RARECast

548 Episodio

1. Crowdsourcing Therapeutic Approaches for an Ultra-Rare Disease

   Pubblicato: 05/02/2020
2. Delivering Oligonucleotide Therapies to Any Cell Type

   Pubblicato: 29/01/2020
3. Protalix Looks Beyond Biobetters

   Pubblicato: 22/01/2020
4. Driving N-of-1 Therapies for Ultra-Rare Disease Patients

   Pubblicato: 15/01/2020
5. Cutting the Time and Cost of Drug Discovery with MicroOrgans

   Pubblicato: 08/01/2020
6. Acquisition Combines Two Pipelines for Rare Skin Diseases

   Pubblicato: 02/01/2020
7. Programming Cells to Produce Neuroprotective Factors to Treat ALS

   Pubblicato: 26/12/2019
8. Origin's Rapid Path to Seek Approval for Treatment of Ultra-Rare Metabolic Condition

   Pubblicato: 18/12/2019
9. Developing a Common Language for Rare Diseases

   Pubblicato: 11/12/2019
10. Why Payers Lag Drug Developers and Regulators in Embracing Real-World Evidence

    Pubblicato: 04/12/2019
11. How a Brother's Love Is Forging a Path for Customized Therapies for Rare Disease Patients

    Pubblicato: 27/11/2019
12. Addressing the Barriers to Accessing Experimental Therapies

    Pubblicato: 20/11/2019
13. A Journey to Advocacy

    Pubblicato: 13/11/2019
14. Turning Chronic Illness into a Fashion Statement

    Pubblicato: 06/11/2019
15. Connecting Young Adults with Rare and Chronic Conditions

    Pubblicato: 30/10/2019
16. Helping Caregivers Care for Themselves

    Pubblicato: 23/10/2019
17. A Festival of Moving Pictures

    Pubblicato: 16/10/2019
18. Deep Genomics Boasts an AI First in Drug Discovery

    Pubblicato: 09/10/2019
19. How to Live with a Disability with Your Mojo Intact

    Pubblicato: 03/10/2019
20. Why a Big Pharma Exec Embraced Rare Neurological Diseases

    Pubblicato: 25/09/2019