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Research & Development

Recordati continuously develops new specialties originating either internally or acquired through development agreements with other pharmaceutical companies and research institutes.

 

Commitment, scientific rigour, capability and highly specialized personnel allow the Group to develop new treatments and to build an innovative product pipeline.

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

We are uniquely structured with multiple opportunities across our R&D team including CMC, preclinical, regulatory, patient safety, QA, clinical operations, clinical development, medical affairs. We are continuously growing, with a focus on developing new specialties, new treatments – and investing in medical innovations that bring a brighter future.

Interested in joining our team?

We foster an entrepreneurial environment where high-performing individuals are empowered to make a difference across our organisation.

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