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Expert Interview

Slingshot members are talking to an expert! The topic is:

Evaluating Vertex Pharmaceuticals Incorporated's VX-880 for the Treatment of Type 1 Diabetes (T1D) with Impaired Hypoglycemic Awareness and Severe Hypoglycemia

Ticker(s): VRTX

Who's the expert?

Institution: UT Southwestern Medical Center

  • Board-certified endocrinologist, Professor of medicine, and Director of the Diabetes Clinic at UT Southwestern Medical Center and Parkland Hospital.
  • Currently manages 200 patients with Type 1 Diabetes and 10 patients that use the Omnipod System.
  • Clinical research interests include diabetes management, prevention, and novel treatments while serving as the chair of Biomedical research.

Interview Questions
Q1.

Can you tell us your impression about the mechanism of action of VX-880 and how it differentiates from other treatments available for T1D, especially in patients with impaired hypoglycemic awareness and SHEs?

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Q2.

Based on the results from the ongoing Phase 1/2 study, how does VX-880's efficacy compare to other T1D treatments? Are there any specific outcomes from the study that highlight its effectiveness, particularly in glucose control and insulin independence?

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Q3.

Given that VX-880 has the potential to restore the body’s ability to regulate glucose levels by restoring pancreatic islet cell function, how does it address the unmet medical needs in T1D therapy?

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Q4.

With the PRIME designation by the European Medicines Agency and Fast Track Designation by the U.S. FDA, how do you see the competitive landscape shaping up for VX-880 in the T1D market? Are there any potential competitors or emerging treatments that might challenge its position?

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Q5.

From the data presented, how would you characterize the safety profile of VX-880? Are there any significant adverse events or side effects that clinicians should be aware of?

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Q6.

Given the ongoing medical advancements in T1D and the potential of stem cell-derived therapies, where do you position VX-880 in the broader treatment paradigm for T1D?

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Q7.

With the expansion of the VX-880 trial to additional sites across multiple countries, what are your expectations for the global reception and potential adoption of this therapy?

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Q8.

As VX-880 cells are foundational for the VX-264 cells-plus-device program, can you provide insights into the potential of VX-264 and its role in the future of T1D treatment?

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Q9.

Considering the limitations and complexities of current insulin delivery systems, how transformative do you believe VX-880 could be in changing the standard of care for T1D patients?

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