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Therapeutic Education

This section provides educational resources designed to support healthcare professionals using RRD products in rare disease management.

Hematology

Products
Product: Sutimlimab-jome

Sutimlimab-jome

Prescribing Information

Sutimlimab Mechanism of Action (MOA)

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CAD Mechanism of Disease (MOD)

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Sutimlimab-jome (Enjaymo) for the Management of Hemolysis in Cold Agglutinin Disease (CAD) - Positive Quality Intervention (PQi)

*See disclaimer

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Sutimlimab-jome (Enjaymo) for the Management of Hemolysis in Cold Agglutinin Disease (CAD) - Positive Quality Intervention (PQi) in Action

*See disclaimer

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Metabolic

Products
Product: Hemin for injection

Hemin for injection

Prescribing Information

Hemin for Injection: Dosing and Administration Infographic

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Endocrinology

Products
Product: Pasireotide for injectable suspensionPasireotide injection

Pasireotide for injectable suspension

Prescribing Information

Optimizing Treatment in Acromegaly: A Patient-Centric Approach

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Pasireotide-Associated Hyperglycemia: Molecular Mechanism in Cushing’s Disease and Acromegaly

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Understanding Acromegaly and Cushing's Disease

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Pasireotide injection

Prescribing Information

Pasireotide-Associated Hyperglycemia: Molecular Mechanism in Cushing’s Disease and Acromegaly

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Understanding Acromegaly and Cushing's Disease

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Oncology

Products
Product: Siltuximab

Siltuximab

Prescribing Information

Siltuximab (Sylvant®) in Patients with Idiopathic Multicentric Castleman Disease - Positive Quality Intervention (PQI)

*See disclaimer

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Siltuximab (Sylvant®) in Patients with Idiopathic Multicentric Castleman Disease - Positive Quality Intervention (PQI) in Action

*See disclaimer

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*Disclaimer: This educational content was independently developed by Network for Collaborative Oncology Development & Advancement (NCODA) and participating authors. Recordati Rare Diseases provided funding but did not direct the development of the content. Experiences and perspectives shared in the “PQi in Action” section are solely those of the participating healthcare professionals and reflect their individual views and clinical experience. Please refer to the approved Prescribing Information for complete product information.

Scientific Library

Explore select presentations and posters from Congress events and access publications related to Recordati Rare Diseases products categorized by therapeutic area.
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Clinical Trials

Clinical trials are essential for developing safe and effective treatment for our patients. Our goal is to broaden efforts in the rare disease space, striving to improve our products.

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Medical Inquiries

Use this form to submit your medical inquiry. Pharmacists from our Medical Information team will respond to your request as quickly as possible.
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WELCOME TO THE RRD MEDICAL INFORMATION WEBSITE

This Website is intended to help health care professionals in the United States and its territories find scientifically-balanced information and educational resources related to RRD treatments and therapeutic areas of interest, including clinical data, research developments, congress materials and publications. The Website is made available by RRD’s Medical Affairs organization and is provided as an educational resource for informational, non-promotional and scientific exchange purposes.

This Website may contain information about products or uses that have not been approved by the U.S. Food and Drug Administration. RRD does not recommend the use of its products other than as described in the approved prescribing information. The content of this Website is not medical advice and does not replace independent medical judgment. Healthcare providers are responsible for individual patient care on the basis of their professional knowledge, experience, and licensure.

Unless expressly noted on the applicable resource, please do not download or distribute content from this website . No further reproduction or distribution is permitted without permission from RRD or the applicable copyright owner(s). By selecting continue below, you acknowledge and certify that you are a US Healthcare Professional.

Please report any adverse events related to any of our products by calling us at 1-888-575-8344 (M-F 8 AM-6 PM CST). If you prefer, you may email us as well at .

You are encouraged to report side effects of prescription drugs to the FDA. Call 1-800-FDA-1088 or visit www.fda.gov/medwatch.

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A clean environment is essential for people’s well-being: the health of the planet and the health of people is tightly interconnected. Environmental elements, such as air, water, land and climate, all have an impact on the well-being of humans. Placing a focus on people’s health and being sustainable therefore also means prioritising environmental protection and a responsibility towards future generations. This is why the Group ensures that it conducts business in a socially responsible manner and in accordance with sustainable practices, national and international laws, and the expectations of stakeholders.
Recordati for the community
We believe that contributing to the well-being of the community and dedicating part of our resources to acts of solidarity is not merely the fulfilment of company obligations or professional duty, but rather a moral imperative, an essential part of a healthy business capable of growth but at the same time able to support and develop the community in which it operates and make its employees proud.
Value and diversity of our people
At Recordati, we believe in equal opportunities and we guarantee that everyone can achieve their potential. We see diversity as a value and will not tolerate any discrimination based on ethnicity, nationality, gender, sexual orientation, disability, age, political or religious belief, or any other personal characteristics. At Recordati, we work hard to create a safe and inclusive work environment, where we all have our rights to physical and psychological integrity respected on a daily basis, as well as our right to freedom of opinion and association. We recognise that we each have a role to play in the success of our business and we implement staff development policies through which everyone’s contribution and achievements can be appropriately rewarded.
Multiple opportunities
Recordati is uniquely structured to bring treatment options across specialty and primary care, consumer healthcare, and rare diseases. We have fully integrated operations across research and development, chemical and finished product manufacturing through to commercialisation and licensing.
Luigi Longinotti
Managing Director and General Manager EMEA

Luigi Longinotti is Managing Director and General Manager for EMEA at Recordati Rare Diseases, leading the European and Middle Eastern Commercial Operations. He is responsible for Marketing, Medical, Market Access, Regulatory, Manufacturing and Logistics, as well as the enabling functions to support the business, including Compliance and Quality.

 

He joined Recordati in July 2014 as Corporate Portfolio Management Director for Orphan Drugs. In such a role he has been responsible for driving the growth of the rare disease portfolio at Recordati, with his duties ranging from business development to strategic marketing and pipeline project management.

 

Before he joined Recordati, he held senior business and corporate development roles at Chiesi Farmaceutici and Menarini Group where he executed several key asset deals and transactions.

Luigi gained a degree in Economics from the University of Florence and a Master’s degree in Business Innovation from Sant’Anna School of Advanced Studies in Pisa.

Bruno Parenti
Head of LAC Region, Head of Global Endocrinology Franchise

Bruno Parenti is Head of LAC Region at Recordati Rare Diseases, leading the business in Latin America, Asia Pacific and Russia. He has been in this position since 2011, where he spearheaded the expansion of operations around the globe. He recently assumed the additional role of Head of Global Endocrinology Franchise, establishing the new HQ in Basel and building a dedicated organization.

 

Prior to these positions, Bruno spent two years at Recordati Ireland overseeing international sales in the Asia-Pacific region. He served at Chiesi Farmaceutici for two years as Area Manager for the Far East. Earlier in his career, he held commercial roles at Kedrion Biopharmaceuticals where he was responsible for international markets with a focus on Latin America and the Middle East.

Mohamed Ladha
President and General Manager, North America

Mohamed Ladha is the President and General Manager at Recordati Rare Diseases where he is   responsible for the US and Canadian business. During his career,  Mohamed has held numerous leadership positions globally in hematology/oncology and specialty care to oversee business in the US, Canada, EU, China, Emerging Markets, and Japan.

 

Mohamed  joins Recordati Rare Diseases from Oncopeptides, where he was the General Manager and Executive Vice President for the US Region Business Unit. Prior to Oncopeptides, he served in a series of leadership positions of increasing responsibility at companies including Vertex Pharmaceuticals, Pfizer, Schering-Plough, Merck & Company, Hospira, ARIAD Pharmaceuticals, Takeda Oncology, and Tocagen. He started his career in basic science research focused in oncology at the Dana-Farber Cancer Institute.

 

Mohamed graduated from Hampshire College with a Bachelor of Arts degree. He also holds professional/graduate degrees from Harvard University’s Kennedy School of Government and Northwestern University’s Kellogg School of Management.

 

Changing to first name to be consistent with bio below, also feel that first name as opposed to Mr has a more informal and friendly tone.   [EC1]

Scott Pescatore
Executive Vice President

Scott Pescatore is Vice President and Head of Global Operations at Recordati Rare Diseases.

He holds a Doctor of Pharmacy degree and completed his post-doctoral fellowship in Pharmacology and Drug Development. Dr Pescatore has spent over 20 years working internationally in the pharmaceutical industry, specializing in oncology, haematology and rare diseases.

 

He joined Novartis Oncology US in 2001 where he served in various medical, sales and marketing roles of increasing responsibility. In 2008, he moved to Novartis Oncology UK as Business Franchise Head for solid tumours where he also managed the New Products portfolio. In 2010 he moved to Milan to manage the Region Europe Haematology Franchise where he led the joint venture between Novartis Oncology and Incyte to launch a novel treatment for myeloproliferative disorders. In 2014 he was appointed the Oncology General Manager in Ireland and after three years returned to Milan as General Manager of the Region Europe Rare Disease Business Unit, overseeing operations in 37 markets and focusing on the endocrinology portfolio.

 

Prior to joining Recordati Rare Diseases in 2020, he was Vice President Oncology Business Unit for AstraZeneca Italy where he was responsible for the portfolio of oncology/haematology products including two joint ventures with MSD and Daiichi Sankyo.