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Ricerca e sviluppo

Recordati è dedita ad un’attività continuativa di sviluppo di nuovi prodotti specialistici, sia internamente che tramite collaborazioni di sviluppo con altre aziende farmaceutiche e istituti di ricerca.

La devozione al rigore scientifico, le competenze e il personale altamente specializzato consentono al gruppo di sviluppare nuove opzioni terapeutiche e di avere sempre in cantiere idee per prodotti innovativi.

Life Cycle Management

Products

Originator

Name

Therapeutic area

Development Stage

Discover/
Preclinical

Proof of
Concept

Late
Stage

Registration

Post
Marketing

Originator:

Recordati

Molecule Name:

CARBAGLU®

Therapeautic Area:

Metabolic and other

Hyperammonaemia due to NAGS deficiency and to the main organic acidaemias

Phase/Status:

Registration

Development Details:

Regulatory Approval recently obtained in China in NAGS deficiency and organic acidaemias

Originator:

Recordati

Molecule Name:

CYSTADROPS®

Therapeautic Area:

Metabolic and other

Corneal cystine crystal deposits in patients with cystinosis

Phase/Status:

Late Stage

Development Details:

New Container Closure System

Originator:

Tolmar

Molecule Name:

ELIGARD®

Therapeautic Area:

SPC

Hormone-dependent prostate cancer

Phase/Status:

Late Stage

Development Details:

New device post-approval activities

Originator:

Novartis / Recordati

Molecule Name:

ISTURISA®*

Therapeautic Area:

Endocrinology

Endogenous Cushing's syndrome/Cushing's disease

Phase/Status:

Late Stage

Development Details:

Real World Evidence (LINC-7)/Label extension

Originator:

Apeiron / Recordati

Molecule Name:

QARZIBA®*

Therapeautic Area:

Oncology

Treatment of high-risk neuroblastoma patients who achieved at least a partial response at the chemotherapeutical induction, followed by myeloablative therapy and stem cell transplantation, and of patients with relapsed or refractory neuroblastoma

Phase/Status:

Late Stage

Development Details:

Relapsed/Refractory Induction in US

Originator:

Apeiron / Recordati

Molecule Name:

QARZIBA®

Therapeautic Area:

Oncology

Treatment of high-risk neuroblastoma patients who achieved at least a partial response at the chemotherapeutical induction, followed by myeloablative therapy and stem cell transplantation, and of patients with relapsed or refractory neuroblastoma

Phase/Status:

Late Stage

Development Details:

Frontline Induction in EU

Originator:

Novartis / Recordati

Molecule Name:

Pasireotide

Therapeautic Area:

Endocrinology

Post-Bariatric Hypoglycaemia

Phase/Status:

Proof of Concept

Development Details:

Phase II

Originator:

Recordati

Molecule Name:

SYLVANT®*

Therapeautic Area:

Oncology

Treatment of idiopathic Multicentric Castleman Disease (iMCD)

Phase/Status:

Proof of Concept

Development Details:

IL-6 induced diseases (CRS/ICANs)

Products

Originator

Molecule Name

Therapeutic area

Development Stage

Discover/
Preclinical

Proof of
Concept

Late
Stage

Registration

Post
Marketing

Originator:

Recordati / AP-HP

Molecule Name:

REC 0545 / MAAPLIV*

Therapeautic Area:

Metabolic and other

Acute decompensation episodes in Maple Syrup Urine Disease (MSUD) or leucinosis

Phase/Status:

Registration

Development Details:

Filing in EU in 2023, registration stage ongoing.

Originator:

Recordati / MimeTech

Molecule Name:

REC 0559*

Therapeautic Area:

Metabolic and other

Neurotrophic Keratitis

Phase/Status:

Proof of Concept

Development Details:

Phase 2 in progress

Products

Originator

Molecule Name

Therapeutic area

Development Stage

Discover/
Preclinical

Proof of
Concept

Late
Stage

Registration

Post
Marketing

Originator:

Novartis / Recordati

Molecule Name:

ISTURISA®

Therapeautic Area:

Endocrinology

Endogenous Cushing's syndrome/Cushing's disease

Phase/Status:

Post Marketing

Development Details:

Non-Interventional Study (LINC-6)

Originator:

Novartis / Recordati

Molecule Name:

ISTURISA®

Therapeautic Area:

Endocrinology

Endogenous Cushing's syndrome/ Cushing's disease

Phase/Status:

Post Marketing

Development Details:

Paediatric post-approval development plan

Originator:

Gedeon Richter

Molecule Name:

REAGLIA®

Therapeautic Area:

CNS

Schizophrenia

Phase/Status:

Post Marketing

Development Details:

Post marketing regulation studies

*= will result in new product indication

La struttura di Recordati è unica, con opportunità in tutti i team di ricerca e sviluppo, inclusi CMC, pre-clinico, regolatorio, della farmacovigilanza, del controllo della qualità, delle operazioni cliniche, dello sviluppo clinico e il team medico. Siamo in continua crescita, e i nostri obiettivi sono incentrati sullo sviluppo di nuovi prodotti specialistici, nuove opzioni terapeutiche e sull’investimento nelle innovazioni mediche che possano offrire un futuro migliore.

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INFORMATION ON PERSONAL DATA PROTECTION PURSUANT TO ARTICLE 13 OF LEGISLATIVE DECREE NO. 196/2003

The personal data that you provide by compiling this form will be used by Recordati Industria Chimica e Farmaceutica S.p.A. (“Recordati”) – the “Data Controller” – solely for performing activities connected with the provision of the email alert service and it will be processed manually, by computer and via the internet in a manner that will guarantee its security and confidentiality. It is not compulsory for you to give your data, however, if you refuse to allow it to be processed, then it will be impossible for Recordati to provide you with the above-mentioned service. Your personal data may be passed on to other companies that belong to the RECORDATI Group or to associate companies of the Group and to third parties that Recordati uses to provide the service to you.

 

In any event we assure you that your data will be processed solely for the above purposes and using the above methods.

 

The company Tech Style S.r.l. has been appointed as external Data Processor in accordance with Art. 29 of the Privacy Code, because it has been engaged to maintain the technological part of the website. The Director of Investor Relations and Corporate Communication of Recordati S.p.a. has been appointed as internal Data Processor of Recordati in accordance with article 29 of the Privacy Code.

 

A data subject shall have the right to obtain at any moment confirmation of whether or not data is held on him/her, to know its content and origin, to check its accuracy or to ask for it to be added to, updated or rectified (article 7 of the Privacy Code).

 

Requests must be sent to the Data Processor of Recordati:
   by email, to the address: ;
   or by ordinary mail to Recordati Industria Chimica e Farmaceutica S.p.A. – Director of Investor Relations and Corporate Communications – 1 Via Civitali – 20148 Milan.

 

In accordance with article 23 of Legislative Decree No. 196/03 on personal data protection, having read the above information, I hereby authorise Recordati S.p.A. to process my personal data for the purposes set out in that same information. I am aware that if I refuse, Recordati will not be able to enable its email alert service for me.

 

Subsequent withdrawal of consent to the data processing mentioned in the preceding paragraph will result in the cancellation of the subscription request or cancellation of the subscription to the email alert service.