi | CLEVIPREX | clevidipine | EMULSION;INTRAVENOUS | 022156-001 | Aug 1, 2008 | 5,856,346 | ⤷ 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 | Tablets | 500 mg | ➤ Subscribe | 2016-01-29 |
| ➤ 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 |
International Patents for Chiesi Drugs
| Country | Patent Number | Estimated Expiration |
|---|---|---|
| Canada | 2975599 | ⤷ Start Trial |
| Moldova, Republic of | 3253401 | ⤷ Start Trial |
| World Intellectual Property Organization (WIPO) | 2009140407 | ⤷ Start Trial |
| Israel | 245172 | ⤷ 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 | 132014902228079 | Italy | ⤷ Start Trial | PRODUCT NAME: LOMITAPIDE E OGNI SUA FORMA TERAPEUTICAMENTE EQUIVALENTE COME PROTETTA DAL BREVETTO BASE(LOJUXTA); AUTHORISATION NUMBER(S) AND DATE(S): EU/1/13/851/001/-003, 20130805 |
| 2515855 | 201740046 | Slovenia | ⤷ Start Trial | PRODUCT NAME: COMBINATION OF GLYCOPYRRONIUM BROMIDE, FORMOTEROL OR ITS SALT AND BECLOMETASONE DIPROPIONATE; NATIONAL AUTHORISATION NUMBER: EU/1/17/1208/001-005; DATE OF NATIONAL AUTHORISATION: 20170717; AUTHORITY FOR NATIONAL AUTHORISATION: EU |
| 2515855 | LUC00060 | Luxembourg | ⤷ Start Trial | PRODUCT NAME: COMBINAISON DE BROMURE DE GLYCOPYRRONIUM, FORMOTEROL OU UN SEL DE CELUI-CI ET DIPROPIONATE DE BECLOMETASONE; AUTHORISATION NUMBER AND DATE: EU/1/17/1208 20170719 |
| 2515855 | 1890005-0 | Sweden | ⤷ Start Trial | PRODUCT NAME: A COMBINATION OF GLYCOPYRRONIUM BROMIDE, FORMOTEROL OR A SALT THEREOF AND BECLOMETASONE DIPROPIONATE.; FIRST MARKETING AUTHORIZATION NUMBER SE: EG EU/1/17/1208, 2017-07-19; DEN 2025-05-19 MEDDELADE PRV BESLUT OM RAETTAD SKYDDSTID FOER FOELJANDE TILLAEGGSSKYDD: 1590005-3,1890005-0 |
| >Patent Number | >Supplementary Protection Certificate | >SPC Country | >SPC Expiration | >SPC Description |
Similar Applicant Names
Here is a list of applicants with similar names.

