Our Mission

The Rare Collective partners with industry, patient organizations, and researchers to guide the development, commercialization, and adoption of innovative therapies and devices for rare disease communities.

Many people living with a rare disease have no cure or effective treatment. But, there’s hope.

Biopharmaceutical companies, academia, government agencies and patient organizations are working to better understand and treat more of the estimated 7,000 rare diseases. Their research is yielding impressive results, with more orphan drug designations and regulatory approvals each year.

Orphan Drug Approvals in U.S.

Mission

Source: FDA

We strive to serve our community by speeding the development and delivery of orphan drugs for rare diseases.

The Rare Collective helps its clients navigate every facet of orphan-drug development, including:

  • Market forecasting
  • Determining medical need
  • Quantifying disease burden
  • Identifying patients
  • Educating physicians
  • Advising patient advocacy groups
  • Defining regulatory pathways
  • Building support among stakeholders
  • Ensuring market access
  • Patient advocacy best practices

Our team of experts shares knowledge across disciplines and taps a vast network of experts to give clients the tools and resources needed to advance rare disease therapies. We know the rapidly evolving orphan space, and have real world, hands-on experience supporting our clients so they can focus on the big picture.