Capturing the Burden of​ Prader-Willi Syndrome on Patients and the Healthcare System: A Real-World Analysis of United States Claims Data​.

Resuming Diazoxide Choline Extended-Release (DCCR) after 16-week Randomized Withdrawal is Associated with Significant Improvements in Hyperphagia and Behavioral Symptoms in PWS (Study C614)

Long-term Administration of Diazoxide Choline Extended-Release (DCCR) Tablets in People with Prader-Willi Syndrome: Changes in Lean Body Mass and Lean Mass Index

Pediatric Endocrine Society, 2025

Academy of Managed Care Pharmacy, 2025

Design of a Randomized Withdrawal Period Following Long-Term Administration of Diazoxide Choline Extended-Release Tablets to People with Prader-Willi Syndrome​

Withdrawal of Diazoxide Choline Extended-Release (DCCR) Tablets Worsens Hyperphagia and Increases Weight and BMI in a 16-Week Double-Blind, Placebo-Controlled, Randomized Withdrawal Period in Patients With Prader-Willi Syndrome

Long-Term Safety of Diazoxide Choline Extended-Release (DCCR) Tablets in Participants with Prader-Willi Syndrome from the Completed C601 Randomized Double-Blind Placebo-Controlled Study (DESTINY PWS) and C602 Open Label Extension (OLE) Study

Relaxation of Food Control Parameters Based on Improvements in the Food Safe Zone Questionnaire Occurs with Reduction of Hyperphagia in Clinical Trials of Diazoxide Choline Extended Release (DCCR) in Participants with Prader-Willi Syndrome.