The MC4R pathway

Learn about the role of the MC4R pathway, how it can be disrupted and the subsequent consequences

Rare acquired MC4R pathway disease

Learn more about the root causes of aHO and how to recognise the signs

Bardet-Biedl syndrome & other genetic diseases

Key clinical features, like hyperphagia and early-onset obesity, in paediatric patients

How to recognise undiagnosed adults with Bardet-Biedl syndrome

The important role of an ophthalmologist in the early identification of Bardet-Biedl syndrome

Resources & events

Explore a collection of educational videos, handouts and resources

Upcoming events related to rare MC4R pathway diseases

Precision medicine

The first and only approved medicine which targets a root cause of rare MC4R pathway diseases

Rare genetic MC4R pathway disease

Learn more about IMCIVREE's role in the treatment of patients from 2–<6 years of age

Explore the role of IMCIVREE for patients with Bardet-Biedl syndrome

Learn more about IMCIVREE’s role in treating patients living with POMC, PCSK1 and LEPR deficiencies

Resources & events

For more information, explore our collection of videos, handouts and resources

Guidance on the recommended IMCIVREE dose titration for your patients

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